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Overlooked roles of high-valence Sn in SnS2 loaded on gC3N4 for enhanced photocatalytic H2O2 production: Mechanism, DFT, and techno-economic analysis study
- Title
- Overlooked roles of high-valence Sn in SnS2 loaded on gC3N4 for enhanced photocatalytic H2O2 production: Mechanism, DFT, and techno-economic analysis study
- Authors
- Choong C.E.; Hong K.; Wong K.T.; Kong Z.; Yang A.; Mohd Jais F.; Yoon Y.; Choi E.; Jang M.
- Ewha Authors
- 윤여민
- SCOPUS Author ID
- 윤여민

- Issue Date
- 2025
- Journal Title
- Journal of Energy Chemistry
- ISSN
- 2095-4956
- Citation
- Journal of Energy Chemistry vol. 108, pp. 154 - 164
- Keywords
- Hydrogen Peroxide; In Situ Sers; Oxygen Reduction Reaction; Z-scheme; Decay (organic); Green Synthesis; Photocatalytic Activity; Density-functional-theory; In Situ Surface-enhanced Raman Spectroscopy; Isopropanol; Novel Methods; Photo-catalytic; Production Mechanisms; Surface Enhanced Raman Spectroscopy; Techno-economic Analysis; Electrolytic Reduction
- Publisher
- Elsevier B.V.
- Indexed
- SCIE; SCOPUS

- Document Type
- Article
- Abstract
- Solar-driven photocatalysis with charge-transfer modulation is a green approach for enhancing the oxygen reduction reaction (ORR) to generate hydrogen peroxide (H<inf>2</inf>O<inf>2</inf>). In this study, we introduced a novel method for synthesizing high-valence Snδ+ in SnS<inf>2</inf>, combined with gC<inf>3</inf>N<inf>4</inf> to create gC<inf>3</inf>N<inf>4</inf>/SnS<inf>2</inf>. Density functional theory (DFT) calculations exhibited that the interface between SnS<inf>2</inf> and gC<inf>3</inf>N<inf>4</inf> creates interband states through strong hybridization, revealing that photoexcited electrons flowed from C in gC<inf>3</inf>N<inf>4</inf> to S in SnS<inf>2</inf>, forming a Z-scheme heterojunction. The optimal gC<inf>3</inf>N<inf>4</inf>/SnS<inf>2</inf>-2 (2% SnS<inf>2</inf> loaded) achieved a high H<inf>2</inf>O<inf>2</inf> production rate of 7.186 mmol g−1 h−1 and an apparent quantum efficiency (AQE) of 33.8% at 405 nm with isopropanol (IPA), converting 88.8% IPA to acetone in 2 h. The gC<inf>3</inf>N<inf>4</inf>/SnS<inf>2</inf> composite improved the charge transfer resistance and elongated the non-radiative electron decay time. Notably, SnS<inf>2</inf> doping of gC<inf>3</inf>N<inf>4</inf> decreased the antibonding orbital occupancy and lowered the energy barrier for O<inf>2</inf> and OOH* adsorption. In situ surface-enhanced Raman spectroscopy (SERS) analysis confirmed the generation of OOH* on gC<inf>3</inf>N<inf>4</inf>/SnS<inf>2</inf> during light irradiation. A techno-economic analysis (TEA) was conducted to evaluate the economic viability of photocatalytic H<inf>2</inf>O<inf>2</inf> production, revealing that it was not economically feasible owing to challenges in the separation process. This study provides unique perspectives on the approaches to inducing a high valence state of Snδ+ for enhancing photocatalytic H<inf>2</inf>O<inf>2</inf> generation and the challenge of commercializing H<inf>2</inf>O<inf>2</inf> production via photocatalysis. © 2025 Elsevier B.V., All rights reserved.
- DOI
- 10.1016/j.jechem.2025.03.069
- Appears in Collections:
- 공과대학 > 환경공학과 > Journal papers
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