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用于在0.6V电压下驱动的耐用、非易失性电致变色器件的含四(-甲基苯并咪唑基)联吡啶的钌(II)基金属超分子聚合物

Ru(II)-Based Metallo-Supramolecular Polymer with Tetrakis(-methylbenzimidazolyl)bipyridine for a Durable, Nonvolatile, and Electrochromic Device Driven at 0.6 V.

作者信息

Santra Dines Chandra, Mondal Sanjoy, Yoshida Takefumi, Ninomiya Yoshikazu, Higuchi Masayoshi

机构信息

Electronic Functional Macromolecules Group, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba 305-0044, Japan.

出版信息

ACS Appl Mater Interfaces. 2021 Jul 7;13(26):31153-31162. doi: 10.1021/acsami.1c07275. Epub 2021 Jun 26.

DOI:10.1021/acsami.1c07275
PMID:34176261
Abstract

Low-voltage operation, high durability, and long memory time are demanded for electrochromic (EC) display device applications. Metallo-supramolecular polymers (MSPs), composed of a metal ion and ditopic ligand, are one of the recently developed EC materials, and the ligand modification is expected to tune the redox potential of MSP. In order to lower the redox potential of MSP, tetrakis(-methylbenzimidazolyl)bipyridine () was designed as an electronically rich ligand. Ru-based MSP () was successfully synthesized by 1:1 complexation of RuCl(DMSO) with . The molecular weight () was high (8.8 × 10 Da) enough to provide a simple H NMR spectrum, of which the proton peaks could be assigned by the comparison with the spectrum of the corresponding mono-Ru complex. The redox potential () between Ru(II/III) was 0.51 V Ag/Ag, which was much lower than the redox potential of previously reported Ru-based MSP with bis(terpyridyl)benzene (0.95 V Ag/Ag). The polymer film exhibited reversible, distinct color changes between violet and light green-yellow upon applying very low potentials of 0 and 0.6 V Ag/Ag, respectively. The appearance and disappearance of the metal-to-ligand charge transfer absorption by the electrochemical redox between Ru(II/III) were confirmed using spectro-electrochemical measurement. A solid-state EC device with was revealed to have large optical contrast (Δ 54%), fast response time (1.37 s for bleaching and 0.67 s for coloration), remarkable coloration efficiency (571 cm/C), and high durability for the repeated color changes more than 20,000 cycles. The device also showed a long optical memory time of up to 19 h to maintain 40% to the initial contrast under the open circuit conditions. It is considered that the stabilization of the Ru(III) state by suppressed the self-coloring to Ru(II) inside the device.

摘要

电致变色(EC)显示设备应用需要低电压操作、高耐久性和长记忆时间。由金属离子和双齿配体组成的金属超分子聚合物(MSP)是最近开发的EC材料之一,预计配体修饰可调节MSP的氧化还原电位。为了降低MSP的氧化还原电位,设计了四(-甲基苯并咪唑基)联吡啶()作为富电子配体。通过RuCl(DMSO)与的1:1络合成功合成了Ru基MSP()。分子量()很高(8.8×10 Da),足以提供简单的1H NMR光谱,通过与相应单Ru络合物的光谱比较可以归属质子峰。Ru(II/III)之间的氧化还原电位()为0.51 V vs Ag/Ag,远低于先前报道的含双(三联吡啶基)苯的Ru基MSP的氧化还原电位(0.95 V vs Ag/Ag)。该聚合物膜在分别施加0和0.6 V vs Ag/Ag的极低电位时,在紫色和浅绿黄色之间表现出可逆且明显的颜色变化。通过光谱电化学测量证实了Ru(II/III)之间电化学氧化还原导致的金属-配体电荷转移吸收的出现和消失。具有的固态EC器件显示出大的光学对比度(Δ 54%)、快速响应时间(漂白1.37 s,着色0.67 s)、显著的着色效率(571 cm2/C)以及超过20,000次循环的重复颜色变化的高耐久性。该器件还显示出长达19 h的长光学记忆时间,在开路条件下可保持初始对比度的40%。据认为,通过对Ru(III)状态的稳定抑制了器件内部向Ru(II)的自着色。

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引用本文的文献

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