4.8 Article

Revealing the Double-Edged Sword Role of Graphene on Boosted Charge Transfer versus Active Site Control in TiO2 Nanotube Arrays@RGO/MoS2 Heterostructure

Journal

SMALL
Volume 14, Issue 21, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201704531

Keywords

active sites; charge transfer; double-edged sword role; heterostructures; photoredox

Funding

  1. National Natural Science Foundation of China [U1463204, 20903023, 21173045]
  2. Award Program for Minjiang Scholar Professorship
  3. Independent Research Project of State Key Laboratory of Photocatalysis on Energy and Environme [2014A05]
  4. 1st Program of Fujian Province for Top Creative Young Talents
  5. Open Research Project of State Key Laboratory of Physical Chemistry of Solid Surfaces of Xiamen University [201519]
  6. Natural Science Foundation (NSF) of Fujian Province [2017J07002]
  7. Program for Returned High-Level Overseas Chinese Scholars of Fujian province

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Charge separation/transfer is generally believed to be the most key factor affecting the efficiency of photocatalysis, which however will be counteracted if not taking the active site engineering into account for a specific photoredox reaction. Here, a 3D heterostructure composite is designed consisting of MoS2 nanoplatelets decorated on reduced graphene oxide-wrapped TiO2 nanotube arrays (TNTAs@RGO/MoS2). Such a cascade configuration renders a directional migration of charge carriers and controlled immobilization of active sites, thereby showing much higher photoactivity for water splitting to H-2 than binary TNTAs@RGO and TNTAs/MoS2. The photoactivity comparison and mechanistic analysis reveal the double-edged sword role of RGO on boosted charge separation/transfer versus active site control in this composite system. The as-observed inconsistency between boosted charge transfer and lowered photoactivity over TNTAs@RGO is attributed to the decrease of active sites for H-2 evolution, which is significantly different from the previous reports in literature. The findings of the intrinsic relationship of balanced benefits from charge separation/transfer and active site control could promote the rational optimization of photocatalyst design by cooperatively manipulating charge flow and active site control, thereby improving the efficiency of photocatalysis for target photoredox processes.

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