4.7 Article

Biomass-Assisted Synthesis of CeO2 Nanorods for CO2 Photoreduction under Visible Light

期刊

ACS APPLIED NANO MATERIALS
卷 4, 期 4, 页码 4226-4237

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c00720

关键词

biomass-assisted synthesis; crystal phase engineering; CeO2 photocatalyst; visible light; CO2 photoreduction

资金

  1. National Natural Science Foundation of China [21871124]
  2. Shantou University (Shantou, China) [130-09419024]
  3. fund for Innovative Talents of Higher Learning Institutions of Liaoning Province, China (2018)

向作者/读者索取更多资源

This study successfully synthesized a highly efficient photocatalyst for converting CO2 into high-valued fuels by utilizing commercial chemicals and plant leaves. The amount of plant leaves introduced during the synthesis process had a significant impact on the growth morphology of the resulting CeO2 nanocrystals.
CO2 photoreduction into high-valued fuels is considered as a promising route to alleviate the clash between the environment and energy. Morphology-dependent CeO2 nanocrystallines with special crystal planes and increased amounts of specific surface areas, structural defects, and active sites have recently demonstrated excellent performance in catalysis. In this article, a biomass-assisted synthesis of CeO2 (BC) photocatalyst is successfully synthesized via a simple yet effective hydrothermal-calcining method by using commercial Ce(NO3)(3) as a precursor and leaves of Alternanthera philoxeroides (LAP) as a crystal growth modifier. The amount of LAP introduced into the precursor has a significant effect on regulating the growth of the formed CeO2 from nanocubes to nanorods for the resulting BCs. Owing to the emergence of the just right microenvironment for regulating the growth of the CeO2 nanocrystalline, the optimal sample of BC-15 with a morphology of nanorods is found to be the most efficient one as a photocatalyst for CO2 reduction under visible light. As the major product, the CO yield (126.8 mu mol g(-1) at a reaction time of 6 h) of BC-15 is similar to 7.4-fold of the reference CeO2 nanocubes synthesized without LAP in the precursor. In addition, the underlying evolution process of the nanorods and detailed mechanism insight into the boosted CO2 photoreduction performance are investigated by means of a series of experimental characterizations and results. The present work provides a meaningful protocol to utilize the crystal phase engineering strategy to design morphology dependence of photocatalysts and assisted synthesis with renewable biomass materials for solar-to-fuel conversion.

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