Engineering the coordination environment of Ni and Pd dual active sites for promoting the oxygen reduction reaction

被引:0
|
作者
Li, Lei [1 ,2 ]
Wu, Xiaoxia [1 ,2 ]
Zhang, Ruotong [1 ,2 ]
Bai, Narsu [1 ,2 ]
Zhang, Min [1 ,2 ]
Wen, Yuhua [3 ]
机构
[1] Inner Mongolia Normal Univ, Coll Phys & Elect Informat, Hohhot 010022, Peoples R China
[2] Inner Mongolia Key Lab Phys & Chem Funct Mat, Hohhot 010022, Peoples R China
[3] Xiamen Univ, Dept Phys, Xiamen 361005, Peoples R China
来源
SCIENTIFIC REPORTS | 2025年 / 15卷 / 01期
关键词
Oxygen reduction reaction; Graphene; Edge termination; O doping; Density-functional theory; TOTAL-ENERGY CALCULATIONS; GRAPHENE; ELECTROCATALYSTS; CHALLENGES; EFFICIENCY; CATALYSTS; DESIGN;
D O I
10.1038/s41598-025-93115-0
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
Precisely regulating active sites is vital for promoting the oxygen reduction reaction (ORR) activity. Here we reported highly active Ni-Pd co-doped N-coordinated graphene towards ORR achieved by edge termination and O doping. Our first-principles calculations demonstrated that edge termination effectively boost the ORR activity, and armchair-edge termination was energetically more favorable than zigzag-edge termination. Notably, after O doping Ni-Pd active center, armchair edge-terminated Ni-Pd active site exhibited better ORR activity, and the lowest overpotential was only 0.31 V. This improvement in activity was attributed to the shift of the d-band center of Ni atom toward the Fermi-level and the shift of the d-band center of Pd atom away from the Fermi-level, thus regulating the *OH adsorption strength. This work paves the way for developing highly active graphene-based dual-atom catalysts for ORR through edge and doping engineering.
引用
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页数:9
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