TY - JOUR
T1 - Air-Stable Perylene Diimide Trimer Material for N-Type Organic Electrochemical Transistors
AU - Nguyen-Dang, Tung
AU - Bao, Si Tong
AU - Kaiyasuan, Chokchai
AU - Li, Kunyu
AU - Chae, Sangmin
AU - Yi, Ahra
AU - Joy, Syed
AU - Harrison, Kelsey
AU - Kim, Jae Young
AU - Pallini, Francesca
AU - Beverina, Luca
AU - Graham, Kenneth R.
AU - Nuckolls, Colin
AU - Nguyen, Thuc Quyen
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/6/13
Y1 - 2024/6/13
N2 - A new method is reported to make air-stable n-type organic mixed ionic-electronic conductor (OMIEC) films for organic electrochemical transistors (OECTs) using a solution-processable small molecule helical perylene diimide trimer, hPDI[3]-C11. Alkyl side chains are attached to the conjugated core for processability and film making, which are then cleaved via thermal annealing. After the sidechains are removed, the hPDI[3] film becomes less hydrophobic, more ordered, and has a deeper lowest unoccupied molecular orbital (LUMO). These features provide improved ionic transport, greater electronic mobility, and increased stability in air and in aqueous solution. Subsequently, hPDI[3]-H is used as the active material in OECTs and a device with a transconductance of 44 mS, volumetric capacitance of ≈250 F cm−3, µC* value of 1 F cm−1 V−1 s−1, and excellent stability (> 5 weeks) is demonstrated. As proof of their practical applications, a hPDI[3]-H-based OECTs as a glucose sensor and electrochemical inverter is utilized. The approach of side chain removal after film formation charts a path to a wide range of molecular semiconductors to be used as stable, mixed ionic-electronic conductors.
AB - A new method is reported to make air-stable n-type organic mixed ionic-electronic conductor (OMIEC) films for organic electrochemical transistors (OECTs) using a solution-processable small molecule helical perylene diimide trimer, hPDI[3]-C11. Alkyl side chains are attached to the conjugated core for processability and film making, which are then cleaved via thermal annealing. After the sidechains are removed, the hPDI[3] film becomes less hydrophobic, more ordered, and has a deeper lowest unoccupied molecular orbital (LUMO). These features provide improved ionic transport, greater electronic mobility, and increased stability in air and in aqueous solution. Subsequently, hPDI[3]-H is used as the active material in OECTs and a device with a transconductance of 44 mS, volumetric capacitance of ≈250 F cm−3, µC* value of 1 F cm−1 V−1 s−1, and excellent stability (> 5 weeks) is demonstrated. As proof of their practical applications, a hPDI[3]-H-based OECTs as a glucose sensor and electrochemical inverter is utilized. The approach of side chain removal after film formation charts a path to a wide range of molecular semiconductors to be used as stable, mixed ionic-electronic conductors.
KW - mixed ionic-electronic conductors
KW - n-type semiconductors
KW - organic electrochemical transistors
KW - sidechain engineering
KW - small molecules
UR - http://www.scopus.com/inward/record.url?scp=85188927918&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85188927918&partnerID=8YFLogxK
U2 - 10.1002/adma.202312254
DO - 10.1002/adma.202312254
M3 - Article
C2 - 38521992
AN - SCOPUS:85188927918
SN - 0935-9648
VL - 36
JO - Advanced Materials
JF - Advanced Materials
IS - 24
M1 - 2312254
ER -