A strategy of stabilization via active energy-exchange for bistable electrochromic displays was written by Gu, Chang;Wang, Xiaojun;Jia, Ai-Bo;Zheng, Hongzhi;Zhang, Weiran;Wang, Yuyang;Li, Minjie;Zhang, Yu-Mo;Zhang, Sean Xiao-An. And the article was included in CCS Chemistry in 2022.Computed Properties of C9H15F6N2P This article mentions the following:
As future energy-saving optoelectronics, bistable electrochromic (EC) materials/devices have high energy efficiency for potential applications as smart windows, displays, and information/energy storage, due to their ability to maintain optical states without consuming energy. However, further development is hindered by the lack of in-depth understanding of related key factors and universally applicable design strategies to achieve bistability. Herein, we report a new strategy based on active energyexchange with the aid of proton-coupled electron transfer, which can dynamically adjust the HOMO /LUMO energy levels of materials to obtain good bistability from traditional nonbistable materials. This strategy was thoroughly studied and proven by taking quinone derivatives and bromocresol green derivatives as examples. The device obtained after further polymerization and optimization showed remarkable bistability, coloration efficiency, and application potential for energy-saving flexible displays. The success, challenges, and cognitive gains of this strategy not only accelerate the development of various energysaving optoelectronic materials/devices, but are also likely to stimulate progress in physics, chem., and materials. In the experiment, the researchers used many compounds, for example, 1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9Computed Properties of C9H15F6N2P).
1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Computed Properties of C9H15F6N2P
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem