Tae‐Hyuk Kwon
UNIST 공과대학 · 공학
Tae-Hyuk Kwon 교수의 연구실은 유기 및 무기 광물질을 기반으로 한 고효율 광전기 소자 개발에 중점을 두고 있습니다. 특히 이르리듐 복합체를 활용한 색채널링 가능한 발광 소자, 광수집 및 에너지 저장 기반의 인Door용 배터리, 그리고 다이아이오드화 스니트 기반의 페로브스카이트 소재를 활용한 태양전지 등 다양한 에너지 변환 및 저장 기술을 연구하고 있습니다. 또한, 전자 이동성과 안정성을 향상시키기 위한 신소재 설계 및 전기화학적 메커니즘 규명도 핵심 과제입니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Various iridium complexes consisting of phenylpyrazole (ppz) ligands and isoquinolinecarboxylic acids (iq) as ancillary ligands were designed by energy band-gap calculations via ab initio calculations and synthesized to give rise to various emission wavelengths as expected. Fine color tuning was achieved through varying the position of the methyl substituent on the phenylpyrazole moiety with HOMO electron densities. Additional color tuning was made possible by altering the LUMO through the use o
A series of efficient light-harvesting systems (FIr3mGx, x = 1−3) based on dendrimer donor (mCP: N,N‘-dicarbazolyl-3,5-benzene) derivatives coupled with a sky blue phosphorescent acceptor (FIrpic: iridium(III) bis[(4,6-difluorophenyl)pyridinato-N,C2‘]-3-hydroxypicolinate derivative) were prepared, and their photophysical properties were investigated. The light-harvesting ability of FIr3mGx (x = 1−3) increases with the number of energy donor mCP units. The acceptor PL intensity of the donor−accep
Dye-sensitized photo-rechargeable battery (DSPB) harvests and stores dim light efficiently, realizing indoor-light-harvesting battery to operate IoT devices successfully without sun light.
A one-pot synthesis of 2,6-dibromodithieno[3,2-b;2',3'-d]thiophene (dibromo-DTT, 4) was developed. A key step was bromodecarboxylation of DTT-2,6-dicarboxylic acid, obtained by saponification of the diester 1. The donor-acceptor dye DAHTDTT (13), based on a central 2,6-bis[2'-(3'-hexylthienyl)]dithieno[3,2-b;2',3'-d]thiophene core (9), was prepared and incorporated in a dye-sensitized solar cell (DSC), which exhibited an energy conversion efficiency of 7.3% with V(oc) of 697 mV, J(sc) of 14.4 mA
Abstract Here, a new method is presented to increase the turn‐on time and stability of light‐emitting electrochemical cells (LECs). To this end, a neutral iridium complex ( 5 ) containing a pendant Na + ion that is generally known to have a faster mobility in the solid film than bulky anions is introduced, instead of the classic ionic transition metal complex (iTMC) with counter anion ( 7 ). Synthesis, photophysical and electrochemical studies of these complexes are reported. In the device confi
Abstract A vacancy‐ordered double perovskite, Cs 2 SnI 6 , has emerged as a promising lead‐free perovskite in the optoelectronic field. However, the charge transfer kinetics mediated by its surface state remains unclear. Here, the charge transfer mechanism of Cs 2 SnI 6 is reported and the role of its surface state in the presence of a redox mediator is clarified. Specifically, charge transfer through the surface state of Cs 2 SnI 6 and its subsequent surface state charging are demonstrated by c
An ensemble sensor system that exhibited selective luminescence enhancement upon binding to thymidine 5'-triphosphate (TTP) in HEPES buffer over other nucleotides was developed. The ensemble system consisted of an energy acceptor (FIrpic-bis(Zn2+-dipicolylamine conjugate, FIrpic=bis[(4,6-difluorophenyl)-pyridinato-N,C2+]picolinate) derivative) and an energy donor (mCP-Zn2+-cyclen, mCP=N,N'-dicarbazolyl-3,5-benzene). Among the nucleotides, the selective recognition and luminescence enhancement fo
Aggregates of amyloidogenic peptides are involved in the pathogenesis of several degenerative disorders. Herein, an iridium(III) complex, Ir-1, is reported as a chemical tool for oxidizing amyloidogenic peptides upon photoactivation and subsequently modulating their aggregation pathways. Ir-1 was rationally designed based on multiple characteristics, including 1) photoproperties leading to excitation by low-energy radiation; 2) generation of reactive oxygen species responsible for peptide oxidat
The direct formation of CN and CO bonds from inert gases is essential for chemical/biological processes and energy storage systems. However, its application to carbon nanomaterials for improved energy storage remains technologically challenging. A simple and very fast method to form CN and CO bonds in reduced graphene oxide (RGO) and carbon nanotubes (CNTs) by an ultrasonic chemical reaction is described. Electrodes of nitrogen- or oxygen-doped RGO (N-RGO or O-RGO, respectively) are fabricat
A neutral tripod system for biotin-avidin assays, which is composed of biotin, FIrpic as an energy acceptor, and mCP as an energy donor, offers remarkable sensitivity over traditional transition metal based protein probes due to the intramolecular energy transfer and increased hydrophobicity associated with the avidin binding site and neutral probe 1.
Amyloidogenic peptides are considered central pathological contributors towards neurodegeneration as observed in neurodegenerative disorders [<i>e.g.</i>, amyloid-β (Aβ) peptides in Alzheimer's disease (AD)]; however, their roles in the pathologies of such diseases have not been fully elucidated since they are challenging targets to be studied due to their heterogeneous nature and intrinsically disordered structure. Chemical approaches to modify amyloidogenic peptides would be valuable in advanc
Conjugated microporous polymers (CMPs) are promising energy storage materials owing to their rigid and cross-linked microporous structures. However, the fabrication of nano- and microstructured CMP films for practical applications is currently limited by processing challenges. Herein, we report that combined sono-cavitation and nebulization synthesis (SNS) is an effective method for the synthesis of CMP films from a monomer precursor solution. Using the SNS, the scalable fabrication of microporo
Efficient and selective production of CH<sub>4</sub> through the CO<sub>2</sub> reduction reaction (CO2RR) is a challenging task due to the high amount of energy consumption and various reaction pathways. Here, we report the synthesis of Zn-based polyoxometalate (ZnPOM) and its application in the photocatalytic CO2RR. Unlike conventional Zn-based catalysts that produce CO, ZnPOM can selectively catalyze the production of CH<sub>4</sub> in the presence of an Ir-based photosensitizer (TIr3) throug
We report a 10% enhancement of the photovoltaic performance of polymer bulk heterojunction solar cells composed of an iridium complex, P3HT, PEO and PCBM.