4.7 Article

N-N type core-shell heterojunction engineering with MoO3 over ZnO nanorod cores for enhanced solar energy harvesting application in a photoelectrochemical cell

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 791, Issue -, Pages 739-746

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2019.03.292

Keywords

Photoelectrochemical cell; Nanorods; Heterojunction; Photoanode; Hydrogen generation

Funding

  1. CSIR
  2. Department of Science and Technology (DST) [2015/IF150237]
  3. SNBNCBS

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Herein, we report an easy and scalable chemical bath deposition and spin coating route of n-n hetero architecture engineering to fabricate MoO3-ZnO core-shell nanorods (NRs) based photoanode, which is indeed the first time demonstration of this particular nano-heterojunction for solar energy conversion and hydrogen energy generation in a photoelectrochemical (PEC) cell. We further tune the MoO3 shell thickness by varying spin coated layer thickness. An average thickness similar to 100 nm of MoO3 over 450 nm ZnO NRs significantly improves the photocurrent from 3.3 to 27.6 mu Acm(-2). A 7.5 fold increase in applied bias photon to current conversion efficiency (ABPE) value is achieved upon visible light illumination (Visible light, 10 mWcm(-2)) with a maximum value of 0.15% than bare ZnO NRs (0.02%). In addition, hydrogen gas (5 mu molcm(-2)) is evolved even at no external potential applied to the PEC cell with this MoO3-ZnO. The physical insight of the enhanced PEC performance is also elucidated. We find the n-n hetero-architecture to provide a suitable solution to maximize solar light absorption along with enhanced charge carrier separation which also boosts the charge transportation and mobility in the junction region due to suitable core-shell interfacial band alignment and modulation of interfacial electronic structure. Mainly, the MoO3 shell provides a potential solution to get more catalytically active sites and the outer Mo-O dipole layer transfers holes to the electrolyte for easy oxidation of water. (C) 2019 Published by Elsevier B.V.

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