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MOF-on-MOF Strategy to Construct a Nitrogen-Doped Carbon-Incorporated CoP@Fe-CoP Core-Shelled Heterostructure for High-Performance Overall Water Splitting.
- Source :
-
Inorganic chemistry [Inorg Chem] 2022 Jan 17; Vol. 61 (2), pp. 1159-1168. Date of Electronic Publication: 2021 Dec 28. - Publication Year :
- 2022
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Abstract
- The design and preparation of efficient and low-cost catalysts for water electrolysis are crucial and highly desirable to produce eco-friendly and sustainable hydrogen fuel. Herein, we prepared nitrogen-doped carbon-incorporated CoP@Fe-CoP core-shelled nanorod arrays grown on Ni foam (CoP@Fe-CoP/NC/NF) through phosphorization of ZIF-67@Co-Fe Prussian blue analogue (ZIF-67@CoFe-PBA). The hierarchical nanorod arrays combined with the core-shelled structure offer favorable mass/electron transport capacity and maximize the active sites, thus enhancing the electrochemically active surface area. The synergistic effect of the bimetallic components and the nitrogen-doped carbon matrix endow the composite with an optimized electronic structure. Benefiting from the above superiorities of morphological and chemical compositions, this self-supported CoP@Fe-CoP/NC/NF heterostructure can drive alkaline hydrogen evolution reaction and oxygen evolution reaction with overpotentials of 97 and 270 mV to yield 100 mA cm <superscript>-2</superscript> , respectively. The two-electrode alkaline electrolyzer constructed by this heterostructure shows a low cell voltage of 1.58 V to yield 10 mA cm <superscript>-2</superscript> , superior to the precious-metal-based electrocatalyst apparatus (IrO <subscript>2</subscript> ∥Pt/C). This study offers a feasible and facile approach to develop efficient electrocatalysts for water electrolysis, which applies to other electrochemical energy conversion and storage applications.
Details
- Language :
- English
- ISSN :
- 1520-510X
- Volume :
- 61
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Inorganic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34962378
- Full Text :
- https://doi.org/10.1021/acs.inorgchem.1c03498