TY - JOUR
T1 - Separation in the Roles of Carrier Transport and Light Emission in Light-Emitting Organic Transistors with a Bilayer Configuration
AU - Shang, Hui
AU - Shimotani, Hidekazu
AU - Kanagasekaran, Thangavel
AU - Tanigaki, Katsumi
N1 - Funding Information:
*E-mail: shimotani@tohoku.ac.jp (Hidekazu Shimotani). *E-mail: tanigaki@m.tohoku.ac.jp (K.T.). ORCID Hidekazu Shimotani: 0000-0003-3238-9420 Present Addresses ⊥T.K.: Department of Physics, Indian Institute of Science Education and Research (IISER), Tirupati 517507, India §Institute of Condensed Matter and Nanosciences (IMCN/ NAPS), Université catholique de Louvain, 1348 Louvain-la-Neuve, Belgium. Author Contributions H. Shang and H. Shimotani conceived the experiments. H. Shimotani and K.T. supervised the project. H. Shang carried out almost all the experiments and wrote the manuscript. H. Shimotani performed theoretical calculation. T.K. provided technique of CsF and TTC thin-film deposition. Funding This work was supported by JSPS KAKENHI grant numbers 24684023 and 25610084. H. Shang is grateful for the CSC scholarship from Chinese government as well as the Tohoku University President Scholarship for Research and Education. Notes The authors declare no competing financial interest.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/6/5
Y1 - 2019/6/5
N2 - To develop high-performance organic light-emitting organic field-effect transistors (LE-OFETs), a fundamental problem in organic semiconductors is to compromise light luminescent efficiency for high carrier mobility and vice versa. Therefore, LE-OFETs can avoid this problem by separating the light-emission and carrier-transport functions. Here, a bilayer LE-OFET composed of a tetracene crystal as a carrier transporter (bottom crystal) and a 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran (DCM1)-doped tetracene crystal as a light emitter (top crystal) was fabricated. Red light-emission color, which is distinct from the green emission color of tetracene, was detected in the top crystal. Light emission from the top layer was prohibited when an insulating thin film was inserted between the two crystals. These observations indicate that excitons are formed in the bottom crystal and transferred to the top crystal, emitting reddish light. Bilayer LE-OFETs have the advantage of providing both high current density and a bright emission for high-performance light-emitting FETs.
AB - To develop high-performance organic light-emitting organic field-effect transistors (LE-OFETs), a fundamental problem in organic semiconductors is to compromise light luminescent efficiency for high carrier mobility and vice versa. Therefore, LE-OFETs can avoid this problem by separating the light-emission and carrier-transport functions. Here, a bilayer LE-OFET composed of a tetracene crystal as a carrier transporter (bottom crystal) and a 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran (DCM1)-doped tetracene crystal as a light emitter (top crystal) was fabricated. Red light-emission color, which is distinct from the green emission color of tetracene, was detected in the top crystal. Light emission from the top layer was prohibited when an insulating thin film was inserted between the two crystals. These observations indicate that excitons are formed in the bottom crystal and transferred to the top crystal, emitting reddish light. Bilayer LE-OFETs have the advantage of providing both high current density and a bright emission for high-performance light-emitting FETs.
KW - bilayer device structure
KW - delayed fluorescence
KW - energy transfer
KW - long exciton diffusion length
KW - organic light-emitting transistor
KW - separated functions
KW - singlet fission
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U2 - 10.1021/acsami.9b02298
DO - 10.1021/acsami.9b02298
M3 - Article
C2 - 31124645
AN - SCOPUS:85066406224
SN - 1944-8244
VL - 11
SP - 20200
EP - 20204
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 22
ER -