• 제목/요약/키워드: Tandem cell

검색결과 152건 처리시간 0.029초

Tandem cell 적용을 위한 narrow band gap을 갖는 a-Si 태양전지 개발 (Development of amorphous Si solar cell with narrow band gap for Tandem cell)

  • 김선호;유동주;안세원;이헌민;김동환
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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    • pp.63.1-63.1
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    • 2010
  • 실리콘 박막 태양전지의 효율을 향상시키기 위해 밴드갭이 다른 흡수층을 적용한 tandem형 적층 태양전지를 이용하고 있다. 일반적으로 1.7eV이상의 밴드갭이 큰 비정질 실리콘을 이용하여 단파장의 빛을 흡수하고, 상대적으로 낮은 1.1eV 정도의 밴드갭을 갖는 미세결정 실리콘 층으로 장파장을 흡수하게 된다. 이렇게 연결된 tandem형 태양전지의 효율을 극대화하기 위해서는 각 태양전지에서 발생하는 전류 밀도를 일치시키는 것이 필요하다. 이를 위해 비정질 실리콘의 두께가 증가되는 경우가 있는데 이러한 경우 비정질 실리콘의 광열화 특성(Lihgt-induced degradation)으로 안정화 효율이 감소하게 된다. 따라서 비정질 실리콘 태양전지의 전류 밀도를 향상 시켜 두께를 최소화하는 것이 매우 중요하다. Tandem형 태양전지에서 비정질 실리콘 태양전지의 전류 밀도를 향상시키기 위해 두 개의 전지사이에 광 반사층을 적용하여 태양전지를 제조하게 된다. 이러한 경우 비정질 실리콘의 전류 밀도는 증가하지만, 광 반사 층의 장파장 흡수로 인하여 하부 태양전지의 전류 밀도 감소가 더 커지게 되어 전체 발생 전류 밀도는 오히려 감소하게 된다. 본 논문에서는 비정질 실리콘의 밴드갭을 제어하여 광 흡수 파장 영역 확대로 전류 밀도를 향상시키는 연구를 진행하였다. PECVD의 RF power 조건을 제어하여 1.75eV에서 1.67eV까지 밴드갭을 변화시켰다. 이와 같은 조건의 박막을 광 흡수층으로 갖는 p-i-n 구조의 비정질 실리콘 태양전지를 제작하였다. i층의 밴드갭이 감소됨에 따라 장파장 영역의 흡수가 확대되어 전류 밀도가 증가 하였지만, Voc의 감소가 컸다. 이는 i층의 밴드갭이 좁아짐에 따라 p층과의 불연속성이 커졌기 때문이다. 이러한 악영향을 줄이기 위해 p층과 i층 사이에 buffer층을 삽입하여 태양전지를 제작하였다. 이와 같은 최적의 buffer층 삽입을 통하여 불연속성을 줄임으로써 Voc의 상승효과를 확인하였다. 본 연구의 결과로 좁은 밴드갭을 갖는 광 흡수 층을 적용하여 전류 밀도를 향상시키고, 최적화된 buffer층 삽입으로 Voc를 향상시킴으로써 고효율의 비정질 실리콘 태양전지를 제작하였다. 이를 tandem형 태양전지에 적용할 경우 초기 효율뿐만 아니라 얇은 두께에서 제조할 수 있기 때문에 광열화 특성이 향상되어 안정화 효율의 증가를 가져올 수 있다.

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핵치환에 의한 cloning, stem cell, 그리고 효소 telomerase (Mammalian Cloning by Nuclear transfer, Stem Cell, and Enzyme Telomerase)

  • 한창열
    • 식물조직배양학회지
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    • 제27권6호
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    • pp.423-428
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    • 2000
  • In 1997 when cloned sheep Dolly and soon after Polly were born, it had become head-line news because in the former the nucleus that gave rise to the lamb came from cells of six-year-old adult sheep and in the latter case a foreign gene was inserted into the donor nucleus to make the cloned sheep produce human protein, factor IX, in e milk. In the last few years, once the realm of science fiction, cloned mammals especially in livestock have become almost commonplace. What the press accounts often fail to convey, however, is that behind every success lie hundreds of failures. Many of the nuclear-transferred egg cells fail to undergo normal cell divisions. Even when an embryo does successfully implant in the womb, pregnancy often ends in miscarriage. A significant fraction of the animals that are born die shortly after birth and some of those that survived have serious developmental abnormalities. Efficiency remains at less than one % out of some hundred attempts to clone an animal. These facts show that something is fundamentally wrong and enormous hurdles must be overcome before cloning becomes practical. Cloning researchers now tent to put aside their effort to create live animals in order to probe the fundamental questions on cell biology including stem cells, the questions of whether the hereditary material in the nucleus of each cell remains intact throughout development, and how transferred nucleus is reprogrammed exactly like the zygotic nucleus. Stem cells are defined as those cells which can divide to produce a daughter cell like themselves (self-renewal) as well as a daughter cell that will give rise to specific differentiated cells (cell-differentiation). Multicellular organisms are formed from a single totipotent stem cell commonly called fertilized egg or zygote. As this cell and its progeny undergo cell divisions the potency of the stem cells in each tissue and organ become gradually restricted in the order of totipotent, pluripotent, and multipotent. The differentiation potential of multipotent stem cells in each tissue has been thought to be limited to cell lineages present in the organ from which they were derived. Recent studies, however, revealed that multipotent stem cells derived from adult tissues have much wider differentiation potential than was previously thought. These cells can differentiate into developmentally unrelated cell types, such as nerve stem cell into blood cells or muscle stem cell into brain cells. Neural stem cells isolated from the adult forebrain were recently shown to be capable of repopulating the hematopoietic system and produce blood cells in irradiated condition. In plants although the term$\boxDr$ stem cell$\boxUl$is not used, some cells in the second layer of tunica at the apical meristem of shoot, some nucellar cells surrounding the embryo sac, and initial cells of adventive buds are considered to be equivalent to the totipotent stem cells of mammals. The telomere ends of linear eukaryotic chromosomes cannot be replicated because the RNA primer at the end of a completed lagging strand cannot be replaced with DNA, causing 5' end gap. A chromosome would be shortened by the length of RNA primer with every cycle of DNA replication and cell division. Essential genes located near the ends of chromosomes would inevitably be deleted by end-shortening, thereby killing the descendants of the original cells. Telomeric DNA has an unusual sequence consisting of up to 1,000 or more tandem repeat of a simple sequence. For example, chromosome of mammal including human has the repeating telomeric sequence of TTAGGG and that of higher plant is TTTAGGG. This non-genic tandem repeat prevents the death of cell despite the continued shortening of chromosome length. In contrast with the somatic cells germ line cells have the mechanism to fill-up the 5' end gap of telomere, thus maintaining the original length of chromosome. Cem line cells exhibit active enzyme telomerase which functions to maintain the stable length of telomere. Some of the cloned animals are reported prematurely getting old. It has to be ascertained whether the multipotent stem cells in the tissues of adult mammals have the original telomeres or shortened telomeres.

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텐덤형 태양전지를 위한 InAs 다중 양자점과 InGaAs 다중 양자우물에 관한 연구 (Design and Growth of InAs Multi-Quantum Dots and InGaAs Multi-Quantum Wells for Tandem Solar Cell)

  • 조중석;김상효;황보수정;장재호;최현광;전민현
    • 한국진공학회지
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    • 제18권5호
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    • pp.352-357
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    • 2009
  • 본 연구에서는 1.1 eV의 에너지대역을 흡수할 수 있는 InAs 양자점구조와 1.3 eV의 에너지 대역을 흡수 할 수 있는 InGaAs 양자우물구조를 이용한 텐덤형 태양전지의 구조를 1D poisson을 이용해 설계하고, 분자선 에피택시 장비를 이용하여 각각 5, 10, 15층씩 쌓은 양자점 및 양자우물구조를 삽입하여 p-n접합을 성장하였다. Photoluminescence (PL) 측정을 이용한 광학적특성 평가에서 양자점 5층 및 양자우물 10층을 삽입한 구조의 PL 피크가 가장 높은 상대발광강도를 나타냈으며, 각각 1.1 eV 및 1.3 eV에서 57.6 meV 및 12.37 meV의 Full Width at Half Maximum을 나타내었다. 양자점의 밀도 및 크기는 Reflection High-Energy Electron Diffraction system과 Atomic Force Microscope를 이용해 분석하였다. 그리고 GaAs/AlGaAs층을 이용한 터널접합에서는 I-V 측정을 통하여 GaAs층의 두께(20, 30, 50 nm)에 따른 터널링 효과를 평가하였다. GaAs 층의 두께가 30 nm 및 50 nm의 터널접합에서는 backward diode 특성을 나타낸 반면, 20 nm GaAs층의 GaAs/AlGaAs 터널접합에서는 다이오드 특성 곡선을 확인하였다.

A Novel Approach to Investigating Protein/Protein Interactions and Their Functions by TAP-Tagged Yeast Strains and its Application to Examine Yeast Transcription Machinery

  • Jung, Jun-Ho;Ahn, Yeh-Jin;Kang, Lin-Woo
    • Journal of Microbiology and Biotechnology
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    • 제18권4호
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    • pp.631-638
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    • 2008
  • Tandem affinity purification (TAP) method combined with LC-MS/MS is the most accurate and reliable way to study the interaction of proteins or proteomics in a genome-wide scale. For the first time, we used a TAP-tag as a mutagenic tool to disrupt protein interactions at the specific site. Although lots of commonly used mutational tools exist to study functions of a gene, such as deletional mutations and site-directed mutagenesis, each method has its own demerit. To test the usefulness of a TAP-tag as a mutagenic tool, we applied a TAP-tag to RNA polymerase II, which is the key enzyme of gene expression and is controlled by hundreds of transcription factors even to transcribe a gene. Our experiment is based on the hypothesis that there will be interrupted interactions between Pol II and transcription factors owing to the TAP-tag attached at the C-terminus of each subunit of Pol II, and the abnormality caused by interrupted protein interactions can be observed by measuring a cell-cycle of each yeast strain. From ten different TAP-tagged strains, Rpb7- and Rpb12-TAP-tagged strains show severe defects in growth rate and morphology. Without a heterodimer of Rpb4/Rpb7, only the ten subunits Pol II can conduct transcription normally, and there is no previously known function of Rpb7. The observed defect of the Rpb7-TAP-tagged strain shows that Rpb7 forms a complex with other proteins or compounds and the interruption of the interaction can interfere with the normal cell cycle and morphology of the cell and nucleus. This is a novel attempt to use a TAP-tag as a proteomic tool to study protein interactions.

WTAP 단백질의 안정성을 통한 CCDC98 단백질의 cyclin B1 발현 조절 (Coiled-Coil Domain-Containing Protein 98 (CCDC98) Regulates Cyclin B1 Expression by Affecting WTAP Protein Stability)

  • 오윤정;이은희;이일규;김경수;김홍태
    • 생명과학회지
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    • 제21권8호
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    • pp.1067-1075
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    • 2011
  • CCDC98 단백질은 BRCA1-A 복합체를 DNA 손상 부위로 이동시킴으로써 DNA손상에 의하여 유도되는 G2/M cell cycle checkpoint에 중요한 역할을 한다고 알려져 있다. 하지만 많은 연구에도 불구하고 CCDC98 단백질의 기능에 대해서 알려진 바가 거의 없다. 본 연구는 CCDC98 단백질의 기능을 밝히고자 tandem affinity purification 방법을 수행하였다. 그 결과 Wilms tumor 1-associating protein (WTAP)을 CCDC98의 결합 단백질로 분리 동정하였다. 이들 단백질의 결합을 in vivo and in vitro binding assays를 통하여 확인하였다. 또한, CCDC98 단백질이 cyclin B1의 발현을 억제함을 확인하였는데, 이는 WTAP 단백질의 발현을 조절함으로써 이루어진다는 것을 확인하였다. 이는 CCDC98 단백질이 새로운 세포주기 조절자라는 것을 증명하는 결과이다.

Differential Protein Quantitation in Mouse Neuronal Cell Lines using Amine-Reactive Isobaric Tagging Reagents with Tandem Mass Spectrometry

  • Cho, Kun;Park, Gun-Wook;Kim, Jin-Young;Lee, Sang-Kwang;Oh, Han-Bin;Yoo, Jong-Shin
    • Mass Spectrometry Letters
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    • 제1권1호
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    • pp.25-28
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    • 2010
  • The high-throughput identification and accurate quantification of proteins are essential strategies for exploring cellular functions and processes in quantitative proteomics. Stable isotope tagging is a key technique in quantitative proteomic research, accompanied by automated tandem mass spectrometry. For the differential proteome analysis of mouse neuronal cell lines, we used a multiplexed isobaric tagging method, in which a four-plex set of amine-reactive isobaric tags are available for peptide derivatization. Using the four-plex set of isobaric tag for relative and absolute quantitation (iTRAQ) reagents, we analyzed the differential proteome in several stroke time pathways (0, 4, and 8 h) after the mouse neuronal cells have been stressed using a glutamate oxidant. In order to obtain a list of the differentially expressed proteins, we selected those proteins which had apparently changed significantly during the stress test. With 95% of the peptides showing only a small variation in quantity before and after the test, we obtained a list of eight up-regulated and four down-regulated proteins for the stroke time pathways. To validate the iTRAQ approach, we studied the use of oxidant stresses for mouse neuronal cell samples that have shown differential proteome in several stroke time pathways (0, 4, and 8 h). Results suggest that histone H1 might be the key protein in the oxidative injury caused by glutamate-induced cytotoxicity in HT22 cells.

RF-마그네트론 스퍼터링으로 증착된 산화주석 전자수송층의 광학적 및 전기적 특성에 대한 증착 전력의 영향 (Effect of Sputtering Power on Optical and Electrical Properties of SnOx Electron Transport Layer Deposited by RF-magnetron Sputtering)

  • 황지성;이원규;황재근;이상원;현지연;이솔희;정석현;강윤묵;김동환;이해석
    • Current Photovoltaic Research
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    • 제9권1호
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    • pp.1-5
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    • 2021
  • The properties of the electron transport layer (ETL) have a great effect on perovskite solar cell performance. Depositing conformal SnO2 ETL on bottom textured silicon cells is essential to increase current density in terms of the silicon-perovskite tandem solar cells. In the recent study, the SnO2 electron transport layer deposited by the sputtering method showed an efficiency of 19.8%. Also, an electron transport layer with a sputtered TiO2 electron transport layer in a 4-terminal tandem solar cell has been reported. In this study, we synthesized SnOx ETL with a various sputtering power range of 30-60W by Radio-frequency (RF)-magnetron sputtering. The properties of SnOx thin film were characterized using ellipsometer, UV-vis spectrometer, and IV measurement. With a sputtering power of 50W, the solar cell showed the highest efficiency of 13.3%, because of the highest fill factor by the conductivity of SnOx film.

Sound Propagation in 5CB Liquid Crystals Homogeneously Confined in a Planar Cell

  • Ko, Jae-Hyeon;Hwang, Yoon-Hwae;Kim, Jong-Hyun
    • Journal of Information Display
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    • 제10권2호
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    • pp.72-75
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    • 2009
  • The Brillouin spectrum of 4'-n-pentyl-4-cyano-biphenyl (5CB) liquid crystals homogeneously confined in a planar liquid crystal (LC) cell was measured using a 6-pass tandem Fabry-Perot interferometer. By adopting a special right-angle scattering geometry, the sound velocity of 5CB was estimated from the Brillouin shift without knowing the refractive index. The sound velocity of the longitudinal wave propagating along the direction of the directors aligned parallel to the glass plates of the LC cell was 1784${\pm}$7 m/s at 300 K. The attenuation coefficient $\alpha$ was estimated to be approximately $1.9{\times}10^6m^{-1}$, which is about twice as large as that of the longitudinal sound wave propagating along the direction perpendicular to the directors. The present method may be very useful in the evaluation of the elastic properties of the materials used in display devices, whose refractive indices are not known.

High-Power Conversion Efficiency of Photovoltaic Cells Fabricated with a Small-molecular and Polymer Donating Blend Layer

  • Kim, Ji-Heon;Park, Jea-Gun
    • Current Photovoltaic Research
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    • 제2권2호
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    • pp.48-52
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    • 2014
  • A photovoltaic cell of CuPc:P3HT:PCBM was introduced to extend the light absorption in the visible wavelength between 300~500 and 550~800 nm. By fabricating the photovoltaic cells of ITO / PEDOT:PSS / CuPc:P3HT:PCBM / BCP / Al with small-molecular and polymer donating materials blended layer, we demonstrated a high PCE of 4.20% with high Jsc of $10.05mA/cm^2$. This performance of photovoltaic cell with the blended layer of small-molecular and polymer can be competitive with that of tandem cells.

Possible Roles of LAMMER Kinase Lkh1 in Fission Yeast by Comparative Proteome Analysis

  • Cho, Soo-Jin;Kim, Young-Hwan;Park, Hee-Moon;Shin, Kwang-Soo
    • Mycobiology
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    • 제38권2호
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    • pp.108-112
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    • 2010
  • To investigate the possible roles of LAMMER kinase homologue, Lkh1, in Schizosaccharomyces pombe, whole proteins were extracted from wild type and lkh1-deletion mutant cells and subjected to polyacrylamide gel electrophoresis. Differentially expressed proteins were identified by tandem mass spectrometry (MS/MS) and were compared with a protein database. In whole-cell extracts, 10 proteins were up-regulated and 9 proteins were down-regulated in the mutant. In extracellular preparations, 6 proteins were up-regulated in the lkh1+ null mutant and 4 proteins successfully identified: glycolipid anchored surface precursor, $\beta$-glucosidase (Psu1), cell surface protein, glucan 1,3-$\beta$-glucosidase (Bgl2), and exo-1,3 $\beta$-glucanase (Exg1). These results suggest that Lkh1 is involved in regulating cell wall assembly.