Pd single atoms guided proton transfer along an interfacial hydrogen bond network for efficient electrochemical hydrogenation

Electrochemical hydrogenation (ECH) of unsaturated carbon-heteroatom bonds is essential for chemical transformations but is often limited by a barrier-intensive surface hydrogen transfer process. The interfacial hydrogen bond (HB) network offers a promising pathway for proton transfer but requires addressing the challenge of nondirectional proton shuttling in three-dimensional space. Here, we create hydrophilic CuO<i><sub>x</sub></i> islands on Cu foam (CF) and load electron-enriched Pd (Pd<sup>δ-</sup>) single atoms as proton traps (Pd<sub>1</sub>-CuO<i><sub>x</sub></i>/CF) to guide a fast proton transfer along a modified HB network to enhance ECH efficiency. During ECH, hydrophilic CuO<i><sub>x</sub></i> islands dissociate H<sub>2</sub>O into protons and reconstruct the interfacial HB network for facile proton transfer, while the Pd<sup>δ-</sup> single atoms reorient H<sub>2</sub>O molecules to electrostatically attract and reduce protons to active hydrogen, enabling efficient substrate hydrogenation. With guided proton transfer, Pd<sub>1</sub>-CuO<i><sub>x</sub></i>/CF achieves 99% hydrogenation efficiency for C─Cl bonds, outperforming Pd<sub>1</sub>-CF (69%) and CuO<i><sub>x</sub></i>/CF (57%), and demonstrates high selectivity and Faradaic efficiency in hydrogenating C═O and C≡N bonds to produce valuable chemicals.

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Publication Details

Journal
Science Advances
Published
2025-08-08
DOI
https://doi.org/10.1126/sciadv.adu1602
Citations
41
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
14.90
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article

Pd single atoms guided proton transfer along an interfacial hydrogen bond network for efficient electrochemical hydrogenation

Zhiwei Hu, Jie Dai, Ruizhao Wang, Cheng‐Wei Kao et al.
41 citations
Science Advances
Electrocatalysts for Energy Conversion
14.90
article

Pd single atoms guided proton transfer along an interfacial hydrogen bond network for efficient electrochemical hydrogenation

Zhiwei Hu, Jie Dai, Ruizhao Wang, Cheng‐Wei Kao, Xiang‐Kui Gu, Jiaxian Wang, Yancai Yao, Xingyue Zou, Qi Wang, Kaiyuan Wang, Long Zhao, Wenhuai Li, Ting‐Shan Chan, Lizhi Zhang, Qian Zheng, Rui Zhao
article en
41 citations

Abstract

Electrochemical hydrogenation (ECH) of unsaturated carbon-heteroatom bonds is essential for chemical transformations but is often limited by a barrier-intensive surface hydrogen transfer process. The interfacial hydrogen bond (HB) network offers a promising pathway for proton transfer but requires addressing the challenge of nondirectional proton shuttling in three-dimensional space. Here, we create hydrophilic CuO<i><sub>x</sub></i> islands on Cu foam (CF) and load electron-enriched Pd (Pd<sup>δ-</sup>) single atoms as proton traps (Pd<sub>1</sub>-CuO<i><sub>x</sub></i>/CF) to guide a fast proton transfer along a modified HB network to enhance ECH efficiency. During ECH, hydrophilic CuO<i><sub>x</sub></i> islands dissociate H<sub>2</sub>O into protons and reconstruct the interfacial HB network for facile proton transfer, while the Pd<sup>δ-</sup> single atoms reorient H<sub>2</sub>O molecules to electrostatically attract and reduce protons to active hydrogen, enabling efficient substrate hydrogenation. With guided proton transfer, Pd<sub>1</sub>-CuO<i><sub>x</sub></i>/CF achieves 99% hydrogenation efficiency for C─Cl bonds, outperforming Pd<sub>1</sub>-CF (69%) and CuO<i><sub>x</sub></i>/CF (57%), and demonstrates high selectivity and Faradaic efficiency in hydrogenating C═O and C≡N bonds to produce valuable chemicals.

Science AdvancesVol. 11(32)
Nanjing Tech University (CN), Yunnan University (CN), Wuhan University (CN), National Synchrotron Radiation Research Center (TW), Max Planck Institute for Chemical Physics of Solids (DE)
Openalex Percentile: Top 1%
Electrocatalysts for Energy Conversion
14.90
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