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作 者:Fengjun Yin Hong Liu
机构地区:[1]Chongqing Institute of Green and Intelligent Technology,Chinese Academy of Sciences,Chongqing 400714,China [2]Key Laboratory of Reservoir Aquatic Environment,Chinese Academy of Sciences,Chongqing 400714,China [3]University of Chinese Academy of Sciences,Beijing 100049,China
出 处:《Journal of Energy Chemistry》2020年第11期339-343,共5页能源化学(英文版)
基 金:the National Natural Science Foundation of China(51525805,51727812,51808526)。
摘 要:For aqueous interfacial reactions involving H+and OH-, the interfacial pH varies dynamically during the reaction process, which is a key factor determining the reaction performance. Herein, the kinetic relevance between the interfacial pH and reaction rate is deciphered owing to the success in establishing the transport equations of H+/OH- in unbuffered solutions, and is charted as a current(j)–pH diagram in the form of an electrochemical response. The as-described j–pH interplay is experimentally verified by the oxygen reduction and hydrogen evolution reactions. This diagram serves to form a panoramic graphic view of pH function working on the interfacial reactions in conjunction with the Pourbaix’s potential–pH diagram, and particularly enables a kinetic understanding of the transport effect of H+and OH-on the reaction rate and valuable instruction toward associated pH control and buffering manipulation.
关 键 词:j–pH diagram Interfacial reaction pH gradient H^+and OH^-transports Electrode reaction
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