Ecofriendly AgBiS2 Nanocrystal Photoanode for Highly Efficient Visible-Light-Driven Photoelectrochemical Water Splitting
Source abstract
Abstract
Photoelectrochemical (PEC) hydrogen production via water splitting is a promising sustainable energy conversion method. However, most semiconductors used as photoanodes in PEC splitting exhibit several drawbacks, including ultraviolet (UV)-limited activity, toxic components, and complicated material processing. To address these issues, this study presents a photoanode design strategy for visible-light-driven PEC water splitting in aqueous Na 2 SO 4 solution using a solution-processable AgBiS 2 nanocrystal (NC) photoanode. It was observed that the characteristics of the ligand used for the AgBiS 2 NC photoanode are crucial in determining its PEC water splitting performance. Moreover, the thiol ligand-capped AgBiS 2 NC photoanode shows a higher photocurrent density ( J ph ) in both 1 sun and visible light than typical TiO 2 or Bi 2 S 3 NC photoanodes owing to its excellent electron collection ability and low interfacial charge transfer resistance. The AgBiS 2 NC photoanode emits 91% of J ph under visible and near-IR light, whereas the Bi 2 S 3 NC photoanodes exhibited a J ph of 67% under the same conditions, demonstrating the superiority of AgBiS 2 NC materials for application in highly efficient visible-light-driven PEC devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · Electrocatalysts for Energy Conversion · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Energy Science and Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Republic of Korea
Department of Chemistry, Research Institute for Natural Sciences, and Research Institute for Convergence of Basic Science, Hanyang University, Seoul 04763, Republic of Korea
Department of Chemistry, Kookmin University, Seoul 02707, Republic of Korea
Funding
Ministry of Science and ICT, South Korea · National Research Foundation of Korea
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