过电位
电解
双功能
制氢
尿素
阳极
分解水
化学
无机化学
普鲁士蓝
电解水
碱性水电解
催化作用
电催化剂
析氧
材料科学
化学工程
电极
电化学
有机化学
物理化学
工程类
光催化
电解质
作者
Thangjam Ibomcha Singh,G. Rajeshkhanna,Soram Bobby Singh,Tolendra Kshetri,Nam Hoon Kim,Joong Hee Lee
出处
期刊:Chemsuschem
[Wiley]
日期:2019-10-15
卷期号:12 (21): 4810-4823
被引量:79
标识
DOI:10.1002/cssc.201902232
摘要
Hollow-structured Fex Co2-x P, Fex Co3-x O4 , and Prussian blue analogue (FeCo-PBA) microbuilding arrays on Ni foam (NF) are derived from Co-based metal-organic frameworks (Co-MOF) using a simple room temperature and post-heat-treatment route. Among them, Fex Co2-x P/NF shows excellent bifunctional catalytic activities by demonstrating very low oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) overpotentials of 255/114 mV at a current density of 20/10 mA cm-2 respectively, whereas Fex Co3-x O4 /NF and FeCo-PBA/NF demand higher overpotentials. Remarkably, for water electrolysis, Fex Co2-x P/NF requires only 1.61 V to obtain 10 mA cm-2 . In contrast to water electrolysis, urea electrolysis reduces overpotential and simultaneously purifies the urea-rich wastewater. The urea oxidation reaction at the Fex Co2-x P/NF anode needs just 1.345 V to achieve 20 mA cm-2 , which is 140 mV less than the 1.48 V potential required for OER. Moreover, the generation of H2 through urea electrolysis needs only 1.42 V to drive 10 mA cm-2 .
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