Chinese Journal of Catalysis ›› 2026, Vol. 82: 238-250.DOI: 10.1016/S1872-2067(25)64919-9

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Synergistic Pd species anchored in ordered macroporous In2O3 boosting solar-driven CO2 and H2O conversion

Fuhao Yina,1, Qianyu Zhanga,1, Mao Xua,1, Shupeng Weia, Yi Lia, Pengzuo Chena, Yanying Zhaob,*(), Benxia Lia,*()   

  1. aSchool of Chemistry and Chemical Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, China
    bSchool of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, Zhejiang, China
  • Received:2025-07-17 Accepted:2025-10-10 Online:2026-03-18 Published:2026-03-05
  • Contact: * E-mail: libx@zstu.edu.cn (B. Li),yyzhao@zstu.edu.cn (Y. Zhao).
  • About author:1 Contributed equally to this work.
  • Supported by:
    National Natural Science Foundation of China(22371257);Joint Funds of the Zhejiang Provincial Natural Science Foundation of China(LZY23B030006)

Abstract:

Achieving efficient photocatalytic CO2 reduction using H2O as a hydrogen source requires the synergistic optimization of both charge and proton transfer between CO2 reduction and H2O oxidation half-reactions. However, conventional studies mostly focused on enhancing these half-reactions independently, overlooking the intrinsic interdependence between them. Herein, this work develops a photothermal catalyst (denoted as Pd1+c/3DOM-In2O3) through engineering synergistic Pd single atoms (Pd1) and Pd clusters (Pdc) in three-dimensional ordered macroporous (3DOM) In2O3 framework. The mechanistic study reveals that the coexistence of Pd single atoms and clusters not only offers synergistic active sites to promote the reaction of CO2 and H2O, but also substantially improves the separation and transfer efficiencies of photogenerated electrons and holes. The Pd clusters facilitate H2O dissociation to ensure an adequate supply of active hydrogen species as well as synergistically enhance the adsorption and activation of CO2 at Pd single-atom sites. Furthermore, the enhanced photoabsorption in visible and near-infrared regions, attributed to the localized surface plasmon resonance of Pd clusters, leads to a significant increase in catalyst temperature under simulated solar irradiation. The integration of photocatalysis with the photothermal effect affords an intensified driving force for the selective conversion of CO2 and H2O into CO, thereby accelerating the reaction kinetics of the overall photocatalytic CO2 reduction process. As a result, the Pd1+c/3DOM-In2O3 catalyst exhibits excellent performance for solar-driven CO2 reduction with H2O vapor, achieving a remarkable CO production rate of 192.52 μmol g-1 h-1, which is 19.8-fold and 12.2-fold higher than those of pure 3DOM-In2O3 and Pd1/3DOM-In2O3, respectively. This study provides valuable insights into the synergistic effect of metal single atoms and clusters toward both efficient photocatalysis and photothermal effect for solar-driven CO2 reduction.

Key words: Photocatalytic CO2 reduction, Photothermal effect, Pd species, Synergistic active sites, H2O activation