4.7 Article

Macroscopic graphitic carbon nitride monolith for efficient hydrogen production by photocatalytic reforming of glucose under sunlight

期刊

CHEMOSPHERE
卷 283, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.131174

关键词

Graphitic carbon nitride; Photoreforming; Hydrogen; Crystallization; Glucose

资金

  1. R&D Convergence Program of NST (National Research Council of Science & Technology) of the Republic of Korea [CAP-15-02-KBSI]
  2. National Research Foundation of Korea (NRF) - Korean government (MSIT) [2019R1C1C1007745]
  3. Smart Civil Infrastructure Research Program - Ministry of Land, Infrastructure and Transport of the Korean government [21SCIP-B145909-04]
  4. National Research Foundation of Korea (NRF) - Korean government (Ministry of Science, ICT & Future Planning) [2019R1A4A2001527]
  5. National Research Foundation of Korea [2019R1C1C1007745] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

This study develops monodisperse organic single-crystal monoliths with controllable dimensions, which are transformed into g-CN by thermal polycondensation, showcasing the potential to efficiently produce hydrogen via photoreforming. The dimensional tunability of the photocatalysts enables tailored catalytic activity for practical use and the formation of value-added products without compromising photocatalytic effectiveness in wastewater treatment.
Large particulate photocatalysts allow efficient recovery or installation into the substrate, while limiting possible light-catalyst interaction or mass/charge-transfer. In this study, we developed monodisperse organic singlecrystal monoliths with controllable dimensions in the range of 10-100 mu m. These were prepared on a 10-g scale by a solution-processed molecular cooperative assembly between melamine (M) and trithiocyanuric acid (TCA) and then transformed into the corresponding g-CN (MTCA-CN) by thermal polycondensation. Molecular precursors that are tightly bound in the crystal undergo polycondensation without losing their macroscopic properties depending on the dimensions of MTCA, thereby changing the microstructure, electronic structure, and photocatalytic activity. Such dimensional tunability enables the fulfillment of various catalytic requirements such as particle size, light absorption, charge separation, band edge potential, and mass transfer. As a proof-ofconcept, it was shown that MTCA-CN is tailored to have a high rate of evolution of hydrogen (3.19 mu mol/h) from glucose via photoreforming under AM1.5G by using MTCA-100 crystals, leading to the formation of g-CN with the more positive highest occupied molecular orbital (HOMO) level. This study highlights the possibility of developing photocatalysts for practical use and obtaining value-added products (VAPs) without losing the photocatalytic activity relevant for wastewater treatment.

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