Vertically Phase-Separated PEDOT:PSS Film via Solid-Liquid Interface Doping for Flexible Organic Electrochemical Transistors.

ACS Appl Mater Interfaces

MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, 310027 Hangzhou, China.

Published: March 2025

Organic electrochemical transistors (OECTs) are seen as some of the most promising devices in organic bioelectronics. Recent interest in OECTs is sparked by the high performance of an organic semiconductor channel material, i.e., poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS). The capability of ion penetration and charge transport of the channel determines the performance of the OECTs. However, the uniform structure of the PEDOT:PSS channel always makes it difficult to achieve a well-balanced between the two functions. Here, we report a novel PEDOT:PSS film with a vertical phase separation structure (VPSS-P), where PSS accumulates at the surface, and PEDOT enriches at the bottom of the film. Such a unique structure improves the electrochemical stability and reduces the contact resistance, significantly enhancing OECT performance with high transconductance (70.5 mS), product of mobility (μ) and volumetric capacitance (*) (μ* ∼ 479 F cm V s), and ultralow contact resistance (∼0.79 Ω cm). Flexible OECT devices with VPSS-P show robust performance against deformation. Our findings highlight a new class of high-performance transistors and provide guidelines for designing state-of-the-art channel materials.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.5c01311DOI Listing

Publication Analysis

Top Keywords

pedotpss film
8
organic electrochemical
8
electrochemical transistors
8
contact resistance
8
vertically phase-separated
4
pedotpss
4
phase-separated pedotpss
4
film solid-liquid
4
solid-liquid interface
4
interface doping
4

Similar Publications

TiO-Nanobelt-Enhanced, Phosphorescent, Organic Light-Emitting Diodes.

Nanomaterials (Basel)

January 2025

Department of Materials Science and Engineering, National Tsing Hua University, 101, Sec. 2, Kuang-Fu Road, Hsinchu 30013, Taiwan.

This study investigates the enhancement of organic light-emitting diode (OLED) performance through the integration of titanium dioxide (TiO) nanocomposites within a poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT/PSS) matrix. The nanocomposite films were prepared using a controlled dispersion of TiO belts into the PEDOT/PSS solution, followed by their incorporation into the OLED hole-injection layer (HIL). Our results demonstrate a significant improvement in device efficiency, attributed to the optimized charge carrier mobility and reduced recombination losses, which were achieved by the presence of TiO.

View Article and Find Full Text PDF

An electro- and optically favorable quaternary nanocomposite film was produced by solution-casting nickel oxide nanoparticles (NiO NPs) into polyvinyl alcohol (PVA), polyvinyl pyrrolidone (PVP), and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT/PSS). Based on transmission electron microscopy (TEM) and X-ray diffraction (XRD) observations, the synthesized NiO NPs have a cubic phase and a diameter between 10 and 45 nm. The complexity and interactions observed through XRD patterns, UV-visible spectra, and FTIR measurements suggest that the NPs are not just dispersed within the polymer matrix, but are interacting with it, leading to enhanced dielectric properties and AC electrical conductivity.

View Article and Find Full Text PDF

Superior Hole Injection Material PEGDT/TPF/PVDF with p-Doping Capability for Highly Efficient Solution-Processed Organic Light-Emitting Diode.

ACS Appl Mater Interfaces

October 2024

School of Advanced Materials and School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, Peking University, Shenzhen 518055, China.

Article Synopsis
  • The performance of OLED devices heavily relies on the ability to efficiently inject charge, particularly holes, through the anode interface.
  • An innovative p-doping hole injection material, PEGDT/TPF/PVDF, is introduced, achieving impressive metrics like a maximum current efficiency of 56.4 Cd A and an external quantum efficiency (EQE) of 19.8%.
  • The material enhances the anode's work function by 0.2 eV, significantly improving hole injection and offering a viable alternative to the commonly used PEDOT/PSS.
View Article and Find Full Text PDF

Carbon nanotube (CNT) films are extensively researched as a promising material for wearable thermoelectric generators (TEGs) owing to their good flexibility and high thermoelectric conversion ability. Miniaturizing a pair of p- and n-type thermocouples and increasing the number of repeating elements can effectively increase the power of TEGs. However, conventional p-n patterning methods, such as dipping and printing, have a coarse resolution at the submillimeter level, thereby limiting the miniaturization rate.

View Article and Find Full Text PDF

PEDOT:Nafion for Highly Efficient Supercapacitors.

ACS Appl Mater Interfaces

April 2024

Department of Environmental and Prevention Sciences, University of Ferrara, Ferrara 44121, Italy.

Supercapacitors offer notable properties as energy storage devices, providing high power density and fast charging and discharging while maintaining a long cycling lifetime. Although poly(3,4-ethylenedioxythiophene) doped with poly(4-styrenesulfonate) (PEDOT/PSS) has become a gold standard among organic electronics materials, researchers are still investigating ways to further improve its capacitive characteristics. In this work, we introduced Nafion as an alternative polymeric counterion to PSS to form highly capacitive PEDOT/Nafion; its advantageous supercapacitive properties were further improved by treatment with either dimethyl sulfoxide or ethylene glycol.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!