In Hwan Jung
한양대학교 융합전자공학과 · 공학
이 교수의 연구실은 주로 유기 반도체 소재 및 고성능 유기 광전소자에 초점을 맞추고 있습니다. 특히 저 bandgap 폴리머를 활용한 태양전지, 페인트형 열전소자, 그리고 풀폴리머 태양전지의 구조-성능 상관관계를 연구하며, 전자 수용체 및 기증체 모노머의 설계를 통해 전자적 성질을 정밀하게 조절하는 데 기여하고 있습니다. 다양한 유기 반도체 고분자 합성과 전자구조 제어를 기반으로 에너지 변환 및 저장 기술의 혁신을 추구하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
We have synthesized four types of cyclopentadithiophene (CDT)-based low-bandgap copolymers, poly[{4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-2,6-diyl}-alt-(2,2'-bithiazole-5,5'-diyl)] (PehCDT-BT), poly[(4,4-dioctyl-4H-cyclopenta[2,1-b:3,4-b']dithiophene-2,6-diyl)-alt-(2,2'-bithiazole-5,5'-diyl)] (PocCDT-BT), poly[{4,4-bis(2-ethylhexyl)-4H-cyclopenta[2,1-b:3,4-b']dithiophene-2,6-diyl}-alt-{2,5-di(thiophen-2-yl)thiazolo[5,4-d]thiazole-5,5'-diyl}] (PehCDT-TZ), and poly[(4,4-diocty
We studied the thermoelectric properties of a diketopyrrolopyrrole-based semiconductor (PDPP3T) via a precisely tuned doping process using Iron (III) chloride. In particular, the doping states of PDPP3T film were linearly controlled depending on the dopant concentration. The outstanding Seebeck coefficient of PDPP3T assisted the excellent power factors (PFs) over 200 μW m<sup>-1</sup>K<sup>-2</sup> at the broad range of doping concentration (3-8 mM) and the maximum PF reached up to 276 μW m<sup>
New electron withdrawing monomers, thieno[2′,3′:5′,6′]pyrido[3,4-g]thieno[3,2-c]isoquinoline-5,11(4H,10H)-dione (TPTI) and fluorenedicyclopentathiophene dimalononitrile (CN), have been developed and used to form 12 alternating polymers having different monomer combinations: (a) weak donating monomer–strong accepting monomer, (b) weak accepting monomer–strong accepting monomer, (c) weak accepting monomer–weak accepting monomer, and (d) strong donating monomer–strong accepting monomer. It was foun
We studied fullerene-free organic solar cells using rhodanine-terminated BDT3TR and O-IDTBR.
Several electron accepting polymers having weak accepting–strong accepting (WA-SA) and strong accepting–strong accepting (SA-SA) monomer alternation were synthesized for studies of structure/property relationship in all-polymer solar cells. Two kinds of cyclic amide monomers, 4,10-bis(2-butyloctyl)-thieno[2′,3′:5,6]pyrido[3,4-g]thieno-[3,2-c]isoquinoline-5,11-dione (TPTI) and 5,11-bis(2-butyloctyl)-thieno[2′,3′:4,5]pyrido[2,3-g]thieno[3,2-c]quinoline-4,10-dione (TPTQ), were synthesized as weak a
Abstract We synthesized two fluorene‐based copolymers poly[(2,5‐bis(4‐hexylthiophen‐2‐yl)thiazolo[5,4‐day]thiazole‐5,5′‐diyl)‐alt‐(9,9′‐dioctylfluorene‐2,7‐diyl)] ( PF‐TTZT), and poly[(5,5′‐bis(4‐hexylthiophen‐2‐yl)‐2,2′‐bithiazole‐5,5′‐diyl)‐alt‐(9,9′‐dioctylfluorene‐2,7‐diyl)] (PF‐TBTT), which contain the electron‐withdrawing moieties, thiazolothiazole, and bithiazole, respectively. Through electrochemical studies, we found that these two polymers exhibit stable reversible oxidation and reduct
A near-infrared-harvesting n-type porphyrin-based acceptor for organic photovoltaics (OPVs) was developed. The n-type acceptor, PDI-P<sub>Zn</sub>-PDI, was designed by connecting a zinc porphyrin (P<sub>Zn</sub>) core to two perylenediimide (PDI) wings through ethyne bridges. A narrow bandgap of 1.27 eV was achieved through the extended π-conjugation and intramolecular charge transfer between the strongly electron-donating P<sub>Zn</sub> core and the electron-accepting PDI wings. A bulk heteroju
While hole extraction is crucial for the external quantum efficiency of conventional n-i-p colloidal quantum dot (CQD) solar cells (CQDSCs), sulfur-passivated p-type CQDs (pCQDs) have been the best hole-transport material (HTM) to date. In this work, we developed organic π-conjugated polymers (π-CPs) that can achieve substantially improved HTM performance compared with conventional pCQDs. A weakly electron-withdrawing triisopropylsilylethynyl (TIPS) group was employed with a weak donor moiety, b
Organic photodetectors (OPDs) are attracting attention for use in flexible and portable electronic applications such as image sensors, remote sensing, optical communications, and medical sensors because of their strong photon responsivity in thin films over a broad range of wavelengths. In particular, the efficient photon-to-current conversion of OPDs under visible light allows their use in indirect X-ray detectors using scintillators to convert X-rays to visible light. The polymer poly(4,8-bis(
The susceptibility of porphyrin derivatives to light-harvesting and charge-transport operations have enabled these materials to be employed in solar cell applications. The potential of porphyrin derivatives as hole-transporting materials (HTMs) for perovskite solar cells (PSCs) has recently been demonstrated, but knowledge of the relationships between the porphyrin structure and device performance remains insufficient. In this work, a series of novel zinc porphyrin (PZn) derivatives has been dev
While the outstanding charge transport and sunlight-harvesting properties of porphyrin molecules are highly attractive as active materials for organic photovoltaic (OPV) devices, the development of n-type porphyrin-based electron acceptors has been challenging. In this work, we developed a high-performance porphyrin-based electron acceptor for OPVs by substitution of four naphthalene diimide (NDI) units at the perimeter of a Zn-porphyrin (P<sub>Zn</sub>) core using ethyne linkage. Effective π-co
Abstract We have synthesized two cyclopentadithiophene (CDT)‐based low bandgap copolymers, poly[(4,4‐bis(2‐ethyl‐hexyl)‐4 H ‐cyclopenta[2,1‐ b :3,4‐ b ′]dithiophene‐2,6‐diyl)‐ alt ‐(benzo[ c ][1,2,5]selenadiazole‐4,7‐diyl)] (PCBSe) and poly[(4,4‐bis(2‐ethyl‐hexyl)‐4 H ‐cyclopenta[2,1‐ b :3,4‐ b ′]dithiophene‐2,6‐diyl)‐ alt ‐(4,7‐dithiophen‐2‐yl‐benzo[ c ][1,2,5]selenadiazole‐5,5′‐diyl)] (PCT2BSe), for use in photovoltaic applications. Through the internal charge transfer interaction between the
Porphyrin derivatives have recently emerged as hole transport layers (HTLs) because of their electron-rich characteristics. Although several successes with porphyrin-based HTLs have been recently reported, achieving excellent solar cell performance, the chances to improve this further by molecular engineering are still open. In this work, Zn porphyrin (P<sub>Zn</sub>)-based HTLs were developed by conjugating fluorinated triphenylamine (FTPA) wings at the perimeter of the P<sub>Zn</sub> core for
Abstract Perovskite nanocrystals (PNCs) are attractive photoactive materials in various optoelectronic devices including light‐emitting diodes, solar cells, and photodetectors. However, the weakly bound surface ligands on PNCs reduce colloidal stability and cause film formation and patterning difficulties, severely restricting their practical applications. Herein, a rationally designed photocrosslinkable zwitterionic (PZ) ligand is introduced to obtain directly patternable CsPbBr 3 PNCs with enh
Abstract Ternary organic photovoltaic (OPV) devices with multiple light‐absorbing active materials have emerged as an efficient strategy for realizing further improvements in the power conversion efficiency (PCE) without building complex multijunction structures. However, the third component often acts as recombination centers and, hence, the optimization of ternary blend morphology poses a major challenge to improving the PCE of these devices. In this work, the performance of OPVs is enhanced t