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Journal ArticleDOI

Atomically Dispersed Indium-Copper Dual-Metal Active Sites Promoting C-C Coupling for CO2 Photoreduction to Ethanol.

TLDR
In this paper , a dual-metal photocatalyst consisted of atomically dispersed Indium-Copper anchored on polymeric carbon nitride (InCu/PCN), on which the photoreduction of CO 2 delivered an excellent ethanol production rate of 28.5 μmol·g −1 ·h -1 with a high selectivity of 92%.
Abstract
Photoreduction of CO 2 to C 2+ solar fuel is a promising carbon-neutral technology for renewable energy. This strategy is challenged by its low productivity due to low efficiency in multielectron utilization and slow C-C coupling kinetics. This work reports a dual-metal photocatalyst consisted of atomically dispersed Indium-Copper anchored on polymeric carbon nitride (InCu/PCN), on which the photoreduction of CO 2 delivered an excellent ethanol production rate of 28.5 μmol·g -1 ·h -1 with a high selectivity of 92%. Coupled experimental investigation with DFT calculation, this study unveils the following mechanisms underpinning the high performance of this catalyst. Essentially, In-Cu interaction enhances the charge separation by accelerating charge transfer from PCN to metal sites. In also transfers electrons to neighboring Cu via Cu-N-In bridges, increasing the electron density of Cu active sites. Furthermore, In-Cu dual-metal sites promote the adsorption of *CO intermediates and lower the energy barrier of C-C coupling.

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

TL;DR: 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.
Journal ArticleDOI

Microenvironment Engineering of Single/Dual-atom Catalysts for Electrocatalytic Application.

TL;DR: In this article , a review summarizes the latest progress in microenvironment engineering of single/dual-atom active sites via a comprehensive comparison of single-atom catalyst (SACs) and dual-atom catalysts (DACs), in terms of design principles, modulation strategy and theoretical understanding of structure-performance correlations.
Journal ArticleDOI

Oxygen vacancy engineering of zinc oxide for boosting piezo-electrocatalytic hydrogen evolution

TL;DR: In this paper , the defect engineering is applied in the hydrothermally-synthesized ZnO by heat treatment to fabricate ZnOs catalysts with various concentrations of oxygen vacancy.
Journal ArticleDOI

Isolated Electron Trap-Induced Charge Accumulation for Efficient Photocatalytic HydrogenProduction.

TL;DR: In this paper , isolated Mo atoms in a high oxidation state have been incorporated into the lattice of Cd0.5Zn 0.5S (CZS@Mo) nanorods, which exhibit photocatalytic hydrogen evolution rate of 11.32 mmol g-1/h-1 (226.4 µmol h-1; catalyst dosage 20 mg).
Journal ArticleDOI

Highly Selective Ethylene Production from Solar-Driven CO2 Reduction on the Bi2S3@In2S3 Catalyst with In–SV–Bi Active Sites

TL;DR: In this article , the Bi2S3@InS3 heterostructure catalyst is fabricated via one-step solvothermal synthesis, where Bi 2S3 serves as a photothermal material and synchronously affords photoexcited charge carriers.
References
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Journal ArticleDOI

A metal-free polymeric photocatalyst for hydrogen production from water under visible light

TL;DR: It is shown that an abundant material, polymeric carbon nitride, can produce hydrogen from water under visible-light irradiation in the presence of a sacrificial donor.
Journal ArticleDOI

CO2 electroreduction to ethylene via hydroxide-mediated copper catalysis at an abrupt interface

TL;DR: A copper electrocatalyst at an abrupt reaction interface in an alkaline electrolyte reduces CO2 to ethylene with 70% faradaic efficiency at a potential of −0.55 volts versus a reversible hydrogen electrode (RHE).
Journal ArticleDOI

Atomically dispersed Fe3+ sites catalyze efficient CO2 electroreduction to CO.

TL;DR: Electrochemical data suggest that the Fe3+ sites derive their superior activity from faster CO2 adsorption and weaker CO absorption than that of conventional Fe2+ sites, whereas non–precious metal catalysts have shown low to modest activity.
Journal ArticleDOI

Selective visible-light-driven photocatalytic CO 2 reduction to CH 4 mediated by atomically thin CuIn 5 S 8 layers

TL;DR: In this article, the authors show that the formation of a highly stable Cu-C-O-In intermediate at the Cu-In dual sites is the key feature determining selectivity.
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