High Current-density Organic Electrochemical Diodes Enabled by Asymmetric Active Layer Design
Type
ArticleAuthors
Kim, YoungseokKim, Gunwoo
Ding, Bowen
Jeong, Dahyun
Lee, Inho
Park, Sungjun
Kim, Bumjoon J.
McCulloch, Iain

Heeney, Martin

Yoon, Myung-Han

KAUST Department
Chemical Science ProgramKAUST Solar Center (KSC)
Date
2021-12Embargo End Date
2022-12-01Permanent link to this record
http://hdl.handle.net/10754/674004
Metadata
Show full item recordAbstract
Owing to outstanding electrical/electrochemical performance, operational stability, mechanical flexibility, and decent biocompatibility, organic mixed ionic-electronic conductors have shown great potential as implantable electrodes for neural recording/stimulation and as active channels for signal switching/amplifying transistors. Nonetheless, no studies exist on the general design rule for high-performance electrochemical diodes, which are essential for highly functional circuit architectures. Herein, we report on generalizable electrochemical diodes with very high current density over 30 kAcm-2 by introducing an asymmetric active layer based on organic mixed ionic-electronic conductors. The underlying mechanism on polarity-sensitive balanced ionic doping/dedoping is elucidated by numerical device analysis and in operando spectroelectrochemical potential mapping, while the general material requirements for electrochemical diode operation are deduced using various types of conjugated polymers. In parallel, analog signal rectification and digital logic processing circuits are successfully demonstrated to show the broad impact of organic electrochemical diode-incorporated circuits. We expect that organic electrochemical diodes will play vital roles in realizing multifunctional soft bioelectronic circuitry in combination with organic electrochemical transistors. This article is protected by copyright. All rights reserved.Citation
Kim, Y., Kim, G., Ding, B., Jeong, D., Lee, I., Park, S., … Yoon, M. (2021). High Current-density Organic Electrochemical Diodes Enabled by Asymmetric Active Layer Design. Advanced Materials, 2107355. doi:10.1002/adma.202107355Sponsors
The authors thank the Engineering and Physical Sciences Research Council (EPSRC) (EP/T028513/1), the Royal Society and the Wolfson Foundation (Royal Society Wolfson Fellowship) for funding. This work was also supported by a National Research Foundation (NRF) grant funded by the Korean government (MSIT) (NRF-2021R1A2C1013015, NRF-2018M3A7B4070988, NRF-2020M3D1A1030660 and NRF-2020M1A2A2080748), the Global Research Laboratory program (NRF-2017K1A1A2013153) and GIST Research Institute (GRI) grant by the GIST in 2021.Publisher
WileyJournal
Advanced MaterialsPubMed ID
34852181Additional Links
https://onlinelibrary.wiley.com/doi/10.1002/adma.202107355ae974a485f413a2113503eed53cd6c53
10.1002/adma.202107355
Scopus Count
Related articles
- Designing Polymeric Mixed Conductors and Their Application to Electrochemical-Transistor-Based Biosensors.
- Authors: Kim JH, Kim SM, Kim G, Yoon MH
- Issue date: 2020 Nov
- Functionalized Organic Thin Film Transistors for Biosensing.
- Authors: Wang N, Yang A, Fu Y, Li Y, Yan F
- Issue date: 2019 Feb 19
- High-Performance Integrated Iontronic Circuits Based on Single Nano/Microchannels.
- Authors: Li J, Li M, Zhang K, Hu L, Li D
- Issue date: 2023 Jun
- Fibriform Organic Electrochemical Diodes with Rectifying, Complementary Logic and Transient Voltage Suppression Functions for Wearable E-Textile Embedded Circuits.
- Authors: Choi KH, Kim SJ, Kim H, Jang HW, Yi H, Park MC, Choi C, Ju H, Lim JA
- Issue date: 2023 Mar 28
- Asymmetric Nafion-Coated Nanopore Electrode Arrays as Redox-Cycling-Based Electrochemical Diodes.
- Authors: Fu K, Han D, Kwon SR, Bohn PW
- Issue date: 2018 Sep 25
Related items
Showing items related by title, author, creator and subject.
-
A flexible organic active matrix circuit fabricated using novel organic thin film transistors and organic light-emitting diodesGutiérrez-Heredia, Gerardo; González, Luis A.; Alshareef, Husam N.; Gnade, Bruce E.; Quevedo-López, Manuel Angel Quevedo (Semiconductor Science and Technology, IOP Publishing, 2010-10-04) [Article]We present an active matrix circuit fabricated on plastic (polyethylene naphthalene, PEN) and glass substrates using organic thin film transistors and organic capacitors to control organic light-emitting diodes (OLEDs). The basic circuit is fabricated using two pentacene-based transistors and a capacitor using a novel aluminum oxide/parylene stack (Al2O3/ parylene) as the dielectric for both the transistor and the capacitor. We report that our circuit can deliver up to 15 μA to each OLED pixel. To achieve 200 cd m-2 of brightness a 10 μA current is needed; therefore, our approach can initially deliver 1.5× the required current to drive a single pixel. In contrast to parylene-only devices, the Al2O 3/parylene stack does not fail after stressing at a field of 1.7 MV cm-1 for >10 000 s, whereas 'parylene only' devices show breakdown at approximately 1000 s. Details of the integration scheme are presented. © 2010 IOP Publishing Ltd.
-
Polarization Energies at Organic–Organic Interfaces: Impact on the Charge Separation Barrier at Donor–Acceptor Interfaces in Organic Solar CellsRyno, Sean; Fu, Yao-Tsung; Risko, Chad; Bredas, Jean-Luc (ACS Applied Materials & Interfaces, American Chemical Society (ACS), 2016-06-08) [Article]We probe the energetic landscape at a model pentacene/fullerene-C60 interface to investigate the interactions between positive and negative charges, which are critical to the processes of charge separation and recombination in organic solar cells. Using a polarizable force field, we find that polarization energy, i.e. the stabilization a charge feels due to its environment, is larger at the interface than in the bulk for both a positive and a negative charge. The combination of the charge being more stabilized at the interface and the Coulomb attraction between the charges, results in a barrier to charge separation at the pentacene-C60 interface that can be in excess of 0.7 eV for static configurations of the donor and acceptor locations. However, the impact of molecular motions, i.e., the dynamics, at the interface at room temperature results in a distribution of polarization energies and in charge separation barriers that can be significantly reduced. The dynamic nature of the interface is thus critical, with the polarization energy distributions indicating that sites along the interface shift in time between favorable and unfavorable configurations for charge separation.
-
Roles of singlet oxygen and triplet excited state of dissolved organic matter formed by different organic matters in bacteriophage MS2 inactivationRosado-Lausell, Sahid L.; Wang, Hanting; Gutiérrez, Leonardo A.; Romero-Maraccini, Ofelia C.; Niu, Xi-Zhi; Gin, Karina; Croue, Jean-Philippe; Nguyen, Thanh Ha (Water Research, Elsevier BV, 2013-09) [Article]Inactivation of bacteriophage MS2 by reactive oxygen species (ROS) and triplet excited state of dissolved organic matter (3DOM*) produced by irradiation of natural and synthetic sensitizers with simulated sunlight of wavelengths greater than 320nm was investigated. Natural sensitizers included purified DOM isolates obtained from wastewater and river waters, and water samples collected from Singapore River, Stamford Canal, and Marina Bay Reservoir in Singapore. Linear correlations were found between MS2 inactivation rate constants (kobs) and the photo-induced reaction rate constants of 2,4,6-trimethylphenol (TMP), a probe compound shown to react mainly with 3DOM*. Linear correlations between MS2 kobs and singlet oxygen (1O2) concentrations were also found for both purified DOM isolates and natural water samples. These correlations, along with data from quenching experiments and experiments with synthetic sensitizers, Rose Bengal (RB), 3'-methoxyacetophenone (3'-MAP), and nitrite (NO2-), suggest that 1O2, 3DOM*, and hydroxyl radicals (•OH) could inactivate bacteriophage MS2. Linear correlations between MS2 kobs and Specific Ultraviolet Absorption determined at 254nm (SUVA254) were also found for both purified DOM isolates and natural samples. These results suggest the potential use of TMP as a chemical probe and SUVA254 as an indicator for virus inactivation in natural and purified DOM water samples. © 2013 Elsevier Ltd.