Photo Responsive Electron and Proton Conductivity within a Hydrogen-Bonded Organic Framework

被引:56
作者
Chen, Shimin [1 ]
Ju, Yan [1 ]
Zhang, Hao [1 ]
Zou, Yingbing [1 ]
Lin, Si [1 ]
Li, Yunbin [1 ]
Wang, Shuaiqi [1 ]
Ma, En [2 ]
Deng, Weihua [1 ]
Xiang, Shengchang [1 ]
Chen, Banglin [1 ]
Zhang, Zhangjing [1 ]
机构
[1] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Prov Key Lab Polymer Mat, Fuzhou 350117, Peoples R China
[2] Chinese Acad Sci, Haixi Inst, Xiamen Inst Rare Earth Mat, Xiamen Key Lab Rare Earth Photoelect Funct Mat, Xiamen 361000, Peoples R China
基金
中国国家自然科学基金;
关键词
Coupled Proton-Electron Transfer; D-A & pi; -& pi; Stacking; Hydrogen-Bonded Organic Framework; METHYL VIOLOGEN; DESIGN; STABILITY;
D O I
10.1002/anie.202308418
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rational design of crystalline porous materials with coupled proton-electron transfer has not yet been reported to date. Herein, we report a donor-acceptor (D-A) p-p stacking hydrogen-bonded organic framework (HOF; HOF-FJU-36) with zwitterionic 1,1 & PRIME;-bis(3-carboxybenzyl)-4,4 & PRIME;-bipyridinium (H2L2+) as acceptor and 2,7-naphthalene disulfonate (NDS2-) as donor to form a two-dimensional (2D) layer. Three water molecules were situated in the channels to connect with acidic species through hydrogen bonding interactions to give a 3D framework. The continuous p-p interactions along the a axis and the smooth H-bonding chain along the b axis provide the electron and proton transfer pathways, respectively. After 405 nm light irradiation, the photogenerated radicals could simultaneously endow HOF-FJU-36 with photoswitchable electron and proton conductivity due to coupled electron-proton transfer. By single-crystal X-ray diffraction (SCXRD) analyses, X-ray photoelectron spectroscopy (XPS), transient absorption spectra and density functional theory (DFT) calculations, the mechanism of the switchable conductivity upon irradiation has been demonstrated.
引用
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页数:7
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