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羟基辅助的氢溢流作用于Ru-MoTiC以实现高效碱性析氢反应。

HO assisted hydrogen spillover over Ru-MoTiC for efficient alkaline hydrogen evolution.

作者信息

Liu Xiaojing, Xie Fangxia, Xi Qing, Wang Yawen, Wang Yunfang, Li Houfen, Li Rui, Fan Caimei, Liu Jianxin, Wang Jiancheng

机构信息

Shanxi Key Laboratory of Complex Air Pollution Control and Carbon Reduction, College of Environmental and Ecology, Taiyuan University of Technology, Taiyuan 030024, PR China; Key Laboratory of Coal Science and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, PR China.

Shanxi Key Laboratory of Complex Air Pollution Control and Carbon Reduction, College of Environmental and Ecology, Taiyuan University of Technology, Taiyuan 030024, PR China; Key Laboratory of Coal Science and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, PR China.

出版信息

J Colloid Interface Sci. 2025 Sep 15;694:137738. doi: 10.1016/j.jcis.2025.137738. Epub 2025 Apr 28.

Abstract

The limited supply capacity and high transport kinetic energy barrier of H* hinder the implementation of the alkaline hydrogen evolution reaction (HER). Constructing an HO environment can effectively enhance the concentration and diffusion kinetics of H*, thereby alleviating the associated limiting factors. Here we report a novel Ru nanoclusters supported by 2D MoTiC nanosheets (Ru-MoTiC) as an effective HER electrocatalyst in alkaline environments. Results indicate that H* is rapidly generated at the Ru site due to the efficient water dissociation capability of Ru-MoTiC, subsequently combining with water molecules to form HO. HO then rapidly diffuses to the -O group on MXene, which can release H* and act as active sites for H evolution, facilitated by the lower migration energy barrier of HO. This strategy simultaneously enhances both the supply and transfer of H*, facilitating synergistic catalysis between Ru and MXene. Consequently, Ru-MoTiC exhibits an overpotential of 47 mV at 10 mA cm, lower than that observed in acidic media (108 mV). This paper introduces a new approach for the development of catalytic materials aimed at achieving efficient and pH-universal electrochemical H evolution.

摘要

H* 的有限供应能力和高传输动能势垒阻碍了碱性析氢反应(HER)的实施。构建一个HO环境可以有效地提高H的浓度和扩散动力学,从而缓解相关的限制因素。在此,我们报道了一种由二维MoTiC纳米片负载的新型Ru纳米团簇(Ru-MoTiC),作为碱性环境中一种有效的HER电催化剂。结果表明,由于Ru-MoTiC具有高效的水离解能力,H在Ru位点迅速生成,随后与水分子结合形成HO。然后,HO迅速扩散到MXene上的-O基团,该基团可以释放H并作为析氢的活性位点,这得益于HO较低的迁移能垒。该策略同时增强了H的供应和转移,促进了Ru和MXene之间的协同催化。因此,Ru-MoTiC在10 mA cm时的过电位为47 mV,低于在酸性介质中观察到的过电位(108 mV)。本文介绍了一种开发催化材料的新方法,旨在实现高效且pH通用的电化学析氢。

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