TY - JOUR
T1 - Pentacene derivative/DTTCNQ cocrystals
T2 - Alkyl-confined mixed heterojunctions with molecular alignment and transport property tuning
AU - Ma, Yudong
AU - Zhou, Yecheng
AU - Jin, Jianqun
AU - Wang, Wei
AU - Liu, Xitong
AU - Xu, Haixiao
AU - Zhang, Jing
AU - Huang, Wei
N1 - Publisher Copyright:
This journal is © The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Organic cocrystals are formed via the self-assembly of donor and acceptor constituents, which are mixed together through weak noncovalent interactions. Although they reveal unique physical features, their synthesis still faces major drawbacks for the introduction of more potential semiconductors. Herein, we first report soluble pentacene derivative (TMTES-P) based complexes, with suitable alkyl terminal groups, enabling the location of 4,8-bis(dicyanomethylene)-4,8-dihydrobenzo[1,2-b:4,5-b′]-dithiophene (DTTCNQ) in the crystal lattice, thereby allowing the cocrystallization of a binary system on demand. To our surprise, via varying growth conditions, molecular disorders could be removed due to existing short-contacts as the locking force, and even the carrier charge could be changed. This organic donor-acceptor system presents unconventional insights: charge polarity control over (opto)electronic devices with a supramolecular driving force as the directional alignment guide.
AB - Organic cocrystals are formed via the self-assembly of donor and acceptor constituents, which are mixed together through weak noncovalent interactions. Although they reveal unique physical features, their synthesis still faces major drawbacks for the introduction of more potential semiconductors. Herein, we first report soluble pentacene derivative (TMTES-P) based complexes, with suitable alkyl terminal groups, enabling the location of 4,8-bis(dicyanomethylene)-4,8-dihydrobenzo[1,2-b:4,5-b′]-dithiophene (DTTCNQ) in the crystal lattice, thereby allowing the cocrystallization of a binary system on demand. To our surprise, via varying growth conditions, molecular disorders could be removed due to existing short-contacts as the locking force, and even the carrier charge could be changed. This organic donor-acceptor system presents unconventional insights: charge polarity control over (opto)electronic devices with a supramolecular driving force as the directional alignment guide.
UR - http://www.scopus.com/inward/record.url?scp=85076818242&partnerID=8YFLogxK
U2 - 10.1039/c9sc04807c
DO - 10.1039/c9sc04807c
M3 - 文章
AN - SCOPUS:85076818242
SN - 2041-6520
VL - 10
SP - 11125
EP - 11129
JO - Chemical Science
JF - Chemical Science
IS - 48
ER -