Lithium niobate has received interest in nonlinear frequency conversion due to its wide transparency window,from ultraviolet to mid-infrared spectral regions,and large second-order nonlinear susceptibility.However,its...Lithium niobate has received interest in nonlinear frequency conversion due to its wide transparency window,from ultraviolet to mid-infrared spectral regions,and large second-order nonlinear susceptibility.However,its nanostructure is generally difficult to etch,resulting in low-Q resonance and lossy nanostructures for second harmonic generation.By applying the concept of bound states in the continuum,we performed theoretical and experimental investigations on high-Q resonant etchless thin-film lithium niobate with Si O_(2) nanostructures on top for highly efficient second harmonic generation.In the fabricated nanostructured devices,a resonance with a Q factor of 980 leads to the strong enhancement of second harmonic generation by over 1500 times compared with that in unpatterned lithium niobate thin film.Although the pump slightly deviates from central resonance,an absolute conversion efficiency of 6.87×10^(-7) can be achieved with the fundamental pump peak intensity of 44.65 MW/cm^(2),thus contributing to the normalized conversion efficiency of 1.54×10^(-5)cm^(2)/GW.Our work establishes an etchless lithium niobate device for various applications,such as integrated nonlinear nanophotonics,terahertz frequency generation,and quantum information processing.展开更多
Mo_(2)C is an excellent electrocatalyst for hydrogen evolution reaction(HER).However,Mo_(2)C is a poor electrocatalyst for oxygen evolution reaction(OER).Herein,two different elements,namely Co and Fe,are incorporated...Mo_(2)C is an excellent electrocatalyst for hydrogen evolution reaction(HER).However,Mo_(2)C is a poor electrocatalyst for oxygen evolution reaction(OER).Herein,two different elements,namely Co and Fe,are incorporated in Mo_(2)C that,therefore,has a finely tuned electronic structure,which is not achievable by incorporation of any one of the metals.Consequently,the resulting electrocatalyst Co_(0.8)Fe_(0.2)-Mo_(2)C-80 displayed excellent OER catalytic performance,which is evidenced by a low overpotential of 214.0(and 246.5)mV to attain a current density of 10(and 50)mA cm^(-2),an ultralow Tafel slope of 38.4 mV dec^(-1),and longterm stability in alkaline medium.Theoretical data demonstrates that Co_(0.8)Fe_(0.2)-Mo_(2)C-80 requires the lowest overpotential(1.00 V)for OER and Co centers to be the active sites.The ultrahigh catalytic performance of the electrocatalyst is attributed to the excellent intrinsic catalytic activity due to high Brunauer-Emmett-Teller specific surface area,large electrochemically active surface area,small Tafel slope,and low chargetransfer resistance.展开更多
Heteronanostructures(HNs)with precise components and interfaces are important for many applications,such as designing efficient and robust solar-to-fuel catalysts via integrating specific semiconductors with favorable...Heteronanostructures(HNs)with precise components and interfaces are important for many applications,such as designing efficient and robust solar-to-fuel catalysts via integrating specific semiconductors with favorable band alignments.However,rationally endowing such features with rigorous framework control remains a synthetic bottleneck.Herein,we report a modular divergent creation of dual-cocatalysts integrated semiconducting sulfide nanotriads(NTds),comprising both isolated Pd_(x)S oxidation(ox)and MoS_(2) reduction(red)domains within each single CdS counterpart,which exhibit superior photocatalytic activity and stability for hydrogen evolution reaction(HER).The stepwise constructed Pd_(x)S_((ox))−CdS−MoS_(2(red)) NTds possess dualinterfaces facilitating continuous charge separation and segregated active sites accelerating redox reactions,respectively,achieving the HER rate up to 9 mmol·h^(−1)·g^(−1),which is about 60 times higher than that of bare CdS,and show no evidence of deactivation after long-term cycling.This design principle and transformation protocol provide predictable retrosynthetic pathways to HNs with increased degree of complexity and more elaborate functionalities that are otherwise inaccessible.展开更多
Humidity is a critical environmental parameter for several production processes and its control/monitoring is of great importance in maintaining the quality of goods and products. In this context, metallic oxide ceram...Humidity is a critical environmental parameter for several production processes and its control/monitoring is of great importance in maintaining the quality of goods and products. In this context, metallic oxide ceramic nanostructures are materials of great technological interest in the fabrication of moisture sensors because they have good chemical/structural stability and high surface area/volume ratio. The electrical response of these sensors relates to the chemisorbed and physisorbed layers of water molecules on the surface of the ceramic particles and to the capillary condensation of water in the microscopic pores between the particles. Based on these aspects, this work presents the fundamentals, electrical/electronic properties, influence of dopants, novel preparation procedure by electrospinning and perspectives of application of TiO2:WO3 metal oxide heteronanostructures as humidity sensors.展开更多
基金supported by the National Natural Science Foundation of China (Grant Nos. 61775084, and 62075088)the National Safety Academic Fund (Grant No. U2030103)+2 种基金the Natural Science Foundation of Guangdong Province (Grant Nos. 2020A1515010791, and 2021A0505030036)the Open Fund of Guangdong Provincial Key Laboratory of Information Photonics Technology of Guangdong University of Technology (Grant No. GKPT20-03)the Fundamental Research Funds for the Central Universities (Grant Nos. 21622107, and 21622403)。
文摘Lithium niobate has received interest in nonlinear frequency conversion due to its wide transparency window,from ultraviolet to mid-infrared spectral regions,and large second-order nonlinear susceptibility.However,its nanostructure is generally difficult to etch,resulting in low-Q resonance and lossy nanostructures for second harmonic generation.By applying the concept of bound states in the continuum,we performed theoretical and experimental investigations on high-Q resonant etchless thin-film lithium niobate with Si O_(2) nanostructures on top for highly efficient second harmonic generation.In the fabricated nanostructured devices,a resonance with a Q factor of 980 leads to the strong enhancement of second harmonic generation by over 1500 times compared with that in unpatterned lithium niobate thin film.Although the pump slightly deviates from central resonance,an absolute conversion efficiency of 6.87×10^(-7) can be achieved with the fundamental pump peak intensity of 44.65 MW/cm^(2),thus contributing to the normalized conversion efficiency of 1.54×10^(-5)cm^(2)/GW.Our work establishes an etchless lithium niobate device for various applications,such as integrated nonlinear nanophotonics,terahertz frequency generation,and quantum information processing.
基金financial support from the SERB-SURE under file number of SUR/2022/003129Jong Hyeok Park acknowledges the support of the National Research Foundation of Korea (NRF)funded by the Ministry of Science and ICT (RS-2023-00302697,RS-2023-00268523).
文摘Mo_(2)C is an excellent electrocatalyst for hydrogen evolution reaction(HER).However,Mo_(2)C is a poor electrocatalyst for oxygen evolution reaction(OER).Herein,two different elements,namely Co and Fe,are incorporated in Mo_(2)C that,therefore,has a finely tuned electronic structure,which is not achievable by incorporation of any one of the metals.Consequently,the resulting electrocatalyst Co_(0.8)Fe_(0.2)-Mo_(2)C-80 displayed excellent OER catalytic performance,which is evidenced by a low overpotential of 214.0(and 246.5)mV to attain a current density of 10(and 50)mA cm^(-2),an ultralow Tafel slope of 38.4 mV dec^(-1),and longterm stability in alkaline medium.Theoretical data demonstrates that Co_(0.8)Fe_(0.2)-Mo_(2)C-80 requires the lowest overpotential(1.00 V)for OER and Co centers to be the active sites.The ultrahigh catalytic performance of the electrocatalyst is attributed to the excellent intrinsic catalytic activity due to high Brunauer-Emmett-Teller specific surface area,large electrochemically active surface area,small Tafel slope,and low chargetransfer resistance.
基金the National Natural Science Foundation of China(Nos.21431006,U1932213,21905261,and 22171065)the National key Research and Development Program of China(Nos.2018YFE0202201 and 2021YFA0715700)+5 种基金the University Synergy Innovation Program of Anhui Province(No.GXXT-2019-028)the Science and Technology Major Project of Anhui Province(No.201903a05020003)S.K.H.acknowledges the Anhui Province Key Research and Development Plan(No.202104e11020005)the Hefei National Laboratory for Physical Sciences at the Microscale(No.KF2020005).C.G.acknowledges the National Postdoctoral Program for Innovative Talents(No.BX20180284)the China Postdoctoral Science Foundation(No.2019M660155).
文摘Heteronanostructures(HNs)with precise components and interfaces are important for many applications,such as designing efficient and robust solar-to-fuel catalysts via integrating specific semiconductors with favorable band alignments.However,rationally endowing such features with rigorous framework control remains a synthetic bottleneck.Herein,we report a modular divergent creation of dual-cocatalysts integrated semiconducting sulfide nanotriads(NTds),comprising both isolated Pd_(x)S oxidation(ox)and MoS_(2) reduction(red)domains within each single CdS counterpart,which exhibit superior photocatalytic activity and stability for hydrogen evolution reaction(HER).The stepwise constructed Pd_(x)S_((ox))−CdS−MoS_(2(red)) NTds possess dualinterfaces facilitating continuous charge separation and segregated active sites accelerating redox reactions,respectively,achieving the HER rate up to 9 mmol·h^(−1)·g^(−1),which is about 60 times higher than that of bare CdS,and show no evidence of deactivation after long-term cycling.This design principle and transformation protocol provide predictable retrosynthetic pathways to HNs with increased degree of complexity and more elaborate functionalities that are otherwise inaccessible.
基金The authors acknowledge the financial support from Bahia State Research Foundation(FAPESB,Project 1252/2018).
文摘Humidity is a critical environmental parameter for several production processes and its control/monitoring is of great importance in maintaining the quality of goods and products. In this context, metallic oxide ceramic nanostructures are materials of great technological interest in the fabrication of moisture sensors because they have good chemical/structural stability and high surface area/volume ratio. The electrical response of these sensors relates to the chemisorbed and physisorbed layers of water molecules on the surface of the ceramic particles and to the capillary condensation of water in the microscopic pores between the particles. Based on these aspects, this work presents the fundamentals, electrical/electronic properties, influence of dopants, novel preparation procedure by electrospinning and perspectives of application of TiO2:WO3 metal oxide heteronanostructures as humidity sensors.
