Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/151046
Title: Exposing unsaturated Cu1-O2 sites in nanoscale Cu-MOF for efficient electrocatalytic hydrogen evolution
Authors: Cheng, Weiren
Zhang, Huabin
Luan, Deyan
Lou, David Xiong Wen
Keywords: Engineering::Materials
Issue Date: 2021
Source: Cheng, W., Zhang, H., Luan, D. & Lou, D. X. W. (2021). Exposing unsaturated Cu1-O2 sites in nanoscale Cu-MOF for efficient electrocatalytic hydrogen evolution. Science Advances, 7(18), eabg2580-. https://dx.doi.org/10.1126/sciadv.abg2580
Project: MOE2019-T2-2-049
NRF-NRFI2016-04
Journal: Science Advances 
Abstract: Conductive metal-organic framework (MOF) materials have been recently considered as effective electrocatalysts. However, they usually suffer from two major drawbacks, poor electrochemical stability and low electrocatalytic activity in bulk form. Here, we have developed a rational strategy to fabricate a promising electrocatalyst composed of a nanoscale conductive copper-based MOF (Cu-MOF) layer fully supported over synergetic iron hydr(oxy)oxide [Fe(OH)x] nanoboxes. Owing to the highly exposed active centers, enhanced charge transfer, and robust hollow nanostructure, the obtained Fe(OH)x@Cu-MOF nanoboxes exhibit superior activity and stability for the electrocatalytic hydrogen evolution reaction (HER). Specifically, it needs an overpotential of 112 mV to reach a current density of 10 mA cm−2 with a small Tafel slope of 76 mV dec−1. X-ray absorption fine structure spectroscopy combined with density functional theory calculations unravels that the highly exposed coordinatively unsaturated Cu1-O2 centers could effectively accelerate the formation of key *H intermediates toward fast HER kinetics.
URI: https://hdl.handle.net/10356/151046
ISSN: 2375-2548
DOI: 10.1126/sciadv.abg2580
Rights: © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Journal Articles

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