过电位
分解水
阳极
析氧
材料科学
钙钛矿(结构)
电流密度
碱性水电解
电解
化学工程
阴极
交换电流密度
电解水
无机化学
电极
纳米技术
催化作用
化学
电化学
物理化学
工程类
物理
塔菲尔方程
生物化学
电解质
光催化
量子力学
作者
Jiayi Tang,Xiaomin Xu,Tony P. Tang,Yijun Zhong,Zongping Shao
标识
DOI:10.1002/smtd.202201099
摘要
Abstract Development of cost‐effective water splitting technology that allows low‐overpotential operation at high current density with non‐precious catalysts is the key for large‐scale hydrogen production. Herein, it is demonstrated that the versatile perovskite‐based oxides, usually applied for operating at low current density and room temperature in alkaline solution, can be developed into low‐cost, highly active and durable electrocatalysts for operating at high current densities in a zero‐gap anion exchange membrane electrolyzer cell (AEMEC). The composite perovskite with mixed phases of Ruddlesden–Popper and single perovskite is applied as the anode in AEMEC and exhibits highly promising performance with an overall water‐splitting current density of 2.01 A cm −2 at a cell voltage of only 2.00 V at 60 °C with stable performance. The elevated temperature to promote anion diffusion in membrane boosts oxygen evolution kinetics by enhancing lattice‐oxygen participation. The bifunctionality of perovskites further promises the more cost‐effective symmetrical AEMEC configuration, and a primary cell with the composite perovskite as both electrodes delivers 3.00 A cm −2 at a cell voltage of only 2.42 V. This work greatly expands the use of perovskites as robust electrocatalysts for industrial water splitting at high current density with great practical application merit.
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