An exsolution constructed FeNi/NiFe2O4 composite: preferential breaking of octahedral metal-oxygen bonds in a spinel oxide

被引:25
作者
Guo, Xiaoyan [1 ]
Yao, Lu [1 ]
Hou, Xiangyan [1 ]
Wu, Xiaofeng [1 ]
Zhang, Yaowen [1 ]
Zhu, Qian [1 ]
Guo, Zhangtao [1 ]
Li, Shuting [1 ]
Jiang, Yilan [2 ]
Feng, Shouhua [1 ]
Huang, Keke [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Jilin Prov Int Cooperat Key Lab Adv Inorgan Solid, Qianjin St 2699, Changchun 130012, Peoples R China
[2] Hohai Univ, Coll Environm, Key Lab Integrated Regulat & Resource Dev Shallow, Minist Educ, Nanjing 210098, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE ANODE; MAGNETIC-PROPERTIES; EVOLUTION REACTION; FE NANOPARTICLES; NICKEL FERRITE; NIFE2O4; GROWTH; ELECTROCATALYSTS; REDUCTION; MECHANISM;
D O I
10.1039/d2sc02149h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Exsolution is an ingenious strategy for the in situ construction of metal- or alloy-decorated oxides and, due to its promising energy related catalysis applications, has advanced from use in perovskites to use in spinels. Despite its great importance for designing target composites, the ability to identify whether active metal ions at octahedral or tetrahedral sites will preferentially exsolve in a spinel remains unexplored. Here, an inverse spinel NiFe2O4 (NFO) was employed as a prototype and FeNi/NFO composites were successfully constructed via exsolution. The preferential breaking of octahedral metal-oxygen bonds in the spinel oxide was directly observed using Mossbauer and X-ray absorption spectroscopy. This was further verified from the negative segregation energies calculated based on density-functional theory. One exsolved FeNi/NFO composite exhibits enhanced electrochemical activity with an overpotential of 283 mV at 10 mA cm(-2) and a long stability time for the oxygen evolution reaction. This work offers a unique insight into spinel exsolution based on the preferential breaking of chemical bonds and may be an effective guide for the design of new composite catalysts where the desired metal ions are deliberately introduced to octahedral and/or tetrahedral sites.
引用
收藏
页码:9440 / 9449
页数:10
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