Accelerating Kinetics of Alkaline Hydrogen Oxidation Reaction on Ru through Engineering Oxophilicity

Benefiting from its hydrogen binding energy being similar to that of platinum (Pt), ruthenium (Ru) is expected to replace Pt in the alkaline hydrogen oxidation reaction (HOR). Unfortunately, the adsorbed hydroxyl groups tend to cover Ru surfaces, making Ru unable to adsorb hydrogen, resulting in sluggish HOR kinetics. In this work, we demonstrate that alkaline HOR kinetics on Ru can be accelerated by combining it with highly oxophilic MoO2. Resulting from the stronger oxophilicity of MoO2, hydroxyl groups preferentially adsorb on MoO2, allowing Ru sites to adsorb hydrogen, thus facilitating HOR kinetics. Guided by the theoretical calculations, we synthesize a Ru/MoO2 catalyst for HOR, achieving a mass activity of 5.17 A mgPGM–1, which is 13.6 times greater than that of commercial 20% Pt/C. Notably, a peak power density of 1.09 W cm–2 is achieved using this Ru/MoO2 catalyst as the anode in an anion exchange membrane fuel cell (AEMFC).

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Publication Details

Journal
ACS Materials Letters
Published
2024-08-30
DOI
https://doi.org/10.1021/acsmaterialslett.4c01346
Citations
11
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.13

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article

Accelerating Kinetics of Alkaline Hydrogen Oxidation Reaction on Ru through Engineering Oxophilicity

Qianwang Chen, Zhiyu Cheng, Pin Meng, Jitang Chen et al.
11 citations
ACS Materials Letters
Electrocatalysts for Energy Conversion
1.13
article

Accelerating Kinetics of Alkaline Hydrogen Oxidation Reaction on Ru through Engineering Oxophilicity

Qianwang Chen, Zhiyu Cheng, Pin Meng, Jitang Chen, Qian Wang, Chenyang Bi, Jiahe Yang, Changlai Wang, Yang Yang, Pengcheng Wang, Dongdong Wang, Xingyan Chen, Hongda Shi, Hao Wu
article en
11 citations

Abstract

Benefiting from its hydrogen binding energy being similar to that of platinum (Pt), ruthenium (Ru) is expected to replace Pt in the alkaline hydrogen oxidation reaction (HOR). Unfortunately, the adsorbed hydroxyl groups tend to cover Ru surfaces, making Ru unable to adsorb hydrogen, resulting in sluggish HOR kinetics. In this work, we demonstrate that alkaline HOR kinetics on Ru can be accelerated by combining it with highly oxophilic MoO2. Resulting from the stronger oxophilicity of MoO2, hydroxyl groups preferentially adsorb on MoO2, allowing Ru sites to adsorb hydrogen, thus facilitating HOR kinetics. Guided by the theoretical calculations, we synthesize a Ru/MoO2 catalyst for HOR, achieving a mass activity of 5.17 A mgPGM–1, which is 13.6 times greater than that of commercial 20% Pt/C. Notably, a peak power density of 1.09 W cm–2 is achieved using this Ru/MoO2 catalyst as the anode in an anion exchange membrane fuel cell (AEMFC).

ACS Materials LettersVol. 6(10)
University of Science and Technology of China (CN), Fuyang Normal University (CN), Hefei National Center for Physical Sciences at Nanoscale (CN), Nagoya University (JP)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 25%
Electrocatalysts for Energy Conversion
1.13
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