过电位
析氧
材料科学
分解水
催化作用
阳极
非阻塞I/O
电解
氧化物
阴极
交换电流密度
镍
氧化镍
化学工程
无机化学
电化学
电极
冶金
化学
物理化学
塔菲尔方程
生物化学
光催化
工程类
电解质
作者
Deok‐Hye Park,Min‐Ha Kim,Hak‐Joo Lee,Woo‐Jun Lee,Jeong‐Hyeon Byeon,Ji‐Hwan Kim,Jae‐Sung Jang,Kyung‐Won Park
标识
DOI:10.1002/admi.202102063
摘要
Abstract In water splitting, anode catalysts for the oxygen evolution reaction (OER), which is the rate‐determining step, are more critical than cathode catalysts. Herein, the authors prepare Ni‐IrO x composite catalysts consisting of NiO and IrO 2 for the OER by a solid‐state reaction with different ratios of NiO to IrO 2 and reaction temperatures. In particular, Ni‐IrO x ‐400 with a molar ratio of NiO/IrO 2 = 1:1 heated at 400 ° C shows the best OER performance. In the overall water splitting test using an anion exchange membrane (AEM) water electrolyzer, the single cell with Ni‐IrO x ‐400 as the anode catalyst shows current densities of 1454.8 mA cm −2 , respectively, measured at 1.8 V. Furthermore, the stability tests of the AEM single cells are carried out at 50 ° C under a constant current density of 500 mA cm −2 . The single cell with Ni‐IrO x ‐400 shows only a slight increase in the overpotential (rate: 2.0 mV h −1 ) for 100 h owing to the enhanced stability of Ni‐IrO x ‐400 compared to IrO 2 (12.5 mV h −1 ). The improved OER performance of the Ni‐IrO x ‐400 may be attributed to a composite structure that can prevent particle agglomeration and thus preserve the active sites during the OER.
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