Issue 38, 2014

“Nano to nano” electrodeposition of WO3 crystalline nanoparticles for electrochromic coatings

Abstract

A “nano to nano” electrodeposition approach for preparing nano-structured thin films from the dispersion of nano-objects is reported. A typical WO3 system is demonstrated, where nanocrystalline films are electrodeposited onto transparent conductive electrodes such as ITO and Ag grid printed PET (Ag grid/PET) from the water dispersion of WO3 nanoparticles without applying high potential, adding surfactants or polymers. The process is based on the reduction of WO3, which eliminates the electrostatic repulsion between the nanoparticles causing film deposition on the cathode. The reduced WO3 (HWO3) is conductive, thus it allows further film growth towards higher thickness and coverage. The electrodeposited films consist of stacked crystalline nanoparticles, which provide a highly active surface area, facilitate the penetration of electrolyte and the intercalation/deintercalation of Li+ in the nanocrystals and therefore result in outstanding electrochromic performance and stability (92% contrast, 9 s coloring and 15 s bleaching, retaining 76% contrast after 1000 coloring–bleaching cycles). The thickness, electrochromic performance and surface coverage of the films are well tuned by potential and time. This novel “nano to nano” electrodeposition approach based on the electrochemical redox of nano-objects can be extended to various transition metal oxide nano-objects with different sizes and shapes.

Graphical abstract: “Nano to nano” electrodeposition of WO3 crystalline nanoparticles for electrochromic coatings

Supplementary files

Article information

Article type
Paper
Submitted
05 Jul 2014
Accepted
31 Jul 2014
First published
31 Jul 2014

J. Mater. Chem. A, 2014,2, 16224-16229

Author version available

“Nano to nano” electrodeposition of WO3 crystalline nanoparticles for electrochromic coatings

L. Liu, M. Layani, S. Yellinek, A. Kamyshny, H. Ling, P. S. Lee, S. Magdassi and D. Mandler, J. Mater. Chem. A, 2014, 2, 16224 DOI: 10.1039/C4TA03431G

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