4.8 Article

P-Type AsP Nanosheet as an Electron Donor for Stable Solar Broad-Spectrum Hydrogen Evolution

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 46, Pages 55102-55111

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c16670

Keywords

artificial photosynthesis; plasmon resonance; electron donor; hydrogen evolution; NIR region

Funding

  1. NSFC [51802157, 61725402, 22172077]
  2. Natural Science Foundation of Jiangsu Province of China [BK20211573]
  3. Jiangsu International Science and Technology Cooperation Program [BZ2020063]
  4. China Postdoctoral Science Foundation [2020M671496]
  5. Fundamental Research Funds for the Central Universities [30921011216]

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The researchers have developed a novel AsP nanosheets that can serve as a stable electron donor for water reductive hydrogen in the near-infrared region. By coupling with Au nanorods and 1T-MoS2 nanosheets, a ternary heterojunction MoS2-Au-AsP was constructed with optimal H2 production rate.
Although research progress on mimicking natural photosynthesis for solar-to-fuel conversion has been continuously made, exploring broadband spectral-responsive materials with suitable band positions and high stability still remains a huge challenge. Herein, we, for the first time, report novel AsP nanosheets (NSs) with P-type semiconducting property and enough negative conduction band, which can work as a stable near-infrared (NIR) region-responsive electron donor for water reductive hydrogen (H-2) production. To mimic photosystem I, Au nanorods (NRs) act as electron transport media, which are also responsible for the enhanced electric field nearby, and 1T-MoS2 NSs as a hydrogen evolution catalyst are orderly coupled with AsP NSs with a sheet-rod-sheet structure by electrostatic self-assembly. The cascaded band level alignment enables unidirectional electron flow from AsP to Au and then to MoS2, and the optimum H-2 production rate of the MoS2-Au-AsP ternary heterojunction reaches 125.52 mu mol g(-1) h(-1) with good stability even after being stored for several months under light irradiation with a wavelength longer than 700 nm. This work provides a platform that is energetically tailored to drive a solar broad-spectrum fuel generation, including CO2 reduction and N-2 fixation.

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