Making Nonconjugated Small-Molecule Organic Radicals Conduct

Authors
Yu, IlhwanJo, YerinKo, JaehyoungKim, Dae-YoonSohn, DaewonJoo, Yongho
Issue Date
2020-07-08
Publisher
AMER CHEMICAL SOC
Citation
NANO LETTERS, v.20, no.7, pp.5376 - 5382
Abstract
Charge neutral, nonconjugated organic radicals have emerged as extremely useful active materials for solid-state electronic applications. This previous achievement confirmed the potential of radical-based macromolecules in organic electronic devices; however, charge transport in radical molecules has not been studied in great detail from a fundamental perspective. Here we demonstrate the charge transport in a nonconjugated organic small radical, 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (h-TEMPO). The chemical component of this radical molecule allows us to form a single crystal via physical vapor deposition (PVD). While the charge transport of this macroscopic open-shell single crystal is rather low, thermal annealing of the well-defined single crystal enables the molecule to have a rapid charge transfer reaction due to the electronic communication of open-shell sites with each other, which results in electrical conductivities greater than 0.05 S m(-1). This effort demonstrates a drastically different model than the commonly accepted conjugated polymers or molecules for the creation of next-generation conductors.
Keywords
PHYSICAL VAPOR GROWTH; FIELD-EFFECT-TRANSISTOR; CHARGE-TRANSPORT; THIN-FILM; SEMICONDUCTORS; POLYMER; ORGANIZATION; PERFORMANCE; NONVOLATILE; CRYSTALS; PHYSICAL VAPOR GROWTH; FIELD-EFFECT-TRANSISTOR; CHARGE-TRANSPORT; THIN-FILM; SEMICONDUCTORS; POLYMER; ORGANIZATION; PERFORMANCE; NONVOLATILE; CRYSTALS; Nonconjugated conductor; stable radical; small-molecule conductor; Single-crystal
ISSN
1530-6984
URI
https://pubs.kist.re.kr/handle/201004/118393
DOI
10.1021/acs.nanolett.0c01730
Appears in Collections:
KIST Article > 2020
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE