Neighbouring Synergy in High-Density Single Ir Atoms on CoGaOOH for Efficient Alkaline Electrocatalytic Oxygen Evolution

被引:22
作者
Ma, Peiyu [1 ]
Cao, Heng [1 ]
Hao, Qi [4 ]
Wang, Ruyang [1 ]
Liu, Wanting [2 ]
Zuo, Ming [2 ]
Jia, Chuanyi [3 ]
Zhang, Zhirong [2 ]
Bao, Jun [1 ]
机构
[1] Univ Sci & Technol China, iChEM Collaborat Innovat Ctr Chem Energy Mat, Natl Synchrotron Radiat Lab, Key Lab Precis & Intelligent Chem, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Key Lab Surface & Interface Chem & Energy Catalysi, Hefei Natl Res Ctr Phys Sci Microscale, Dept Chem Phys,Key Lab Strongly Coupled Quantum Ma, R China, Hefei 230026, Anhui, Peoples R China
[3] Guizhou Educ Univ, Inst Appl Phys, Guizhou Prov Key Lab Comp Nanomat Sci, Guiyang 550018, Guizhou, Peoples R China
[4] Westlake Univ, Sch Engn, Hangzhou 310030, Zhejiang, 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
SCALING RELATION; CATALYSTS; SITES; STRAIN; OXIDES;
D O I
10.1002/anie.202404418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The catalytic performance of single-atom catalysts was strictly limited by isolated single-atom sites. Fabricating high-density single atoms to realize the synergetic interaction in neighbouring single atoms could optimize the adsorption behaviors of reaction intermediates, which exhibited great potential to break performance limitations and deepen mechanistic understanding of electrocatalysis. However, the catalytic behavior governed by neighbouring single atoms is particularly elusive and has yet to be understood. Herein, we revealed that the synergetic interaction in neighbouring single atoms contributes to superior performance for oxygen evolution relative to isolated Ir single atoms. Neighbouring single atoms was achieved by fabricating high-density single atoms to narrow the distance between single atoms. Electrochemical measurements demonstrated that the Nei-Ir1/CoGaOOH with neighbouring Ir single atoms exhibited a low overpotential of 170 mV at a current density of 10 mA cm-2, and long-durable stability over 2000 h for oxygen evolution. Mechanistic studies revealed that neighbouring single atoms synergetic stabilized the *OOH intermediates via extra hydrogen bonding interactions, thus significantly reducing the reaction energy barriers, as compared to isolated Ir single atoms. The discovery of the synergetic interaction in neighbouring single atoms could offer guidance for the development of efficient electrocatalysts, thus accelerating the world's transition to sustainable energy. The catalytic performance of single-atom catalysts was strictly limited by isolated single-atom sites. Fabricating high-density single atoms to realize the synergetic interaction in neighbouring single atoms exhibited great potential to break performance limitations. Herein, we revealed that the synergetic interaction in neighbouring Ir single atoms contributes to enhanced performance for oxygen evolution relative to isolated Ir single atoms.+ image
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页数:10
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共 57 条
[1]   Synergistic effects of mixing and strain in high entropy spinel oxides for oxygen evolution reaction [J].
Baek, Jihyun ;
Hossain, Md Delowar ;
Mukherjee, Pinaki ;
Lee, Junghwa ;
Winther, Kirsten T. ;
Leem, Juyoung ;
Jiang, Yue ;
Chueh, William C. ;
Bajdich, Michal ;
Zheng, Xiaolin .
NATURE COMMUNICATIONS, 2023, 14 (01)
[2]   Double-atom catalysts as a molecular platform for heterogeneous oxygen evolution electrocatalysis [J].
Bai, Lichen ;
Hsu, Chia-Shuo ;
Alexander, Duncan T. L. ;
Chen, Hao Ming ;
Hu, Xile .
NATURE ENERGY, 2021, 6 (11) :1054-1066
[3]   Comparison of Fe-enhanced oxygen evolution electrocatalysis in amorphous and crystalline nickel oxides to evaluate the structural contribution [J].
Bak, Jumi ;
Yun, Tae Gyu ;
An, Ji-Sang ;
Bae, Hyung Bin ;
Chung, Sung-Yoon .
ENERGY & ENVIRONMENTAL SCIENCE, 2022, 15 (02) :610-620
[4]  
Banger KK, 2011, NAT MATER, V10, P45, DOI [10.1038/nmat2914, 10.1038/NMAT2914]
[5]   Improving the Oxygen Evolution Reaction on Fe3O4(001) with Single-Atom Catalysts [J].
Bianchetti, Enrico ;
Perilli, Daniele ;
Di Valentin, Cristiana .
ACS CATALYSIS, 2023, 13 (07) :4811-4823
[6]   Altering Hydrogenation Pathways in Photocatalytic Nitrogen Fixation by Tuning Local Electronic Structure of Oxygen Vacancy with Dopant [J].
Bo, Yanan ;
Wang, Haiyun ;
Lin, Yunxiang ;
Yang, Tian ;
Ye, Run ;
Li, Yu ;
Hu, Canyu ;
Du, Pengye ;
Hu, Yangguang ;
Liu, Zhi ;
Long, Ran ;
Gao, Chao ;
Ye, Bangjiao ;
Song, Li ;
Wu, Xiaojun ;
Xiong, Yujie .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (29) :16085-16092
[7]   Beyond the top of the volcano? - A unified approach to electrocatalytic oxygen reduction and oxygen evolution [J].
Busch, Michael ;
Halck, Niels B. ;
Kramm, Ulrike I. ;
Siahrostami, Samira ;
Krtil, Petr ;
Rossmeisl, Jan .
NANO ENERGY, 2016, 29 :126-135
[8]   Ultrahigh Oxygen Evolution Reaction Activity Achieved Using Ir Single Atoms on Amorphous CoOx Nanosheets [J].
Cai, Chao ;
Wang, Maoyu ;
Han, Shaobo ;
Wang, Qi ;
Zhang, Qing ;
Zhu, Yuanmin ;
Yang, Xuming ;
Wu, Duojie ;
Zu, Xiaotao ;
Sterbinsky, George E. ;
Feng, Zhenxing ;
Gu, Meng .
ACS CATALYSIS, 2021, 11 (01) :123-130
[9]   Carbon-Defect-Driven Electroless Deposition of Pt Atomic Clusters for Highly Efficient Hydrogen Evolution [J].
Cheng, Qingqing ;
Hu, Chuangang ;
Wang, Guoliang ;
Zou, Zhiqing ;
Yang, Hui ;
Dai, Liming .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2020, 142 (12) :5594-5601
[10]   In-situ structure and catalytic mechanism of NiFe and CoFe layered double hydroxides during oxygen evolution [J].
Dionigi, Fabio ;
Zeng, Zhenhua ;
Sinev, Ilya ;
Merzdorf, Thomas ;
Deshpande, Siddharth ;
Lopez, Miguel Bernal ;
Kunze, Sebastian ;
Zegkinoglou, Ioannis ;
Sarodnik, Hannes ;
Fan, Dingxin ;
Bergmann, Arno ;
Drnec, Jakub ;
de Araujo, Jorge Ferreira ;
Gliech, Manuel ;
Teschner, Detre ;
Zhu, Jing ;
Li, Wei-Xue ;
Greeley, Jeffrey ;
Roldan Cuenya, Beatriz ;
Strasser, Peter .
NATURE COMMUNICATIONS, 2020, 11 (01)