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Review
. 2021 Sep 30:9:734108.
doi: 10.3389/fchem.2021.734108. eCollection 2021.

Recent Advances in Quantum Dots for Photocatalytic CO2 Reduction: A Mini-Review

Affiliations
Review

Recent Advances in Quantum Dots for Photocatalytic CO2 Reduction: A Mini-Review

Young Ho Park et al. Front Chem. .

Abstract

Solar energy-driven carbon dioxide (CO2) reduction to valuable solar fuels/chemicals (e.g., methane, ethanol, and carbon monoxide) using particulate photocatalysts is regarded as one of the promising and effective approaches to deal with energy scarcity and global warming. The growth of nanotechnology plays an eminent role in improving CO2 reduction (CO2R) efficiencies by means of offering opportunities to tailor the morphology of photocatalysts at a nanoscale regime to achieve enhanced surface reactivity, solar light absorption, and charge separation, which are decisive factors for high CO2R efficiency. Notably, quantum dots (QDs), tiny pieces of semiconductors with sizes below 20 nm, offering a myriad of advantages including maximum surface atoms, very short charge migration lengths, size-dependent energy band positions, multiple exciton generation effect, and unique optical properties, have recently become a rising star in the CO2R application. In this review, we briefly summarized the progress so far achieved in QD-assisted CO2 photoreduction, highlighting the advantages of QDs prepared with diverse chemical compositions such as metal oxides, metal chalcogenides, carbon, metal halide perovskites, and MXenes.

Keywords: CO2 reduction; MXene; carbon quantum dot; metal oxide; perovskite; photocatalyst; quantum dots; transition metal chalcogenide.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Schematic illustration of the (A) photocatalytic CO2 conversion method, (B) CO2 conversion by semiconducting photocatalyst, (C) density of states modification under different degrees of quantum confinement, and (D) the advantages of the QDs for the photocatalytic reduction of CO2.
FIGURE 2
FIGURE 2
TEM images of CsPbBr3 QDs with particle sizes of (A) 3.8 nm, (B) 6.1 nm, (C) 8.5 nm, and (D) 11.6 nm (inset crystal structures). Photocatalytic CO2R for QDs with (E) 8.5 nm CsPbBr3 QDs and (F) CsPbBr3 QDs of different sizes (reproduced with permission from (Hou et al., 2017)). (G) Schematic illustration for synthesis of Ti3C2 QDs and Ti3C2 QDs/Cu2O NWs/Cu heterostructure, FE-SEM images of (H) Cu2O NWs/Cu, (i) Ti3C2 QDs/Cu2O NWs/Cu heterostructures, (J) CH3OH yield as a function of time, and (K) energy level diagram of Ti3C2 QDs/Cu2O NWs/Cu and Ti3C2 sheets/Cu2O NWs/Cu heterostructures (reproduced with permission from (Zeng et al., 2019)).

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