A strongly coupled Ru-CrOx cluster-cluster heterostructure for efficient alkaline hydrogen electrocatalysis

被引:103
|
作者
Zhang, Bingxing [1 ,2 ]
Wang, Jianmei [1 ]
Liu, Guimei [2 ]
Weiss, Catherine M. [3 ]
Liu, Danqing [1 ]
Chen, Yaping [1 ]
Xia, Lixue [4 ]
Zhou, Peng [5 ]
Gao, Mingxia [1 ]
Liu, Yongfeng [1 ]
Chen, Jian [6 ]
Yan, Yushan [3 ]
Shao, Minhua [2 ,7 ,8 ]
Pan, Hongge [1 ,6 ]
Sun, Wenping [1 ,9 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Kowloon, Hong Kong, Peoples R China
[3] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE USA
[4] Wuhan Univ Technol, Int Sch Mat Sci & Engn, State Key Lab Silicate Mat Architectures, Wuhan, Hubei, Peoples R China
[5] Peking Univ, Sch Environm & Energy, Shenzhen Grad Sch, Shenzhen, Peoples R China
[6] Xian Technol Univ, Inst Sci & Technol New Energy, Xian, Peoples R China
[7] Hong Kong Univ Sci & Technol, Energy Inst, Kowloon, Hong Kong, Peoples R China
[8] Hong Kong Univ Sci & Technol, Chinese Natl Engn Res Ctr Control & Treatment Heav, Kowloon, Hong Kong, Peoples R China
[9] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
OXIDATION REACTION; MEDIA;
D O I
10.1038/s41929-024-01126-3
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
Constructing well-defined heterostructure interfaces in catalysts is an efficient strategy to break the so-called scaling relationships and to accelerate the reactions involving multiple intermediates. Here a cluster-cluster heterostructure catalyst composed of crystalline ruthenium cluster and amorphous chromium oxide cluster is designed to realize high-performance alkaline hydrogen electrocatalysis. The strongly coupled cluster-cluster heterostructure interface induces a unique interfacial interpenetration effect, which simultaneously optimizes the adsorption of intermediates on each cluster. The resulting catalyst exhibits impressive catalytic activities for the hydrogen oxidation reaction (exchange current density of 2.8 A mg-1Ru) and the hydrogen evolution reaction (mass activity of 23.0 A mg(-1)Ru at the overpotential of 100 mV) in alkaline media. The hydroxide exchange membrane fuel cell delivers a mass activity of 22.4 A mg(-1)Ru at 0.65 V and outstanding durability with no voltage loss over 105 h operation at 500 mA cm(-2). The present work demonstrates the superiority of cluster-cluster heterostructure interface towards the development of advanced catalysts.
引用
收藏
页码:441 / 451
页数:11
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