Trifunctional Single-Atomic Ru Sites Enable Efficient Overall Water Splitting and Oxygen Reduction in Acidic Media

被引:182
作者
Peng, Xianyun [1 ,2 ]
Zhao, Shunzheng [3 ]
Mi, Yuying [1 ,2 ]
Han, Lili [4 ]
Liu, Xijun [1 ,2 ]
Qi, Defeng [1 ,2 ]
Sun, Jiaqiang [5 ]
Liu, Yifan [6 ]
Bao, Haihong [1 ,2 ]
Zhuo, Longchao [7 ]
Xin, Huolin L. [4 ]
Luo, Jun [1 ,2 ]
Sun, Xiaoming [8 ]
机构
[1] Tianjin Univ Technol, Ctr Electron Microscopy, Tianjin 300384, Peoples R China
[2] Tianjin Univ Technol, Sch Mat Sci & Engn, Inst New Energy Mat & Low Carbon Technol, Tianjin Key Lab Adv Funct Porous Mat, Tianjin 300384, Peoples R China
[3] Univ Sci & Technol Beijing, Dept Environm Engn, Beijing 100083, Peoples R China
[4] Univ Calif Irvine, Dept Phys & Astron, Irvine, CA 92697 USA
[5] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
[6] Shenzhen Univ, Minist Educ & Guangdong Prov, Key Lab Optoelect Devices & Syst, Shenzhen 518060, Peoples R China
[7] Xian Univ Technol, Sch Mat Sci & Engn, Xian 710048, Peoples R China
[8] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
acidic environment; overall water splitting; oxygen reduction; single-atomic Ru sites; trifunctional catalysts; HYDROGEN EVOLUTION; FUEL-CELLS; METAL-FREE; FE SITES; ELECTROCATALYSTS; ELECTRODE; CATALYST; OXIDATION; GRAPHENE;
D O I
10.1002/smll.202002888
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of cost-effective, active trifunctional catalysts for acidic oxygen reduction (ORR) as well as hydrogen and oxygen evolution reactions (HER and OER, respectively) is highly desirable, albeit challenging. Herein, single-atomic Ru sites anchored onto Ti(3)C(2)T(x)MXene nanosheets are first reported to serve as trifunctional electrocatalysts for simultaneously catalyzing acidic HER, OER, and ORR. A half-wave potential of 0.80 V for ORR and small overpotentials of 290 and 70 mV for OER and HER, respectively, at 10 mA cm(-2)are achieved. Hence, a low cell voltage of 1.56 V is required for the acidic overall water splitting. The maximum power density of an H-2-O(2)fuel cell using the as-prepared catalyst can reach as high as 941 mW cm(-2). Theoretical calculations reveal that isolated Ru-O(2)sites can effectively optimize the adsorption of reactants/intermediates and lower the energy barriers for the potential-determining steps, thereby accelerating the HER, ORR, and OER kinetics.
引用
收藏
页数:10
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