4.7 Article

Manganese oxide at cadmium sulfide (MnOx@CdS) shells encapsulated with graphene: A spatially separated photocatalytic system towards superior hydrogen evolution

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 533, Issue -, Pages 452-462

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.08.102

Keywords

Spatially separated; MnOx@CdS; Graphene; Hydrogen evolution; Photocatalytic

Funding

  1. Fundamental Research Funds for the Central Universities of Central South University [2017zzts099]
  2. National Science Foundation of China [11674398]

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Exploring novel, high-efficiency and durable catalysts is of vital importance to expedite current research on photocatalytic H-2 evolution and address the energy and environmental issues. Herein, we rationally designed and synthesized a novel MnOx@CdS@GR photocatalyst with spatially separated dual co-catalysts for efficient visible-light-driven hydrogen production activity. In this spatially separated photocatalytic system, reduced graphene oxide (GR) and MnOx nanoparticles were anchored on the outer and inner surfaces of CdS shells acting as electron and hole collectors, respectively. The composition, microstructure and optical properties of the samples were thoroughly investigated. Photoluminescence spectra and photocurrent response as well as electrochemical impedance spectra were employed to reveal the separation and transfer ability of photo-generated charge carriers in the spatially separated MnOx@CdS@GR catalyst. Benefit from the synergistic effect including boosted light absorption capacity, enlarged specific surface area and increased separation and transfer efficiency of electron/hole pairs, the MnOx@CdS@GR exhibited superior H-2 evolution performance, and the optimized H-2-evolution rate reached a value of 5.45 mmol h(-1) g(-1), which is approximately 7.2 times than that of bare CdS. Moreover, this novel catalyst also displayed a long-term stability without apparent debasement in H-2 evolution activity. Finally, the photocatalytic mechanism was proposed and discussed. (C) 2018 Elsevier Inc. All rights reserved.

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