4.7 Article

Combining carbon dots with WO3-x nanodots for utilizing the full spectrum of solar radiation in photocatalysis

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 428, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.131139

Keywords

Solar energy utilization; Photocatalysis; Oxygen deficient tungsten oxide; Carbon dots; Heterojunction

Funding

  1. Specialized Research Fund for Sanjin Scholars Program of Shanxi Province, China
  2. Program for the Innovative Talents of Higher Education Institutions of Shanxi, China
  3. Key Research and Development Plan (International Cooperation) of Shanxi Province, China [201903D421082]
  4. Transformation of Scientific and Techno-logical Achievements Programs of Higher Education Institutions in Shanxi (TSTAP), China

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The study developed a hybrid system of carbon dots and oxygen-deficient WO3-x nanodots, which can effectively utilize the full spectrum of solar radiation and enhance photocatalytic activity.
Artificial photocatalytic systems represent a promising and available technology to directly convert sunlight into usable energy resources. Unfortunately, the current photocatalysts often absorb an only small range of sunlight spectra, hence greatly limiting the utilization efficiency of solar energy. Herein, we firstly developed a hybrid system that combines carbon dots (CDs) and oxygen-deficient WO3-x nanodots through a mild solvothermal method. This hybrid system features the heterojunction structure with dimensions smaller than 15 nm and can effectively utilize the full spectrum of solar radiation in photocatalytic oxidative reactions. In hybrid system, the CDs can enhance visible light harvesting ability of WO3-x nanodots and deliver their photoinduced carriers to the intermediate energy bands induced by oxygen-deficient of WO3-x. After further excitation with low energy photons, then more chemically useful carriers can be generated to participate fully in catalytic activation and reaction processes, resulting in 3.2 times higher photocatalytic activities of CDs@WO3-x than WO3-x nanodots.

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