(289f) Tungsten Trioxide/Zinc Tungstate Bilayers: Electrochromic Behaviors, Energy Storage and Electron Transfer | AIChE

(289f) Tungsten Trioxide/Zinc Tungstate Bilayers: Electrochromic Behaviors, Energy Storage and Electron Transfer

Authors 

Wei, H. - Presenter, University of Tennessee Knoxville
Ding, D., Lamar University
Yan, X., Lamar University
Guo, J., university of tennessee, knoxville
Chen, H., Texas State University-San Marcos
Shao, L., Harbin Institute of Technology
Wei, S., Lamar University
Guo, Z., Lamar University
Sun, L., University of Connecticut

Materials with integrated functions of energy storage and electrochromism are highly desirable from the point of view of sustainable development.1, 2 Herein, pair-sequentially spin-coated tungsten trioxide (WO3) and zinc tungstate (ZnWO4) bilayer films onto indium tin oxide (ITO) coated glass slides have been prepared via sol-gel methods followed by annealing. The bilayers of ZnWO4/WO3 (the bilayer film consisting of an inner layer of ZnWO4 and an outer layer of WO3 on the ITO glass) and WO3/ZnWO4 (the bilayer film consisting of an inner layer of WO3 and an outer layer of ZnWO4 on the ITO glass) exhibit integrated functions of electrochromic and energy storage behaviors as indicated by the in situ spectroelectrochemistry and cyclic voltammetry (CV) results. Accordingly, blue color was observed for the bilayer films at -1 V in 0.5 M H2SO4 solution. An areal capacitance of 140 and 230 μF/cm2 was obtained for the ZnWO4/WO3, and WO3/ZnWO4 film, respectively, at a scan rate of 0.05 V/s in the CV measurements. The CV results also unveiled the electron transfer behavior between the semiconductor films in the oxidation process, suggesting a sequence-dependent electrochemical response in the bilayer films. Meanwhile, methylene blue (MB) was used as an indicator to study the electron transfer phenomenon during the reduction process at negative potentials of -0.4 and -0.8 V, in 0.5 M Na2SO4. The results indicated that the electrons transfer across the bilayers was enhanced at more negative potentials.

References

1.  H. Wei, X. Yan, S. Wu, Z. Luo, S. Wei and Z. Guo, The Journal of Physical Chemistry C, 2012, 116, 25052-25064.

2.  H. Wei, J. Zhu, S. Wu, S. Wei and Z. Guo, Polymer, 2013, 54, 1820-1831.

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