Bimetallic nanoalloys planted on super-hydrophilic carbon nanocages featuring tip-intensified hydrogen evolution electrocatalysis

The insufficient availability and activity of interfacial water remain a major challenge for alkaline hydrogen evolution reaction (HER). Here, we propose an "on-site disruption and near-site compensation" strategy to reform the interfacial water hydrogen bonding network via deliberate cation penetration and catalyst support engineering. This concept is validated using tip-like bimetallic RuNi nanoalloys planted on super-hydrophilic and high-curvature carbon nanocages (RuNi/NC). Theoretical simulations suggest that tip-induced localized concentration of hydrated K<sup>+</sup> facilitates optimization of interfacial water dynamics and intermediate adsorption. In situ synchrotron X-ray spectroscopy endorses an H* spillover-bridged Volmer‒Tafel mechanism synergistically relayed between Ru and Ni. Consequently, RuNi/NC exhibits low overpotential of 12 mV and high durability of 1600 h at 10 mA cm<sup>‒2</sup> for alkaline HER, and demonstrates high performance in both water electrolysis and chlor-alkali electrolysis. This strategy offers a microscopic perspective on catalyst design for manipulation of the local interfacial water structure toward enhanced HER kinetics.

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Publication Details

Journal
Nature Communications
Published
2024-08-21
DOI
https://doi.org/10.1038/s41467-024-51370-1
Citations
136
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
13.92

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article

Bimetallic nanoalloys planted on super-hydrophilic carbon nanocages featuring tip-intensified hydrogen evolution electrocatalysis

Hsiao‐Tsu Wang, Yu‐Cheng Shao, Xiuyun Wang, Chih‐Wen Pao et al.
136 citations
Nature Communications
Electrocatalysts for Energy Conversion
13.92
article

Bimetallic nanoalloys planted on super-hydrophilic carbon nanocages featuring tip-intensified hydrogen evolution electrocatalysis

Hsiao‐Tsu Wang, Yu‐Cheng Shao, Xiuyun Wang, Chih‐Wen Pao, Lili Han, Yi Feng Xiao, Haihui Hu, Shuwen Zhao, Linjie Zhang, Chen Sun, Dongdong Xiao, Kuan Hung Chen, Wei-Xuan Lin
article en
136 citations

Abstract

The insufficient availability and activity of interfacial water remain a major challenge for alkaline hydrogen evolution reaction (HER). Here, we propose an "on-site disruption and near-site compensation" strategy to reform the interfacial water hydrogen bonding network via deliberate cation penetration and catalyst support engineering. This concept is validated using tip-like bimetallic RuNi nanoalloys planted on super-hydrophilic and high-curvature carbon nanocages (RuNi/NC). Theoretical simulations suggest that tip-induced localized concentration of hydrated K<sup>+</sup> facilitates optimization of interfacial water dynamics and intermediate adsorption. In situ synchrotron X-ray spectroscopy endorses an H* spillover-bridged Volmer‒Tafel mechanism synergistically relayed between Ru and Ni. Consequently, RuNi/NC exhibits low overpotential of 12 mV and high durability of 1600 h at 10 mA cm<sup>‒2</sup> for alkaline HER, and demonstrates high performance in both water electrolysis and chlor-alkali electrolysis. This strategy offers a microscopic perspective on catalyst design for manipulation of the local interfacial water structure toward enhanced HER kinetics.

Nature CommunicationsVol. 15(1)
Tamkang University (TW), Chinese Academy of Sciences (CN), National Synchrotron Radiation Research Center (TW), Fujian Institute of Research on the Structure of Matter (CN), Institute of Physics (CN), Fuzhou University (CN)
National Natural Science Foundation of China, Chinese Academy of Sciences, Natural Science Foundation of Fujian Province, National Synchrotron Radiation Research Center, Fujian Institute of Research on the Structure of Matter, National Key Research and Development Program of China
Clean water and sanitation
Openalex Percentile: Top 0%
Electrocatalysts for Energy Conversion
13.92
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