With a 10%reversible compressive strain in more than 10 deformation cycles,the shape memory polymer composites(SMPCs)could be used for deployable structure and releasing mechanism.In this paper,without traditional ele...With a 10%reversible compressive strain in more than 10 deformation cycles,the shape memory polymer composites(SMPCs)could be used for deployable structure and releasing mechanism.In this paper,without traditional electro-explosive devices or motors/controllers,the deployable SMPC flexible solar array system(SMPC-FSAS)is studied,developed,ground-based tested,and finally on-orbit validated.The epoxy-based SMPC is used for the rolling-out variable-stiffness beams as a structural frame as well as an actuator for the flexible blanket solar array.The releasing mechanism is primarily made of the cyanate-based SMPC,which has a high locking stiffness to withstand 50 g gravitational acceleration and a large unlocking displacement of 10 mm.The systematical mechanical and thermal qualification tests of the SMPC-FSAS flight hardware were performed,including sinusoidal sweeping vibration,shocking,acceleration,thermal equilibrium,thermal vacuum cycling,and thermal cycling test.The locking function of the SMPC releasing mechanisms was in normal when launching aboard the SJ20 Geostationary Satellite on 27 Dec.,2019.The SMPC-FSAS flight hardware successfully unlocked and deployed on 5 Jan.,2020 on geostationary orbit.The triggering signal of limit switches returned to ground at the 139 s upon heating,which indicated the successful unlocking function of SMPC releasing mechanisms.A pair of epoxy-based SMPC rolled variable-stiffness tubes,which clapped the flexible blanket solar array,slowly deployed and finally approached an approximate 100%shape recovery ratio within 60 s upon heating.The study and on-orbit successful validation of the SMPC-FSAS flight hardware could accelerate the related study and associated productions to be used for the next-generation releasing mechanisms as well as space deployable structures,such as new releasing mechanisms with low-shocking,testability and reusability,and ultra-large space deployable solar arrays.展开更多
Two-dimensional(2D)transition-metal selenides,espe-cially MoSe_(2),is considered to be an excellent alternative electrocatalyst for the hydrogen evolution reaction(HER).However,it still features high overpotential in ...Two-dimensional(2D)transition-metal selenides,espe-cially MoSe_(2),is considered to be an excellent alternative electrocatalyst for the hydrogen evolution reaction(HER).However,it still features high overpotential in HER due to the low density of active sites,which limits its practical application.Herein,the hydrogen evolution reaction activity of MoSe_(2)is enhanced by the incorporation of metal-cation,tungsten,which succeeds in taking the place of Mo in the lattice of MoSe_(2),inducing the spacing expansion and bringing new flexural edges to serve as active sites.In addition,the incorporated metal also facil-itates electron transport from Mo active center toward W and Se atoms with auspicious hydrogen adsorption prop-erties.展开更多
Owing to the unique structure,anode-free lithium metal batteries(AFLMBs)have higher energy density and lower production cost than traditional lithium metal batteries(LMBs)or lithium-ion batteries(LIBs),However,AFLMBs ...Owing to the unique structure,anode-free lithium metal batteries(AFLMBs)have higher energy density and lower production cost than traditional lithium metal batteries(LMBs)or lithium-ion batteries(LIBs),However,AFLMBs suffer from an inherently finite Li reservoir and exhibit poor cycle stability,low Coulombic efficiency(CE)and severe dendrite growth.In this work,polydiallyl lithium disulfide(PDS-Li)was successfully synthesized and coated on Cu current collector by electrochemical polymerization.The PDS-Li acts as an additional lithium resource to compensate for the irreversible loss of lithium during cycling.In addition,the special structure and lithiophilicity of PDS-Li contribute to lower nucleation overpotential and uniform lithium deposition.When coupled with Li-rich manganese-based(LRM)cathode of Li1.2Mn0.54Ni0.13Co0.13O2,the anode-free full cell exhibits significantly improved cycle stability over 100 cycles and capacity retention of 63.3%and 57%after 80 and 100 cycles,respectively.We believe that PDS-Li can be used to ensure stable cycling performance and high-energy-density in AFLMBs.展开更多
Lithium metal is regarded as the most promising anode material for next generation high energy density lithium batteries due to its high theoretical capacity and lowest potential versus standard hydrogen electrode.How...Lithium metal is regarded as the most promising anode material for next generation high energy density lithium batteries due to its high theoretical capacity and lowest potential versus standard hydrogen electrode.However,lithium dendrite growth and huge volume change during cycling hinder its practical application.It is of great importance to design advanced Li metal anodes to solve these problems.Herein,we report a ZnO-coated Zn foam as the host matrix to pre-store lithium through thermal infusing,achieving a Zn@ZnO foam supported Li composite electrode(LZO).Needlelike ZnO nanofibers grown on the Zn foam greatly increase the surface area and enhance the lithiophilicity of the Zn foam.In situ formed synaptic LiZn layer after lithium infusion can disperse local current density and lower Li diffusion barrier effectively,leading to homogeneous Li deposition behavior,thus suppressing dendrite formation.The porous Zn foam skeleton can accommodate volume variation of the electrode during longterm cycling.Benefiting from these merits,the LZO anode exhibits much better cycle stability and rate capability in both symmetrical and full cells with low voltage hysteresis than the bare Li anode.This work opens a new opportunity in designing high performance composite Li anode for lithium-metal batteries.展开更多
Solid oxide electrolysis cells(SOECs)provide a promising way for converting renewable energy into chemical fuels.Traditionally,NiO/CGO(nickel-gadolinium doped ceria)cermet has shown its excellent properties in ionic a...Solid oxide electrolysis cells(SOECs)provide a promising way for converting renewable energy into chemical fuels.Traditionally,NiO/CGO(nickel-gadolinium doped ceria)cermet has shown its excellent properties in ionic and electronic conductivity under reducing conditions.Herein,we developed a novel 1D NiO/CGO cathode through a cerium metal-organic framework(MOF)derived process.The cathode’s 1D nanostructure integrated with a microchannel scaffold facilitates enhanced mass transport,providing vertically aligned pathways for CO_(2)and H_(2)O diffusion.Additionally,the 1D framework increases the number of interfacial sites and reduces ion diffusion distances,thereby simplifying electron/ion transport.Consequently,this advanced cathode achieved a significant breakthrough in SOEC performance,maintaining efficient CO_(2)and H_(2)O electrolysis at an extraordinary current density of 1.41 A/cm^(2)at 1.5 V and excellent stability over 24 h at 850℃.The enhanced performance of this newly developed cathode not only achieves a remarkable 100%improvement compared to those of NiO/CGO cathodes with varying geometrical configurations but also surpasses those of commercial NiO/CGO catalysts by an outstanding 40%when tested under identical conditions.The development of the 1D NiO/CGO enhances the efficiency and durability of ceramic cathodes for CO_(2)and H_(2)O co-electrolysis in SOECs and improves the scalability and effectiveness of SOECs in renewable energy applications.展开更多
Recent advances in utilizing ^(17)O isotopic labeling methods for solid-state nuclear magnetic resonance(NMR)investigations of metal oxides for lithium-ion batteries have yielded extensive insights into their structur...Recent advances in utilizing ^(17)O isotopic labeling methods for solid-state nuclear magnetic resonance(NMR)investigations of metal oxides for lithium-ion batteries have yielded extensive insights into their structural and dynamic details.Herein,we commence with a brief introduction to recent research on lithium-ion battery oxide materials studied using ^(17)O solid-state NMR spectroscopy.Then we delve into a review of ^(17)O isotopic labeling methods for tagging oxygen sites in both the bulk and surfaces of metal oxides.At last,the unresolved problems and the future research directions for advancing the ^(17)O labeling technique are discussed.展开更多
The insurmountable charge transfer impedance at the Li metal/solid polymer electrolytes(SPEs)interface at room temperature as well as the ascending risk of short circuits at the operating temperature higher than the m...The insurmountable charge transfer impedance at the Li metal/solid polymer electrolytes(SPEs)interface at room temperature as well as the ascending risk of short circuits at the operating temperature higher than the melting point,dominantly limits their applications in solid-state batteries(SSBs).Although the inorganic filler such as CeO_(2)nanoparticle content of composite solid polymer electrolytes(CSPEs)can significantly reduce the enormous charge transfer impedance at the Li metal/SPEs interface,we found that the required content of CeO_(2)nanoparticles in SPEs varies for achieving a decent interfacial charge transfer impedance and the bulk ionic conductivity in CSPEs.In this regard,a sandwich-type composited solid polymer electrolyte with a 10%CeO_(2)CSPEs interlayer sandwiched between two 50%CeO_(2)CSPEs thin layers(sandwiched CSPEs)is constructed to simultaneously achieve low charge transfer impedance and superior ionic conductivity at 30℃.The sandwiched CSPEs allow for stable cycling of Li plating and stripping for 1000 h with 129 mV polarized voltage at 0.1 mA cm^(-2)and 30℃.In addition,the LiFePO_(4)/Sandwiched CSPEs/Li cell also exhibits exceptional cycle performance at 30℃and even elevated120℃without short circuits.Constructing multi-layered CSPEs with optimized contents of the inorganic fillers can be an efficient method for developing all solid-state PEO-based batteries with high performance at a wide range of temperatures.展开更多
The use of lithium-sulfur batteries under high sulfur loading and low electrolyte concentrations is severely restricted by the detrimental shuttling behavior of polysulfides and the sluggish kinetics in redox processe...The use of lithium-sulfur batteries under high sulfur loading and low electrolyte concentrations is severely restricted by the detrimental shuttling behavior of polysulfides and the sluggish kinetics in redox processes.Two-dimensional(2D)few layered black phosphorus with fully exposed atoms and high sulfur affinity can be potential lithium-sulfur battery electrocatalysts,which,however,have limitations of restricted catalytic activity and poor electrochemical/chemical stability.To resolve these issues,we developed a multifunctional metal-free catalyst by covalently bonding few layered black phosphorus nanosheets with nitrogen-doped carbon-coated multiwalled carbon nanotubes(denoted c-FBP-NC).The experimental characterizations and theoretical calculations show that the formed polarized P-N covalent bonds in c-FBP-NC can efficiently regulate electron transfer from NC to FBP and significantly promote the capture and catalysis of lithium polysulfides,thus alleviating the shuttle effect.Meanwhile,the robust 1D-2D interwoven structure with large surface area and high porosity allows strong physical confinement and fast mass transfer.Impressively,with c-FBP-NC as the sulfur host,the battery shows a high areal capacity of 7.69 mAh cm^(−2) under high sulfur loading of 8.74 mg cm^(−2) and a low electrolyte/sulfur ratio of 5.7μL mg^(−1).Moreover,the assembled pouch cell with sulfur loading of 4 mg cm^(−2) and an electrolyte/sulfur ratio of 3.5μL mg^(−1) shows good rate capability and outstanding cyclability.This work proposes an interfacial and electronic structure engineering strategy for fast and durable sulfur electrochemistry,demonstrating great potential in lithium-sulfur batteries.展开更多
Lithium-ion batteries(LIBs)have greatly facilitated our daily lives since 1990s[1,2].To meet the ever-increasing demand on energy density,Li metal is seen as the ultimate anode because of its ultra-high specific capac...Lithium-ion batteries(LIBs)have greatly facilitated our daily lives since 1990s[1,2].To meet the ever-increasing demand on energy density,Li metal is seen as the ultimate anode because of its ultra-high specific capacity(3860 m Ah/g)and the lowest electrochemical potential(-3.04 V vs.the standard hydrogen electrode)[3–6].However,issues of Li metal anode,such as Li dendrite formation and large volume change during plating/stripping。展开更多
As a promising solid electrolyte for thin-film lithium batteries,the amorphous Li_(0.33)La_(0.56)TiO_(3)(LLTO)thin film has gained great interest.However,enhancing ionic conductivity remains challenging in the field.H...As a promising solid electrolyte for thin-film lithium batteries,the amorphous Li_(0.33)La_(0.56)TiO_(3)(LLTO)thin film has gained great interest.However,enhancing ionic conductivity remains challenging in the field.Here,a systematical study was performed to improve the ionic conductivity of sputter-deposited LLTO thin films via the optimization of processing atmosphere and temperature.By combining the optimized oxygen partial pressure(30%),annealing temperature(300℃),and annealing atmosphere(air),an amorphous LLTO thin film with an ionic conductivity of 5.32910^(-5)·S·cm^(-1) at room temperature and activation energy of 0.26 eV was achieved.The results showed that,first,the oxygen partial pressure should be high enough to compensate for the oxygen loss,but low enough to avoid the abusive oxygen scattering effect on lithium precursors that results in a lithium-poor composition.The oxygen partial pressure needs to achieve a balance between lithium loss and oxygen defects to improve the ionic conductivity.Second,a proper annealing temperature reduces the oxygen defects of LLTO thin films while maintaining its amorphous state,which improves the ionic conductivity.Third,the highest ionic conductivity for the LLTO thin films that were annealed in air(a static space without a gas stream)occurs because of the decreased lithium loss and oxygen defects during annealing.These findings show that the lithium-ion concentration and oxygen defects affect the ionic conductivity for amorphous LLTO thin films,which provides insight into the optimization of LLTO thin-film solid electrolytes,and generates new opportunities for their application in thinfilm lithium batteries.展开更多
Argyrodites,Li_(6)PS_(5)X(X=Cl,Br,I),have piqued the interest of researchers by offering promising lithium ionic conductivity for their application in all-solid-state batteries(ASSBs).However,other than Li_(6)PS_(5)Cl...Argyrodites,Li_(6)PS_(5)X(X=Cl,Br,I),have piqued the interest of researchers by offering promising lithium ionic conductivity for their application in all-solid-state batteries(ASSBs).However,other than Li_(6)PS_(5)Cl(651Cl)and Li_(6)PS_(5)Br(651Br),Li_(6)PS_(5)I(651I)shows poor ionic conductivity(10^(-7)S cm^(-1)at 298 K).Herein,we present Al-doped 651I with I^(-)/S^(2-)site disordering to lower activation energy(Ea)and improve ionic conductivity.They formed argyrodite-type solid solutions with a composition of(Li_(6–3x)Al_(x))PS_(5)I in 0≤x≤0.10,and structural analysis revealed that Al^(3+)is located at Li sites.Also,the Al-doped samples contained anion I^(-)/S^(2-)site disorders in the crystal structures and smaller lattice parameters than the non-doped samples.Impedance spectroscopy measurements indicated that Al-doping reduced the ionic diffusion barrier,Ea,and increased the ionic conductivity to 10^(-5)S cm^(-1);the(Li5.7Al0.1)PS5I had the highest ionic conductivity in the studied system,at 2.6×10^(-5)S cm^(-1).In a lab-scale ASSB,with(Li_(5.7)Al_(0.1))PS_(5)I functioned as a solid electrolyte,demonstrating the characteristics of a pure ionic conductor with negligible electronic conductivity.The evaluated ionic conduction is due to decreased Li+content and I^(-)/S^(2-)disorder formation.Li-site cation doping enables an in-depth understanding of the structure and provides an additional approach to designing betterperforming SEs in the argyrodite system.展开更多
Ti_(2)AlC has been demonstrated as the promising protective layer material for thermal barrier coatings(TBCs)against calcium-magnesium-alumina-silicate(CMAS)attack.In this study,the reliability of Ti_(2)AlC coatings a...Ti_(2)AlC has been demonstrated as the promising protective layer material for thermal barrier coatings(TBCs)against calcium-magnesium-alumina-silicate(CMAS)attack.In this study,the reliability of Ti_(2)AlC coatings against the CMAS corrosion was explored,and new Ti_(2)AlC/YSZ TBCs more efficiently resistant to CMAS were designed.The fabricated Ti_(2)AlC coatings inevitably contain some impurity phases(TiC and Al2Ti3),the contents of which were minimized by optimizing the spraying distance.Corrosion tests revealed that Ti_(2)AlC/YSZ TBCs yielded higher resistance to the CMAS attack than YSZ TBCs,but with long-term exposure to CMAS,the Ti_(2)AlC protective coating exhibited microstructure degradation due to the presence of the impurity phases,which caused the formation of a layer mixed with Al_(2)O_(3)and TiO_(2)rather than a continuous compact Al_(2)O_(3)layer on the surface.Pre-oxidation schemes were designed in air or with a controlled oxygen partial pressure,which revealed that the pre-oxidation at an oxygen partial pressure of~630 Pa could promote a continuous Al_(2)O_(3)layer formed on the Ti_(2)AlC protective coating surface.Furthermore,a vacuum heat treatment at 867℃for 10 h before pre-oxidation was beneficial for the formation of the compact Al_(2)O_(3)layer.Through the above scheme design,new Ti_(2)AlC/YSZ TBCs were obtained,which had reduced impurity phase contents and a pre-oxide layer with an ideal structure on the surface.New TBCs exhibit higher microstructure stability exposed to CMAS and more efficient CMAS resistance.展开更多
During long-term service in space,Gallium Arsenide(GaAs)solar cells are directly exposed to electron irradiation which usually causes a dramatic decrease in their performance.In the multilayer structure of solar cells...During long-term service in space,Gallium Arsenide(GaAs)solar cells are directly exposed to electron irradiation which usually causes a dramatic decrease in their performance.In the multilayer structure of solar cells,the germanium(Ge)layer occupies the majority of the thickness as the substrate.Due to the intrinsic brittleness of semiconductor material,there exist various defects during the preparation and assembly of solar cells,the influences of which tend to be intensified by the irradiation effect.In this work,first,Ge specimens for mechanical tests were prepared at scales from microscopic to macroscopic.Then,after different doses of electron irradiation,the mechanical properties of the Ge specimens were investigated.The experimental results demonstrate that electron irradiation has an obvious effect on the mechanical property variation of Ge in diverse scales.The four-point bending test indicates that the elastic modulus,fracture strength,and maximum displacement of the Ge specimens all increase,and reach the maximum value at the irradiation dose of 1×10^(15)e/cm^(2).The micrometer scale cantilever and nanoindentation tests present similar trends for Ge specimens after irradiation.Atomic Force Microscope(AFM)also observed the change in surface roughness.Finally,a fitting model was established to characterize the relation between modulus change and electron irradiation dose.展开更多
Highly active and durable Pd-based electrocatalysts for ethanol oxidation reaction(EOR)play a crucial role in the commercialization of direct ethanol fuel cells(DEFCs).However,the poisonous intermediates(especially ad...Highly active and durable Pd-based electrocatalysts for ethanol oxidation reaction(EOR)play a crucial role in the commercialization of direct ethanol fuel cells(DEFCs).However,the poisonous intermediates(especially adsorbed CO species(COad))formed during the EOR process can easily adsorb and block the active sites on Pd electrodes,which in turn limits the catalytic efficiency.Hence,we present a series of Pd-based composites with a strong coupling interface consisting of Pd nanosheets and amorphous Bi(OH)_(3)species.The incorporation of Bi(OH)3 can induce an electron-rich state adjacent to the Pd sites and effectively separate the Pd ensemble,leading to excellent CO tolerance.The optimal Pd-Bi(OH)_(3)NSs catalyst manifests a mass activity of 2.2 A·mgPd^(-1),which is 5.7 and 2.0 times higher than that of Pd NSs and commercial Pd/C catalyst,respectively.Further CO-stripping experiments and CO-DRIFTS tests confirm the excellent CO tolerance on Pd-Bi(OH)3 NSs electrode,leading to the enhanced EOR durability.展开更多
Electrochromic asymmetric supercapacitors(EASs), incorporating electrochromic and energy storage into one platform, are extremely desirable for next-generation civilian portable and smart electronic devices. However, ...Electrochromic asymmetric supercapacitors(EASs), incorporating electrochromic and energy storage into one platform, are extremely desirable for next-generation civilian portable and smart electronic devices. However, the crucial challenge of their fast self-discharge rate is often overlooked, although it plays an important role in practical application. Unfortunately, very limited research on EAS has focused on this critical problem. Here, an ultrathin all-inorganic EAS with excellent anti-self-discharge performance and superior electrochromic behavior is designed and manufactured by introducing a thin nanofunctional layer at the electrode/electrolyte interface. The prototype all-inorganic EAS exhibited a wide working voltage of 2.2 V, a high energy/power density(81.2mWh·cm^(-3)/0.688 W·cm^(-3)and 30.6 mWh·cm^(-3)/11.02W·cm^(-3)), along with outstanding electrochemical and electrochromic performance even at high temperatures.Remarkably, the introduced Ta2O5layer can efficiently prohibit the redistribution and diffusion of the movable ions at the fully charged state, endowing the all-inorganic EAS with a tardy self-discharge rate of 12.6 mV·g^(-1),which is an extremely low value when compared with previous reported research. Significantly, the ultrathin allinorganic EASs could also well maintain a slow self-discharge rate and their original electrochemical characteristics under various environmental temperatures. We envision that the novel strategy of electrode/electrolyte interface engineering can effectively deal with the severe self-discharge challenge of EAS, and provide more opportunities for their practical applications.展开更多
The increasing demand for versatile and high-quality near-field radiative heat transfer(NFRHT) has created a critical need for a design approach that can handle numerous candidate structures. In this work, we employ a...The increasing demand for versatile and high-quality near-field radiative heat transfer(NFRHT) has created a critical need for a design approach that can handle numerous candidate structures. In this work, we employ and develop an adaptive hybrid Bayesian optimization(AHBO) algorithm to design the high-quality quasi-monochromatic NFRHT. The candidate materials include hexagonal boron nitride, silicon carbide, and doped silicon. The high-quality quasi-monochromatic NFRHT is optimized over 1.0 × 10^(8) candidate structures to maximize the evaluation factor. It is worth noting that only 2.6% of the candidate structures needed to be calculated to identify the optimal structure. The optimal structure of quasi-monochromatic NFRHT is an aperiodic multilayer metamaterial that differs from conventional periodic multilayer structures. Moreover, we investigate the robustness and mechanisms of the optimal quasi-monochromatic NFRHT with respect to the vacuum gap distance and the temperature difference between the emitter and receiver. In addition, the high-quality multi-peak NFRHT is designed using the AHBO algorithm by improving the definition of the evaluation factor. The results demonstrate that the AHBO algorithm is efficient in designing high-quality quasi-monochromatic and multi-peak NFRHT, and it can be further expanded to other structural designs in the field of energy conversion.展开更多
Adding alloying elements is always considered as an effective method to enhance the resistance against hydrogen embrittlement in steels.Nb and V were added into 22MnB5 hot stamping steel,and then their influences on h...Adding alloying elements is always considered as an effective method to enhance the resistance against hydrogen embrittlement in steels.Nb and V were added into 22MnB5 hot stamping steel,and then their influences on hydrogen permeation of 22MnB5 steel suffering from corrosion in 3.5%NaCl aqueous solution were investigated.The results showed that the addition of Nb/V could reduce the hydrogen permeation content due to solution corrosion.Electrochemical techniques including electrochemical impedance spectroscopy and overpotential stepping hydrogen permeation test con-firmed that compared to the original 22MnB5 steel,22MnB5-NbN steel owned a higher corrosion resistance and a higher hydrogen diffusion resistance.Furthermore,it was confirmed that Nb-V-alloyed 22MnB5 steel showed higher resistance against hydrogen embrittlement than the Nb-V-free counterpart,which should be related to the presentence of nanoscaled Nb/V-containing precipitates as the irreversible trapping sites for hydrogen detected by thermal desorption spectroscopy.Finally,the lattice diffusion coefficient of hydrogen DL was determined in steels with and without Nb and V.展开更多
Surface deterioration occurs more easily in nickel-rich cathode materials with the increase of nickel content.To simultaneously pre-vent deterioration of active cathode materials and improve the electrochemical perfor...Surface deterioration occurs more easily in nickel-rich cathode materials with the increase of nickel content.To simultaneously pre-vent deterioration of active cathode materials and improve the electrochemical performance of the nickel-rich cathode material,the surface of nickel-rich LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode material is decorated with the stable structure and conductive Li_(3)PO_(4)by a facile method.The LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)-1wt%,2wt%,3wt%Li_(3)PO_(4)samples deliver a high-capacity retention of more than 85%after 100 cycles at 1 C under a high voltage of 4.5 V.The effect of different coating amounts(0-5wt%)for the LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode is analyzed in detail.Results show that 2wt%coating of Li_(3)PO_(4)gives better performance compared to other coating concentrations.Detailed analysis of the structure of the samples during the charge−discharge process is performed by in-situ X-ray diffraction.It is indicated that the modification for LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode could protect the well-layered structure under high voltages.In consequence,the electrochemical performance of modified samples is greatly improved.展开更多
A full-duplex radiant energy converter based on both betavoltaic and photovoltaic effects in an easyto-implement way is an attractive alternative for the autonomous wireless sensor microsystem.Here,we report a novel b...A full-duplex radiant energy converter based on both betavoltaic and photovoltaic effects in an easyto-implement way is an attractive alternative for the autonomous wireless sensor microsystem.Here,we report a novel beta/photovoltaic cell based on free-standing Zn O nanorod arrays(ZNRAs)modified with metallic single-walled carbon nanotubes(m-SWCNTs),using radioisotope63 Ni as beta-emitting source.The ZNRAs were grown on Al-doped Zn O(AZO)conductive glass using hydrothermal method.The optimum length and diameter of Zn O nanorods were determined by Monte Carlo simulation for beta energy deposition in ZNRAs.The m-SWCNTs were anchored into the ZNRAs to form a three-dimensional(3-D)Schottky junction structure for effectively separating the beta/photo-excited electron-hole pairs.Experimentally,the betavoltaic and photovoltaic effects were confirmed through the I-V measurements of beta/photovoltaic cells under beta/UV/Vis irradiations,respectively.It is suggested that the m-SWCNTs play key role for the enhancement of beta/photovoltaic performance through the formation of extensive3-D Schottky junction,the conductive network for hole transport,and the surface plasmon resonance exciton absorption for visible light.展开更多
Betavoltaic cells(BCs)are promising self-generating power cells with long life and high power density.However,the low energy conversion efficiency(ECE)has limitations in practical engineering applications.Widebandgap ...Betavoltaic cells(BCs)are promising self-generating power cells with long life and high power density.However,the low energy conversion efficiency(ECE)has limitations in practical engineering applications.Widebandgap semiconductors(WBGSs)with three-dimensional(3-D)nanostructures are ideal candidates for increasing the ECE of BCs.This paper proposes hydrothermally grown ZnO nanorod arrays(ZNRAs)for ^(63)Ni-powered BCs.A quantitative model was established for simulation using the parameter values of the dark characteristics,which were obtained from the experimental measurements for a simulated BC based on a Ni-incorporated ZNRAs structure.Monte Carlo(MC)modeling and simulation were conducted to obtain the values of the β energy deposited in ZNRAs with different nanorod spacings and heights.Through the simulation and optimization of the 3-D ZNRAs and 2-D ZnO bulk structures,the performance of the ^(63)Ni-powered BCs based on both structures was evaluated using a quantitative model.The BCs based on the 3-D ZNRAs structure and 2-D ZnO bulk structure achieved a maximum ECE of 10.1%and 4.69%,respectively,which indicates the significant superiority of 3-D nanostructured WBGSs in increasing the ECE of BCs.展开更多
基金supported by the National Natural Science Foundation of China(Grant No.11632005)。
文摘With a 10%reversible compressive strain in more than 10 deformation cycles,the shape memory polymer composites(SMPCs)could be used for deployable structure and releasing mechanism.In this paper,without traditional electro-explosive devices or motors/controllers,the deployable SMPC flexible solar array system(SMPC-FSAS)is studied,developed,ground-based tested,and finally on-orbit validated.The epoxy-based SMPC is used for the rolling-out variable-stiffness beams as a structural frame as well as an actuator for the flexible blanket solar array.The releasing mechanism is primarily made of the cyanate-based SMPC,which has a high locking stiffness to withstand 50 g gravitational acceleration and a large unlocking displacement of 10 mm.The systematical mechanical and thermal qualification tests of the SMPC-FSAS flight hardware were performed,including sinusoidal sweeping vibration,shocking,acceleration,thermal equilibrium,thermal vacuum cycling,and thermal cycling test.The locking function of the SMPC releasing mechanisms was in normal when launching aboard the SJ20 Geostationary Satellite on 27 Dec.,2019.The SMPC-FSAS flight hardware successfully unlocked and deployed on 5 Jan.,2020 on geostationary orbit.The triggering signal of limit switches returned to ground at the 139 s upon heating,which indicated the successful unlocking function of SMPC releasing mechanisms.A pair of epoxy-based SMPC rolled variable-stiffness tubes,which clapped the flexible blanket solar array,slowly deployed and finally approached an approximate 100%shape recovery ratio within 60 s upon heating.The study and on-orbit successful validation of the SMPC-FSAS flight hardware could accelerate the related study and associated productions to be used for the next-generation releasing mechanisms as well as space deployable structures,such as new releasing mechanisms with low-shocking,testability and reusability,and ultra-large space deployable solar arrays.
基金financially supported by the National Natural Science Foundation of China (Nos.52071226, 51872193 and 5192500409)the Natural Science Foundation of Jiangsu Province (Nos.BK20190827 and BK20181168)
文摘Two-dimensional(2D)transition-metal selenides,espe-cially MoSe_(2),is considered to be an excellent alternative electrocatalyst for the hydrogen evolution reaction(HER).However,it still features high overpotential in HER due to the low density of active sites,which limits its practical application.Herein,the hydrogen evolution reaction activity of MoSe_(2)is enhanced by the incorporation of metal-cation,tungsten,which succeeds in taking the place of Mo in the lattice of MoSe_(2),inducing the spacing expansion and bringing new flexural edges to serve as active sites.In addition,the incorporated metal also facil-itates electron transport from Mo active center toward W and Se atoms with auspicious hydrogen adsorption prop-erties.
基金financially supported by the National Natural Science Foundations of China(Nos.52071226,51872193 and U21A20332)the Natural Science Foundations of Jiangsu Province(Nos.BK20181168,BK20201171 and BK20220061)+2 种基金the Key R&D Project funded by Department of Science and Technology of Jiangsu Province(No.BE2020003-3)the Natural Science Foundation of Jiangsu Higher Education Institutions of China(No.19KJA210004)the Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)。
文摘Owing to the unique structure,anode-free lithium metal batteries(AFLMBs)have higher energy density and lower production cost than traditional lithium metal batteries(LMBs)or lithium-ion batteries(LIBs),However,AFLMBs suffer from an inherently finite Li reservoir and exhibit poor cycle stability,low Coulombic efficiency(CE)and severe dendrite growth.In this work,polydiallyl lithium disulfide(PDS-Li)was successfully synthesized and coated on Cu current collector by electrochemical polymerization.The PDS-Li acts as an additional lithium resource to compensate for the irreversible loss of lithium during cycling.In addition,the special structure and lithiophilicity of PDS-Li contribute to lower nucleation overpotential and uniform lithium deposition.When coupled with Li-rich manganese-based(LRM)cathode of Li1.2Mn0.54Ni0.13Co0.13O2,the anode-free full cell exhibits significantly improved cycle stability over 100 cycles and capacity retention of 63.3%and 57%after 80 and 100 cycles,respectively.We believe that PDS-Li can be used to ensure stable cycling performance and high-energy-density in AFLMBs.
基金supported by the National Natural Science Foundation of China(No.52071085)Shanghai Aerospace Science and Technology Innovation Fund(No.SAST2020-102).
文摘Lithium metal is regarded as the most promising anode material for next generation high energy density lithium batteries due to its high theoretical capacity and lowest potential versus standard hydrogen electrode.However,lithium dendrite growth and huge volume change during cycling hinder its practical application.It is of great importance to design advanced Li metal anodes to solve these problems.Herein,we report a ZnO-coated Zn foam as the host matrix to pre-store lithium through thermal infusing,achieving a Zn@ZnO foam supported Li composite electrode(LZO).Needlelike ZnO nanofibers grown on the Zn foam greatly increase the surface area and enhance the lithiophilicity of the Zn foam.In situ formed synaptic LiZn layer after lithium infusion can disperse local current density and lower Li diffusion barrier effectively,leading to homogeneous Li deposition behavior,thus suppressing dendrite formation.The porous Zn foam skeleton can accommodate volume variation of the electrode during longterm cycling.Benefiting from these merits,the LZO anode exhibits much better cycle stability and rate capability in both symmetrical and full cells with low voltage hysteresis than the bare Li anode.This work opens a new opportunity in designing high performance composite Li anode for lithium-metal batteries.
基金supported by the National Natural Science Foundation of China(Nos.22275121,21931005,22105122,52272265)the National Key R&D Program of China(No.2023YFA1506300)+1 种基金the Shanghai Municipal Science and Technology Major Project of China,the Open Foundation Commission of Shaoxing Research Institute of Renewable Energy and Molecular Engineering,China(No.JDSX2022038)the Project of Jiangxi Academy of Sciences,China(No.2023YSTZX01).
文摘Solid oxide electrolysis cells(SOECs)provide a promising way for converting renewable energy into chemical fuels.Traditionally,NiO/CGO(nickel-gadolinium doped ceria)cermet has shown its excellent properties in ionic and electronic conductivity under reducing conditions.Herein,we developed a novel 1D NiO/CGO cathode through a cerium metal-organic framework(MOF)derived process.The cathode’s 1D nanostructure integrated with a microchannel scaffold facilitates enhanced mass transport,providing vertically aligned pathways for CO_(2)and H_(2)O diffusion.Additionally,the 1D framework increases the number of interfacial sites and reduces ion diffusion distances,thereby simplifying electron/ion transport.Consequently,this advanced cathode achieved a significant breakthrough in SOEC performance,maintaining efficient CO_(2)and H_(2)O electrolysis at an extraordinary current density of 1.41 A/cm^(2)at 1.5 V and excellent stability over 24 h at 850℃.The enhanced performance of this newly developed cathode not only achieves a remarkable 100%improvement compared to those of NiO/CGO cathodes with varying geometrical configurations but also surpasses those of commercial NiO/CGO catalysts by an outstanding 40%when tested under identical conditions.The development of the 1D NiO/CGO enhances the efficiency and durability of ceramic cathodes for CO_(2)and H_(2)O co-electrolysis in SOECs and improves the scalability and effectiveness of SOECs in renewable energy applications.
基金supported by National Key R&D Program of China(2021YFA1502803)the National Natural Science Foundation of China(NSFC)(21972066,91745202)+3 种基金NSFC-Royal Society Joint Program(21661130149)L.P.thanks the Royal Society and Newton Fund for a Royal Society-Newton Advanced Fellowshipsupported by the Research Funds for the Frontiers Science Centre for Critical Earth Material Cycling,Nanjing Universitya Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions.
文摘Recent advances in utilizing ^(17)O isotopic labeling methods for solid-state nuclear magnetic resonance(NMR)investigations of metal oxides for lithium-ion batteries have yielded extensive insights into their structural and dynamic details.Herein,we commence with a brief introduction to recent research on lithium-ion battery oxide materials studied using ^(17)O solid-state NMR spectroscopy.Then we delve into a review of ^(17)O isotopic labeling methods for tagging oxygen sites in both the bulk and surfaces of metal oxides.At last,the unresolved problems and the future research directions for advancing the ^(17)O labeling technique are discussed.
基金supported by the National Key R&D Program of China(2021YFB2400400)the National Natural Science Foundation of China(Grant No.22379120,22179085)+5 种基金the Key Research and Development Plan of Shanxi Province(China,Grant No.2018ZDXM-GY-135,2021JLM-36)the National Natural Science Foundation of China(Grant No.22108218)the“Young Talent Support Plan”of Xi’an Jiaotong University(71211201010723)the Qinchuangyuan Innovative Talent Project(QCYRCXM-2022-137)the“Young Talent Support Plan”of Xi’an Jiaotong University(HG6J003)the“1000-Plan program”of Shaanxi Province。
文摘The insurmountable charge transfer impedance at the Li metal/solid polymer electrolytes(SPEs)interface at room temperature as well as the ascending risk of short circuits at the operating temperature higher than the melting point,dominantly limits their applications in solid-state batteries(SSBs).Although the inorganic filler such as CeO_(2)nanoparticle content of composite solid polymer electrolytes(CSPEs)can significantly reduce the enormous charge transfer impedance at the Li metal/SPEs interface,we found that the required content of CeO_(2)nanoparticles in SPEs varies for achieving a decent interfacial charge transfer impedance and the bulk ionic conductivity in CSPEs.In this regard,a sandwich-type composited solid polymer electrolyte with a 10%CeO_(2)CSPEs interlayer sandwiched between two 50%CeO_(2)CSPEs thin layers(sandwiched CSPEs)is constructed to simultaneously achieve low charge transfer impedance and superior ionic conductivity at 30℃.The sandwiched CSPEs allow for stable cycling of Li plating and stripping for 1000 h with 129 mV polarized voltage at 0.1 mA cm^(-2)and 30℃.In addition,the LiFePO_(4)/Sandwiched CSPEs/Li cell also exhibits exceptional cycle performance at 30℃and even elevated120℃without short circuits.Constructing multi-layered CSPEs with optimized contents of the inorganic fillers can be an efficient method for developing all solid-state PEO-based batteries with high performance at a wide range of temperatures.
基金Jiangsu Provincial Department of Science and Technology,Grant/Award Number:BK20201190Fundamental Research Funds for“Young Talent Support Plan”of Xi'an Jiaotong University,Grant/Award Number:HG6J003+1 种基金“1000-Plan program”of Shaanxi Province and the Velux Foundations through the research center V-Sustain,Grant/Award Number:9455National Key R&D Program of China,。
文摘The use of lithium-sulfur batteries under high sulfur loading and low electrolyte concentrations is severely restricted by the detrimental shuttling behavior of polysulfides and the sluggish kinetics in redox processes.Two-dimensional(2D)few layered black phosphorus with fully exposed atoms and high sulfur affinity can be potential lithium-sulfur battery electrocatalysts,which,however,have limitations of restricted catalytic activity and poor electrochemical/chemical stability.To resolve these issues,we developed a multifunctional metal-free catalyst by covalently bonding few layered black phosphorus nanosheets with nitrogen-doped carbon-coated multiwalled carbon nanotubes(denoted c-FBP-NC).The experimental characterizations and theoretical calculations show that the formed polarized P-N covalent bonds in c-FBP-NC can efficiently regulate electron transfer from NC to FBP and significantly promote the capture and catalysis of lithium polysulfides,thus alleviating the shuttle effect.Meanwhile,the robust 1D-2D interwoven structure with large surface area and high porosity allows strong physical confinement and fast mass transfer.Impressively,with c-FBP-NC as the sulfur host,the battery shows a high areal capacity of 7.69 mAh cm^(−2) under high sulfur loading of 8.74 mg cm^(−2) and a low electrolyte/sulfur ratio of 5.7μL mg^(−1).Moreover,the assembled pouch cell with sulfur loading of 4 mg cm^(−2) and an electrolyte/sulfur ratio of 3.5μL mg^(−1) shows good rate capability and outstanding cyclability.This work proposes an interfacial and electronic structure engineering strategy for fast and durable sulfur electrochemistry,demonstrating great potential in lithium-sulfur batteries.
基金financial support by the National Natural Science Foundation of China(No.51802224)“Shanghai Rising-Star Program”(19QA1409300)Shanghai Aerospace Science and Technology Innovation Fundation(SISP2018)。
文摘Lithium-ion batteries(LIBs)have greatly facilitated our daily lives since 1990s[1,2].To meet the ever-increasing demand on energy density,Li metal is seen as the ultimate anode because of its ultra-high specific capacity(3860 m Ah/g)and the lowest electrochemical potential(-3.04 V vs.the standard hydrogen electrode)[3–6].However,issues of Li metal anode,such as Li dendrite formation and large volume change during plating/stripping。
基金This study was financially supported by the National Natural Science Funds of China(No.21905040)the Startup Funds from the University of Electronic Science and Technology of China,the National Key Research and Development Program of China(Nos.2017YFB0702802 and 2018YFB0905400)Shanghai Venus Project(No.18QB1402600).
文摘As a promising solid electrolyte for thin-film lithium batteries,the amorphous Li_(0.33)La_(0.56)TiO_(3)(LLTO)thin film has gained great interest.However,enhancing ionic conductivity remains challenging in the field.Here,a systematical study was performed to improve the ionic conductivity of sputter-deposited LLTO thin films via the optimization of processing atmosphere and temperature.By combining the optimized oxygen partial pressure(30%),annealing temperature(300℃),and annealing atmosphere(air),an amorphous LLTO thin film with an ionic conductivity of 5.32910^(-5)·S·cm^(-1) at room temperature and activation energy of 0.26 eV was achieved.The results showed that,first,the oxygen partial pressure should be high enough to compensate for the oxygen loss,but low enough to avoid the abusive oxygen scattering effect on lithium precursors that results in a lithium-poor composition.The oxygen partial pressure needs to achieve a balance between lithium loss and oxygen defects to improve the ionic conductivity.Second,a proper annealing temperature reduces the oxygen defects of LLTO thin films while maintaining its amorphous state,which improves the ionic conductivity.Third,the highest ionic conductivity for the LLTO thin films that were annealed in air(a static space without a gas stream)occurs because of the decreased lithium loss and oxygen defects during annealing.These findings show that the lithium-ion concentration and oxygen defects affect the ionic conductivity for amorphous LLTO thin films,which provides insight into the optimization of LLTO thin-film solid electrolytes,and generates new opportunities for their application in thinfilm lithium batteries.
基金supported by the Hundred-Talent Project of Hubei Province,China(Grant No.2021HG01)the Huanggang Young Talent+2 种基金China(Grant No.HRZF2022-5)the Pearl Scholars Research Programs(Grant Nos.P20190218,P20190219)Young Scholars Start-up Research Programs of Huanggang Normal University,China(Grant Nos.Y20190218,Y20190219)。
文摘Argyrodites,Li_(6)PS_(5)X(X=Cl,Br,I),have piqued the interest of researchers by offering promising lithium ionic conductivity for their application in all-solid-state batteries(ASSBs).However,other than Li_(6)PS_(5)Cl(651Cl)and Li_(6)PS_(5)Br(651Br),Li_(6)PS_(5)I(651I)shows poor ionic conductivity(10^(-7)S cm^(-1)at 298 K).Herein,we present Al-doped 651I with I^(-)/S^(2-)site disordering to lower activation energy(Ea)and improve ionic conductivity.They formed argyrodite-type solid solutions with a composition of(Li_(6–3x)Al_(x))PS_(5)I in 0≤x≤0.10,and structural analysis revealed that Al^(3+)is located at Li sites.Also,the Al-doped samples contained anion I^(-)/S^(2-)site disorders in the crystal structures and smaller lattice parameters than the non-doped samples.Impedance spectroscopy measurements indicated that Al-doping reduced the ionic diffusion barrier,Ea,and increased the ionic conductivity to 10^(-5)S cm^(-1);the(Li5.7Al0.1)PS5I had the highest ionic conductivity in the studied system,at 2.6×10^(-5)S cm^(-1).In a lab-scale ASSB,with(Li_(5.7)Al_(0.1))PS_(5)I functioned as a solid electrolyte,demonstrating the characteristics of a pure ionic conductor with negligible electronic conductivity.The evaluated ionic conduction is due to decreased Li+content and I^(-)/S^(2-)disorder formation.Li-site cation doping enables an in-depth understanding of the structure and provides an additional approach to designing betterperforming SEs in the argyrodite system.
基金sponsored by the National Natural Science Foundation of China(Grant No.51971156).
文摘Ti_(2)AlC has been demonstrated as the promising protective layer material for thermal barrier coatings(TBCs)against calcium-magnesium-alumina-silicate(CMAS)attack.In this study,the reliability of Ti_(2)AlC coatings against the CMAS corrosion was explored,and new Ti_(2)AlC/YSZ TBCs more efficiently resistant to CMAS were designed.The fabricated Ti_(2)AlC coatings inevitably contain some impurity phases(TiC and Al2Ti3),the contents of which were minimized by optimizing the spraying distance.Corrosion tests revealed that Ti_(2)AlC/YSZ TBCs yielded higher resistance to the CMAS attack than YSZ TBCs,but with long-term exposure to CMAS,the Ti_(2)AlC protective coating exhibited microstructure degradation due to the presence of the impurity phases,which caused the formation of a layer mixed with Al_(2)O_(3)and TiO_(2)rather than a continuous compact Al_(2)O_(3)layer on the surface.Pre-oxidation schemes were designed in air or with a controlled oxygen partial pressure,which revealed that the pre-oxidation at an oxygen partial pressure of~630 Pa could promote a continuous Al_(2)O_(3)layer formed on the Ti_(2)AlC protective coating surface.Furthermore,a vacuum heat treatment at 867℃for 10 h before pre-oxidation was beneficial for the formation of the compact Al_(2)O_(3)layer.Through the above scheme design,new Ti_(2)AlC/YSZ TBCs were obtained,which had reduced impurity phase contents and a pre-oxide layer with an ideal structure on the surface.New TBCs exhibit higher microstructure stability exposed to CMAS and more efficient CMAS resistance.
基金co-supported by the Joint Fund of Advanced Aerospace Manufacturing Technology Research,China(No.U1937601)the Research Fund of State Key Laboratory of Mechanics and Control of Mechanical Structures+1 种基金China(No.MCMS-I-0221Y01)National Natural Science Foundation of China for Creative Research Groups(No.51921003).
文摘During long-term service in space,Gallium Arsenide(GaAs)solar cells are directly exposed to electron irradiation which usually causes a dramatic decrease in their performance.In the multilayer structure of solar cells,the germanium(Ge)layer occupies the majority of the thickness as the substrate.Due to the intrinsic brittleness of semiconductor material,there exist various defects during the preparation and assembly of solar cells,the influences of which tend to be intensified by the irradiation effect.In this work,first,Ge specimens for mechanical tests were prepared at scales from microscopic to macroscopic.Then,after different doses of electron irradiation,the mechanical properties of the Ge specimens were investigated.The experimental results demonstrate that electron irradiation has an obvious effect on the mechanical property variation of Ge in diverse scales.The four-point bending test indicates that the elastic modulus,fracture strength,and maximum displacement of the Ge specimens all increase,and reach the maximum value at the irradiation dose of 1×10^(15)e/cm^(2).The micrometer scale cantilever and nanoindentation tests present similar trends for Ge specimens after irradiation.Atomic Force Microscope(AFM)also observed the change in surface roughness.Finally,a fitting model was established to characterize the relation between modulus change and electron irradiation dose.
基金This work was supported by the National Natural Science Foundation of China(Nos.51922073 and 21902109)the Natural Science Foundation of Jiangsu Province(Nos.BK20200960 and BK20180097)+1 种基金the Natural Science Foundation of Higher Education in Jiangsu Province(No.20KJB150041)the Natural Science Foundation of Nantong University for High-Level Talent(No.03083033).
文摘Highly active and durable Pd-based electrocatalysts for ethanol oxidation reaction(EOR)play a crucial role in the commercialization of direct ethanol fuel cells(DEFCs).However,the poisonous intermediates(especially adsorbed CO species(COad))formed during the EOR process can easily adsorb and block the active sites on Pd electrodes,which in turn limits the catalytic efficiency.Hence,we present a series of Pd-based composites with a strong coupling interface consisting of Pd nanosheets and amorphous Bi(OH)_(3)species.The incorporation of Bi(OH)3 can induce an electron-rich state adjacent to the Pd sites and effectively separate the Pd ensemble,leading to excellent CO tolerance.The optimal Pd-Bi(OH)_(3)NSs catalyst manifests a mass activity of 2.2 A·mgPd^(-1),which is 5.7 and 2.0 times higher than that of Pd NSs and commercial Pd/C catalyst,respectively.Further CO-stripping experiments and CO-DRIFTS tests confirm the excellent CO tolerance on Pd-Bi(OH)3 NSs electrode,leading to the enhanced EOR durability.
基金financially supported by the National Natural Science Foundation of China (Nos. 62205311, 52073007, 61875005 and 52011540389)the Fundamental Research Program of Shanxi Province (No. 202103021223177)。
文摘Electrochromic asymmetric supercapacitors(EASs), incorporating electrochromic and energy storage into one platform, are extremely desirable for next-generation civilian portable and smart electronic devices. However, the crucial challenge of their fast self-discharge rate is often overlooked, although it plays an important role in practical application. Unfortunately, very limited research on EAS has focused on this critical problem. Here, an ultrathin all-inorganic EAS with excellent anti-self-discharge performance and superior electrochromic behavior is designed and manufactured by introducing a thin nanofunctional layer at the electrode/electrolyte interface. The prototype all-inorganic EAS exhibited a wide working voltage of 2.2 V, a high energy/power density(81.2mWh·cm^(-3)/0.688 W·cm^(-3)and 30.6 mWh·cm^(-3)/11.02W·cm^(-3)), along with outstanding electrochemical and electrochromic performance even at high temperatures.Remarkably, the introduced Ta2O5layer can efficiently prohibit the redistribution and diffusion of the movable ions at the fully charged state, endowing the all-inorganic EAS with a tardy self-discharge rate of 12.6 mV·g^(-1),which is an extremely low value when compared with previous reported research. Significantly, the ultrathin allinorganic EASs could also well maintain a slow self-discharge rate and their original electrochemical characteristics under various environmental temperatures. We envision that the novel strategy of electrode/electrolyte interface engineering can effectively deal with the severe self-discharge challenge of EAS, and provide more opportunities for their practical applications.
基金supported by the National Natural Science Foundation of China (Grant Nos. 52120105009 and 51906144)the Science and Technology Commission of Shanghai Municipality (Grant Nos. 20JC1414800 and 22ZR1432900)the Open Fund of Key Laboratory of Thermal Management and Energy Utilization of Aircraft of Ministry of Industry and Information Technology (Grant No. CEPE2020015)。
文摘The increasing demand for versatile and high-quality near-field radiative heat transfer(NFRHT) has created a critical need for a design approach that can handle numerous candidate structures. In this work, we employ and develop an adaptive hybrid Bayesian optimization(AHBO) algorithm to design the high-quality quasi-monochromatic NFRHT. The candidate materials include hexagonal boron nitride, silicon carbide, and doped silicon. The high-quality quasi-monochromatic NFRHT is optimized over 1.0 × 10^(8) candidate structures to maximize the evaluation factor. It is worth noting that only 2.6% of the candidate structures needed to be calculated to identify the optimal structure. The optimal structure of quasi-monochromatic NFRHT is an aperiodic multilayer metamaterial that differs from conventional periodic multilayer structures. Moreover, we investigate the robustness and mechanisms of the optimal quasi-monochromatic NFRHT with respect to the vacuum gap distance and the temperature difference between the emitter and receiver. In addition, the high-quality multi-peak NFRHT is designed using the AHBO algorithm by improving the definition of the evaluation factor. The results demonstrate that the AHBO algorithm is efficient in designing high-quality quasi-monochromatic and multi-peak NFRHT, and it can be further expanded to other structural designs in the field of energy conversion.
基金The authors are grateful to the financial support of the National Key R&D Program of China(No.2021YFB3702401)National Natural Science Foundation of China(U1937601).
文摘Adding alloying elements is always considered as an effective method to enhance the resistance against hydrogen embrittlement in steels.Nb and V were added into 22MnB5 hot stamping steel,and then their influences on hydrogen permeation of 22MnB5 steel suffering from corrosion in 3.5%NaCl aqueous solution were investigated.The results showed that the addition of Nb/V could reduce the hydrogen permeation content due to solution corrosion.Electrochemical techniques including electrochemical impedance spectroscopy and overpotential stepping hydrogen permeation test con-firmed that compared to the original 22MnB5 steel,22MnB5-NbN steel owned a higher corrosion resistance and a higher hydrogen diffusion resistance.Furthermore,it was confirmed that Nb-V-alloyed 22MnB5 steel showed higher resistance against hydrogen embrittlement than the Nb-V-free counterpart,which should be related to the presentence of nanoscaled Nb/V-containing precipitates as the irreversible trapping sites for hydrogen detected by thermal desorption spectroscopy.Finally,the lattice diffusion coefficient of hydrogen DL was determined in steels with and without Nb and V.
基金This work was financially supported by the Guangdong Key Laboratory of Battery Safety(No.2019B121203008)the National Natural Science Foundation of China(No.52072036),NSAF(No.U1930113)+2 种基金the Beijing Natural Science Foundation(No.L182022)the 13th Five-Year Plan of Advance Research and Sharing Techniques by Equipment Department(No.41421040202)the China Postdoctoral Science Foundation(No.2021TQ0034).
文摘Surface deterioration occurs more easily in nickel-rich cathode materials with the increase of nickel content.To simultaneously pre-vent deterioration of active cathode materials and improve the electrochemical performance of the nickel-rich cathode material,the surface of nickel-rich LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode material is decorated with the stable structure and conductive Li_(3)PO_(4)by a facile method.The LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)-1wt%,2wt%,3wt%Li_(3)PO_(4)samples deliver a high-capacity retention of more than 85%after 100 cycles at 1 C under a high voltage of 4.5 V.The effect of different coating amounts(0-5wt%)for the LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode is analyzed in detail.Results show that 2wt%coating of Li_(3)PO_(4)gives better performance compared to other coating concentrations.Detailed analysis of the structure of the samples during the charge−discharge process is performed by in-situ X-ray diffraction.It is indicated that the modification for LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)cathode could protect the well-layered structure under high voltages.In consequence,the electrochemical performance of modified samples is greatly improved.
基金the financial support of the project from the National Natural Science Foundation of China(Grant No.61574117)the Natural Science Foundation of Guangdong Province(Grant No.2018B030311002)the China Scholarship Council(Grant No.201806310044)。
文摘A full-duplex radiant energy converter based on both betavoltaic and photovoltaic effects in an easyto-implement way is an attractive alternative for the autonomous wireless sensor microsystem.Here,we report a novel beta/photovoltaic cell based on free-standing Zn O nanorod arrays(ZNRAs)modified with metallic single-walled carbon nanotubes(m-SWCNTs),using radioisotope63 Ni as beta-emitting source.The ZNRAs were grown on Al-doped Zn O(AZO)conductive glass using hydrothermal method.The optimum length and diameter of Zn O nanorods were determined by Monte Carlo simulation for beta energy deposition in ZNRAs.The m-SWCNTs were anchored into the ZNRAs to form a three-dimensional(3-D)Schottky junction structure for effectively separating the beta/photo-excited electron-hole pairs.Experimentally,the betavoltaic and photovoltaic effects were confirmed through the I-V measurements of beta/photovoltaic cells under beta/UV/Vis irradiations,respectively.It is suggested that the m-SWCNTs play key role for the enhancement of beta/photovoltaic performance through the formation of extensive3-D Schottky junction,the conductive network for hole transport,and the surface plasmon resonance exciton absorption for visible light.
基金supported by the National Natural Science Foundation of China(Nos.12175190 and U2241284)the National Key R&D Program of China(Nos.SQ2022YFB190165)+1 种基金the Natural Science Foundation of Fujian Province,China(No.2022J02006)the Special Funds for Central Government Guiding Shenzhen Development in Science and Technology,China(No.2021Szvup066).
文摘Betavoltaic cells(BCs)are promising self-generating power cells with long life and high power density.However,the low energy conversion efficiency(ECE)has limitations in practical engineering applications.Widebandgap semiconductors(WBGSs)with three-dimensional(3-D)nanostructures are ideal candidates for increasing the ECE of BCs.This paper proposes hydrothermally grown ZnO nanorod arrays(ZNRAs)for ^(63)Ni-powered BCs.A quantitative model was established for simulation using the parameter values of the dark characteristics,which were obtained from the experimental measurements for a simulated BC based on a Ni-incorporated ZNRAs structure.Monte Carlo(MC)modeling and simulation were conducted to obtain the values of the β energy deposited in ZNRAs with different nanorod spacings and heights.Through the simulation and optimization of the 3-D ZNRAs and 2-D ZnO bulk structures,the performance of the ^(63)Ni-powered BCs based on both structures was evaluated using a quantitative model.The BCs based on the 3-D ZNRAs structure and 2-D ZnO bulk structure achieved a maximum ECE of 10.1%and 4.69%,respectively,which indicates the significant superiority of 3-D nanostructured WBGSs in increasing the ECE of BCs.
