Chinese Journal of Catalysis ›› 2026, Vol. 90: 130-144.DOI: 10.1016/S1872-2067(26)65192-3

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Boron-incorporation-mediated interfacial water orientation for boosting CO2 electroreduction to CH4

Yue Shena, Bing Chena, Jielian Yanga, Qi Wua, Yuemei Liaoa, Liya Zhoua,*(), Naixin Lyub, Jin Guoa, Xuetang Xua,*(), Anxiang Guana,*(), Zaiwang Zhaoc,*()   

  1. a School of Chemistry and Chemical Engineering, State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Guangxi Key Laboratory of Electrochemical Energy Materials, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development. Guangxi University, Nanning 530004, Guangxi, China
    b Department of Chemical Engineering, Carnegie Mellon University, Pittsburgh 15213, Pennsylvania, United States
    c College of Energy Materials and Chemistry, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010070, Inner Mongolia, China
  • Received:2026-04-21 Accepted:2026-06-15 Online:2026-11-18 Published:2026-11-19
  • About author:First author contact:

    Study concept and design: Yue Shen. Sample processing and characterization: Yue Shen, Bing Chen, Jielian Yang. Data analysis and interpretation: Yue Shen, Qi Wu, Yuemei Liao, Naixin Lyu, Jin Guo. Funding acquisition: Liya Zhou, Xuetang Xu, Anxiang Guan. Manuscript draft: Yue Shen, Anxiang Guan, Zaiwang Zhao. Manuscript review and editing: Liya Zhou, Xuetang Xu, Anxiang Guan, Zaiwang Zhao. All authors read and approved the final manuscript.

  • Supported by:
    National Natural Science Foundation of China(22465006);Natural Science Foundation of Guangxi Province(2026GXNSFAA00640424);Guangxi Science and Technology Major Program(Guike)(AA24263003);Guangxi Youth Talent Inclusive Support Policy Research Launch Fund(ZX02080030425009)

Abstract:

Precisely regulating interfacial water orientation to optimize proton supply and intermediate stabilization remains a critical challenge for efficient and selective electrochemical CO2 reduction to CH4, a high-value energy carrier with complex eight-proton-coupled electron transfer kinetics. Herein, we address this challenge by developing a boron (B) incorporation strategy to engineer the interfacial water microenvironment of Cu-doped CeO2 catalysts, where heteroatom B doping reorients interfacial water from an O-down to H-down configuration. The optimized 1.25BC-Cu catalyst achieves a maximum Faradaic efficiency (FE) of 74.9% for CH4 at −1.7 V vs. reversible hydrogen electrode (RHE), accompanied by a high partial current density of −582.4 mA cm-2, outperforming most previous CO2-to-CH4 catalysts. This catalyst also exhibits exceptional long-term stability, with negligible current decay and well-retained CH4 FE after 30 h of continuous electrolysis. Systematic experimental characterizations, including in-situ attenuated total reflection infrared spectroscopy, in-situ Raman spectroscopy, and electrochemical measurements, confirm that the H-down water alignment accelerates water dissociation for efficient *H generation and facilitates key CO2RR intermediates hydrogenation. Ab initio molecular dynamics and density functional theory calculations further reveal that B and Cu co-doping modulates the electronic structure of CeO2, upshifting the d-band center to enhance intermediate adsorption affinity, and reduces the free energy barrier of the rate-determining step for CH4 formation. The B incorporation drives ordered H-down water arrangement, optimizing proton transfer kinetics and suppressing competitive side reactions. Our findings establish heteroatom-mediated interfacial water orientation as a pivotal design principle for tailoring CO2RR selectivity, providing a new avenue for the rational synthesis of high-performance electrocatalysts for efficient CO2 methanation and energy storage.

Key words: Water orientation, O-down, H-down, CO2 electroreduction, B doping