Issue 28, 2017

High-efficiency photoelectrochemical hydrogen generation enabled by p-type semiconductor nanoparticle-decorated n-type nanotube arrays

Abstract

TiO2 nanotube arrays (TNTAs) were decorated with NiO nanoparticles via a sequential chemical bath deposition (CBD) approach to yield NiO@TNTA photoanodes. In sharp contrast to pure TNTAs, NiO@TNTAs displayed increased absorption and decreased photoluminescence. Interestingly, NiO@TNTA photoanodes exhibited a higher photoelectrochemical activity for hydrogen production than pure TNTAs. The incident-photon-to-current-conversion efficiency (IPCE) of the optimized NiO@TNTA photoanode was calculated to be 62.8%, and remarkably, the maximum hydrogen production rate reached 37.8 μmol h−1 cm−2, approximately 5.0 times faster than pure TNTAs. Such markedly enhanced photoelectrochemical efficiency can be attributed primarily to the efficient separation of photogenerated charge carriers at the p–n junction of the two dissimilar semiconductors, that is, p-type NiO and n-type TiO2, in conjunction with the implementation of nanosized NiO particles with large surface area which enables a shortened charge transfer distance and in turn increased probability of reaction of charge carriers with water molecules.

Graphical abstract: High-efficiency photoelectrochemical hydrogen generation enabled by p-type semiconductor nanoparticle-decorated n-type nanotube arrays

Supplementary files

Article information

Article type
Paper
Submitted
26 Nov 2016
Accepted
06 Mar 2017
First published
21 Mar 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 17551-17558

High-efficiency photoelectrochemical hydrogen generation enabled by p-type semiconductor nanoparticle-decorated n-type nanotube arrays

L. Sun, Z. Wu, S. Xiang, J. Yu, Y. Wang, C. Lin and Z. Lin, RSC Adv., 2017, 7, 17551 DOI: 10.1039/C6RA27388B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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