Electrocatalytic water splitting provides an efficient method for the production of hydrogen.In electrocatalytic water splitting,the oxygen evolution reaction(OER)involves a kinetically sluggish four-electron transfer...Electrocatalytic water splitting provides an efficient method for the production of hydrogen.In electrocatalytic water splitting,the oxygen evolution reaction(OER)involves a kinetically sluggish four-electron transfer process,which limits the efficiency of electrocatalytic water splitting.Therefore,it is urgent to develop highly active OER catalysts to accelerate reaction kinetics.Coupling single atoms and clusters in one system is an innovative approach for developing efficient catalysts that can synergistically optimize the adsorption and configuration of intermediates and improve catalytic activity.However,research in this area is still scarce.Herein,we constructed a heterogeneous single-atom cluster system by anchoring Ir single atoms and Co clusters on the surface of Ni(OH)_(2)nanosheets.Ir single atoms and Co clusters synergistically improved the catalytic activity toward the OER.Specifically,Co_(n)Ir_(1)/Ni(OH)_(2)required an overpotential of 255 mV at a current density of 10 mA·cm^(−2),which was 60 mV and 67 mV lower than those of Co_(n)/Ni(OH)_(2)and Ir1/Ni(OH)_(2),respectively.The turnover frequency of Co_(n)Ir_(1)/Ni(OH)_(2)was 0.49 s^(−1),which was 4.9 times greater than that of Co_(n)/Ni(OH)_(2)at an overpotential of 300 mV.展开更多
This research elaborates magnetohydrodynamics (MHD) impact on non-Newtonian (Williamson) fluid flow by stretchable rotating disks.Both disks are rotating with different angular velocities and different stretching rate...This research elaborates magnetohydrodynamics (MHD) impact on non-Newtonian (Williamson) fluid flow by stretchable rotating disks.Both disks are rotating with different angular velocities and different stretching rates.Viscous dissipation aspect is considered for energy expression formulation.Entropy generation analysis is described via implementation of thermodynamic second law.Chemical processes (heterogeneous and homogeneous) subjected to entropy generation are introduced first time in literature.Boundary-layer approach is employed for modeling.Apposite variables are introduced for non-dimensionalization of governing systems.Homotopy procedure yields convergence of solutions subjected to computations of highly nonlinear expressions.The significant characteristics of sundry factors against thermal,velocity and solutal fields are described graphically.Besides,tabular results are addressed for engineering quantities (skin-friction coefficient,Nusselt number).The outcomes certify an increment in temperature distribution for Weissenberg (We) and Eckert (Ec) numbers.展开更多
A practical catalytic method to oxidize α-ionone with molecular oxygen using N-hydroxyphthalimide(NHPI)combined with acetylacetone cobatt(Ⅱ)(Co(acac)2)was developed,and the probable catalytic mechanism was proposed....A practical catalytic method to oxidize α-ionone with molecular oxygen using N-hydroxyphthalimide(NHPI)combined with acetylacetone cobatt(Ⅱ)(Co(acac)2)was developed,and the probable catalytic mechanism was proposed.The influences of the reaction conditions on conversion of α-ionone and the selectivity of the major product(5-keto-α-ionone)were investigated,and the technical parameters for 5-keto-α-ionone were optimized.The results show that the primary product is 5-keto-α-ionone,and by-products include epoxy-α-ionone,as well as rearrangement products 4-keto-β-ionone and epoxy-β-ionone,which are characterized by infrared spectra,proton nuclear magnetic resonance spectra,mass spectra and elemental analysis.The selectivity of 5-keto-α-ionone and the conversion of α-ionone are 55.0% and 97.0%,respectively,when 30%(molar fraction)NHPI,1.0%(molar fraction)Co(acac)2 and no solvent are employed under O2 pressure of 1.0 MPa and the reaction temperature of 65℃for 11 h.The procedure shows good reproducibility in the parallel experiments.展开更多
Magneli phase titanium sub-oxide conductive ceramic Tin O2n-1 was used as the support for Pt due to its excellent resistance to electrochemical oxidation, and Pt/Tin O2n-1 composites were prepared by the impregnation-...Magneli phase titanium sub-oxide conductive ceramic Tin O2n-1 was used as the support for Pt due to its excellent resistance to electrochemical oxidation, and Pt/Tin O2n-1 composites were prepared by the impregnation-reduction method. The electrochemical stability of Tin O2n-1 was investigated and the results show almost no change in the redox region after oxidation for 20 h at 1.2 V(vs NHE) in 0.5 mol/L H2SO4 aqueous solution. The catalytic activity and stability of the Pt/Tin O2n-1 toward the oxygen reduction reaction(ORR) in 0.5 mol/L H2SO4 solution were investigated through the accelerated aging tests(AAT), and the morphology of the catalysts before and after the AAT was observed by transmission electron microscopy. At the potential of 0.55 V(vs SCE), the specific kinetic current density of the ORR on the Pt/Tin O2n-1 is about 1.5 times that of the Pt/C. The LSV curves for the Pt/C shift negatively obviously with the half-wave potential shifting about 0.02 V after 8000 cycles AAT, while no obvious change takes place for the LSV curves for the Pt/Tin O2n-1. The Pt particles supported on the carbon aggregate obviously, while the morphology of the Pt supported on Tin O2n-1 remains almost unchanged, which contributes to the electrochemical surface area loss of Pt/C being about 2times that of the Pt/Tin O2n-1. The superior catalytic stability of Pt/Tin O2n-1 toward the ORR could be attributed to the excellent stability of the Tin O2n-1 and the electronic interaction between the metals and the support.展开更多
基金supported by the National Key Research and Development Program of China(2021YFA1500500,2019-YFA0405600)the CAS Project for Young Scientists in Basic Research(YSBR-051)+6 种基金the National Science Fund for Distinguished Young Scholars(21925204)the National Natural Science Foundation of China(22202192,U19A2015,22221003,22250007,22163002)the Collaborative Innovation Program of Hefei Science Center,CAS(2022HSCCIP004)the International Partnership,the DNL Cooperation Fund,CAS(DNL202003)the USTC Research Funds of the Double First-Class Initiative(YD9990002016,YD999000-2014)the Program of Chinese Academy of Sciences(123GJHZ2022101GC)the Fundamental Research Funds for the Central Universities(WK9990000095,WK999000-0124).
文摘Electrocatalytic water splitting provides an efficient method for the production of hydrogen.In electrocatalytic water splitting,the oxygen evolution reaction(OER)involves a kinetically sluggish four-electron transfer process,which limits the efficiency of electrocatalytic water splitting.Therefore,it is urgent to develop highly active OER catalysts to accelerate reaction kinetics.Coupling single atoms and clusters in one system is an innovative approach for developing efficient catalysts that can synergistically optimize the adsorption and configuration of intermediates and improve catalytic activity.However,research in this area is still scarce.Herein,we constructed a heterogeneous single-atom cluster system by anchoring Ir single atoms and Co clusters on the surface of Ni(OH)_(2)nanosheets.Ir single atoms and Co clusters synergistically improved the catalytic activity toward the OER.Specifically,Co_(n)Ir_(1)/Ni(OH)_(2)required an overpotential of 255 mV at a current density of 10 mA·cm^(−2),which was 60 mV and 67 mV lower than those of Co_(n)/Ni(OH)_(2)and Ir1/Ni(OH)_(2),respectively.The turnover frequency of Co_(n)Ir_(1)/Ni(OH)_(2)was 0.49 s^(−1),which was 4.9 times greater than that of Co_(n)/Ni(OH)_(2)at an overpotential of 300 mV.
文摘This research elaborates magnetohydrodynamics (MHD) impact on non-Newtonian (Williamson) fluid flow by stretchable rotating disks.Both disks are rotating with different angular velocities and different stretching rates.Viscous dissipation aspect is considered for energy expression formulation.Entropy generation analysis is described via implementation of thermodynamic second law.Chemical processes (heterogeneous and homogeneous) subjected to entropy generation are introduced first time in literature.Boundary-layer approach is employed for modeling.Apposite variables are introduced for non-dimensionalization of governing systems.Homotopy procedure yields convergence of solutions subjected to computations of highly nonlinear expressions.The significant characteristics of sundry factors against thermal,velocity and solutal fields are described graphically.Besides,tabular results are addressed for engineering quantities (skin-friction coefficient,Nusselt number).The outcomes certify an increment in temperature distribution for Weissenberg (We) and Eckert (Ec) numbers.
基金Project(50573019)supported by the National Natural Science Foundation of China
文摘A practical catalytic method to oxidize α-ionone with molecular oxygen using N-hydroxyphthalimide(NHPI)combined with acetylacetone cobatt(Ⅱ)(Co(acac)2)was developed,and the probable catalytic mechanism was proposed.The influences of the reaction conditions on conversion of α-ionone and the selectivity of the major product(5-keto-α-ionone)were investigated,and the technical parameters for 5-keto-α-ionone were optimized.The results show that the primary product is 5-keto-α-ionone,and by-products include epoxy-α-ionone,as well as rearrangement products 4-keto-β-ionone and epoxy-β-ionone,which are characterized by infrared spectra,proton nuclear magnetic resonance spectra,mass spectra and elemental analysis.The selectivity of 5-keto-α-ionone and the conversion of α-ionone are 55.0% and 97.0%,respectively,when 30%(molar fraction)NHPI,1.0%(molar fraction)Co(acac)2 and no solvent are employed under O2 pressure of 1.0 MPa and the reaction temperature of 65℃for 11 h.The procedure shows good reproducibility in the parallel experiments.
基金Project(21406273)supported by the National Natural Science Foundation of China
文摘Magneli phase titanium sub-oxide conductive ceramic Tin O2n-1 was used as the support for Pt due to its excellent resistance to electrochemical oxidation, and Pt/Tin O2n-1 composites were prepared by the impregnation-reduction method. The electrochemical stability of Tin O2n-1 was investigated and the results show almost no change in the redox region after oxidation for 20 h at 1.2 V(vs NHE) in 0.5 mol/L H2SO4 aqueous solution. The catalytic activity and stability of the Pt/Tin O2n-1 toward the oxygen reduction reaction(ORR) in 0.5 mol/L H2SO4 solution were investigated through the accelerated aging tests(AAT), and the morphology of the catalysts before and after the AAT was observed by transmission electron microscopy. At the potential of 0.55 V(vs SCE), the specific kinetic current density of the ORR on the Pt/Tin O2n-1 is about 1.5 times that of the Pt/C. The LSV curves for the Pt/C shift negatively obviously with the half-wave potential shifting about 0.02 V after 8000 cycles AAT, while no obvious change takes place for the LSV curves for the Pt/Tin O2n-1. The Pt particles supported on the carbon aggregate obviously, while the morphology of the Pt supported on Tin O2n-1 remains almost unchanged, which contributes to the electrochemical surface area loss of Pt/C being about 2times that of the Pt/Tin O2n-1. The superior catalytic stability of Pt/Tin O2n-1 toward the ORR could be attributed to the excellent stability of the Tin O2n-1 and the electronic interaction between the metals and the support.
