Felix Sunjoo Kim

ORCID: 0000-0002-3286-6146
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Research Areas
  • Conducting polymers and applications
  • Organic Electronics and Photovoltaics
  • Perovskite Materials and Applications
  • Advanced Sensor and Energy Harvesting Materials
  • Organic Light-Emitting Diodes Research
  • Advanced Memory and Neural Computing
  • Thin-Film Transistor Technologies
  • Analytical Chemistry and Sensors
  • Semiconductor materials and devices
  • Photonic and Optical Devices
  • Photorefractive and Nonlinear Optics
  • Semiconductor materials and interfaces
  • Nanowire Synthesis and Applications
  • Fullerene Chemistry and Applications
  • Advanced Photocatalysis Techniques
  • Advanced Thermoelectric Materials and Devices
  • Advanced Fiber Laser Technologies
  • Carbon Nanotubes in Composites
  • TiO2 Photocatalysis and Solar Cells
  • Nanocluster Synthesis and Applications
  • Quantum Dots Synthesis And Properties
  • Gas Sensing Nanomaterials and Sensors
  • Advancements in Semiconductor Devices and Circuit Design
  • Carbon and Quantum Dots Applications
  • Advanced Nanomaterials in Catalysis

Chung-Ang University
2015-2024

Government of the Republic of Korea
2015-2019

University of Seoul
2014-2016

University of Washington
2008-2014

University of Kentucky
2009

This paper presents a comprehensive review of the literature on one-dimensional (1D) nanostructures (nanowires, nanoribbons, nanotubes, nanobelts, and nanofibers) π-conjugated small molecules, oligomers, polymers. The diverse methods used in assembling molecular building blocks into 1D functional nanodevices are discussed, including hard soft template-assisted synthesis, electrospinning, nanolithography, self-assembly solution at interfaces, physical vapor transport, other strategies....

10.1021/cm102772x article EN Chemistry of Materials 2010-12-01

Poly(3-butylthiophene) (P3BT) nanowires, prepared by solution-phase self-assembly, have been used to construct highly efficient P3BT/fullerene nanocomposite solar cells. The fullerene/P3BT films showed an electrically bicontinuous nanoscale morphology with average field-effect hole mobilities as high 8.0 x 10(-3) cm2/Vs due the interconnected P3BT nanowire network revealed TEM and AFM imaging. power conversion efficiency of devices was 3.0% (at 100 mW/cm2, AM1.5) in air found be identical...

10.1021/ja800411b article EN Journal of the American Chemical Society 2008-04-01

High-performance ambipolar transistors and inverters are demonstrated using a new donor–acceptor copolymer semiconductor. The show electron hole mobilities of up to 0.04 0.003 cm2 V−1 s−1, respectively. Voltage transfer curves the made on common gold electrodes showed sharp switching with gain 30. Detailed facts importance specialist readers published as "Supporting Information". Such documents peer-reviewed, but not copy-edited or typeset. They available submitted by authors. Please note:...

10.1002/adma.200901819 article EN Advanced Materials 2009-08-11

Our results indicate that a well-designed simple post-processing process can boost the efficiency of thermoelectric power generators made conjugated polymer thin films.

10.1039/c3ta14960a article EN Journal of Materials Chemistry A 2014-01-01

A series of nine alternating donor–acceptor copolymer semiconductors based on naphthalene diimide (NDI) acceptor and seven different thiophene moieties with varied electron-donating strength conformations has been synthesized, characterized, used in n-channel ambipolar organic field-effect transistors (OFETs). The NDI copolymers had moderate to high molecular weights, most them exhibited crystallinity thin films fibers. LUMO energy levels the copolymers, at −3.9 −3.8 eV, were constant as...

10.1021/cm2034273 article EN Chemistry of Materials 2012-04-02

Abstract High power conversion efficiency (PCE), long‐term stability, and mechanical robustness are prerequisites for the commercial applications of organic solar cells (OSCs). In this study, a new star‐shaped trimer acceptor (TYT‐S) is developed high‐performance OSCs with PCE 19.0%, high photo‐stability ( t 80% lifetime = 2600 h under 1‐sun illumination), crack‐onset strain (COS) 21.6% achieved. The isotropic molecular structure TYT‐S affords efficient multi‐directional charge transport...

10.1002/aenm.202303872 article EN Advanced Energy Materials 2024-01-02

The synthesis and characterization of two new thiophene copolymers with backbone phthalimide units is reported. Thin-film optical wide-angle X-ray diffraction measurements indicate extended electronic conjugation close intermolecular pi-stacking for both polymers. Ambient carrier mobility thin-film transistors prepared from these polymers as high 0.28 cm(2)/(V s) an on/off ratio greater than 10(5).

10.1021/ja810050y article EN Journal of the American Chemical Society 2009-05-11

Abstract New thiazolothiazole‐dithienosilole copolymer semiconductors bearing side chains of different type, size, and topology were synthesized used to demonstrate the influence on morphology, charge transport photovoltaic properties. The field effect mobility holes varied from 0.01‐0.03 cm 2 V −1 s in PSOTT PSEHTT 0.12 PSOxTT. average power conversion efficiency solar cells under 1.0 sun illumination could be 2.1% PSOxTT 4.1% 5.0% PSEHTT. highest achieved PSEHTT, that has all‐branched...

10.1002/aenm.201100215 article EN Advanced Energy Materials 2011-06-14

We report the synthesis, characterization, solution-phase assembly of nanowires, field-effect charge transport, and photovoltaic properties regioregular poly(3-pentylthiophene) (P3PT), first poly(3-alkylthiophene) with an odd-numbered alkyl side chain length to be so investigated. Two samples P3PT weight-average molecular weights 61 800 77 000 1.4−1.5 polydispersity index have comparable solubility processability in organic solvents as poly(3-hexylthiophene) (P3HT) but a higher melting...

10.1021/ma901829d article EN Macromolecules 2009-10-26

A homologous series of six novel oligothiophene–naphthalene diimide-based oligomer semiconductors with a donor–acceptor architecture, NDI-nTH (n = 1, 2, 3, 4) and NDI-nT 3), was synthesized used to explore set criteria for the design non-fullerene electron acceptor materials organic solar cells. Thin films had optical band gaps that varied from 2.1 eV in NDI-1TH 1.6 NDI-3TH 1.4 NDI-4TH, demonstrating good potential light harvesting exciton generation. The LUMO energy levels were similar (ca....

10.1021/cm2019668 article EN Chemistry of Materials 2011-09-30

We report studies of bulk heterojunction solar cells composed self-assembled poly(3-butylthiophene) nanowires (P3BT-nw) as the donor component with a fullerene acceptor. show that nanostructure these devices is single most important variable determining their performance, and we use combination solvent thermal annealing to control it. A conductive photoconductive atomic force microscopy provides direct connections between local overall device performance. Films dense random web cause...

10.1021/nn9014906 article EN ACS Nano 2010-03-11

11-Ring heterocyclic diimides were synthesized and found to be planar exhibit a slipped face-to-face π stacking. Variation of the substituents tunes electronic structure properties. In n-channel organic field-effect transistors, new semiconductors have high electron mobility. When they used as acceptor material in polymer solar cells, power conversion efficiency 1.8 % was obtained. As service our authors readers, this journal provides supporting information supplied by authors. Such...

10.1002/anie.201210085 article EN Angewandte Chemie International Edition 2013-04-15

Bulk heterojunction solar cells based on blends of regioregular poly(3-butylthiophene) (P3BT) and phenyl-C61-butyric acid methyl ester (PC61BM) were created by in situ self-assembly P3BT nanowires the morphology photovoltaic properties investigated as a function blend composition. Transmission electron microscopy imaging revealed an interconnected network 11−15 nm width 5−10 μm length amorphous continuous PC61BM phase. The photocurrent density, fill factor, power conversion efficiency...

10.1021/cm801324m article EN Chemistry of Materials 2008-09-23

Synergic effects of conducting polymers, carbon nanotubes, and graphene result in the enhanced thermoelectric properties nanocomposites.

10.1039/c4ta06710j article EN Journal of Materials Chemistry A 2015-01-01

High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain in lateral direction, leading to unipolar n-channel transport field-effect transistors. The electron mobilities of up 0.30 cm(2)/(V s), is among highest values for polymers. Complementary inverters incorporating...

10.1021/ja407471b article EN Journal of the American Chemical Society 2013-09-25

Mechanical properties of conducting polymers are an essential consideration in the design flexible and stretchable electronics, but guidelines for material having both high mechanical electrical remain limited. Here we provide important guideline mechanically robust, electroactive polymer thin films terms molecular weight polymers. These studies based on a highly efficient, representative n-type conjugated (P(NDI2OD-T2)) revealed marked enhancement across narrow range, highlighting existence...

10.1021/acs.chemmater.8b05114 article EN Chemistry of Materials 2019-04-23

A series of 11 organometallic conjugated polymer semiconductors bearing a platinum (Pt) center have been synthesized and their electronic band structures, field-effect charge transport, use in bulk heterojunction solar cells were evaluated. The Pt-bridged donor−acceptor poly(aryleneethynylene)s by Sonogashira-type polycondensation are exemplified poly[4-(5′-trans-bis(tributylphosphine)platinum ethynyl-thiophen-2′-yl)-7-(5′′-ethynyl-thiophen-2′′-yl)-benzo[1,2,5]thiadiazole] (BT-BTPt),...

10.1021/ma8016508 article EN Macromolecules 2009-01-13

Three new donor−acceptor conjugated polymers incorporating thieno[3,4-c]pyrrole-4,6-dione (TPD) acceptor and dialkoxybithiophene or cyclopentadithiophene units as donor have been synthesized explored in bulk heterojunction (BHJ) solar cells organic field-effect transistors (OFETs). The TPD-containing had optical band gaps of 1.50−1.70 eV HOMO levels −4.85 to −5.26 eV. highly electron-rich character P1 P2 destabilizes their HOMOs which significantly affects the photovoltaic efficiency....

10.1021/ma101878w article EN Macromolecules 2010-12-23

Abstract Designing polymers that facilitate exciton dissociation and charge transport is critical for the production of highly efficient all‐polymer solar cells (all‐PSCs). Here, development a new class high‐performance naphthalenediimide (NDI)‐based with large dipole moment change (Δ µ ge ) delocalized lowest unoccupied molecular orbital (LUMO) as electron acceptors all‐PSCs reported. A series NDI‐based copolymers incorporating electron‐withdrawing cyanovinylene groups into backbone...

10.1002/aenm.201701436 article EN Advanced Energy Materials 2017-09-18

Abstract Flexible and mechanically robust gas sensors are the key technologies for wearable implantable electronics. Herein, authors demonstrate high‐performance, flexible nitrogen dioxide (NO 2 ) chemiresistors using a series of n‐type conjugated polymers (CPs: PNDIT2/IM‐ x polymer dopant (poly(ethyleneimine), PEI). Imine double bonds (C = N) incorporated into backbones CPs with different imine contents ( to facilitate strong selective interactions NO . The PEI provides doping stability,...

10.1002/advs.202200270 article EN cc-by Advanced Science 2022-03-20

Five conjugated pyrido[3,4-b]pyrazine-based donor−acceptor copolymers were synthesized by Suzuki and Stille coupling polymerizations, their photophysical electrochemical properties field-effect carrier mobilities characterized. The copolymer semiconductors include poly(pyrido[3,4-b]pyrazine-alt-9,9-dioctyl-2,7-fluorene) (PPPzF), poly(thiophene-2,5-diyl-alt-2,3-diheptyl-pyrido[3,4-b]pyrazine-5,8-diyl) (PTHPPz), poly(thiophene-2,5-diyl-alt-2,3-didecyl-pyrido[3,4-b]pyrazine-5,8-diyl) (PTDPPz),...

10.1021/ma801348b article EN Macromolecules 2008-09-12

Bulk heterojunction solar cells based on blends of the new low band gap donor–acceptor copolymer, poly(N-(dodecyl)-3,6-bis(4-dodecyloxythiophen-2-yl)phthalimide) (PhBT12), and fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) or [6,6]-phenyl-C71-butyric (PC71BM) were systematically investigated. The PhBT12/fullerene blend films found to exhibit a crystalline nanoscale morphology with space-charge-limited mobility holes as high 4.0 × 10−4 cm2/Vs without thermal...

10.1039/b900073a article EN Journal of Materials Chemistry 2009-01-01

Six new donor–acceptor copolymers based on benzobisthiazole and various donor moieties (dithienosilole, dithienopyrrole, cyclopentadithiophene, carbazole, benzodithiophene, bithiophene) were synthesized, characterized, used in field-effect transistors solar cells. The series of polybenzobisthiazoles with architecture have optical band gaps 1.83–2.18 eV, identical LUMO energy levels (∼−3.3 eV), a HOMO level that varied from −4.79 eV PBTDTP to −5.71 PBTHDDT. X-ray diffraction the...

10.1021/ma201128x article EN Macromolecules 2011-08-22

ADVERTISEMENT RETURN TO ISSUEPREVCommunication to the...Communication the EditorNEXTBenzobisthiazole−Thiophene Copolymer Semiconductors: Synthesis, Enhanced Stability, Field-Effect Transistors, and Efficient Solar CellsEilaf Ahmed, Felix S. Kim, Hao Xin, Samson A. Jenekhe*View Author Information Department of Chemical Engineering Chemistry, University Washington, Seattle, Washington 98195-1750*Corresponding author. E-mail: [email protected]Cite this: Macromolecules 2009, 42, 22,...

10.1021/ma9015278 article EN Macromolecules 2009-11-03

We identify and characterize the mesoscale morphology of poly(3-hexylthiophene) (P3HT) fibers crystallized through colloidal self-assembly in various aromatic solvents. The network structure P3HT is evaluated situ small-angle neutron scattering (SANS) ultra (USANS) experiments by electron microscopy. Through model fitting to data, we are able determine that forms structures solution prior deposition. directly obtain structural parameters such as fraction nanofiber form, cross-sectional fiber...

10.1021/ma2000515 article EN Macromolecules 2011-05-02
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