TY - JOUR
T1 - Energy Level, Crystal Morphology and Fluorescence Emission Tuning in Cocrystals via Molecular-Level Engineering
AU - Zhang, Jing
AU - Chen, Jinqiu
AU - Yang, Bo
AU - Ma, Shuang
AU - Yin, Lina
AU - Liu, Zhiqi
AU - Xiang, Wenxin
AU - Liu, Hongguang
AU - Zhao, Jianfen
AU - Sheng, Peng
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2023/2/16
Y1 - 2023/2/16
N2 - Organic donor-acceptor complexes as new organic semiconductor class have attracted wide attention, due to their potential applications in functional optoelectronics. Herein, we present two new charge transfer cocrystals of di-cyanodiazafluorene -perylene (DCPE) and di-cyanodiazaflfluorene-pyrene (DCPY) through a rational cocrystal-engineering strategy. Although they are both 1 : 1 mixed stacking cocrystals with similar chemical structures, the DCPE cocrystal possesses a non-centrosymmetric space group and narrower band gap compared to DCPY cocrystal, because of the non-covalent bonding variation. The electrostatic potential accumulated in the lateral facets leads to highly twisted DCPE nanobelts, and the small band gap causes near infrared fluorescence. Meanwhile, the DCPY crystals with centrosymmetric space groups and weaker intermolecular interactions exhibited an untwisted morphology and red emission. This study will be helpful for the design and understanding of functional cocrystal materials that can be used in flexible micro/nano-mechanics, mechanical energy, and optical devices.
AB - Organic donor-acceptor complexes as new organic semiconductor class have attracted wide attention, due to their potential applications in functional optoelectronics. Herein, we present two new charge transfer cocrystals of di-cyanodiazafluorene -perylene (DCPE) and di-cyanodiazaflfluorene-pyrene (DCPY) through a rational cocrystal-engineering strategy. Although they are both 1 : 1 mixed stacking cocrystals with similar chemical structures, the DCPE cocrystal possesses a non-centrosymmetric space group and narrower band gap compared to DCPY cocrystal, because of the non-covalent bonding variation. The electrostatic potential accumulated in the lateral facets leads to highly twisted DCPE nanobelts, and the small band gap causes near infrared fluorescence. Meanwhile, the DCPY crystals with centrosymmetric space groups and weaker intermolecular interactions exhibited an untwisted morphology and red emission. This study will be helpful for the design and understanding of functional cocrystal materials that can be used in flexible micro/nano-mechanics, mechanical energy, and optical devices.
KW - cocrystal engineering
KW - electrostatic energy
KW - fluorescence emission
KW - nanohelix
KW - self-assembly
UR - http://www.scopus.com/inward/record.url?scp=85145449523&partnerID=8YFLogxK
U2 - 10.1002/chem.202202915
DO - 10.1002/chem.202202915
M3 - 文章
C2 - 36404599
AN - SCOPUS:85145449523
SN - 0947-6539
VL - 29
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 10
M1 - e202202915
ER -