Two Types of Single-Atom FeN4 and FeN5 Electrocatalytic Active Centers on N-Doped Carbon Driving High Performance of the SA-Fe-NC Oxygen Reduction Reaction Catalyst

被引:73
作者
Liang, Xiao [1 ]
Li, Zeyu [1 ]
Xiao, Hong [1 ]
Zhang, Tengfei [1 ]
Xu, Peng [1 ]
Zhang, Hang [1 ]
Gao, Qiuming [1 ]
Zheng, Lirong [1 ,2 ]
机构
[1] Beihang Univ, Beijing Adv Innovat Ctr Biomed Engn, Sch Chem,Minist Educ, Key Lab Bioinspired Smart Interfacial Sci & Techn, Beijing 100191, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; HETEROGENEOUS CATALYSIS; EFFICIENT; SITES; EVOLUTION; GRAPHENE; IRON; HYDROGEN; NANOPARTICLES; FRAMEWORK;
D O I
10.1021/acs.chemmater.1c00235
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
A novel SA-Fe-NC single-atom catalyst is prepared via a spatial isolation strategy. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) analysis indicates that Fe atomically disperses on SA-Fe-NC. Both Xray photoelectron spectroscopy (XPS) and X-ray absorption near-edge spectroscopy (X-ANES) analyses show that the Fe3+/Fe2+ ratio is 0.3/0.7. Extended X-ray absorption fine structure (EXAFS) fitting presents that the isolated Fe is coordinated with 4.4 N atoms on average, corresponding to the coexistence of Fe-N-4 (60%) and Fe-N-5 (40%). The SA-Fe-NC electrochemical catalyst presents high ORR activity (E-onset/E-1/2 = 1.04/0.88 V vs reversible hydrogen electrode (RHE) and J(L) = 5.62 mA cm(-2)), superhigh durability (no obvious loss after 30 000 cycles), and absolute tolerance to methanol in alkaline media. The SA-Fe-NC-based primary Zn-air battery (ZAB) shows a high specific capacity of 806 mAh g(Zn)(-1), a high energy density of 1048 Wh kg(Zn)(-1), and a high power density of 164 mW cm(-2) due to the high electrocatalytic activity of SA-Fe-NC. The ZAB shows a superlong lifetime of 320 h at 10 mA cm(-2) resulting from the superhigh stability of the SA-Fe-NC catalyst.
引用
收藏
页码:5542 / 5554
页数:13
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