Changduk Yang 교수

A record breaking PCE of 12.1% is achieved by incorporating 25 wt% of DR3TSBDT into a PTB7-Th:PC₇₁BM host matrix.

The synthesis of two well-solubilized [60]methanofullerene derivatives ( p- EHO-PCBM and p- EHO-PCBA) is presented for usage in organic solar cells and in field-effect transistors. The para position of the PCBM's phenyl ring was substituted with a branched alkoxy side chain, which contributes to higher solubility, facilitating synthesis, purification, and processing. We find a small change of the open-circuit voltage ( V oc) as a slight improvement in performance upon application in P3HT/[60]met

Abstract Flexible and stretchable organic solar cells (OSCs) have attracted enormous attention due to their potential applications in wearable and portable devices. To achieve flexibility and stretchability, many efforts have been made with regard to mechanically robust electrodes, interface layers, and photoactive semiconductors. This has greatly improved the performance of the devices. State‐of‐the‐art flexible and stretchable OSCs have achieved a power conversion efficiency of 15.21% (16.55%

Abstract A new n‐type organic semiconductor (n‐OS) acceptor IDTPC with n ‐hexyl side chains is developed. Compared to side chains with 4‐hexylphenyl counterparts (IDTCN), such a design endows the acceptor of IDTPC with higher electron mobility, more ordered face‐on molecular packing, and lower band gap. Therefore, the IDTPC‐based polymer solar cells (PSCs) with a newly developed wide bandgap polymer PTQ10 as donor exhibit the maximum power conversion efficiency (PCE) of 12.2%, a near 65% improve

Compared with conventional organic solar cells (OSCs) based on single donor-acceptor pairs, terpolymer- and ternary-based OSCs featuring multiple donor-acceptor pairs are promising strategies for enhancing the performance while maintaining an easy and simple synthetic process. Using multiple donor-acceptor pairs in the active layer, the key photovoltaic parameters (i.e., short-circuit current density, open-circuit voltage, and fill factor) governing the OSC characteristics can be simultaneously

Based on the integrated consideration and engineering of both conjugated backbones and flexible side chains, solution‐processable polymeric semiconductors consisting of a diketopyrrolopyrrole (DPP) backbone and a finely modulated branching side chain ( ε ‐branched chain) are reported. The subtle change in the branching point from the backbone alters the π−π stacking and the lamellar distances between polymer backbones, which has a significant influence on the charge‐transport properties and in t

Abstract Despite rapid advances in the field of nonfullerene polymer solar cells (NF‐PSCs), successful examples of random polymer‐based NF‐PSCs are limited. In this study, it is demonstrated that random donor polymers based on thieno[2′,3′:5′,6′]pyrido[3,4‐ g ]thieno[3,2‐ c ]isoquinoline‐5,11(4 H ,10 H )‐dione (TPTI) containing two simple thiophene (T) and bithiophene (2T) electron‐rich moieties (PTTI‐T x ) can be promising materials for the fabrication of highly efficient NF‐PSCs. With negligib

Introduction of an n-type macromolecular additive (P(NDI2OD-T2) polymer) in organic solar cells brings significant improvements in power conversion efficiency along with robust thermal stability.

A synergetic effect of molecular weight ( M n ) and fluorine (F) on the performance of all‐polymer solar cells (all‐PSCs) is comprehensively investigated by tuning the M n of the acceptor polymer poly(( N,N′ ‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl)‐ alt ‐5,5′‐(2,2′‐bithiophene)) (P(NDI2OD‐T2)) and the F content of donor polymer poly(2,3‐bis‐(3‐octyloxyphenyl)quinoxaline‐5,8‐dyl‐ alt ‐thiophene‐2,5‐diyl). Both M n and F variations strongly influence the charge transpo

The emerging energy crisis has focused significant worldwide attention on solar cells. Although crystalline silicon solar cells are currently widely used, their high cost limits the development of solar power generation. Consequently, hybrid solar cells are becoming increasingly important, especially organic-Si hybrid solar cells (HSCs). Organic-Si HSCs combine a mature technology and high efficiency with the low-temperature manufacturing process and tunable optoelectronic properties of organic

Abstract Considering the potential applications of all‐polymer solar cells (all‐PSCs) as wearable power generators, there is an urgent need to develop photoactive layers that possess intrinsic mechanical endurance, while maintaining a high power‐conversion efficiency (PCE).Herein a strategy is demonstrated to simultaneously control the intercalation behavior and nanocrystallite size in the polymer–polymer blend by using a newly developed, high‐viscosity polymeric additive, poly(dimethylsiloxane‐

Abstract A narrow bandgap polymeric semiconductor, BOC‐PTDPP , comprising alkyl substituted diketopyrrolopyrrole (DPP) and tert ‐butoxycarbonyl ( t ‐BOC)‐protected DPP, is synthesized and used in organic field‐effect transistors (OFETs). The polymer films are prepared by solution deposition and thermal annealing of precursors featuring thermally labile t ‐BOC groups. The effects of the thermal cleavage on the molecular packing structure in the polymer thin films are investigated using thermograv

Abstract Systematic creation of polymeric semiconductors from novel building blocks is critical for improving charge transport properties in organic field‐effect transistors (OFETs). A series of ultralow‐bandgap polymers containing thienoisoindigo (TIIG) as a thiophene analogue of isoindigo (IIG) is synthesized. The UV‐Vis absorptions of the TIIG‐based polymers ( PTIIG‐T , PTIIG‐Se , and PTIIG‐DT ) exhibit broad bands covering the visible to near‐infrared range of up to 1600 nm. All the polymers

Intrinsically stretchable, electroactive materials featuring self-healing abilities will allow for a variety of next-generation stretchable electronics. Here, we synthesize diketopyrrolopyrrole-based “alternating” copolymers with urethane-containing side chains, that is, PDPPurethane copolymers, and use them as active layers in intrinsically stretchable and self-healable plastic transistors. The long-branched urethane side chains possessing moderate H-bonding strength enable sufficient solubilit