http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Rashid Md Al Mamunur,Kim Junkyu,Long Dang Xuan,Kwak Kyungwon,Hong Jongin 대한화학회 2022 Bulletin of the Korean Chemical Society Vol.43 No.5
Density functional theory (DFT), time-dependent DFT, and Marcus theory were used to probe the optoelectronic and charge-transport properties of compounds obtained by inserting long-chain aliphatic alkenes or condensed aromatic rings between the planar quinacridone core and the terminal donor diphenylamine moiety of a reference hole-transporting material (HTM). Compared to the reference HTM, its newly designed derivatives showed lower-lying highest occupied molecular orbitals that were well matched in energy with the valence band maximum of a representative perovskite absorber. HTMs obtained via the insertion of condensed aromatic rings showed higher hole mobilities than those obtained via the insertion of aliphatic alkenes. Overall, hole mobility was mainly influenced by the charge-transfer integral, while other factors, such as the hole reorganization energy, hole hopping rate, and centroid distance, had only minor effects.
Long, Dang Xuan,Noh, Yong-Young American Scientific Publishers 2017 Journal of Nanoscience and Nanotechnology Vol.17 No.8
<P>We report on high-performance organic field-effect transistors (OFETs) with low-cost Mo source/drain electrode by water base solution-processed hybrid PEI:V2O5 interlayers. We were success control of the metal electrode's work function (W-f) by ratio of mixture of contact interlayers and obtain the work function of the Mo electrodes progressively changed from 4.16 to 4.9 eV to reduce energy barriers of ambipolar semiconductor. With the insertion of the mixed layer, OFETs gained significantly improved performance for ambipolar 3,6-Bis-(5bromo-thiophen-2-yl)-N, N-bis (2-octyl-1-dodecyl)-1,4-dioxo-pyrrolo[3,4-c]pyrrole (DPPT-TT) polymer semiconductors, OFETs on the basis DPPT-TT with hybid mixed interlayer/Mo electrodes exhibit field-effect mobilities of 0.8 and 1.9 cm(2)/Vs for electron and hole mobility, respectively.</P>
Long, Dang Xuan,Xu, Yong,Wei, Huai-xin,Liu, Chuan,Noh, Yong-Young The Royal Society of Chemistry 2015 Physical chemistry chemical physics Vol.17 No.31
<P>A simply and facilely synthesized MoO<SUB>3</SUB> solution was developed to fabricate charge injection layers for improving the charge-injection properties in p-type organic field-effect transistors (OFETs). By dissolving MoO<SUB>3</SUB> powder in ammonium (NH<SUB>3</SUB>) solvent under an air atmosphere, an intermediate ammonium molybdate ((NH<SUB>4</SUB>)<SUB>2</SUB>MoO<SUB>4</SUB>) precursor is made stable, transparent and spin-coated to form the MoO<SUB>3</SUB> interfacial layers, the thickness and morphology of which can be well-controlled. When the MoO<SUB>3</SUB> layer was applied to OFETs with a cost-effective molybdenum (Mo) electrode, the field-effect mobility (<I>μ</I><SUB>FET</SUB>) was significantly improved to 0.17 or 1.85 cm<SUP>2</SUP> V<SUP>−1</SUP>s<SUP>−1</SUP> for polymer semiconductors, regioregular poly(3-hexylthiophene) (P3HT) or 3,6-bis-(5bromo-thiophen-2-yl)-<I>N</I>,<I>N</I>′-bis(2-octyl-1-dodecyl)-1,4-dioxo-pyrrolo[3,4-<I>c</I>]pyrrole (DPPT-TT), respectively. Device analysis indicates that the MoO<SUB>3</SUB>-deposited Mo contact exhibits a contact resistance <I>R</I><SUB>C</SUB> of 1.2 MΩ cm comparable to that in a device with the noble Au electrode. Kelvin-probe measurements show that the work function of the Mo electrode did not exhibit a dependence on the thickness of MoO<SUB>3</SUB> film. Instead, ultraviolet photoemission spectroscopy results show that a doping effect is probably induced by casting the MoO<SUB>3</SUB> layer on the P3HT semiconductor, which leads to the improved hole injection.</P> <P>Graphic Abstract</P><P>A simply synthesized MoO<SUB>3</SUB> is used as charge injection layers for printed p-type organic field-effect transistors (OFETs). <IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c5cp03369a'> </P>
Long, Dang Xuan,Choi, Eun-Young,Noh, Yong-Young American Chemical Society 2017 ACS APPLIED MATERIALS & INTERFACES Vol.9 No.29
<P>We report a new p-type dopant, manganese oxide (Mn3O4) nanoparticle, to enhance the performance of organic field-effect transistors (OFETs) with conjugated polymers, including poly(3-hexylthiophene-2,5-diyl), poly[[N,N 9-bis(2-octyldodecyl)-naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,59-(2,29-bithiophene)], and poly[[2,5-bis(2-octyldodecyl)-2,3,5,6-tetrahydro-3,6-dioxopyrrolo[3,4-c]pyrrole-1,4-diyl]-alt-[[2,2'-(2,5-thiophene)bis-thieno(3,2b) thiophene]-5,5'-diyl]] (DPPT-TT). Incorporating a small amount of Mn3O4 nanoparticles in the semiconductor film significantly improved the hole mobility and decreased the threshold voltage for all OFETs, indicating efficient Mn3O4 nanoparticle p-type doping. The Mn3O4 nanoparticle showed a better doping efficiency than the widely used FeCl3 dopant due to better mixability with the host conjugated polymers. In particular, doped DPPT-TT OFETs showed significantly improved mobility up to 2.35 (+/- 0.4) cm(2)/(V.s) with enhanced air and operational stability at 0.1 wt % doping concentration from 1.2 cm(2)/(V.s) for pristine devices.</P>
Long, Dang Xuan,Karakawa, Makoto,Noh, Yong-Young The Royal Society of Chemistry 2016 Physical chemistry chemical physics Vol.18 No.34
<P>The high performance of soluble [60]fulleropyrrolidine upon its use as the active layer of n-channel organic field-effect transistors (OFETs) is reported. The two materials, N-phenyl derivatives C60-fused-N-phenyl-2-phenylpyrrolidine ([C60]PhNPh) and C60-fused N-phenyl-2-hexylpyrrolidine ([C60]HexNPh), have well-controlled molecular structures with a modification of the pyrrolidine ring, with no increase in the LUMO level, achieving a high mobility and highly ambient stable n-type OFET. The top-gate, bottom-contact device shows a high electron charge-carrier mobility of up to 0.14 and 0.08 cm(2) V-1 s(-1) for [C60]PhNPh and [C60]HexNPh, respectively, (I-on/I-off = 10(6)) with the commonly used CYTOP dielectric. Excess carriers introduced by a small amount of chemical doping of polyethyleneimine (PEI) compensate traps by shifting the Fermi level (E-F) toward the respective transport energy levels and therefore increase charge-carrier mobility (0.26 and 0.1 cm(2) V-1 s(-1)) and provide good ambient operational stability compared with pristine devices.</P>
Baking soda: an ultra-cheap and air stable electron injection layer for organic electronic devices
Long, Dang Xuan,Noh, Yong-Young The Royal Society of Chemistry 2018 Journal of materials chemistry. C, Materials for o Vol.6 No.47
<P>To realize high performance printed organic optoelectronic devices, the development of air-stable, cheap, and solution-processable electron injection layers (EILs) is urgently required to avoid the use of a low work-function metal electrode with poor air stability. We report sodium bicarbonate (baking soda, NaHCO3) as an efficient, low-cost, air-stable, and environmentally friendly EIL material in various printed organic electronic devices including organic solar cells (OSCs), organic light-emitting diodes (OLEDs), organic photodiodes (OPDs) and n-channel organic thin film transistors (OFETs). UV photoelectron spectroscopy results indicated that the work-function of various common electrodes used for organic devices such as ITO, Au, Al and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) decreased significantly by more than 1 eV following deposition of a thin NaHCO3 film. The performance and stability of these organic devices improved by around 15% overall with ultra-cheap, air stable EILs. In particular, high performance OSCs based on PTB7:PC71BM with a power conversion efficiency of 8.40% and solution processed OLEDs based on PVK:PBD:Ir(ppy)3 with light emitting efficiencies of 68.5 cd A<SUP>−1</SUP> and 20 lm A<SUP>−1</SUP> were achieved by applying a NaHCO3 interlayer.</P>
Kim, Yiho,Long, Dang Xuan,Lee, Junghoon,Kim, Gyoungsik,Shin, Tae Joo,Nam, Kyung-Wan,Noh, Yong-Young,Yang, Changduk American Chemical Society 2015 Macromolecules Vol.48 No.15
<P>Structure–property relationships associated with a hybrid siloxane-terminated hexyl chain (SiC6), photophysics, molecular packing, thin-film morphology, and charge carrier transport are reported for two novel naphthalene diimide (NDI)-based polymers; P(NDI2SiC6-T2) consists of NDI and bithiophene (T2) repeating units, while for P(NDI2SiC6-TVT), the (<I>E</I>)-2-(2-(thiophen-2-yl)-vinyl)thiophene (TVT) units are introduced into the NDI-based backbone. The analysis of the optical spectra shows that the preaggregation of these polymers in solution is highly sensitive to the choice of solvent such that the films prepared by using different solvents can be “tuned” with regard to their degrees and types of the aggregates. In-depth morphology investigations (atomic force microscopy (AFM), grazing incidence X-ray diffraction (GIXD), and near-edge X-ray absorption fine structure (NEXAFS)) combined with device optimization studies are used to probe the interplay between molecular structure, molecular packing, and OFET mobility. It is found that the polymer films cast as a coating from chloroform (CF) solvent favor a mixed face-on and edge-on orientation, while 1-chloronaphthalene (CN)-cast films favor an almost entirely edge-on orientation, resulting in a difference in mobility between CF- and CN-cast devices. Within this work, the annealed P(NDI2SiC6-T2) device fabricated from CF, despite showing a less densely packed organization, shows the highest electron mobility of up to 1.04 cm<SUP>2</SUP>/V·s due to a highly balanced face-on to edge-on ratio. This work, for the first time, advances our understanding for how the balanced face-on to edge-on ratio plays a dramatic role in facilitating charge transport, opening a new charge-transport mechanism in electronic devices.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/mamobx/2015/mamobx.2015.48.issue-15/acs.macromol.5b01012/production/images/medium/ma-2015-01012k_0009.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ma5b01012'>ACS Electronic Supporting Info</A></P>