• Title/Summary/Keyword: electron donor

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Energy Generation Coupled to Azoreduction by Membranous Vesicles from Shewanella decolorationis S12

  • Hong, Yi-Guo;Guo, Jun;Sun, Guo-Ping
    • Journal of Microbiology and Biotechnology
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    • v.19 no.1
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    • pp.37-41
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    • 2009
  • Previous studies have demonstrated that Shewanella decolorationis S12 can grow on the azo compound amaranth as the sole electron acceptor. Thus, to explore the mechanism of energy generation in this metabolism, membranous vesicles (MVs) were prepared and the mechanism of energy generation was investigated. The membrane, which was fragmentized during preparation, automatically formed vesicles ranging from 37.5-112.5 nm in diameter under electron micrograph observation. Energy was conserved when coupling the azoreduction by the MVs of an azo compound or Fe(III) as the sole electron acceptor with $H_2$, formate, or lactate as the electron donor. The amaranth reduction by the vesicles was found to be inhibited by specific respiratory inhibitors, including $Cu^{2+}$ ions, dicumarol, stigmatellin, and metyrapone, indicating that the azoreduction was indeed a respiration reaction. This finding was further confirmed by the fact that the ATP synthesis was repressed by the ATPase inhibitor N,N'-dicyclohexylcarbodiimide (DCCD). Therefore, this study offers solid evidence of a mechanism of microbial dissimilatory azoreduction on a subcell level.

Density Functional Theory Study on D-π-A-type Organic Dyes Containing Different Electron-Donors for Dye-Sensitized Solar Cells

  • Song, Jing;Xu, Jie
    • Bulletin of the Korean Chemical Society
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    • v.34 no.11
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    • pp.3211-3217
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    • 2013
  • Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations have been employed to investigate the molecular structures and absorption spectra of three D-${\pi}$-A-type organic dyes (C1-1, D5 and TH208) containing identical ${\pi}$-spacers and electron acceptors, but different aromatic amine electron-donating groups (tetrahydroquinoline, triphenylamine and phenothiazine). The coplanar geometries indicate that the strong conjugation is formed in the dyes. The electronic structures suggest that the intramolecular charge transfer from the donor to the acceptor occurs, and the electron-donating ability of tetrahydroquinoline is stronger than those of triphenylamine and phenothiazine. The computed orbital energy levels of these dyes confirm that the electrons could be injected from the excited dyes to the semiconductor conduction band and the oxidized dyes could be reduced effectively by electrolyte. The TD-DFT results show that the CAM-B3LYP/6-31+G(d, p) is suitable for calculating the absorption spectra. The first absorption band for these dyes is assigned to the HOMO${\rightarrow}$LUMO and HOMO-1${\rightarrow}$LUMO transitions.

Electron Acceptors in Organic Solar Cells (유기태양전지의 전자 받개 물질들)

  • Kong, Jaemin;Nam, Sang-Yong
    • Applied Chemistry for Engineering
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    • v.33 no.2
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    • pp.119-125
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    • 2022
  • The power conversion efficiency of organic solar cells has reached over 18%. The rapid increase in the efficiency is largely associated with the development of electron acceptors paired with proper electron donor polymers. In this mini review, the progress of organic solar cells is reviewed in terms of the development of electron acceptors. In the first part of the review, fullerene-based electron acceptors that have led the first half of organic solar cell development were dealt with. In the second part of it, nonfullerene-based electron acceptors, which have potentials to overcome the demerits of fullerene-based electron acceptors and opened a new era of organic solar cells, were introduced. Lastly, some suggestions to tackle the efficiency barrier of 20% are given with the summary of the review in the closing section.

Growth of CdS Single Crystal Thin Films by HWE Method (HWE법에 의한 CdS 단결정 박막의 성장)

  • 양동익;최용대;김진배
    • Journal of the Korean Vacuum Society
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    • v.1 no.3
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    • pp.353-359
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    • 1992
  • 본 연구에서는 HWE 방법에 의하여 GaAs(100) 기판위에 입방정의 단결정 박막을 성장하였다. 성장된 CdS 단결정 박막의 결정구조와 방향을 ECP(electron channeling pattern)로 결정하였다. CdS 박막의 (400)면이 기판과 평행하게 성장됨을 알았다. CdS 박 막의 photoluminescence를 20K에서 측정하였는데, free exception, bound exception 및 donor-acceptor pair에 의한 발광이 관측되었다.

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Synthesis and Characterization of New Push-Pull Chromophores Containing BF2-Azopyrrole Derivatives

  • Ko, HayeMin
    • Journal of the Korean Chemical Society
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    • v.60 no.1
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    • pp.21-27
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    • 2016
  • Novel push-pull chromophores containing 5’-(4-(bis(9,9-dimethyl-9H-fluoren-2-yl)aniline (bisDMFA) as a donor and phenylazo-methylpyrrolyl-boron difluoride (PhAPy-BF2) as an acceptor were designed and synthesized by the Knoevenagel condensation reaction for organic solar cells. Various electron withdrawing moieties were effectively introduced using 2,4-dimethyl-1H-pyrrole to afford new asymmetric BF2-azopyrrole molecules that were characterized by UV-vis spectroscopy and cyclic voltammetry measurements.

Stability of Bulk Heterojunction Organic Solar Cells with Different Blend Ratios of P3HT:PCBM

  • Kwon, Moo-Hyun
    • Transactions on Electrical and Electronic Materials
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    • v.13 no.2
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    • pp.98-101
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    • 2012
  • I studied the stability of organic photovoltaic cells in terms of P3HT:PCBM-71 blend ratio as a function of storage time. I obtained the best cell performance by optimizing the blend ratio of electron donor and electron acceptor within the active layer. In this study, I found that the more the P3HT:PCBM ratio increases within the active layer, the more the cell efficiency decreases as the storage time increases. As a result, the best optimized blend ratio was the 1:0.6 ratio of P3HT:PCBM-71, and cell efficiency of the device with the 1:0.6 blend ratio was 4.49%. The device with the best cell efficiency showed good stability.

2-amino-3-[(E)-4-(diethylamino)-2-alkoxy-benzylideneamino]- fumaronitrile 유도체 ICT 화합물의 결정 구조

  • Kim, Byung-Soon;Matsumoto, Shinya;Son, Young-A
    • Proceedings of the Korean Society of Dyers and Finishers Conference
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    • 2011.03a
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    • pp.62-62
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    • 2011
  • Intramolecular charge transfer (ICT) system has received great attentions due to their promising optoelectronic properties For the efficient ICT of the chromophore, their organic compound mainly consists of strong electron donors (e.g. $NR_2$ or OR groups) and acceptors (e.g. CN or $NO_2$ groups). According to the molecular design and synthesis, the ICT compounds can be extended in many application fields. In this study, we have synthesized ICT compounds having a strong electron acceptor and donor. These novel ICT compounds were easily synthesized by a previously described method with some modifications. Their single crystals were grown and their structures were solved and described in this presentation.

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Irradiation Induced Defects in a Si-doped GaN Single Crystal by Neutron Irradiation

  • Park, Il-Woo
    • Journal of the Korean Magnetic Resonance Society
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    • v.12 no.2
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    • pp.74-80
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    • 2008
  • The local structure of defects in undoped, Si-doped, and neutron irradiated free standing GaN bulk crystals, grown by hydride vapor phase epitaxy, has been investigated by employing electron magnetic resonance(EMR), Raman scattering and cathodoluminescence. The GaN samples were irradiated to a dose of $2{\times}10^{17}$ neutrons in an atomic reactor at Korea Atomic Energy Research Institute. There was no appreciable change in the Raman spectra for undoped GaN samples before and after neutron irradiation. However, a forbidden transition, $A_1$(TO) mode, appeared for a neutron irradiated Si-doped GaN crystal. Cathodoluminescence spectrum for the neutron irradiated Si-doped GaN crystal became much broader or was much more broadened than that for the unirradiated one. The observed EMR center with the g value of 1.952 in a neutron irradiated Si-doped GaN may be assigned to a Si-related complex donor.

Reduction of Azobenzene by Purified Bovine Liver Quinone Reductase

  • Kim, Kyung-Soon;Shin, Hae-Yong
    • BMB Reports
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    • v.33 no.4
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    • pp.321-325
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    • 2000
  • Quinone reductase was purified to homogeneity from bovine liver by using ammonium sulfate fractionation, ionexchange chromatography, and gel filtration chromatography. The enzyme utilized either NADH or NADPH as the electron donor. The enzyme catalyzed the reduction of several quinones and other artificial electron acceptors. Furthermore, the enzyme catalyzed NAD(P)H-dependent reduction of azobenzene. The apparent Km for 1,4-benzoquinone and azobenzene was 1.64 mM and 0.524 mM, respectively. The reduction of azobenzene by quinone reductase was almost entirely inhibited by dicumarol or Cibacron blue 3GA, potent inhibitors of the mammalian quinone reductase. In the presence of 1.0${\mu}M$ Cibacron blue 3GA, azoreductase activity was lowered by 45%, and almost complete inhibition was seen above 2.0 ${\mu}M$ Cibacron blue 3GA.

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Synthesis and Photovoltaic Properties of Organic Photosensitizers for Application of Dye Sensitized Solar Cells (페노시아진을 이용한 염료감응형 태양전지 고효율 염료합성)

  • Yang, Hyun Sik;Shin, So Yeon;Kim, Yeun Ji;Kim, Jae Hong
    • 한국신재생에너지학회:학술대회논문집
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    • 2011.05a
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    • pp.119.2-119.2
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    • 2011
  • Dye-sensitized solar cells (DSSC) are currently attracting wide spread academic and commercial interest for the conversion of sunlight into electricity because of their easy manufacturing process and high efficiency. The solar energy conversion efficiencies of DSSC are strongly dependent on dye molecules adsorbed on the TiO2 surface which used for photosensitization of sun light, since an excited state of dye could inject an electron into the conduction band of semiconductor. We have developed novel organic dyes which have phenothiazine moieties as an electron donor in their charge-transfer chromophore for application of DSSCs. We had synthesized a series of phenothiazine derivatives which have different wave length absorbing chromophore in the molecule with high molar extinction coefficient. The photovoltaic performance of DSSC composed of organic chromophores with broad wavelength absorption property were measured and evaluated by comparison with that of pristine ruthenium dye.

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