4.7 Article

Urchinlike W18O49/g-C3N4 Z-Scheme Heterojunction for Highly Efficient Photocatalytic Reduction of CO2 under Full Spectrum Light

Journal

ENERGY & FUELS
Volume 35, Issue 14, Pages 11468-11478

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.1c01241

Keywords

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Funding

  1. National Key RAMP
  2. D Program of China [2018YFB0605002]
  3. National Natural Science Foundation of China [21546014, 50616114]

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In this study, an urchinlike W18O49/g-C3N4 composite was fabricated via a simple hydrothermal process and exhibited superior photocatalytic behavior under full spectrum and near-infrared light. The enhanced activity was attributed to the tight contact between W18O49 and g-C3N4, as well as the formation of a Z-scheme heterojunction. Additionally, the local surface plasmonic resonance of W5+ also contributed to efficient photocatalysis under near-infrared light.
In this work, an urchinlike W18O49/g-C3N4 composite was fabricated via a simple hydrothermal process. The photocatalytic CO2 conversion reaction was applied to evaluate the photocatalytic behavior of this catalytic system, and the WOCN-20 wt % heterojunction displayed superior photocatalytic behavior under full spectrum light irradiation, which was 6.46 mu mol.h(-1).g(-1) for CO and 3.97 mu mol.h(-1).g(-1) for CH4, respectively. Furthermore, in the near-infrared region, the composite photocatalysts also displayed excellent photocatalytic performance. A large number of characterizations and testing measures were carried out to study the components, morphology, and physicochemical properties of W18O49/g-C3N4 photocatalyst, which were helpful to exploring and understanding the reasons for the improvement of catalytic performance. The boosted activity resulted from the tight contact between W18O49 and g-C3N4 and the formation of a Z-scheme heterojunction. The local surface plasmonic resonance (LSPR) of W5+ also contributed to the realization of efficient photocatalysis under near-infrared light. The Z-scheme electron transport model could realize the efficient separation of light-induced e(-)-h(+) pairs and reduce the recombination rate, thereby boosting the CO2 photocatalytic reduction process.

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