4.7 Article

Electrochromic behavior of NiO-TiO2 films prepared with sodium dodecyl sulfonate added to the sol

期刊

SOLAR ENERGY MATERIALS AND SOLAR CELLS
卷 114, 期 -, 页码 192-198

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.solmat.2013.03.007

关键词

NiO-TiO2; Electrochromism; Sol-gel; Dip coating; Sodium dodecyl sulfonate

资金

  1. Tianjin University of Science and Technology

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The effects of the surfactant sodium dodecyl sulfonate (SOS) on NiO-TiO2 sols, xerogels and films have been studied. Xerogels and films with Ni concentration of 80 mol% have been prepared using sols containing 3, 6, 9 wt% of SDS added to nickel acetate tetrahydrate (Ni(CH3COO)(2)center dot 4H(2)O) and tetra-n-butyl titanate (TNBT) as precursors in a mixture of ethanol and n-butanol. The thermal analysis of dried xerogels has been measured by thermogravimetry (TG) and differential thermal analysis (DTA) in air up to 500 degrees C. The structural properties of xerogels sintered at 300 degrees C have been determined by XRD and the xerogels consist predominantly of bunsenite nanoparticles embedded in an amorphous TiO2 phase. Single layers have been deposited by dip coating on FTO (fluorine doped tin oxide, SnO2:F) coated glasses and sintered at 300 degrees C. Their thickness is found to increase with the SDS amount while the roughness of the surface is reduced. The electrochromic properties of films deposited on FTO coated glasses have been studied in 1 M KOH aqueous electrolyte via cyclic voltammetry (CV), chronoamperometry (CA) and visible light transmission. The anodic and cathodic peaks in CV cycles and the charge intercalated during CA cycles increase with the SDS content. The transmission in the bleached and colored states as well as the change in optical density remain stable for the film prepared with 9 wt% SDS up to almost 18,000 CA cycles, a great improvement compared to films prepared without surfactant. The coloration efficiency of the film prepared with 9 wt% SDS is about 30 cm(2)/C, a value comparable to that obtained for pure NiO film. (C) 2013 Elsevier B.V. All rights reserved.

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