open access publication

Article, 2024

Size-Dependent Multi-Electron Donation in Metal-Complex Quantum Dots Hybrid Catalyst for Photocatalytic Carbon Dioxide Reduction

Advanced Functional Materials, ISSN 1616-301X, 10.1002/adfm.202315734

Contributors

Zhao Q. [1] Abdellah M. 0000-0002-6875-5886 [2] [3] [4] Cao Y. 0000-0003-4073-6162 [5] Meng J. 0000-0002-3813-5221 [1] [4] Zou X. [1] [4] Ene-mark-Rasmussen K. [1] Lin W. 0000-0003-3623-0353 [4] Li Y. [5] Chen Y. [5] Duan H. [4] [6] Pan Q. [4] Zhou Y. 0000-0001-9995-0652 (Corresponding author) [5] Pullerits T. 0000-0003-1428-5564 [4] Xu H. 0000-0001-7918-1454 [7] Canton S.E. 0000-0003-4337-8129 [1] Niu Y. [4] [6] Zheng K. 0000-0002-7236-1070 (Corresponding author) [1] [4]

Affiliations

  1. [1] Technical University of Denmark
  2. [NORA names: DTU Technical University of Denmark; University; Denmark; Europe, EU; Nordic; OECD];
  3. [2] South Valley University
  4. [NORA names: Egypt; Africa];
  5. [3] United Arab Emirates University
  6. [NORA names: United Arab Emirates; Asia, Middle East];
  7. [4] Lund University
  8. [NORA names: Sweden; Europe, EU; Nordic; OECD];
  9. [5] Southwest Petroleum University
  10. [NORA names: China; Asia, East];

Abstract

The effective conversion of carbon dioxide (CO) into valuable chemical fuels relies significantly on the donation of multiple electrons. Its efficiency is closely linked to both the density and lifetime of excited charge carriers. In this study, a hybrid catalyst system comprising covalently bonded InP/ZnS quantum dots (QDs) and Re-complexes is showcased. The electronic band alignment between the QDs and the Re-complexes is revealed to dominate the multi-electron transfer process for photocatalytic conversion to methane (CH). Notably, the size of the QDs is found to be a determining parameter. Among the three QD sizes investigated, transient absorption spectroscopy studies unveil that rapid multi-electron transfer from the QDs to the Re-catalyst occurs in smaller QDs (2.3 nm) due to the substantial driving force. Consequently, the photocatalytic conversion of CO to CH is significantly enhanced with a turnover number of 6, corresponding to the overall apparent quantum yield of ≈1%. This research underscores the possibilities of engineering multi-electron transfer by manipulating the electronic band alignment within a catalytic system. This can serve as a guide for optimizing photocatalytic CO reduction.

Keywords

methane, multi-electron donation, photocatalytic reduction of CO, quantum dot, size-dependent

Funders

  • Royal Physio‐graphic Society of Lund
  • Vetenskapsrådet
  • China Scholarship Council
  • Villum Fonden
  • Carl Tryggers Stiftelse för Vetenskaplig Forskning
  • National Natural Science Foundation of China

Data Provider: Elsevier