4.5 Article

Synthesis and properties of low-cost, photochromic transparent hydrogel based on ethaline-assisted binary tungsten oxide-molybdenum oxide nanocomposite for optical memory applications

Journal

POLYMERS FOR ADVANCED TECHNOLOGIES
Volume 33, Issue 3, Pages 687-699

Publisher

WILEY
DOI: 10.1002/pat.5400

Keywords

hydrogel; molybdenum oxide; photochromism; reverse fading; tungsten oxide

Funding

  1. China Scholarship Council

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Tungsten oxide-based composites are important for applications such as efficient energy windows, but face challenges in functional hydrogels due to agglomeration. The prepared highly transparent hydrogel shows excellent mechanical properties and notable photochromic response.
Tungsten oxide-based composites are important smart materials for wider usage in efficient energy windows, rewritable inks and other colored displays. However, the problem of agglomeration has made it challenging to be employed in transparent, photo-reversible materials especially in functional hydrogels. We herein report the preparation of high transparent hydrogel using water-soluble tungsten oxide-molybdenum oxide nanocomposites. The hydrogel was characterized with FTIR, TGA, XPS, SEM, and UV-Vis-NIR, while the mechanical properties were also analyzed. The FTIR confirmed that the metal oxides combined with the polymer units via strong metal-oxygen bond. For the TGA, the as-prepared hydrogel was still able to maintain a weight loss of 18.12% at 500 degrees C compared to 10.45% for pristine hydrogel. Also, the EDX mapping revealed microscopic metal oxides particles sizes, without any cluster phenomenon appearance. Additionally, the as-prepared hydrogel revealed good mechanical properties as it could sustain a high deformation ratio (lambda) of 86.3% at a stress of 60.3 MPa due to hydrogen bond crosslinking and ionic bond linkages. Moreover, the hydrogel exhibited high percentage transmittance (T%) of similar to 83%, as well as remarkable photochromic response, with absorption peaks at similar to 490, similar to 630 and similar to 730 nm appearing as the exposure time of the UV light increases. Furthermore, change in color was observed in 5 s, deepening to deep blue-black at 300 s exposure to UV, while complete reverse fading was achieved in similar to 6 h in ambient air without external stimulus, hence making it a good potential for applications in various optical memory, sensors and rewritable devices.

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