Abstract
In this study, the influence of transition metal ion doping and rare earth ion co-doping on the structural, optical, and hydrogen (H2) production properties of nanocrystalline ZnS were estimated. A simple hydrothermal technique was utilized to prepare the ZnS, ZnS:Cr, and ZnS:(Cr,Er) nanoparticles (NPs). Comprehensive structural analysis confirming the effectual incorporation of Cr and Er in the place of Zn in ZnS matrix without disturbing the original structure. An-X-ray photoelectron narrow scans confirming the existence of zinc, sulfur, chromium, and erbium in the prepared sample as 2+, 2−, 3+, and 3+ chemical states, respectively. Surprisingly, the optical bandgap of ZnS was slightly enhanced after doping and co-doping. Anticipatedly, ZnS:(Cr,Er) system displayed highest H2 production than those of ZnS and ZnS:Cr samples beneath artificial solar illumination. The plausible causes behind the enhanced H2 evolution are discussed in detail.
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Acknowledgements
This work was supported by the National Research Foundation Korea funded by the Ministry of Science, ICT and Fusion Research (Grant Nos: NRF- 20201G1A1014959 and NRF-2022R1I1A1A01064248). This work was supported by the Technology development Program (S3038568) funded by the Ministry of SMEs and Startups (MSS, Korea). Researchers supporting project number (RSP2023R348), King Saud University, Riyadh, Saudi Arabia.
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This work was funded by the Technology Development Program (S3038568) funded by the Ministry of SMEs and Startups (MSS, Korea).
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BP and PP: Conceptualization, Methodology, Experimental, Investigation, Graphical Work, and Writing—original draft. MSPR and BAA-A: Methodology, Investigation, Experimental, Graphical Work, Writing—original draft, Resources. PR and SS: Formal Analysis. D-YL: Writing Review, Validation, Editing, and Resources. YLK: Investigation, Formal Analysis, Editing, Writing Review, and Supervision.
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Poornaprakash, B., Puneetha, P., Reddy, M.S.P. et al. Hydrogen evolution properties of Cr doped and (Cr, Er) co-doped ZnS nanoparticles. J Mater Sci: Mater Electron 34, 1614 (2023). https://doi.org/10.1007/s10854-023-11023-3
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DOI: https://doi.org/10.1007/s10854-023-11023-3