TY - JOUR
T1 - Effects of selenium incorporation on the performance of polythiophene based organic electrochemical transistors
AU - Li, Meisi
AU - Feng, Wang
AU - Lan, Yu
AU - Sun, Yimin
AU - Li, Ping
AU - Li, Jianfeng
AU - Yang, Wanli
AU - Li, Hongxiang
AU - Ding, Junqiao
AU - Chen, Jianhua
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/5/8
Y1 - 2024/5/8
N2 - Selenium incorporation is a widely used strategy for achieving high mobility semiconductors for a variety of organic optoelectronic devices, but it has received less attention in organic electrochemical transistors (OECTs). Herein, we developed two polythiophene derivatives (Pg2T-S and Pg2T-SVS) containing different selenophene loadings, as well as a selenophene-free polythiophene (Pg2T-T) as the control. The effects of selenium substitution/incorporation on the optical, electrical, electrochemical, and OECT performance of polythiophene-based organic mixed ionic-electronic conductors are systematically investigated. We discovered that introduction of selenium increases quinoidal character and crystallinity, which is beneficial for charge transport but makes ion penetration more challenging. In contrast, increasing selenium content increases the dipole moment and ion-polymer interaction, which is helpful for ion doping and volumetric capacitance but detrimental to charge transport. Therefore, appropriate selenium content should be evaluated to balance the trade-off between charge transfer and volumetric capacitance. As a result, Pg2T-S with moderate selenium loading achieves a high μC* of 332.7 F cm−1 V−1 s−1 with increased μ of 1.31 cm2 V−1 s−1 and maintains the C* value of 254 F cm−3. It also has a quick τon/τoff of 10.76 ms/5.90 ms and outstanding operational stability. Further introducing selenium boosts the dipole moment and ion-polymer interaction and therefore increased C*, but suppressed μ, resulting in inefficient μC*. We indicated that systematic balancing of the effects of selenium incorporation is necessary for the development of mixed ionic-electronic conductors for high-performance OECTs.
AB - Selenium incorporation is a widely used strategy for achieving high mobility semiconductors for a variety of organic optoelectronic devices, but it has received less attention in organic electrochemical transistors (OECTs). Herein, we developed two polythiophene derivatives (Pg2T-S and Pg2T-SVS) containing different selenophene loadings, as well as a selenophene-free polythiophene (Pg2T-T) as the control. The effects of selenium substitution/incorporation on the optical, electrical, electrochemical, and OECT performance of polythiophene-based organic mixed ionic-electronic conductors are systematically investigated. We discovered that introduction of selenium increases quinoidal character and crystallinity, which is beneficial for charge transport but makes ion penetration more challenging. In contrast, increasing selenium content increases the dipole moment and ion-polymer interaction, which is helpful for ion doping and volumetric capacitance but detrimental to charge transport. Therefore, appropriate selenium content should be evaluated to balance the trade-off between charge transfer and volumetric capacitance. As a result, Pg2T-S with moderate selenium loading achieves a high μC* of 332.7 F cm−1 V−1 s−1 with increased μ of 1.31 cm2 V−1 s−1 and maintains the C* value of 254 F cm−3. It also has a quick τon/τoff of 10.76 ms/5.90 ms and outstanding operational stability. Further introducing selenium boosts the dipole moment and ion-polymer interaction and therefore increased C*, but suppressed μ, resulting in inefficient μC*. We indicated that systematic balancing of the effects of selenium incorporation is necessary for the development of mixed ionic-electronic conductors for high-performance OECTs.
UR - https://www.scopus.com/pages/publications/85193592919
U2 - 10.1039/d4tc01226g
DO - 10.1039/d4tc01226g
M3 - 文章
AN - SCOPUS:85193592919
SN - 2050-7534
VL - 12
SP - 7935
EP - 7942
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 22
ER -