Construction of ZnIn2S4-In2O3 hierarchical tubular heterostructures for efficient CO2 photoreduction

Construction of ZnIn2S4-In2O3 hierarchical tubular heterostructures for efficient CO2 photoreduction

2018 | Wang, Sibo; Guan, Bu Yuan; Lou, Xiong Wen David
The paper by Wang, Guan, and Lou (2018) presents the construction of sandwich-like ZnIn₂S₄-In₂O₃ hierarchical tubular heterostructures for efficient CO₂ photoreduction. The authors designed and fabricated these heterostructures by growing ZnIn₂S₄ nanosheets on both inner and outer surfaces of In₂O₃ microtubes. This unique design integrates In₂O₃ and ZnIn₂S₄ into hierarchical one-dimensional (1D) open architectures with double-heterojunction shells and ultrathin two-dimensional (2D) nanosheet subunits. The structure accelerates the separation and transfer of photogenerated charges, provides a large surface area for CO₂ adsorption, and exposes abundant active sites for surface catalysis. The optimized ZnIn₂S₄-In₂O₃ photocatalyst exhibits excellent performance in reductive CO₂ deoxygenation, with a CO evolution rate of 3075 μmol h⁻¹ g⁻¹ and high stability. The study highlights the importance of intimate interfacial contact and strong interactions in the heterostructures for enhancing the efficiency of CO₂ photoreduction.The paper by Wang, Guan, and Lou (2018) presents the construction of sandwich-like ZnIn₂S₄-In₂O₃ hierarchical tubular heterostructures for efficient CO₂ photoreduction. The authors designed and fabricated these heterostructures by growing ZnIn₂S₄ nanosheets on both inner and outer surfaces of In₂O₃ microtubes. This unique design integrates In₂O₃ and ZnIn₂S₄ into hierarchical one-dimensional (1D) open architectures with double-heterojunction shells and ultrathin two-dimensional (2D) nanosheet subunits. The structure accelerates the separation and transfer of photogenerated charges, provides a large surface area for CO₂ adsorption, and exposes abundant active sites for surface catalysis. The optimized ZnIn₂S₄-In₂O₃ photocatalyst exhibits excellent performance in reductive CO₂ deoxygenation, with a CO evolution rate of 3075 μmol h⁻¹ g⁻¹ and high stability. The study highlights the importance of intimate interfacial contact and strong interactions in the heterostructures for enhancing the efficiency of CO₂ photoreduction.
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