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 language | English |
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Article number | 1704091 |
Journal | Advanced Materials |
Volume | 29 |
Issue number | 47 |
DOIs | |
State | Published - 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.
Funders | Funder number |
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111 Project of Ministry of Education of China | B08021 |
Center for Nanophase Materials Sciences | |
Materials Science and Engineering | |
NSFC for Excellent Youth Scholars | 51722304 |
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 China | 51621002, 21376074, 21507030, 91334203 |
National Natural Science Foundation of China | |
China Scholarship Council | 21703267 |
China Scholarship Council | |
National Key Research and Development Program of China | 2013CB733501 |
National Key Research and Development Program of China |
Keywords
- FeCo alloy nanoparticles
- cobalt nitride
- cyclotetramerization
- in situ coupling
- oxygen evolution reaction