4.8 Article

Defect engineering via ternary nonmetal doping boosts the catalytic activity of ZIF-derived carbon-based metal-free catalysts for photovoltaics and water splitting

期刊

MATERIALS TODAY PHYSICS
卷 27, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.mtphys.2022.100785

关键词

ZIF-derivedcarbon; Heteroatomdoping; Hydrogenevolutionreaction; Defectengineering; Counterelectrodecatalyst; Dye-sensitizedsolarcells

资金

  1. NSFC [51672208]
  2. Key Program for Inter- national S & T Cooperation Projects of Shaanxi Province [2019KWZ-03]
  3. Key Program for Nature Science Foundation of Shaanxi Province [2019JZ-20]
  4. Key Science and Technology Innovation Team of Shaanxi Province [2022TD-34]
  5. Open foundation Project of Key Laboratory of Plateau Green Building and Ecological Community of Qinghai Prov- ince [KLKF-2019-002]

向作者/读者索取更多资源

By doping nonmetal atoms and modifying the structure and electronic structure of the catalyst, the catalytic activity of the catalyst was improved. Nitrogen, boron, and phosphorus/sulfur co-doped carbon catalysts demonstrated improved catalytic performance and excellent performance and stability in photovoltaic devices and alkaline hydrogen evolution reactions. This study presents a promising strategy for designing multivariate-doped non-metal catalysts for new energy applications.
The precise adjustment of the electronic structure of catalysts is an effective but difficult strategy for enhancing their catalytic performance. In this work, a defect engineering strategy was adopted to optimize the electronic structure of zeolitic imidazole zinc framework (ZIF)-derived in-situ nitrogen-doped carbon (N-C) via doping with nonmetal atoms (B and P/S). The doped nonmetal atoms altered the regular geometric construction of the catalyst and redistributed the electrons on the substrate, thus modifying the adsorption properties and catalytic ability of the catalyst. Benefitting from the modified electronic structure, enhanced structural defects, and synergistic effects among the different atoms, the N, B, and P/S co-doped carbon catalysts (BPN???C and BSN-C) exhibited enhanced catalytic activity. The best results were observed for BSN-C, which exhibited excellent catalytic activity for triiodide reduction reaction (IRR) in a photovoltaic device with an efficiency of 8.23%, superior to that of Pt (7.20%). BSN-C also produced a low overpotential of 129.7 mV at the current density of 10 mA cm-2 in an alkaline hydrogen evolution reaction (HER). BPN-C and BSN-C displayed remarkable stability in the IRR and HER. This work presents a promising strategy for designing superior carbon-based metal-free catalysts via multivariate doping with non-metal heteroatoms for new energy applications.

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