Colorless Near-Infrared Absorbing Dyes Based on B-N Fused Donor-Acceptor-Donor π-Conjugated Molecules for Organic Phototransistors

被引:0
作者
Yokoyama, Soichi [1 ,2 ]
Utsunomiya, Sakura [1 ]
Seo, Takuji [1 ]
Saeki, Akinori [2 ,3 ]
Ie, Yutaka [1 ,2 ]
机构
[1] Osaka Univ, Inst Sci & Ind Res SANKEN, 8-1 Mihogaoka, Osaka, Ibaraki 5670047, Japan
[2] Osaka Univ, Inst Open & Transdisciplinary Res Initiat OTRI, Innovat Catalysis Sci Div, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Engn, Dept Appl Chem, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
关键词
colorless characteristics; electronic transitions; NIR absorbing dyes; organic phototransistors; organic semiconductors; DIRADICAL CHARACTER; TRANSPARENT; COMPLEXES; POLYMER; SYSTEMS; BODIPY;
D O I
10.1002/advs.202405656
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The introduction of a colorless function to organic electronic devices allows responses to light in the near-infrared (NIR) region and is expected to broaden the applications of these devices. However, the development of a colorless NIR dye remains a challenge due to the lack of a rational molecular design for controlling electronic transitions. In this study, to suppress the pi-pi* transitions in the visible region, polycyclic donor-acceptor-donor pi-conjugated molecules with boron bridges (Py-FNTz-B and IP-FNTz-B) are designed and synthesized, which contain pyrrole or indenopyrrole as donor units with fluorinated naphthobisthiadiazole (FNTz) as an acceptor unit. The pyrrole end-capped Py-FNTz-B shows an absorption band in the NIR region without distinct visible-light absorption, which has led to the establishment of colorless characteristics. The indenopyrrole end-capped IP-FNTz-B shows a narrow optical energy gap of 0.87 eV in films. Time-resolved microwave conductance and field-effect transistors demonstrate the semiconducting characteristics of these molecules, and Py-FNTz-B-based devices function as NIR phototransistors. Theoretical analyses indicate that the combination of a polyene-like electronic structure with orbital symmetry is important to obtain NIR wavelength-selective absorption. This study suggests that a molecular design based on electronic structures can be effective in the development of colorless NIR-absorbing dyes for organic electronics. To develop a colorless near-infrared (NIR) absorbing dye for organic electronics, polycyclic donor-acceptor-donor types of pi-conjugated molecules with boron bridges are synthesized. These molecules show NIR wavelength-selective absorption, which leads to colorless characteristics. Herein, a rational molecular design is proposed based on theoretical analyses. Semiconducting characteristics including NIR-responsible phototransistors are also described. image
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页数:11
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共 81 条
[1]   Solid-State, Near-Infrared to Visible Photon Upconversion via Triplet-Triplet Annihilation of a Binary System Fabricated by Solution Casting [J].
Abulikemu, Aizitiaili ;
Sakagami, Yusuke ;
Heck, Claire ;
Kamada, Kenji ;
Sotome, Hikaru ;
Miyasaka, Hiroshi ;
Kuzuhara, Daiki ;
Yamada, Hiroko .
ACS APPLIED MATERIALS & INTERFACES, 2019, 11 (23) :20812-20819
[2]  
[Anonymous], Deposition numbers 2353845
[3]   Transparent and colorless DSSCs featuring thienyl-pyrrolopyrrole cyanine sensitizers [J].
Baron, Thibaut ;
Naim, Waad ;
Kurucz, Mate ;
Nikolinakos, Ilias ;
Andrin, Baptiste ;
Pellegrin, Yann ;
Jacquemin, Denis ;
Haacke, Stefan ;
Sauvage, Frederic ;
Odobel, Fabrice .
JOURNAL OF MATERIALS CHEMISTRY A, 2023, 11 (31) :16767-16775
[4]   Transparent and Colorless Dye-Sensitized Solar Cells Based on Pyrrolopyrrole Cyanine Sensitizers [J].
Baron, Thibaut ;
Naim, Waad ;
Nikolinakos, Ilias ;
Andrin, Baptiste ;
Pellegrin, Yann ;
Jacquemin, Denis ;
Haacke, Stefan ;
Sauvage, Frederic ;
Odobel, Fabrice .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2022, 61 (35)
[5]   RELATIONSHIP BETWEEN BAND-GAP AND BOND LENGTH ALTERNATION IN ORGANIC CONJUGATED POLYMERS [J].
BREDAS, JL .
JOURNAL OF CHEMICAL PHYSICS, 1985, 82 (08) :3808-3811
[6]   Tunable electrical conductivity in oriented thin films of tetrathiafulvalene-based covalent organic framework [J].
Cai, Song-Liang ;
Zhang, Yue-Biao ;
Pun, Andrew B. ;
He, Bo ;
Yang, Jinhui ;
Toma, Francesca M. ;
Sharp, Ian D. ;
Yaghi, Omar M. ;
Fan, Jun ;
Zheng, Sheng-Run ;
Zhang, Wei-Guang ;
Liu, Yi .
CHEMICAL SCIENCE, 2014, 5 (12) :4693-4700
[7]   Fluorinated naphtho[1,2-c:5,6-c′]bis[1,2,5] thiadiazole-containing π-conjugated compound: synthesis, properties, and acceptor applications in organic solar cells [J].
Chatterjee, Shreyam ;
Ie, Yutaka ;
Seo, Takuji ;
Moriyama, Taichi ;
Wetzelaer, Gert-Jan A. H. ;
Blom, Paul W. M. ;
Aso, Yoshio .
NPG ASIA MATERIALS, 2018, 10 :1016-1028
[8]   Naphtho[1,2-c:5,6-c′]bis[1,2,5]thiadiazole-Based Nonfullerene Acceptors: Effect of Substituents on the Thiophene Unit on Properties and Photovoltaic Characteristics [J].
Chatterjee, Shreyam ;
Ie, Yutaka ;
Aso, Yoshio .
ACS OMEGA, 2018, 3 (05) :5814-5824
[9]   Visibly Transparent Polymer Solar Cells Produced by Solution Processing [J].
Chen, Chun-Chao ;
Dou, Letian ;
Zhu, Rui ;
Chung, Choong-Heui ;
Song, Tze-Bin ;
Zheng, Yue Bing ;
Hawks, Steve ;
Li, Gang ;
Weiss, Paul S. ;
Yang, Yang .
ACS NANO, 2012, 6 (08) :7185-7190
[10]   Unified theory for light-induced halide segregation in mixed halide perovskites [J].
Chen, Zehua ;
Brocks, Geert ;
Tao, Shuxia ;
Bobbert, Peter A. .
NATURE COMMUNICATIONS, 2021, 12 (01)