Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/170282
Title: Oxygen-bridged stabilization of single atomic W on Rh metallenes for robust and efficient pH-universal hydrogen evolution
Authors: Prabhu, P
Do, Viet-Hung
Peng, Chun Kuo
Hu, Huimin
Chen, San-Yuan
Choi, Jin-Ho
Lin, Yan-Gu
Lee, Jong-Min
Keywords: Engineering::Chemical technology
Issue Date: 2023
Source: Prabhu, P., Do, V., Peng, C. K., Hu, H., Chen, S., Choi, J., Lin, Y. & Lee, J. (2023). Oxygen-bridged stabilization of single atomic W on Rh metallenes for robust and efficient pH-universal hydrogen evolution. ACS Nano, 17(11), 10733-10747. https://dx.doi.org/10.1021/acsnano.3c02066
Project: RG105/19
Journal: ACS Nano 
Abstract: Highly efficient and durable electrocatalysts are of the utmost importance for the sustainable generation of clean hydrogen by water electrolysis. Here, we present a report of an atomically thin rhodium metallene incorporated with oxygen-bridged single atomic tungsten (Rh-O-W) as a high-performance electrocatalyst for pH-universal hydrogen evolution reaction. The Rh-O-W metallene delivers ascendant electrocatalytic HER performance, characterized by exceptionally low overpotentials, ultrahigh mass activities, excellent turnover frequencies, and robust stability with negligible deactivation, in pH-universal electrolytes, outperforming that of benchmark Pt/C, Rh/C and numerous other reported precious-metal HER catalysts. Interestingly, the promoting feature of -O-W single atomic sites is understood via operando X-ray absorption spectroscopy characterization and theoretical calculations. On account of electron transfer and equilibration processes take place between the binary components of Rh-O-W metallenes, fine-tuning of the density of states and electron localization at Rh active sites is attained, hence promoting HER via a near-optimal hydrogen adsorption.
URI: https://hdl.handle.net/10356/170282
ISSN: 1936-0851
DOI: 10.1021/acsnano.3c02066
Schools: School of Chemical and Biomedical Engineering 
Rights: © 2023 American Chemical Society. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
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