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耦合的MoO@CoP异质结构作为一种在高电流密度下用于析氢的pH通用电极。

Coupled MoO@CoP heterostructure as a pH-universal electrode for hydrogen generation at a high current density.

作者信息

Chen Pengzuo, Li Kaixun, Ye Yutong, Wu Doufeng, Tong Yun

机构信息

Department of Chemistry, Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, Zhejiang Sci-Tech University, Hangzhou 310018, China.

出版信息

Dalton Trans. 2023 Feb 21;52(8):2262-2271. doi: 10.1039/d2dt03551k.

Abstract

Developing high-performance and low-cost self-supporting electrodes as pH-universal electrocatalysts for the hydrogen-evolution reaction (HER) and realizing high-quality hydrogen production at a high current density are highly desirable, but are hugely challenging. We created a self-supporting electrode with a coupled hierarchical heterostructure by simple electrodeposition followed by sulfurization. It comprised oxygen-deficient molybdenum oxide (MoO) and cobalt phosphide (CoP) on nickel foam (NF), which represented a highly active pH-universal electrocatalyst for the HER at a high current density. Benefiting from a plethora of catalytic active sites, improved interfacial charge transfer, and strong electronic interaction, this type of MoO@CoP/NF electrode delivered a superior catalytic performance. Overpotentials of only 100 mV, 135 mV, and 400 mV were needed to realize a high current density of 1 A cm in alkaline, acid and neutral media, respectively, which were superior to those of most other well-developed materials based on non-noble metals. Our experimental work demonstrates the synergistic advantages of a MoO@CoP heterostructure for improving the intrinsic catalytic performance but also paves a new path for the rational design of advanced electrodes for hydrogen generation in a wide range of pH conditions.

摘要

开发高性能、低成本的自支撑电极作为析氢反应(HER)的pH通用电催化剂,并在高电流密度下实现高质量产氢是非常理想的,但极具挑战性。我们通过简单的电沉积然后硫化制备了一种具有耦合分级异质结构的自支撑电极。它由泡沫镍(NF)上的缺氧氧化钼(MoO)和磷化钴(CoP)组成,是一种在高电流密度下对HER具有高活性的pH通用电催化剂。得益于大量的催化活性位点、改善的界面电荷转移和强电子相互作用,这种类型的MoO@CoP/NF电极表现出优异的催化性能。在碱性、酸性和中性介质中,分别仅需100 mV、135 mV和400 mV的过电位即可实现1 A cm的高电流密度,这优于大多数其他基于非贵金属的先进材料。我们的实验工作证明了MoO@CoP异质结构在提高本征催化性能方面的协同优势,也为在广泛的pH条件下合理设计用于制氢的先进电极开辟了一条新途径。

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