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Journal ArticleDOI

Interfacial Chemical Bond and Oxygen Vacancy‐Enhanced In2O3/CdSe‐DETA S‐scheme Heterojunction for Photocatalytic CO2 Conversion

TLDR
In this paper , an In�O�Cd bond-modulated S-scheme heterojunction of In2O3/CdSe−DETA is synthesized by a simple microwave assisted hydrothermal method for the accelerated photogenerated electron transfer.
Abstract
The S‐scheme heterojunctions have great potential for photocatalytic carbon dioxide reduction due to their unique carrier migration pathways, superior carrier separation efficiencies, and high redox capacities. However, the precise process of the oriented powerful electron transport remains a great challenge. Herein, an InOCd bond‐modulated S‐scheme heterojunction of In2O3/CdSe‐DETA is synthesized by a simple microwave‐assisted hydrothermal method for the accelerated photogenerated electron transfer. Meanwhile, the oxygen vacancies (Vo) of In2O3 have an electron capture effect. Consequently, thanks to the synergistic effect of this In‐Vo‐In‐O‐Cd structural units at the interface, electrons are extracted and rapidly transferred to the surface‐active sites, which improves the electronic coupling of CO2. This finding precisely adjusts the electron transfer pathway and shortens the electron transfer distance. The synergistic effect of this chemical bond established in the S‐scheme heterostructure with oxygen vacancies in In2O3 (Vo‐In2O3) provides new insights into photocatalytic CO2 reduction.

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2D/2D Janus BiTeCl/GeSe vdW heterostructure as a robust high-performance S-scheme photocatalyst for water splitting

TL;DR: In this article , a 2D/2D vdW heterostructures composed of Janus BiTeCl monolayer (ML) and GeSe ML was proposed, and the photocatalytic performance was investigated using first-principles calculations.
Journal ArticleDOI

Carbon dots modified dendritic TiO2-CdS heterojunction for enhanced photodegradation of rhodamine and hydrogen evolution

TL;DR: In this paper , a dendritic ternary photocatalyst of CdS-TiO2 heterojunction modified by carbon dots (CDs) was prepared by simple hydrothermal method and impregnation method, and the catalysts were characterized by XRD, SEM, TEM, XPS, Uvvis and ESI.
Journal ArticleDOI

Recent advances in heterogeneous catalysis of solar-driven carbon dioxide conversion

TL;DR: In this paper , a review summarizes the basic fundamentals and recent advances in the field of solar-driven CO2 conversion including photocatalytic (PC), photoelectrochemical (PEC), photovoltaic plus electrochemical(PV/EC) systems, offers a renewable and scalable way to produce fuels and high-value chemicals for environment and energy sustainability.
References
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Journal ArticleDOI

Designing a 0D/2D S-Scheme Heterojunction over Polymeric Carbon Nitride for Visible-Light Photocatalytic Inactivation of Bacteria.

TL;DR: A robust way for tailoring the performance and interpreting the mechanism of heterojunction-based photocatalytic system for high-performance photocatalysis is provided, via in-situ wet chemistry with subsequent heat treatment.
Journal ArticleDOI

Emerging S‐Scheme Photocatalyst

TL;DR: In this paper , the state-of-the-art S-scheme heterojunction has demonstrated its superiority in photocatalysis and provided new insights into its general designing criteria.
Journal ArticleDOI

Theoretical Insights into Heterogeneous (Photo)electrochemical CO2 Reduction

TL;DR: This review focuses specifically on the theory of heterogeneous electrocatalysis for CO2 reduction, and proposes strategies and principles for the future design of (photo)electrochemical catalysts to improve the selectivity and reaction kinetics ofCO2 reduction.
Journal ArticleDOI

Two-dimensional sulfur- and chlorine-codoped g-C3N4/CdSe-amine heterostructures nanocomposite with effective interfacial charge transfer and mechanism insight

TL;DR: In this paper, a step-scheme photocatalytic mechanism based on S/Cl-CN/CdSe-D heterostructure was proposed, where the S atom is appropriate to be incorporated into the CN framework to replace N atom, which is beneficial to adjust the band gap.
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