Ru nanoparticles supported on partially reduced TiO2 as highly efficient catalyst for hydrogen evolution

被引:63
|
作者
Chen, Li-Na [1 ]
Wang, Su-Heng [1 ]
Zhang, Peng-Yang [1 ]
Chen, Zhi-Xin [1 ]
Lin, Xiao [2 ]
Yang, Hui-Juan [3 ]
Sheng, Tian [4 ]
Lin, Wen-Feng [5 ]
Tian, Na [1 ]
Sun, Shi-Gang [1 ]
Zhou, Zhi-You [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Collaborat Innovat Ctr Chem Energy Mat, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB3 0AS, England
[3] Xian Univ Technol, Inst Adv Elect Energy, Sch Mat Sci & Engn, Xian 710048, Peoples R China
[4] Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
[5] Loughborough Univ, Dept Chem Engn, Loughborough LE11 3TU, Leics, England
基金
英国工程与自然科学研究理事会;
关键词
Hydrogen evolution; Ru-based Electrocatalyst; Oxygen vacancy; Reduced TiO2; Interfacial structure; PLATINUM; SURFACE; ELECTROCATALYSTS; PERFORMANCE; OXIDATION; DURABILITY; CHEMISTRY; METALS; OXIDE;
D O I
10.1016/j.nanoen.2021.106211
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
The development of low-cost yet highly efficient catalysts for hydrogen evolution reaction (HER) is crucial for large-scale clean and sustainable hydrogen production from water splitting. Tuning the interfacial structure of catalyst has emerged as an effective strategy to optimize the intrinsic catalytic activity. In this study, we demonstrated the deposition of Ru nanoparticles by freshly prepared strong reductive Ti(III) oxide, resulting in Ru/reduced TiO2 interface with oxygen vacancies. The as-prepared Ru/r-TiO2 exhibited a superior HER performance over commercial Pt/C in alkaline media, with only a small overpotential of 15 mV required to deliver the benchmark current density of 10 mA cm(-2) and a high turnover frequency of 8.74 s(-1) achieved at an overpotential of 100 mV. Density functional theory calculation indicates that high electrocatalytic activity of Ru/r-TiO2 is originated from the promotion of water dissociation and weakening OH adsorption by reduced TiO2 , which facilitate the conversion of water to H-2. This work provides an efficient strategy for the design of high-performance HER catalysts.
引用
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页数:10
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