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Highly efficient hydrogen production from methanol by single nickel atoms anchored on defective boron nitride nanosheet.
- Source :
- Nano Research; Jul2023, Vol. 16 Issue 7, p8800-8808, 9p
- Publication Year :
- 2023
-
Abstract
- Exploiting inexpensive and effective nickel-based catalysts that produce hydrogen from liquid organic hydrogen carriers (LOHCs) is crucial to alleviating the global energy and environmental crisis. In this study, we report a rational strategy that can realize atomically dispersed Ni atoms anchored on vacancy-abundant boron nitride nanosheets (Ni<subscript>1</subscript>/h-BNNS) with high specific surface area (up to 622 m<superscript>2</superscript>·g<superscript>−1</superscript>) and abundant hydroxyl groups for high efficient hydrogen production. Methanol dehydrogenation results show an excellent hydrogen production performance catalyzed by this Ni<subscript>1</subscript>/h-BNNS, as evidenced by a remarkably high H<subscript>2</subscript> yield rate (1684.23 ), nearly 100% selectivity toward hydrogen and CO, and high anti-coking performance. Density functional theory (DFT) calculations reveal that the outstanding catalytic performance of Ni<subscript>1</subscript>/h-BNNS primarily originates from the unique coordinated environment of atomically dispersed Ni (Ni-B<subscript>2</subscript>O<subscript>2</subscript>) and the synergistic interaction between Ni single atoms and the h-BNNS support. Specifically, the coordinated O atoms play a decisive role in promoting the activity of Ni, and the neighboring B sites significantly decrease the energy barriers for the adsorption of key intermediates of methanol dehydrogenation. This study offers a novel strategy for developing high-performance and stable single-atom Ni catalysts by precisely controlling single-atom sites on h-BN support for sustainable hydrogen production. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 19980124
- Volume :
- 16
- Issue :
- 7
- Database :
- Complementary Index
- Journal :
- Nano Research
- Publication Type :
- Academic Journal
- Accession number :
- 169750666
- Full Text :
- https://doi.org/10.1007/s12274-023-5515-3