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https://hdl.handle.net/10356/147427
Title: | Trimetallic spinel NiCo2-xFexO4 nanoboxes for highly efficient electrocatalytic oxygen evolution | Authors: | Huang, Yi Zhang, Song Lin Lu, Xue Feng Wu, Zhi-Peng Luan, Deyan Lou, David Xiong Wen |
Keywords: | Engineering::Chemical engineering Engineering::Materials |
Issue Date: | 2021 | Journal: | Angewandte Chemie International Edition | Abstract: | The development of efficient and low-cost electrocatalysts toward the oxygen evolution reaction (OER) is critical for improving the efficiency of several electrochemical energy conversion and storage devices. Here, we report an elaborate design and synthesis of porous Co-based trimetallic spinel oxide nanoboxes ( NiCo 2-x Fe x O 4 NBs ) by a novel meta l- organic framework engaged strategy, which involves chemical etching, cation exchange, and subsequent thermal oxidation processes. Owing to the structural and compositional advantages, the optimized trimetallic NiCo 2-x Fe x O 4 NBs deliver superior electrocatalytic performance for OER with an overpotential of 274 mV at 10 mA cm -2 , a small Tafel slope of 42 mV dec -1 , and good stability in alkaline electrolyte, which is much better than that of Co-based bi/monometallic spinel oxides and even commercial RuO 2 . | URI: | https://hdl.handle.net/10356/147427 | ISSN: | 1433-7851 | DOI: | 10.1002/anie.202103058 | Rights: | This is the peer reviewed version of the following article: Huang, Y., Zhang, S. L., Lu, X. F., Wu, Z.-P., Luan, D., & Lou, D. X. W. (2021). Trimetallic spinel NiCo2-xFexO4 nanoboxes for highly efficient electrocatalytic oxygen evolution. Angewandte Chemie International Edition, 60(21), 11841-11846. doi:10.1002/anie.202103058, which has been published in final form at https://doi.org/10.1002/anie.202103058. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SCBE Journal Articles |
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