Developing Proton-Conductive Metal Coordination Polymer as Highly Efficient Electrocatalyst toward Oxygen Reduction

被引:19
作者
Huang, Xiang [1 ]
Gan, Li-Yong [2 ,3 ]
Wang, Jiong [4 ]
Ali, Sajjad [1 ]
He, Chang-Chun [5 ]
Xu, Hu [6 ,7 ]
机构
[1] Southern Univ Sci & Technol, Dept Phys, Shenzhen 518055, Peoples R China
[2] Chongqing Univ, Inst Struct & Funct, Chongqing 400030, Peoples R China
[3] Chongqing Univ, Dept Phys, Chongqing 400030, Peoples R China
[4] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[5] South China Univ Technol, Dept Phys, Guangzhou 510640, Peoples R China
[6] Southern Univ Sci & Technol, Dept Phys, Guangdong Prov Key Lab Computat Sci & Mat Design, Shenzhen 518055, Peoples R China
[7] Southern Univ Sci & Technol, Shenzhen Key Lab Adv Quantum Funct Mat & Devices, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; ORGANIC-FRAMEWORK; NI; CATALYSTS; GRAPHENE; TRENDS; CARBON; SITES; WATER;
D O I
10.1021/acs.jpclett.1c02665
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
Developing earth-abundant transition metal (TM)-based electrocatalysts toward oxygen reduction reaction (ORR) is significant in overcoming the high cost of fuel cells. Herein, using an as-synthesized proton-conductive coordination polymer (termed TM-DHBQ) as a template, we investigate the ORR performance of a series of such TM-DHBQs via screening 3d, 4d, and 5d TMs. We find that most 3d TM-DHBQs exhibit distinguished durability under ORR turnover conditions. The formation energies of these TM-DHBQs and adsorption free energies of ORR intermediates show a good correlation with the number of outer electrons of TM ions in TM-DHBQs, enabling the formation energy as a robust ORR activity descriptor. The Sabatier-type volcano plot and microkinetic modeling coidentify Fe- and Co-DHBQs as two promising alternatives to Pt-based ORR electrocatalysts. For those TM-DHBQs showing strong bonding to oxygen species, the ORR intermediate is found to combine with the TM ion serving as the active center.
引用
收藏
页码:9197 / 9204
页数:8
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