High temperature shock synthesis of superfine Ru nanoparticles anchored on TiO2 @nitrogen-doped carbon for pH-universal hydrogen evolution reaction

被引:7
作者
Cai, Jinxiu [1 ]
Zong, Lingbo [1 ]
Fan, Kaicai [2 ]
Song, Fuxiang [1 ]
Gao, Jianyang [3 ]
Wang, Zumin [4 ]
Chen, Yanan [5 ]
Wang, Lei [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Key Lab Ecochem Engn, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, 1 North 2nd St,Zhongguancun,Haidian Dist, Beijing 100190, Peoples R China
[5] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
High temperature thermal shock; Ru nanoparticle; Hydrogen evolution reaction; pH-universal; EFFICIENT;
D O I
10.1016/j.jallcom.2023.172279
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Due to energy crisis and environmental pollution, it is urgent to develop efficient and cheap catalysts for hydrogen production from water electrolysis. As a cheaper platinum group metal, Ru, a cheaper platinum group metal, is a highly competitive candidate to Pt because of the similar bond energy of M-H. Herein, TiO2 @nitrogen-doped carbon composite supported superfine Ru nanoparticles was synthesized by high temperature shock in a Joule furnace using Ti-MOF support (Ru/TiO2 @NC-J). In the extremely rapid process, MOF was quickly converted into highly conductive nitrogen-doped carbon with tiny TiO2 dispersed in it, and superfine Ru nanoparticles were generated simultaneously in less than 0.5 s. The obtained Ru/TiO2 @NC-J displays wonderful HER performance in the wide pH range. In 1.0 M KOH solution, the overpotential was as low as 11 mV at 10 mA cm(-2) and a Tafel slope was 39.2 mV dec(-1), which far exceeded the activity of Pt/C and conventional calcined samples as well as most of the recently reported catalysts. The as-developed electrocatalysts also showed excellent stability to accommodate large working current for long term test without obvious activity loss in universal pH range. Experimental investigations suggest that the strong metal-support interaction dominantly facilitate the activity of electrocatalytic hydrogen evolution reaction (HER), and stability of Ru/TiO2 @NC-J. This strategy provides a new and super-fast methodology to prepare low-budget and high-performance HER catalysts for practical applications.
引用
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页数:9
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