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  5. Oxophilic gallium single atoms bridged ruthenium clusters for practical anion-exchange membrane electrolyzer

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Article
en
2024

Oxophilic gallium single atoms bridged ruthenium clusters for practical anion-exchange membrane electrolyzer

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0 Files

en
2024
Vol 15 (1)
Vol. 15
DOI: 10.1038/s41467-024-51200-4

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Lin Gu
Lin Gu

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Chenhui Zhou
Jia Shi
Zhaoqi Dong
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Abstract

The development of highly efficient and durable alkaline hydrogen evolution reaction (HER) catalysts is crucial for achieving high-performance practical anion exchange membrane water electrolyzer (AEMWE) at ampere-level current density. Herein, we report a design concept by employing Ga single atoms as an electronic bridge to stabilize the Ru clusters for boosting alkaline HER performance in practical AEMWE. Experimental and theoretical results collectively reveal that the bridged Ga sites trigger strong metal-support interaction for the homogeneous distribution of Ru clusters with high density, as well as optimize the Ru-H bond strength due to the electron transfer between Ru and Ga for enhanced intrinsic HER activity. Moreover, the oxophilic Ga sites near the Ru clusters tend to adsorb the hydroxyl species and accelerate the water dissociation for sufficient proton supplement in an alkaline medium. The Ru-GaSA/N-C catalyst exhibits a low overpotential of 4 ± 1 mV (10 mA cm-2) and high mass activity of 9.3 ± 0.5 A mg-1Ru at -0.05 V vs RHE. In particular, the Ru-GaSA/N-C-based AEMWE in 1 M KOH delivers a voltage of only 1.74 V to reach an industrial current density of 1 A cm-2, and can steadily operate at 1 A cm-2 for more than 170 h.

How to cite this publication

Chenhui Zhou, Jia Shi, Zhaoqi Dong, Lingyou Zeng, Yan Chen, Ying Han, Lu Li, Wenyu Zhang, Qinghua Zhang, Lin Gu, Fan Lv, Mingchuan Luo, Shaojun Guo (2024). Oxophilic gallium single atoms bridged ruthenium clusters for practical anion-exchange membrane electrolyzer. , 15(1), DOI: https://doi.org/10.1038/s41467-024-51200-4.

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Publication Details

Type

Article

Year

2024

Authors

13

Datasets

0

Total Files

0

Language

en

DOI

https://doi.org/10.1038/s41467-024-51200-4

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