电化学
润湿
气体扩散电极
质子交换膜燃料电池
化学
电解质
电极
扩散
纳米技术
电催化剂
化学工程
电化学电池
催化作用
无机化学
材料科学
有机化学
物理化学
热力学
工程类
物理
作者
Jingwen Wang,Chaolin Li,Muhammad Rauf,Wenhui Wang
标识
DOI:10.1021/acssuschemeng.2c06492
摘要
Efficient electrochemical synthesis of H2O2 via a two-electron oxygen reduction reaction (2e–-ORR) has been intensively pursued in the past few years, yet its potential application is still challenging due to the slow transportation of gaseous reactants and numerous competitive reactions in the electrolytic cell. Herein, we report that efficient electrochemical production of H2O2 can be achieved via tuning the wettability of the gas diffusion electrode (GDE) to the Wenzel–Cassie coexistence state (WCS) and controlling the electrochemical reaction pathway using a proton exchange membrane (PEM) divided cell. By tuning the wettability, the electrogeneration of H2O2 reached to 1326 mM with 59% current efficiency after 120 min. It is revealed that the reaction pathway for 2e–-ORR can be controlled by manipulating the crossover or diffusion of the ions or intermediate reactants via different membranes, and the electrogeneration of H2O2 is about 10 times higher in the PEM-divided cell compared to that in the undivided cell. These findings highlight the importance of GDE surface wettability and the reaction pathway for electrochemical synthesis of H2O2, paving an alternative way to develop efficient electrochemical synthesis systems.
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