Title A Novel Solution-Processable n-Dopant Based on 1,4-Dihydropyridine Motif for High Electrical Conductivity of Organic Semiconductors
Authors Shi, Ke
Lu, Zuo-Yu
Yu, Zi-Di
Liu, Han-Yu
Zou, Ye
Yang, Chi-Yuan
Dai, Ya-Zhong
Lu, Yang
Wang, Jie-Yu
Pei, Jian
Affiliation Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Bioorgan Chem & Mol Engn,Coll Chem & Mol, Minist Educ,Key Lab Polymer Chem & Phys,Ctr Soft, Beijing 100871, Peoples R China.
Chinese Acad Sci, Inst Chem, CAS Key Lab Organ Solids, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China.
Keywords dihydropyridine derivatives
electrical conductivity
n-type dopants
solution-processable devices
AIR-STABLE ORGANOMETALLICS
ELECTRONIC MATERIALS
THIN-FILMS
POLYMER
MOBILITY
TRANSISTORS
REDUCTION
DEVICES
MODEL
Issue Date 2017
Publisher ADVANCED ELECTRONIC MATERIALS
Citation ADVANCED ELECTRONIC MATERIALS. 2017, 3(11,SI).
Abstract p- or n-Dopants have played significant roles in the improvement of organic electronic devices through the controllable doping of organic semiconductors. However, there has been little study of air-stable n-dopants under ambient conditions with strong doping capability due to the low electron affinities of organic semiconductors. Herein, a 1,4-dihydropyridine-based derivative is designed and facilely synthesized as an efficient n-dopant. The doping process is systematically investigated by UV-vis-NIR spectroscopy in solution and ultraviolet photoelectron spectroscopy in the solid state. Excellent conductivities are obtained for a variety of doped n-type semiconductors via a simple solution process without further treatment, suggesting a broad class of 1,4-dihydropyridine derivatives could be used as n-dopants in future organic electronic devices.
URI http://hdl.handle.net/20.500.11897/500959
ISSN 2199-160X
DOI 10.1002/aelm.201700169
Indexed SCI(E)
Appears in Collections: 工学院
生物有机与分子工程教育部重点实验室
高分子化学与物理教育部重点实验室

Files in This Work
There are no files associated with this item.

Web of Science®


0

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.