TY - JOUR
T1 - Self-doping and self-acid-doping of conjugated polymer bioelectronics : the case for accuracy in nomenclature
AU - Fidanovksi, Kristina
AU - Gu, Modi
AU - Travaglini, Lorenzo
AU - Lauto, Antonio
AU - Mawad, Damia
PY - 2024/9/25
Y1 - 2024/9/25
N2 - Conjugated polymers are enabling the development of flexible bioelectronics, largely driven by their organic nature which facilitates modification and tuning to suit a variety of applications. As organic semiconductors, conjugated polymers require a dopant to exhibit electrical conductivity, which in physiological conditions can result in dopant loss and thereby deterioration in electronic properties. To overcome this challenge, “self-doped” and self-acid-doped conjugated polymers having ionized pendant groups covalently bound to their backbone are being developed. The ionized group in a “self-doped” polymer behaves as the counterion that maintains electroneutrality, while an external dopant is required to induce charge transfer. The ionized group in a self-acid-doped polymer induces charge transfer and behaves as the counterion balancing the charges. Despite their doping processes being different, the two terms, self-doped and self-acid-doped, are often used interchangeably in the literature. Here, the differences are highlighted in the doping mechanisms of self-doped and self-acid-doped polymers, and it is proposed that the term “self-doped” should be replaced by “self-compensated,” while reserving the term self-acid-doped for polymers that are intrinsically doped without the need of an external dopant. This is followed by a summary of examples of self-acid-doping in bioelectronics, highlighting their stability in the conductive state under physiological conditions.
AB - Conjugated polymers are enabling the development of flexible bioelectronics, largely driven by their organic nature which facilitates modification and tuning to suit a variety of applications. As organic semiconductors, conjugated polymers require a dopant to exhibit electrical conductivity, which in physiological conditions can result in dopant loss and thereby deterioration in electronic properties. To overcome this challenge, “self-doped” and self-acid-doped conjugated polymers having ionized pendant groups covalently bound to their backbone are being developed. The ionized group in a “self-doped” polymer behaves as the counterion that maintains electroneutrality, while an external dopant is required to induce charge transfer. The ionized group in a self-acid-doped polymer induces charge transfer and behaves as the counterion balancing the charges. Despite their doping processes being different, the two terms, self-doped and self-acid-doped, are often used interchangeably in the literature. Here, the differences are highlighted in the doping mechanisms of self-doped and self-acid-doped polymers, and it is proposed that the term “self-doped” should be replaced by “self-compensated,” while reserving the term self-acid-doped for polymers that are intrinsically doped without the need of an external dopant. This is followed by a summary of examples of self-acid-doping in bioelectronics, highlighting their stability in the conductive state under physiological conditions.
KW - bioelectronics
KW - conjugated polymers
KW - self-acid-doped polymers
KW - self-doped polymers
UR - https://hdl.handle.net/1959.7/uws:73289
UR - http://www.scopus.com/inward/record.url?scp=85176591304&partnerID=8YFLogxK
U2 - 10.1002/adhm.202302354
DO - 10.1002/adhm.202302354
M3 - Article
SN - 2192-2640
VL - 13
JO - Advanced Healthcare Materials
JF - Advanced Healthcare Materials
IS - 24
M1 - 2302354
ER -