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Activating multisite high-entropy alloy nanocrystals via enriching M–pyridinic N–C bonds for superior electrocatalytic hydrogen evolution

Activating multisite high-entropy alloy nanocrystals via enriching M–pyridinic N–C bonds for superior electrocatalytic hydrogen evolution

作     者:Jingyu Wang Jiahao Zhang Yanjie Hu Hao Jiang Chunzhong Li 王靖毓;张家豪;胡彦杰;江浩;李春忠

作者机构:Key Laboratory for Ultrafine Materials of Ministry of EducationFrontiers Science Center for Materiobiology and Dynamic ChemistrySchool of Materials Science and EngineeringEast China University of Science and TechnologyShanghai 200237China Shanghai Engineering Research Center of Hierarchical NanomaterialsSchool of Chemical EngineeringEast China University of Science and TechnologyShanghai 200237China 

基  金:supported by the National Natural Science Foundation of China(21838003,51621002) the Innovation Program of Shanghai Municipal Education Commission the Fundamental Research Funds for the Central Universities 

出 版 物:《Science Bulletin》 (科学通报(英文版))

年 卷 期:2022年第67卷第18期

页      码:1890-1897,M0004页

摘      要:The activation of multisite high-entropy alloy(HEA)electrocatalysts is helpful for improving the atomic utilization of each metal in water electrolysis ***,well-dispersed HEA nanocrystals on Nrich graphene with abundant M–pyridinic N–C bonds were synthesized through an ultrasonic-assisted confinement synthesis *** Raman analysis and density functional theory calculations revealed that the electrocatalysts presented the optimal electronic rearrangement with fast ratedetermined H_(2)O dissociation kinetics and favorable H^(*)adsorption behavior that greatly enhanced hydrogen 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 electronic structure were *** work provides a new avenue toward activating HEA as advanced electrocatalysts and promotes the research on HEA for energy-related electrolysis.

主 题 词:Electrocatalyst Hydrogen evolution reaction High-entropy alloy M–pyridinic N–C Water splitting 

学科分类:081702[081702] 081705[081705] 07[理学] 070205[070205] 08[工学] 0817[工学-轻工类] 080501[080501] 080502[080502] 0805[工学-能源动力学] 0702[理学-物理学类] 

核心收录:

D O I:10.1016/j.scib.2022.08.022

馆 藏 号:203114468...

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