Highly selective conversion of methane(CH_(4))to methanol(CH_(3)OH)is an emerging attractive but challenging process for future development of hydrogen economy,which requires efficient catalysts.Herein,we systematical...Highly selective conversion of methane(CH_(4))to methanol(CH_(3)OH)is an emerging attractive but challenging process for future development of hydrogen economy,which requires efficient catalysts.Herein,we systematically explore the catalytic properties of Pt(111)overlayer on transition metal oxides(TMOs)for CH_(4) conversion by first principles calculations.The Pt(111)monolayer supported by Ce-terminated CeO_(2)(111)substrate exhibits high activity and selectivity for CH_(4) conversion to CH_(3)OH,with the kinetic barrier of rate-limiting step of 1.05 eV.Intriguingly,the surface activity of Pt overlayer is governed by its d-band center relative to the energy of bonding states of adsorbed molecules,which in turn depends on the number of charge transfer between Pt(111)monolayer and underlying TMOs substrates.These results provide useful insights in the design of metal overlayers as catalysts with high-ultra performance and atomic utilization.展开更多
Thermochemical two-step CO_(2) splitting is a potential approach that fixes the sustainable resource into transportable liquid fuels.However,the harsh CO_(2) splitting conditions,the limited oxygen release kinetics an...Thermochemical two-step CO_(2) splitting is a potential approach that fixes the sustainable resource into transportable liquid fuels.However,the harsh CO_(2) splitting conditions,the limited oxygen release kinetics and capacity of metal oxides block further promoted the CO yield and solar-to-fuel energy efficiency.Here,we propose a different carbon cycle assisted by Ni/La_(2)O_(3) via coupling methane decomposition with thermochemical CO_(2) splitting,replacing conventional metal oxides cycle.Superior performance was demonstrated with methane conversion reached around 94%with almost pure H_(2) generation.Encouragingly,CO_(2) conversion of 98%and CO yield of 6.9 mmol g^(-1) derived from CO_(2) were achieved,with peak CO evolution rate(402 mL min^(-1) g^(-1))of orders of magnitude higher than that in metal oxide process and outstanding thermodynamic solar-to-fuel energy efficiency(55.5%vs.18.5%).This was relevant to the synergistic activation of La_(2)O_(3) and Ni for CO_(2) in carbon cycle,thus improving CO_(2) splitting reaction with carbon species.展开更多
While Fe-based oxygen carriers(OC) are regarded to be promising for chemical looping combustion(CLC),the decrease of CO_2 selectivity during deep reduction process and the severe agglomeration of Fe_2O_3 often occur a...While Fe-based oxygen carriers(OC) are regarded to be promising for chemical looping combustion(CLC),the decrease of CO_2 selectivity during deep reduction process and the severe agglomeration of Fe_2O_3 often occur after multiple redox cycles due to the low oxygen mobility.Herein,Fe-substituted Bahexaaluminates(Ba Fe_xAl_(12)– xO_(19),denoted as BF_xA-H,x = 1 and 2) prepared by a modified two-step method exhibited not only higher amount of converted oxygen(Ot) and CH_4 conversion(77% and 81% vs.17%and 75%) than those prepared by the traditional co-precipitation method(BF_xA-C,x = 1 and 2) but also high CO_2 selectivity above 92% during the nearly whole reduction from Fe^(3+) to Fe^(2+).Furthermore,the BFxA-H exhibited the excellent recyclability during 50 cycles.The better performance was ascribed to the markedly enhanced oxygen mobility which resulted from dominant occupancy of Fe cations in Al(5) sites(Fe^5: 71% and 70% vs.49% and 41%) in mirror planes of hexaaluminate leading to larger amount of lattice oxygen coordinated with Fe^5(O–Fe^5)(0.45 and 0.85 mmol/g vs.0.31 and 0.50 mmol/g).The improvement of oxygen mobility also favored the preservation of chemical state of Fe cations in hexaaluminate structure in the re-oxidation step,resulting in the excellent recyclability of BF_xA-H.展开更多
A Pt-Rh three-way catalyst（M-DS） supported on CeO_2-ZrO_2-La_2O_3-Nd_2O_3 and its analogous supported catalyst（DS） were developed via a modified double-solvent method and conventional double-solvent method, respec...A Pt-Rh three-way catalyst（M-DS） supported on CeO_2-ZrO_2-La_2O_3-Nd_2O_3 and its analogous supported catalyst（DS） were developed via a modified double-solvent method and conventional double-solvent method, respectively. The as-prepared catalysts were characterized by N_2 adsorption-desorption, X-ray diffraction（XRD）, CO-chemisorption, X-ray photoelectron spectroscopy（XPS） and hydrogen temperature-programmed reduction（H_2-TPR）. The preformed Pt nanoparticles generated using ethanol as a reducing agent on M-DS presented enhanced Pt dispersion regardless of aging treatment as confirmed by XRD and CO-chemisorption measurements. The textural properties and reduction ability of M-DS were maintained to a large extent after aging treatment. This result was consistent with those of the N_2 adsorption-desorption and H_2-TPR, respectively. Meanwhile, the XPS analysis demonstrated that higher Pt^0 species and larger Ce^（3＋） concentration could be obtained for M-DS. In the conversion of a simulated compressed natural gas（CNG） vehicle exhaust, both fresh and aged M-DS showed a significant enhancement in the activity and N_2-selectivity. Particularly, the complete conversion temperature（T_（90）） of CH_4 over the aged M-DS catalyst was 65 oC lower than that over the aged catalyst by conventional double-solvent method.展开更多
基金supported by the National Natural Science Foundation of China(Nos.11974068,91961204,and 12004065)the Fundamental Research Funds for the Central Universities of China(No.DUT20LAB110)+1 种基金the Liaoning Provincial Natural Science Foundation of China(No.2019JH3/30100002)Key Research and Development Project of Liaoning Province(No.2020JH2/10500003).
文摘Highly selective conversion of methane(CH_(4))to methanol(CH_(3)OH)is an emerging attractive but challenging process for future development of hydrogen economy,which requires efficient catalysts.Herein,we systematically explore the catalytic properties of Pt(111)overlayer on transition metal oxides(TMOs)for CH_(4) conversion by first principles calculations.The Pt(111)monolayer supported by Ce-terminated CeO_(2)(111)substrate exhibits high activity and selectivity for CH_(4) conversion to CH_(3)OH,with the kinetic barrier of rate-limiting step of 1.05 eV.Intriguingly,the surface activity of Pt overlayer is governed by its d-band center relative to the energy of bonding states of adsorbed molecules,which in turn depends on the number of charge transfer between Pt(111)monolayer and underlying TMOs substrates.These results provide useful insights in the design of metal overlayers as catalysts with high-ultra performance and atomic utilization.
基金supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB17020100)the National Key R&D Program of China(2016YFA0202-801)+1 种基金the National Natural Science Foundation of China(NSFC)grants(21676269,21706254,21878283,22022814)the Dalian Institute of Chemical Physics,CAS(DICP I201916)。
文摘Thermochemical two-step CO_(2) splitting is a potential approach that fixes the sustainable resource into transportable liquid fuels.However,the harsh CO_(2) splitting conditions,the limited oxygen release kinetics and capacity of metal oxides block further promoted the CO yield and solar-to-fuel energy efficiency.Here,we propose a different carbon cycle assisted by Ni/La_(2)O_(3) via coupling methane decomposition with thermochemical CO_(2) splitting,replacing conventional metal oxides cycle.Superior performance was demonstrated with methane conversion reached around 94%with almost pure H_(2) generation.Encouragingly,CO_(2) conversion of 98%and CO yield of 6.9 mmol g^(-1) derived from CO_(2) were achieved,with peak CO evolution rate(402 mL min^(-1) g^(-1))of orders of magnitude higher than that in metal oxide process and outstanding thermodynamic solar-to-fuel energy efficiency(55.5%vs.18.5%).This was relevant to the synergistic activation of La_(2)O_(3) and Ni for CO_(2) in carbon cycle,thus improving CO_(2) splitting reaction with carbon species.
基金supported by the National Science Foundation of China (NSFC) (21303137,21406225 and 21676269)the National Key Project for Fundamental Research and Development of China (2016YFA0202801)Postdoctoral Science Foundation of China (2014M561261)
文摘While Fe-based oxygen carriers(OC) are regarded to be promising for chemical looping combustion(CLC),the decrease of CO_2 selectivity during deep reduction process and the severe agglomeration of Fe_2O_3 often occur after multiple redox cycles due to the low oxygen mobility.Herein,Fe-substituted Bahexaaluminates(Ba Fe_xAl_(12)– xO_(19),denoted as BF_xA-H,x = 1 and 2) prepared by a modified two-step method exhibited not only higher amount of converted oxygen(Ot) and CH_4 conversion(77% and 81% vs.17%and 75%) than those prepared by the traditional co-precipitation method(BF_xA-C,x = 1 and 2) but also high CO_2 selectivity above 92% during the nearly whole reduction from Fe^(3+) to Fe^(2+).Furthermore,the BFxA-H exhibited the excellent recyclability during 50 cycles.The better performance was ascribed to the markedly enhanced oxygen mobility which resulted from dominant occupancy of Fe cations in Al(5) sites(Fe^5: 71% and 70% vs.49% and 41%) in mirror planes of hexaaluminate leading to larger amount of lattice oxygen coordinated with Fe^5(O–Fe^5)(0.45 and 0.85 mmol/g vs.0.31 and 0.50 mmol/g).The improvement of oxygen mobility also favored the preservation of chemical state of Fe cations in hexaaluminate structure in the re-oxidation step,resulting in the excellent recyclability of BF_xA-H.
基金supported by the National Key Research and Development Program of China(2016YFC0204902)
文摘A Pt-Rh three-way catalyst（M-DS） supported on CeO_2-ZrO_2-La_2O_3-Nd_2O_3 and its analogous supported catalyst（DS） were developed via a modified double-solvent method and conventional double-solvent method, respectively. The as-prepared catalysts were characterized by N_2 adsorption-desorption, X-ray diffraction（XRD）, CO-chemisorption, X-ray photoelectron spectroscopy（XPS） and hydrogen temperature-programmed reduction（H_2-TPR）. The preformed Pt nanoparticles generated using ethanol as a reducing agent on M-DS presented enhanced Pt dispersion regardless of aging treatment as confirmed by XRD and CO-chemisorption measurements. The textural properties and reduction ability of M-DS were maintained to a large extent after aging treatment. This result was consistent with those of the N_2 adsorption-desorption and H_2-TPR, respectively. Meanwhile, the XPS analysis demonstrated that higher Pt^0 species and larger Ce^（3＋） concentration could be obtained for M-DS. In the conversion of a simulated compressed natural gas（CNG） vehicle exhaust, both fresh and aged M-DS showed a significant enhancement in the activity and N_2-selectivity. Particularly, the complete conversion temperature（T_（90）） of CH_4 over the aged M-DS catalyst was 65 oC lower than that over the aged catalyst by conventional double-solvent method.
