过电位
析氧
电催化剂
电化学
分解水
催化作用
无机化学
电解质
X射线光电子能谱
化学
锰
阳极
电极
化学工程
材料科学
冶金
物理化学
工程类
光催化
生物化学
作者
Iranna Udachyan,Jayesh T. Bhanushali,Amir Mizrahi,Tomer Zidki,Dan Meyerstein
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2022-11-07
卷期号:5 (11): 13903-13912
被引量:8
标识
DOI:10.1021/acsaem.2c02543
摘要
With the growing population and energy demand, there is an urgent need for the production and storage of clean energy obtained from renewable resources. Water splitting electrocatalytically is a major approach to obtain clean H2. The efficiency, stability, and slow kinetics of anode materials developed so far do not fit the commercial application of the water oxidation reaction. To develop an efficient energy conversion catalyst, particularly for the oxygen evolution reaction (OER) herewith, Mn2(CO3)3 was electrodeposited on a Ni foam (NF) electrode surface by the chronoamperometric technique. The deposited Mn2(CO3)3/NF was characterized using various surface characterization techniques. The electrochemical behavior of the Mn2(CO3)3/NF-deposited electrode toward the OER was studied using electrochemical methods in KOH (pH 14) and NaHCO3 (pH 8.3) electrolytes. The Mn2(CO3)3/NF electrode showed a lower overpotential than CO3/NF and NF electrodes in the KOH/NaHCO3 media. The Mn2(CO3)3/NF electrode performs high electrocatalytic water oxidation with an overpotential of 360 mV at a current density of 10 mA·cm–2. This overpotential is much lower than those of CO3/NF (460 mV) and bare NF (520 mV), with good long-term stability in the KOH medium without any catalytic degradation after 100 CV cycles and 15 h chronoamperometric studies. The stability of the electrodeposited Mn2(CO3)3 on the NF electrode was determined by X-ray photoelectron spectroscopy. Thus, the Mn2(CO3)3/NF catalyst is suitable for the oxygen evolution reaction.
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