Publication:
Theoretical study of the electronic structure and properties of alternating donor-acceptor couples of carbazole-based compounds for advanced organic light-emitting diodes (Oled)

dc.contributor.authorMakjan S.
dc.contributor.authorPromkatkaew M.
dc.contributor.authorHannongbua S.
dc.contributor.authorBoonsri P.
dc.date.accessioned2021-04-05T03:04:06Z
dc.date.available2021-04-05T03:04:06Z
dc.date.issued2019
dc.date.issuedBE2562
dc.description.abstractGenerally, it is difficult to generate a high-performance pure blue emission organic light-emitting diode (OLED). That is because the intrinsically wide band-gap makes it hard to inject charges into the emitting layer in such devices. To solve the problem, carbazole derivatives have been widely used because they have more thermal stability, a good hole transporting property, more electron rich (p-type) material, and higher photoconductivity. In the present work, novel copolymers containing donor-acceptor-acceptor-donor (D-A-A-D) blue compounds used for OLEDs were investigated. The theory of the geometrical and electronic properties of N-ethylcarbazole (ECz) as donor molecule (D) coupled to a series of 6 acceptor molecules (A) for advanced OLEDs were investigated. The acceptors were thiazole (TZ), thiadiazole (TD), thienopyrazine (TPZ), thienothiadiazole (TTD), benzothiadiazole (BTD), and thiadiazolothienopyrazine (TDTP). The ground state structure of the copolymers were studied using Density Functional Theory (DFT) at B3LYP/6-31G(d) level. Molecular orbital analysis study indicated 3 investigated copolymers (ECz-diTZ-ECz, ECz-diTD-ECz, ECz-diBTD-ECz) have efficient bipolar charge transport properties for both electron and hole injection to the TiO2 conduction band (4.8 eV). In addition, the excited states electronic properties were calculated using Time-Dependent Density Functional Theory (TD-DFT) at the same level. Among these investigated copolymer ECz-diTZ-ECz and ECz-diTD-ECz showed the maximum absorption wavelengths (λabs) with blue emitting at 429 and 431 nm, respectively. The results suggested that selected D-A-A-D copolymers can improve the electron-and hole-transporting abilities of the devices. Therefore, the designed copolymers would be a promising material for future development of light-emitting diodes, electrochromic windows, photovoltaic cells, and photorefractive materials. © 2019 Trans Tech Publications Ltd, Switzerland.
dc.format.mimetypeapplication/pdf
dc.identifier.citationKey Engineering Materials. Vol 824 KEM, (2019), p.236-244
dc.identifier.doi10.4028/www.scientific.net/KEM.824.236
dc.identifier.issn10139826
dc.identifier.other2-s2.0-85079849089
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5552
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherElectronic equipment
dc.subject.otherElectronic properties
dc.subject.otherElectronic structure
dc.subject.otherEnergy gap
dc.subject.otherGround state
dc.subject.otherHole mobility
dc.subject.otherMolecular orbitals
dc.subject.otherMolecules
dc.subject.otherOrganic light emitting diodes (OLED)
dc.subject.otherOrganic polymers
dc.subject.otherPhotoelectrochemical cells
dc.subject.otherPhotorefractive crystals
dc.subject.otherPhotovoltaic cells
dc.subject.otherPolycyclic aromatic hydrocarbons
dc.subject.otherTitanium dioxide
dc.subject.otherCarbazole
dc.subject.otherDependent Density Functional Theory (TD-DFT)
dc.subject.otherEnergy gab
dc.subject.otherGround-state structures
dc.subject.otherHole-transporting property
dc.subject.otherStructure and properties
dc.subject.otherTime
dc.subject.otherTime dependent density functional theory
dc.subject.otherDensity functional theory
dc.titleTheoretical study of the electronic structure and properties of alternating donor-acceptor couples of carbazole-based compounds for advanced organic light-emitting diodes (Oled)
dc.typeConference Paper
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85079849089&doi=10.4028%2fwww.scientific.net%2fKEM.824.236&partnerID=40&md5=c9f90e398ff7eed54a5301c338e5eff7

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