析氧
分解水
制氢
催化作用
电导率
无机化学
化学
循环伏安法
电化学
化学工程
氧气
氧化还原
材料科学
物理化学
电极
有机化学
工程类
光催化
作者
Kahyun Ham,Jaewon Lee,Ki-Young Lee,Jae-Young Lee
标识
DOI:10.1016/j.jechem.2022.04.034
摘要
Electrochemical water splitting is one of the most reliable approaches for environmental-friendly hydrogen production. Because of their stability and abundance, Mn-based materials have been studied as electrocatalysts for the oxygen evolution reaction (OER), which is a more sluggish reaction in the water splitting system. To increase the OER activity of Mn, it is imperative to facilitate the structural change of Mn oxide to the active phase with Mn3+ species, known as the active site. Here, we present the relationship between the electronic conductivity in the catalyst layer and the formation of the Mn active phase, δ-MnO2, from wrinkled Mn(OH)2. Mn(OH)2 has poor conductivity, and it disrupts the oxidation reaction toward MnOOH or δ-MnO2. Adjacent conductive carbon to Mn(OH)2 enabled Mn(OH)2 to be oxidized to δ-MnO2. Furthermore, after repetitive cyclic voltammetry activation, the more conductive environment resulted in a higher density of δ-MnO2 through the irreversible phase transition, and thus it contributes to the improvement of the OER activity.
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