Published September 15, 2016 | Version v1
Journal article

In situ synthesis of oriented NiS nanotube arrays on FTO as high-performance counter electrode for dye-sensitized solar cells

  • 1. Key Laboratory of Atomic and Molecular Physics & Functional Materials of Gansu Province, College of Physics and Electronic Engineering, Northwest Normal University, Lanzhou, 730070 (China)
  • 2. Laboratory of Clean Energy Chemistry and Materials, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000 (China)

Description

Oriented nickel sulfide (NiS) nanotube arrays were successfully in-situ fabricated on conductive glass substrate and used directly as counter electrode for dye-sensitized solar cells without any post-processing. Compared with Pt counter electrode, for the beneficial effect of electronic transport along the axial direction through the arrays to the substrate, oriented NiS nanotube arrays exhibit both higher electrocatalytic activity for I3 reduction and better electrochemical stability, resulting in a significantly improved power conversion efficiency of 9.8%. Such in-situ grown oriented sulfide semiconductor nanotube arrays is expected to lead a new class structure of composites for highly efficient cathode materials. - Highlights: • In-situ synthesis strategy was proposed to construct oriented NiS nanotube arrays. • Such oriented tube nanostructure benefits the electronic transport along the axial direction of the arrays. • As CE of DSSCs, NiS nanotube arrays exhibit both higher efficiency (9.8%) and electrochemical stability than Pt.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jallcom.2016.04.079

Additional details

Identifiers

DOI
10.1016/j.jallcom.2016.04.079;
PII
S0925-8388(16)31033-7;

Publishing Information

Journal Title
Journal of Alloys and Compounds
Journal Volume
679
Journal Page Range
p. 384-390
ISSN
0925-8388
CODEN
JALCEU

Optional Information

Copyright
Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.