A Cu and Fe dual-atom nanozyme mimicking cytochrome c oxidase to boost the oxygen reduction reaction

被引:134
|
作者
Du, Cheng [1 ,4 ]
Gao, Yijing [2 ]
Chen, Hengquan [3 ]
Li, Ping [1 ,4 ]
Zhu, Shuyun [5 ]
Wang, Jianguo [2 ]
He, Qinggang [3 ]
Chen, Wei [1 ,4 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Zhejiang Univ Technol, Inst Ind Catalysis, State Key Lab Breeding Base Green Chem Synth Tech, Coll Chem Engn, Hangzhou 310032, Peoples R China
[3] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310027, Zhejiang, Peoples R China
[4] Univ Sci & Technol China, Hefei 230029, Anhui, Peoples R China
[5] Qufu Normal Univ, Sch Chem & Chem Engn, Qufu, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
GENERALIZED GRADIENT APPROXIMATION; FUNCTIONAL ANALOGS; FUEL-CELLS; CATALYSTS; EFFICIENT; CARBON; COPPER; SITES; ZN; ELECTROCATALYSTS;
D O I
10.1039/d0ta06485h
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
The intrinsically sluggish kinetics of the oxygen reduction reaction (ORR) and overuse of expensive and unstable Pt-based catalysts have severely hampered the development of clean energy technologies. Herein, a type of non-noble metal nanozyme as an ORR electrocatalyst, with Fe-Cu dual atomic sites embedded in three-dimensional porous N-doped carbon (FeCu-DA/NC), is fabricated by mimicking both the constituents of active centers and enzymatic microenvironment of Cytochrome c oxidase (CcO). The atomically dispersed Fe-Cu single atom sites are clearly identified by direct aberration-corrected transmission electron microscopy imaging, systematic X-ray absorption fine structure (XAFS) analyses, and density functional theory (DFT) calculations. FeCu-DA/NC exhibits a superior ORR activity, with about 30 mV more positive half-wave potential (E-1/2) than that of commercial Pt/C catalysts in a base, and moreover with only anE(1/2)gap of 20 mV to Pt/C in an acid. Importantly, FeCu-DA/NC displays an excellent durability under both acidic and basic conditions, which is much superior to that of Pt/C. DFT calculations further demonstrate that the enhanced performance can be attributed to the unique synergistic effect between Cu and Fe single atoms in which Cu-N(4)serves as the electron donor to increase the electron density of the active centers of Fe-N(4)and thus to facilitate O(2)activation.
引用
收藏
页码:16994 / 17001
页数:8
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