4.8 Article

Hydrothermal Synthesis g-C3N4/Nano-InVO4 Nanocomposites and Enhanced Photocatalytic Activity for Hydrogen Production under Visible Light Irradiation

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 7, Issue 33, Pages 18247-18256

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b05715

Keywords

g-C3N4; InVO4; nanocomposites; interface; H-2 production from water splitting; heterojunction

Funding

  1. National Natural Science Foundation of China [21276116, 21301076, 21303074, 21201085]
  2. Natural Science Foundation of Jiangsu Province [BK2011517]
  3. Special Financial Grant from China Postdoctoral Science Foundation [2013T60501]
  4. Open Project of State Key Laboratory of Rare Earth Resource Utilizations [RERU2014010]
  5. Program for New Century Excellent Talents in University [NCET-13-0835]
  6. Henry Fok Education Foundation [141068]
  7. Six Talents Peak Project in Jiangsu Province [XCL-025]

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We synthesized g-C3N4/nano-InVO4 heterojunction-type photocatalyts by in situ growth of InVO4, nanopartides onto the surface of g-C3N4 sheets via a hydrothermal process. The results of SEM and TEM showed that the obtained InVO4 nanopartides 20 nm in size dispersed uniformly on the surface of g-C3N4 sheets, which revealed that g-C3N4 sheets was probably a promising support for in situ growth of nanosize materials. The achieved intimate interface promoted the charge transfer and inhibited the recombination rate of photogenerated electron hole pairs, which significantly improved the photocatalytic activity. A possible growth process of g-C3N4/nano-InVO4 nanocomposites was proposed based on different mass fraction of g-C3N4 content. The obtained g-C3N4/nano-InVO4 nanocomposites could achieve effective separation of charge-hole pairs and stronger reducing power, which caused enhanced H-2 evolution from water-splitting compared with bare g-C3N4 sheets and g-C3N4/micro-InVO4 composites, respectively. As a result, the g-C3N4/nano-InVO4 nanocomposite with a mass ratio of 80:20 possessed the maximum photocatalytic activity for hydrogen production under visible-light irradiation.

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