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Industrial-level co-electrosynthesis of alkenol and Mg(OH)2 from seawater over Nd1Gd1 dual atomic site on metallene
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  • Published: 15 April 2026

Industrial-level co-electrosynthesis of alkenol and Mg(OH)2 from seawater over Nd1Gd1 dual atomic site on metallene

  • Qiqi Mao1,2 na1,
  • Wenxin Wang1 na1,
  • Ruidong Yang1,
  • Kai Deng1,
  • Hongjie Yu1,
  • Wenzhen Li  ORCID: orcid.org/0000-0002-1020-51872,
  • Liang Wang  ORCID: orcid.org/0000-0003-2971-63041,
  • Hongjing Wang  ORCID: orcid.org/0000-0003-0641-39091 &
  • …
  • Shaojun Guo  ORCID: orcid.org/0000-0002-5941-414X3 

Nature Communications (2026) Cite this article

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Subjects

  • Electrocatalysis
  • Hydrogen energy
  • Two-dimensional materials

Abstract

Industrial-level alkynols electrocatalytic semi-hydrogenation using seawater as hydrogen source offers a sustainable alternative to conventional thermocatalytic routes, yet remains limited by the lack of efficient and robust electrocatalysts. Here, we report the synthesis of Nd1Gd1 dual atomic site on metallene for co-production of alkenol and magnesium hydroxide in the seawater system. Nd1Gd1Pd metallene achieves a selectivity of ≈96.7% and a Faradaic efficiency of ≈87.3% for the conversion of 2-methyl-3-butyn-2-ol to 2-methyl-3-buten-2-ol at −150 mA cm-2 in a flow-cell system, and maintains ≈98.0% selectivity at 1.2 A for over 300 h of continuous operation, achieving the long-term stable co-electrosynthesis of alkenols and magnesium hydroxide in natural seawater at industrial-scale currents. Techno-economic analysis reveals a projected product revenue of at least $8,499 per ton of 2-methyl-3-buten-2-ol, underlining the industrial viability of this process. Mechanism investigations illustrate dual hydrogen-spillover and co-catalytic effects on Nd1Gd1Pd, promoting migration-reaction coupling mechanism of reactive *H to synergize hydrogenation. This work provides a seawater electrocatalytic semi-hydrogenation system and proposes an optimization strategy by atomically engineered dual hydrogen-spillover effect.

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Data availability

All data supporting the findings of this study are available within the article and its Supplementary Information. Source data are provided as a Source data file in the Supplementary Information. Source data are provided with this paper.

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Acknowledgements

This research was supported by the Zhejiang Provincial Natural Science Foundation of China under grant no. LR24B060001 (H.J.W.), and National Natural Science Foundation of China under grant no. 22572173 (L.W.), 22478345 (H.J.W.). Crystal structure visualizations were generated using the VESTA software.

Author information

Author notes
  1. These authors contributed equally: Qiqi Mao, Wenxin Wang.

Authors and Affiliations

  1. State Key Laboratory of Green Chemical Synthesis and Conversion, Zhejiang Key Laboratory of Surface and Interface Science and Engineering for Catalysts, College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, PR China

    Qiqi Mao, Wenxin Wang, Ruidong Yang, Kai Deng, Hongjie Yu, Liang Wang & Hongjing Wang

  2. Department of Chemical and Biological Engineering, Iowa State University, Ames, IA, USA

    Qiqi Mao & Wenzhen Li

  3. School of Materials Science and Engineering, Peking University, Beijing, PR China

    Shaojun Guo

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Contributions

H.J.W., L.W., and Q.M. conceived the idea and designed the experiments. H.J.W., L.W. supervised the project. Q.M., W.X.W., and R.Y. carried out catalyst synthesis and electrochemical experiments. K.D., H.J.Y. performed structural characterizations and analyzed XANES and EXAFS data. R.Y. performed and analyzed DFT calculations. Q.M., W.X.W., and R.Y. conducted in situ FTIR and EPR measurements. H.J.W., L.W., and Q.M. analyzed the results and wrote the paper. W.Z.L., S.G. helped with the revision of the paper. All authors discussed the results and commented on the manuscript.

Corresponding authors

Correspondence to Wenzhen Li, Liang Wang, Hongjing Wang or Shaojun Guo.

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Nature Communications thanks Nikolay Kornienko, Sang Uck Lee, Guangqin Li and the other anonymous reviewer(s) for their contribution to the peer review of this work. A peer review file is available.

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Mao, Q., Wang, W., Yang, R. et al. Industrial-level co-electrosynthesis of alkenol and Mg(OH)2 from seawater over Nd1Gd1 dual atomic site on metallene. Nat Commun (2026). https://doi.org/10.1038/s41467-026-71588-5

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  • Received: 27 August 2025

  • Accepted: 25 March 2026

  • Published: 15 April 2026

  • DOI: https://doi.org/10.1038/s41467-026-71588-5

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