MXenes公司
析氧
催化作用
电化学
钴
材料科学
化学工程
电解
电解水
分解水
过渡金属
纳米颗粒
无机化学
法拉第效率
化学
电极
纳米技术
物理化学
电解质
有机化学
光催化
工程类
作者
Young Sang Park,Ari Chae,Gwan Hyun Choi,Swetarekha Ram,Seung‐Cheol Lee,Satadeep Bhattacharjee,Jiyoon Jung,Hyo Sang Jeon,Cheol‐Hee Ahn,Seung Sang Hwang,Dong‐Yeun Koh,Insik In,Taegon Oh,Seon Joon Kim,Chong Min Koo,Albert S. Lee
标识
DOI:10.1016/j.apcatb.2024.123731
摘要
The role of 2D transition metal carbides, also known as MXenes, as active catalyst supports in Co-based oxygen evolution reaction (OER) catalysts was elucidated through a combination of experimental and computation electrochemistry. Through facile seeding of commericial Co nanoparticles on three different MXene supports (Ti3C2Tx, Mo2Ti2C3Tx, Mo2CTx), Co@MXene catalysts were prepared and their electrochemical properties examined for alkaline OER electrocatalysts. The OER activity enhancement of Co was significantly improved for Mo2CTx and Mo2Ti2C3Tx supports, but marginal on the Ti3C2Tx in rotating disk electrode and membrane electrode assembly tests. The Co@Mo2CTx exhibited the highest anion exchange water electrolysis performance of 2.11 A cm-2 at 1.8 V with over 700 hours of stable performance, exceeding previous benchmarks for non-platinum group (non-PGM) metal OER catalysts. The superior performance was attributed to the strong chemical interaction of Co nanoparticle with the Mo2CTx MXene support. Insights into the electrochemical and chemical oxidation according to MXene type as related to cell durability, as well the effect of electrical conductivity and inherent boosting of electrocatalytic activity of Mo-based MXenes elucidated through density functional theory (DFT) calculations helped explain the performance and durabilty enhancement of Mo-based MXene supports over Ti3C2Tx supports.
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