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铂表面对溶液中离子的特殊响应的机理研究
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作者 邢宝忠 翁筠蓉 高鸿 《齐齐哈尔轻工业学院学报》 1992年第4期49-56,共8页
本文对经适当处理的Pt表面的电位对溶液中阳离子浓度的突变随时间呈峰形变化的机理进行了讨论。
关键词 pt表面结构 机理研究 离子交换
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Restructuring of well-defined Pt-based electrode surfaces under mild electrochemical conditions
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作者 Jie Wei Wei Chen +2 位作者 Da Zhou Jun Cai Yan-Xia Chen 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第11期2792-2801,共10页
Since the 1980s,single-crystal Pt electrodes with well-defined surface structures have been deemed stable under mild electrochemical conditions(e.g.,in the potential region of electric double layers,underpotential dep... Since the 1980s,single-crystal Pt electrodes with well-defined surface structures have been deemed stable under mild electrochemical conditions(e.g.,in the potential region of electric double layers,underpotential deposition of hydrogen,or mild hydrogen evolution/OH adsorption)and have served as model electrodes for unraveling the structure-performance relation in electrocatalysis.With the advancement of in situ electrochemical microscopy/spectroscopy techniques,subtle surface restructuring under mild electrochemical conditions has been achieved in the last decade.Surface restructuring can considerably modify electrocatalytic properties by generating/destroying highly active sites,thereby interfering with the deduction of the structure-performance relation.In this review,we summarize recent progress in the restructuring of well-defined Pt(-based)electrode surfaces under mild electrochemical conditions.The importance of the meticulous structural characterization of Pt electrodes before,during,and after electrochemical measurements is demonstrated using CO adsorption/oxidation,hydrogen adsorption/evolution,and oxygen reduction as examples.The implications of present findings for correctly identifying the reaction mechanisms and kinetics of other electrocatalytic systems are also briefly discussed. 展开更多
关键词 Surface restructuring Well-defined pt electrode surface Structure-performance relation In situ/operando electrochemical characterization ELECTROCATALYSIS
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