In Situ Coupling Strategy for the Preparation of FeCo Alloys and Co4N Hybrid for Highly Efficient Oxygen Evolution

Xiang Zhu, Tian Jin, Chengcheng Tian, Chenbao Lu, Xiaoming Liu, Min Zeng, Xiaodong Zhuang, Shize Yang, Lin He, Honglai Liu, Sheng Dai

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Abstract

An in situ coupling approach is developed to create a new highly efficient and durable cobalt-based electrocatalyst for the oxygen evolution reaction (OER). Using a novel cyclotetramerization, a task-specific bimetallic phthalocyanine-based nanoporous organic framework is successfully built as a precursor for the carbonization synthesis of a nonprecious OER electrocatalyst. The resultant material exhibits an excellent OER activity with a low overpotential of 280 mV at a current density of 10 mA cm−2 and high durability in an alkaline medium. This impressive result ranks among the best from known Co-based OER catalysts under the same conditions. The simultaneous installation of multiple diverse cobalt-based active sites, including FeCo alloys and Co4N nanoparticles, plays a critical role in achieving this promising OER performance. This innovative approach not only enables high-performance OER activity to be achieved but simultaneously provides a means to control the surface features, thereby tuning the catalytic property of the material.

Original languageEnglish
Article number1704091
JournalAdvanced Materials
Volume29
Issue number47
DOIs
StatePublished - Dec 20 2017

Funding

X.Z. and T.J. contributed equally to this work. X.Z., C.T., and S.D. were supported by the Materials Sciences and Engineering Division, Office of Basic Energy Sciences, U.S. Department of Energy under contract with UT-Battelle, LLC. S.Z.Y. was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering. X.Y.L. was supported by the Center for Nanophase Materials Sciences at the Oak Ridge National Laboratory. H.L.L acknowledges the support from the National Basic Research Program of China (2013CB733501), the National Natural Science Foundation of China (No. 91334203, 21376074, and 21507030), the National Natural Science Foundation of China for Innovative Research Groups (No. 51621002), and the 111 Project of Ministry of Education of China (No. B08021). T.J. acknowledges the support from CSC. M.Z. and L.H. were supported by the National Natural Science Foundation of China (21703267). X.Z. acknowledges financial support from NSFC for Excellent Youth Scholars (51722304). The authors gratefully acknowledge Dr. Sujuan Wu for the electron microscopy images.

FundersFunder number
111 Project of Ministry of Education of ChinaB08021
Center for Nanophase Materials Sciences
Materials Science and Engineering
NSFC for Excellent Youth Scholars51722304
U.S. Department of Energy
Office of Science
Basic Energy Sciences
Oak Ridge National Laboratory
Division of Materials Sciences and Engineering
National Natural Science Foundation of China51621002, 21376074, 21507030, 91334203
National Natural Science Foundation of China
China Scholarship Council21703267
China Scholarship Council
National Key Research and Development Program of China2013CB733501
National Key Research and Development Program of China

    Keywords

    • FeCo alloy nanoparticles
    • cobalt nitride
    • cyclotetramerization
    • in situ coupling
    • oxygen evolution reaction

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