Min Ju Cho

ORCID: 0000-0003-1917-1865
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Organic Light-Emitting Diodes Research
  • Luminescence and Fluorescent Materials
  • Perovskite Materials and Applications
  • Thin-Film Transistor Technologies
  • Liquid Crystal Research Advancements
  • Molecular Junctions and Nanostructures
  • Nonlinear Optical Materials Research
  • Advanced Memory and Neural Computing
  • Photochromic and Fluorescence Chemistry
  • Molecular Sensors and Ion Detection
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • TiO2 Photocatalysis and Solar Cells
  • Advanced Photocatalysis Techniques
  • Advanced Sensor and Energy Harvesting Materials
  • Photorefractive and Nonlinear Optics
  • Photonic and Optical Devices
  • Green IT and Sustainability
  • Nonlinear Optical Materials Studies
  • Porphyrin and Phthalocyanine Chemistry
  • Synthesis and properties of polymers
  • Photoreceptor and optogenetics research
  • Nanomaterials and Printing Technologies

Korea University
2016-2025

Asan Medical Center
2023

University of Ulsan
2023

Ulsan College
2023

Government of the Republic of Korea
2015-2021

Seoul Institute
2015-2020

University of Siegen
2019

University at Buffalo, State University of New York
2011-2016

Korea Basic Science Institute
2013

Korea Institute of Science and Technology
2006

Thermally activated delayed fluorescence materials exhibited outstanding external quantum efficiencies in OLEDs along with good CIE color coordinates and improved device stabilities. Hence these are most promising for commercialization of OLEDs.

10.1039/c6tc04377a article EN Journal of Materials Chemistry C 2016-01-01

Despite the high performance of OLEDs consisting host–guest blend systems in emissive layer, containing a single molecule as an emitter layer (<italic>i.e.</italic> non-doped OLEDs) have significant advantages including easy fabrication procedures and enhanced device stability.

10.1039/c8tc06293e article EN Journal of Materials Chemistry C 2019-01-01

A facile approach to make an efficient hybrid bulk heterojunction photovoltaic device with lead sulfide nanocrystals and a low-bandgap polymer is demonstarted, resulting in power conversion efficiency of about 2–3%.

10.1002/adma.201101912 article EN Advanced Materials 2011-07-22

Anthracene-based conjugated molecules are synthesized and J-aggregations clearly observed in a single-crystal structure study. Single-crystal-based field-effect transistors (FETs) exhibit high mobility. They displayed dramatic photoinduced enhancement of the drain current showed unusually photoresponsivity under extremely low intensity light. Due to excitons, single multiple-stage memory operations achieved.

10.1002/adma.201100944 article EN Advanced Materials 2011-05-19

Abstract Ultra‐deep‐blue aggregation‐induced delayed fluorescence (AIDF) emitters (TB‐tCz and TB‐tPCz) bearing organoboron‐based cores as acceptors 3,6‐substituted carbazoles donors are presented. The thermally activated (TADF) properties of the two confirmed by theoretical calculations time‐resolved photoluminescence experiments. TB‐tCz TB‐tPCz exhibit fast reverse intersystem crossing rate constants owing to efficient spin–orbit coupling between singlet triplet states. When applied in...

10.1002/adfm.202102588 article EN Advanced Functional Materials 2021-06-12

Abstract Three new color‐tunable (deep‐blue to sky‐blue) and solution‐processable emitters—9′‐(2,12‐di‐ tert ‐butyl‐5,9‐dioxa‐13 b ‐boranaphtho[3,2,1‐ de ]anthracen‐7‐yl)‐9′ H ‐9,3′:6′,9″‐tercarbazole ( TB‐3Cz) , 9′‐(2,12‐di‐ ]anthracen‐7‐yl)‐9,9″‐diphenyl‐9 ,9′ ,9″ ‐3,3′:6′,3″‐tercarbazole TB‐P3Cz) 9‐(2,12‐di‐ ]anthracen‐7‐yl)‐ N 3 6 ‐tetraphenyl‐9 ‐carbazole‐3,6‐diamine TB‐DACz) —are demonstrated, which are cleverly designed synthesized by appending a boron‐fused entity as an electron...

10.1002/adom.201902175 article EN Advanced Optical Materials 2020-05-25

Recently, all-polymer solar cells (all-PSCs) have made significant progress in terms of efficiency and performance. Using Y-series-based small-molecule acceptors, a new range polymer acceptors for all-PSC has been developed. These synthesized low band gap, broad absorption, easily tunable energy levels, making them suitable n-type candidates efficient all-PSCs. In this review, we summarize some molecular design synthesis strategies used to advance the field innovative materials device...

10.1021/acsenergylett.2c01541 article EN ACS Energy Letters 2022-10-12

We synthesized a highly crystalline DPP-based polymer, DPPBTSPE, which contained 1,2-bis(5-(thiophen-2-yl)selenophen-2-yl)ethene as planar and rigid electron donating group. High- low-molecular weight (MW) DPPBTSPE fractions were collected by Soxhlet extraction employed to investigate their unique charge transport properties in macroscopic films single polymer nanowire (SC-PNW), respectively. The low-MW could provide well-isolated high aspect ratio SC-PNWs, the direction of π–π stacking was...

10.1021/acsnano.5b01982 article EN ACS Nano 2015-05-11

A new tellurophene-based π-conjugated polymer, PDTDPPTe, was synthesized. PDTDPPTe exhibits a smaller optical band gap (Egopt = 1.25 eV) than thiophene-based PDTDPPT 1.30 eV). Thin-film transistors comprising displayed outstanding performance (μmax 1.78 cm2 V−1 s−1, Ion/Ioff 105–6).

10.1039/c3cc41250d article EN Chemical Communications 2013-01-01

A new solution-processable polymeric emitter containing non-conjugated cyclohexane units was developed for high-performing TADF-OLEDs.

10.1039/c7py02113e article EN Polymer Chemistry 2018-01-01

Template-guided solution-shearing (TGSS) is used to fabricate field-effect transistors (FETs) composed of micropatterned prisms as active channels. The comprise highly crystalline PTDPP-DTTE, in which diketopyrrolopyrrole (DPP) flanked by thiophene. FET has a maximum mobility approximately 7.43 cm2 V−1 s−1, much higher than the values thin-film with solution-sheared or spin-coated films PTDPP-DTTE annealed at 200 °C. As service our authors and readers, this journal provides supporting...

10.1002/adma.201401179 article EN Advanced Materials 2014-06-27

We synthesized a novel fully conjugated block copolymer, P3, in which wide-band gap donor (P1) was connected to narrow-band acceptor (P2). As P3 contains P1 with wide bandgap and P2 narrow bandgap, it exhibits very complementary absorption. Transient photoluminescence measurement using dilute solution demonstrated intramolecular charge transfer between the block, not observed P1/P2 blend solution. A thin film showed complete PL quenching because photoinduced inter-/intramolecular states were...

10.1021/acsami.8b03580 article EN ACS Applied Materials & Interfaces 2018-05-15

A highly crystalline conjugated donor (D)-acceptor (A) block copolymer (PBDT2T-b-N2200) that has good solubility in nonhalogenated solvents is successfully synthesized. PBDT2T-b-N2200 shows a broad complementary absorption behavior owing to wide-band gap (PBDT2T) present as D-block and narrow-band acceptor (N2200) an A-block. Polymer solar cells (PSCs) with (CBCP) are fabricated using toluene solution PSC created annealed film showing the highest power conversion efficiency of 6.43%, which...

10.1002/advs.201902470 article EN cc-by Advanced Science 2020-01-09

Herein, a novel core molecule for V-shaped host molecules was synthesized, wherein two carbazoles were directly linked to cyclohexane. Cy-mCP and Cy-mCBP hosts also successfully prepared solution-processable thermally activated delayed fluorescence organic light-emitting diodes (TADF-OLEDs). The contained cyclohexane linker small molecular (mCP mCBP), exhibiting twice the weight while maintaining basic properties of single with improved film-forming ability solubility in solvents. These...

10.1021/acsami.3c01236 article EN ACS Applied Materials & Interfaces 2023-05-31

New isoindigo and di(thienyl)ethylene-containing π-extended conjugated polymers with different branched side-chains molecular weights (MWs) have been synthesized. Octyldodecyl (OD) decyltetradecyl (DT) groups were employed as side chain moieties tethered to units. In addition, the MW of polymer was varied by changing polymerization time. The bearing DT chains showed much better charge transport behavior, compared that OD chains. hole mobility high-MW PIIDDTE-III determined be higher than...

10.1039/c3py00735a article EN Polymer Chemistry 2013-01-01

In this work, three-armed luminogens IAcTr-out and IAcTr-in were synthesized used as emitters bearing triazine indenoacridine moieties in thermally activated delayed fluorescence organic light-emitting diodes (OLEDs). These molecules could form a uniform thin film via the solution process also allowed subsequent deposition of an electron transporting layer either by vacuum or all-solution coating method. Intriguingly, new displayed aggregation-induced emission (AIE), which is unique...

10.1021/acsami.7b19681 article EN ACS Applied Materials & Interfaces 2018-04-09

New thienothiophene-flanked diketopyrrolopyrrole and thiophene-containing π-extended conjugated polymers with various branched alkyl side-chains were successfully synthesized. 2-Octyldodecyl, 2-decyltetradecyl, 2-tetradecylhexadecyl, 2-hexadecyloctadecyl, 2-octadecyldocosyl groups selected as the side-chain moieties anchored to N-positions of unit. All five found be soluble owing bulkiness side chains. The thin-film transistor based on 2-tetradecylhexadecyl-substituted polymer showed highest...

10.1021/am508026s article EN ACS Applied Materials & Interfaces 2015-01-15

A single component polymer solar cell with a CDABP film annealed at 180 °C showed maximum power conversion efficiency of 5.28%, which is much higher than that (2.62%) the device as-cast film.

10.1039/c9ta06107j article EN Journal of Materials Chemistry A 2019-01-01

New M- and V-shaped perylene diimide (PDI)-based small molecules were synthesized as new n-type acceptors for nonfullerene-based polymer solar cells.

10.1039/c6cc04229e article EN Chemical Communications 2016-01-01

New small molecules having modified acceptor strength and π-conjugation length containing dicyanovinylene (DCV) tricyanovinylene (TCV) as a strongly electron-accepting unit with indacenodithiophene, IDT(DCV)2, IDT(TCV)2, IDTT(TCV)2, were synthesized studied in terms of their applicability to polymer solar cells PTB7-Th an electron-donating polymer. Intriguingly, the blended films IDT(TCV)2 IDTT(TCV)2 exhibited superior shelf life stabilities more than 1000 h without any reduction initial...

10.1021/acsami.6b15707 article EN ACS Applied Materials & Interfaces 2017-02-24
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