典型文献
Activating multisite high-entropy alloy nanocrystals via enriching M-pyridinic N-C bonds for superior electrocatalytic hydrogen evolution
文献摘要:
The activation of multisite high-entropy alloy(HEA)electrocatalysts is helpful for improving the atomic utilization of each metal in water electrolysis catalysis.Herein,well-dispersed HEA nanocrystals on N-rich graphene with abundant M-pyridinic N-C bonds were synthesized through an ultrasonic-assisted confinement synthesis method.Operando Raman analysis and density functional theory calculations revealed that the electrocatalysts presented the optimal electronic rearrangement with fast rate-determined H2O dissociation kinetics and favorable H* adsorption behavior that greatly enhanced hydro-gen generation in alkaline electrolyte.A small overpotential of only 138.6 mV was required to obtain the current density of 100 mA cm-2 and the Tafel slope of as low as 33.0 mV dec-1,which was considerably smaller than the overpotentials of the counterpart with poor M-pyridinic N-C bonds(290.4 mV)and commercial Pt/C electrocatalysts(168.6 mV).The atomic structure,coordination environment,and elec-tronic structure were clarified.This work provides a new avenue toward activating HEA as advanced elec-trocatalysts and promotes the research on HEA for energy-related electrolysis.
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作者姓名:
Jingyu Wang;Jiahao Zhang;Yanjie Hu;Hao Jiang;Chunzhong Li
作者机构:
Key Laboratory for Ultrafine Materials of Ministry of Education,Frontiers Science Center for Materiobiology and Dynamic Chemistry,School of Materials Science and Engineering,East China University of Science and Technology,Shanghai 200237,China;Shanghai Engineering Research Center of Hierarchical Nanomaterials,School of Chemical Engineering,East China University of Science and Technology,Shanghai 200237,China
文献出处:
引用格式:
[1]Jingyu Wang;Jiahao Zhang;Yanjie Hu;Hao Jiang;Chunzhong Li-.Activating multisite high-entropy alloy nanocrystals via enriching M-pyridinic N-C bonds for superior electrocatalytic hydrogen evolution)[J].科学通报(英文版),2022(18):1890-1897
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0.642489
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