Charge-enriched RuO2 nanoparticles decorating TiO2 with Ti defects to promote oxygen evolution reaction in acidic media

被引:8
|
作者
Wang, Ye [1 ]
Hao, Yixin [1 ]
Wang, Luqi [1 ]
Li, Chunsheng [2 ,3 ]
Ren, Jianwei [4 ]
Sun, Yan [2 ,3 ]
Hu, Feng [1 ]
Li, Linlin [1 ]
Peng, Shengjie [1 ]
机构
[1] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Peoples R China
[2] Suzhou Univ Sci & Technol, Sch Chem & Life Sci, Suzhou 215009, Jiangsu, Peoples R China
[3] Suzhou Univ Sci & Technol, Key Lab Adv Electrode Mat Novel Solar Cells Petr &, Suzhou 215009, Jiangsu, Peoples R China
[4] Univ Johannesburg, Dept Mech Engn Sci, Cnr Kingsway & Univ Rd, ZA-2092 Johannesburg, South Africa
基金
中国国家自然科学基金;
关键词
WATER OXIDATION; ELECTROCATALYSTS; REDOX; ABUNDANT; OXIDE;
D O I
10.1039/d3qi01203d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Dispersing precious metal oxide nanoparticles on a support is a promising catalyst modification strategy for the oxygen evolution reaction in acidic media, but the rational design of the heterointerface remains challenging. Herein, electron-rich ruthenium dioxide dispersed on the metal-deficient TiO2 is constructed as an efficient electrocatalyst for oxygen evolution. The combination with defective support triggers the charge transfer from the support to RuO2, which optimizes the adsorption/desorption of oxo-intermediates and thus improves the kinetics of the OER reaction. Moreover, the large electron filling in the support, as an auxiliary, accelerates the deprotonation of oxo-intermediates during the acidic OER. As a result, the improved d-TiO2/RuO2 showed excellent OER activity, with an overpotential of 226 mV @10 mA cm(-2) in 0.5 M H2SO4, which was superior to that of commercial RuO2. This study provides an ideal defective support for unique heterojunction catalysts and highlights the development of noble metal catalysts with low cost.
引用
收藏
页码:6015 / 6022
页数:8
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