Single-site Pt-doped RuO2 hollow nanospheres with interstitial C for high-performance acidic overall water splitting

被引:224
|
作者
Wang, Juan [1 ,2 ]
Yang, Hao [3 ]
Li, Fan [4 ]
Li, Leigang [1 ]
Wu, Jianbo [4 ,5 ,6 ]
Liu, Shangheng [1 ]
Cheng, Tao [3 ]
Xu, Yong [7 ]
Shao, Qi [3 ]
Huang, Xiaoqing [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Wenzhou Univ, Coll Chem & Mat Engn, Key Lab Carbon Mat Zhejiang Prov, Wenzhou 325035, Peoples R China
[3] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Jiangsu, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[5] Shanghai Jiao Tong Univ, Ctr Hydrogen Sci, Shanghai 200240, Peoples R China
[6] Shanghai Jiao Tong Univ, Future Mat Innovat Ctr, Zhangjiang Inst Adv Study, Shanghai 200240, Peoples R China
[7] Guangdong Univ Technol, Collaborat Innovat Ctr Adv Energy Mat, Sch Mat & Energy, Guangzhou Key Lab Low Dimens Mat & Energy Storage, Guangzhou 510006, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 中国博士后科学基金;
关键词
HYDROGEN EVOLUTION REACTION; OXYGEN EVOLUTION; BIFUNCTIONAL ELECTROCATALYSTS; EFFICIENT; NANOPARTICLES; CATALYSTS; REDUCTION; GRAPHENE; DESIGN;
D O I
10.1126/sciadv.abl9271
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Realizing stable and efficient overall water splitting is highly desirable for sustainable and efficient hydrogen production yet challenging because of the rapid deactivation of electrocatalysts during the acidic oxygen evolution process. Here, we report that the single-site Pt-doped RuO2 hollow nanospheres (SS Pt-RuO2 HNSs) with interstitial C can serve as highly active and stable electrocatalysts for overall water splitting in 0.5 M H2SO4. The performance toward overall water splitting have surpassed most of the reported catalysts. Impressively, the SS Pt-RuO2 HNSs exhibit promising stability in polymer electrolyte membrane electrolyzer at 100 mA cm(-2) during continuous operation for 100 hours. Detailed experiments reveal that the interstitial C can elongate Ru-O and Pt-O bonds, and the presence of SS Pt can readily vary the electronic properties of RuO2 and improve the OER activity by reducing the energy barriers and enhancing the dissociation energy of *O species.
引用
收藏
页数:11
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