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Near-infrared-driven photocatalytic CO2 reduction to C2 hydrocarbons by bis(terpyridine)-metal functionalized lead halide frameworks
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  • Published: 15 January 2026

Near-infrared-driven photocatalytic CO2 reduction to C2 hydrocarbons by bis(terpyridine)-metal functionalized lead halide frameworks

  • Yukong Li1,
  • Ziyi Wang1,
  • Xiaoyang He1,
  • Chen Sun1,
  • Qikai Zheng1,
  • Yilin Jiang1,
  • Zuofeng Chen  ORCID: orcid.org/0000-0002-2376-21501 &
  • …
  • Honghan Fei  ORCID: orcid.org/0000-0003-1353-99211 

Nature Communications , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Photocatalysis

Abstract

Hybrid lead halides have demonstrated great promise for CO2 photoreduction due to their excellent photophysical properties. However, developing a single-component hybrid lead halide that combines high intrinsic stability with near-infrared absorption remains a significant challenge. Herein, to address both issues, we design a series of nine highly stable lead halide frameworks functionalized by bis(terpyridine)-metal complexes, which exhibit strong light absorption extending into the near-infrared region up to 1150 nm. Unlike their symmetric chloride and bromide analogues, the charge-polarized lead iodide sites in bis(terpyridine)-metal-functionalized frameworks serve as highly efficient C–C coupling centers for C2 production in near-infrared-driven CO2 photoreduction, achieving notable C2 production rates of up to 14.2 μmol g-1 h-1 with electron selectivities as high as 86%. These performances match the state-of-the-art among all reported single-component, near-infrared-responsive photocatalysts. This work highlights the potential of coordination-driven assembly of highly stable lead halide frameworks for near-infrared-driven artificial photosynthesis.

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Data availability

The data supporting the findings of this study are available. The X-ray crystallographic coordinates for structures reported in this study have been deposited at the Cambridge Crystallographic Data Centre (CCDC), under deposition number 2435159 (TJU-59(Cl)-Fe(tpy)2), 2435160 (TJU-59(Cl)-Co(tpy)2), 2435161 (TJU-59(Cl)-Ni(tpy)2), 2435162 (TJU-59(Br)-Fe(tpy)2), 2435163 (TJU-59(Br)-Co(tpy)2), 2435164 (JU-59(Br)-Ni(tpy)2), 2435165 (TJU-60(I)-Fe(tpy)2), 2435166 (TJU-60(I)-Co(tpy)2) and 2435167 (TJU-60(I)-Ni(tpy)2), respectively. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. Source data are provided with this paper.

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Acknowledgements

This work was supported by grants from the National Key R&D Program of China (2024YFA1211004), the National Natural Science Foundation of China (225B2117, 22171214, 22471196), the Recruitment of Global Youth Experts by China, the Xiaomi Young Talents Program, the Fundamental Research Funds for the Central Universities, and the Science & Technology Commission of Shanghai Municipality (19DZ2271500).

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Authors and Affiliations

  1. School of Chemical Science and Engineering, Shanghai Key Laboratory of Chemical Assessment and Sustainability, Tongji University, Shanghai, P. R. China

    Yukong Li, Ziyi Wang, Xiaoyang He, Chen Sun, Qikai Zheng, Yilin Jiang, Zuofeng Chen & Honghan Fei

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Contributions

Y.L., Z.C., and H.F. conceived the project. H.F. and Z.C. supervised the project, and Y.L. performed the majority of experimental studies. Z.W., C.S., Q.Z., and Y.J. assisted in synthesis and photophysical studies. X.H. and Z.C. assisted in computational studies. Y.L., Z.C., and H.F. wrote and revised the manuscript. All authors contributed to the discussion and revisions.

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Correspondence to Zuofeng Chen or Honghan Fei.

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Li, Y., Wang, Z., He, X. et al. Near-infrared-driven photocatalytic CO2 reduction to C2 hydrocarbons by bis(terpyridine)-metal functionalized lead halide frameworks. Nat Commun (2026). https://doi.org/10.1038/s41467-026-68450-z

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  • Received: 20 May 2025

  • Accepted: 05 January 2026

  • Published: 15 January 2026

  • DOI: https://doi.org/10.1038/s41467-026-68450-z

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