Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/155470
Title: Enhancing electrochemical nitrogen reduction with Ru nanowires : via the atomic decoration of Pt
Authors: Zhang, Weiqing
Yang, Liting
An, Changhua
Zhang, Jichao
Zhu, Junfa
Chen, Peng
Keywords: Engineering::Chemical engineering
Issue Date: 2020
Source: Zhang, W., Yang, L., An, C., Zhang, J., Zhu, J. & Chen, P. (2020). Enhancing electrochemical nitrogen reduction with Ru nanowires : via the atomic decoration of Pt. Journal of Materials Chemistry A, 8(47), 25142-25147. https://dx.doi.org/10.1039/d0ta09937f
Project: AMEIRG18- 0016
MOE2017-T2-2- 005
Journal: Journal of Materials Chemistry A
Abstract: Achieving an efficient electrochemical nitrogen reduction reaction (ENRR) remains a great challenge, demanding the development of a new strategy for ENRR catalyst engineering. Herein, we demonstrate a largely improved ENRR by the controlled engineering of Ru nanowires with atomic Pt decoration. Specifically, the readily synthesized Ru88Pt12 nanowires exhibit a high NH3 production rate of 47.1 μg h-1 mgcat-1 and faradaic efficiency of 8.9% at -0.2 V, which are 5.3 and 14.6 times higher than those values for Ru nanowires. They also show outstanding stability, as evidenced by the full preservation of the NH3 yield and faradaic efficiency even after 15 h of electrocatalysis. As revealed by theoretical investigations, the d-band center of Ru atoms is upshifted by the tensile strain due to the presence of Pt atoms, leading to the selective enhancement of N2 adsorption and the stabilization of N2H∗. Such an atomic engineering method may be applied to precisely tailor other metal nanocatalysts for different applications.
URI: https://hdl.handle.net/10356/155470
ISSN: 2050-7496
DOI: 10.1039/d0ta09937f
DOI (Related Dataset): 10.21979/N9/JSICXW
Schools: School of Chemical and Biomedical Engineering 
Rights: © 2020 The Royal Society of Chemistry. All rights reserved. This paper was published in Journal of Materials Chemistry A and is made available with permission of The Royal Society of Chemistry.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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