In Situ Electrochemical Interfacial Polymerization for Covalent Organic Frameworks with Tunable Electrochromism

• Published in: Angewandte Chemie International Edition Vol. 63; no. 46; pp. e202413071 - n/a
• Main Authors: Wang, Ying‐Ao, Wu, Qiong, Wang, Xun, Jiang, Min, Zhang, Rui, Chen, Xiao‐Juan, Liang, Ru‐Ping, Qiu, Jian‐Ding
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 11.11.2024
• Edition: International ed. in English
• Subjects: Chemical synthesis; Covalent organic frameworks; Electrochemistry; Electrochromism; Electrosynthesis; Functional groups; Polymerization; Redox properties; Steric hindrance; Uranium; Covalent organic frameworks; Electrosynthesis; Electrochromism; Uranium
• ISSN: 1433-7851; 1521-3773; 1521-3773
• DOI: 10.1002/anie.202413071

A rapid in situ synthesis of electrochromic covalent organic frameworks (EC‐COFs) was proposed by using green electrochemical interface polymerization of N,N,N’,N’‐tetrakis(4‐aminophenyl)‐1,4‐benzenediamine (TPDA) and 2,5‐dihydroxyterephthalaldehyde (DHBD). The synthetized TPDA‐DHBD films exhibit stable polymorphic color variations under different applied potentials, which can be attributed to the redox state changes of bis(triphenylamine) and imine electroactive functional groups within the COFs skeleton. TPDA‐DHBD represents markedly different electrochromisms from red to cyan due to the steric hindrance effect caused by the presence of UO22+, demonstrating the unique tunability of COFs materials. This work offers a new feasible idea for rapid EC‐COFs synthesis and tunable EC‐COFs realization. Simple and efficient electrochemical interfacial polymerization strategy was utilized to rapidly prepare electrochromic covalent organic frameworks (COFs) films at room temperature, which exhibited stable polymorphic electrochromic properties. Additionally, the electrochromic behavior of COFs films at negative potentials can be regulated by uranium, demonstrating the unique color tunability of COFs.