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Synergistic integration of MXene nanosheets with CdS@TiO2 core@shell S-scheme photocatalyst for augmented hydrogen generation

Authors
Rao, Vempuluru NavakoteswaraKwon, HyungukLee, YongheeRAVI, PARNAPALLEAhn, Chi WonKim, KyeounghakYang, Jun-Mo
Issue Date
Sep-2023
Publisher
ELSEVIER SCIENCE SA
Keywords
Hierarchal structure; Stability; Valence state; Shell thickness; DFT; Mxene photocatalyst
Citation
CHEMICAL ENGINEERING JOURNAL, v.471
Journal Title
CHEMICAL ENGINEERING JOURNAL
Volume
471
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/88765
DOI
10.1016/j.cej.2023.144490
ISSN
1385-8947
1873-3212
Abstract
In order to ensure continuous and stable production of hydrogen (H2), the development of hierarchical nano-structures within a few-layer Mxene nanosheet, incorporating an ultrathin TiO2 shell material, is essential. This shell material plays a crucial role in maintaining the long-term stability of the core and preventing photo-corrosion, thus enabling uninterrupted H2 generation. To evaluate their potential as visible-driven photo-catalysts for high H2 production, we conducted a comparative analysis of CdS cores covered with three different shell transition metal oxides (TiO2@NiO@ZnO), supported by Mxene. Structural and morphological character-izations through XRD and TEM confirmed the formation of pure CdS@TiO2@NiO@ZnO core-shell nano-structures, characterized by spherical shapes with a core diameter of 187 nm and a shell thickness of 19.2 nm. XPS experiments demonstrated the structural integrity of the individual elements within the nanocomposite, existing in their respective oxidation states within the core@shell structure. The hierarchical nanostructure exhibited optical characteristics with an absorption edge ranging from 480 to 580 nm. Among the three different shell materials, TiO2 displayed the highest photocatalytic activity under visible light irradiation, followed by NiO and ZnO. Based on our findings, the CdS@TiO2 core@shell photocatalyst supported by Mxene exhibited the highest efficiency, with a production rate of 16.2 mmol.h- 1.g-1cat. This can be attributed to enhanced charge separation, the spatial distribution of carriers, and favorable structural properties. Our DFT calculations further supported the efficacy of coupling Mxene with CdS/TiO2, as it facilitated efficient water splitting, with CdS favoring H2O dissociation and Mxene favoring HER. These results highlight the potential of developing highly efficient photocatalysts for water splitting by integrating Mxene with CdS/TiO2. Additionally, The prepared CDTM (Mxene@CdS/TiO2) photocatalyst existing S-scheme heterojunction for efficient water splitting. This underscores the system's effective functioning across diverse sceneries, Overall, our study presents a feasible and effective strategy for constructing an S-scheme heterojunction system that utilizes photo charge carrier separa-tion to enhance the utilization and conversion of solar energy.
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RAVI, PARNAPALLE
BioNano Technology (Department of Physics)
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