• Title/Summary/Keyword: 다공성 전극

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Influence of Nanostructured TiO2 Electrode Fabricated with Acid-treated Paste on the Photovoltaic Efficiency of Dye-Sensitized Solar Cells (산처리된 페이스트로 제조한 나노 구조체 TiO2 전극이 염료감응형 태양전지의 효율에 미치는 영향)

  • Lee, Jae-Wook;Hwang, Kyung-Jun;Roh, Sung-Hee;Kim, Sun-Il
    • Applied Chemistry for Engineering
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    • v.18 no.4
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    • pp.356-360
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    • 2007
  • Recently, dye sensitized solar cells (DSSCs) composed of nanoporous $TiO_2$, light-sensitive dyes, electrolytes, and counter electrode have been received much attention. Nanostructured particles with higher surface area for the higher adsorption of Ru (II) dye are required to increase the quantity of light absorption. Also, it has been reported that the key factor to achieve high energy conversion efficiency in the photoelectrode of DSSC is the heat treatment of $TiO_2$ paste with acid addition. In this work, we investigated the influence of acid treatment of $TiO_2$ solar cell on the photovoltaic performance of DSSC. The working electrodes fabricated in this work were characterized by X-ray photoelectron spectroscopy (XPS), extended X-ray absorption fine structure (EXAFS), field emission scanning electron microscope (FE-SEM), and atomic force microscope (AFM). In addition, the influence of nanostructured photoelectrode fabricated with the acid-treated paste on the energy conversion efficiency was investigated on the basis of photocurrent-potential curves. It was found that the influence of acid-treated paste on the photovoltaic efficiency was significant.

Electrochemical Reduction of Perchlorate Ion on Porous Carbon Electrodes Deposited with Iron Nanoparticles (영가철 나노 입자가 전착된 다공성 탄소전극을 이용한 과염소산 이온의 전기화학적 환원)

  • Rhee, Insook;Kim, Eun Yong;Lee, Bokyoung;Paeng, Ki-Jung
    • Journal of the Korean Electrochemical Society
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    • v.18 no.2
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    • pp.81-85
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    • 2015
  • A method for degradation of the perchlorate anion ($ClO{_4}^-$) has been studied using electrochemically generated zero-valent iron (ZVI) deposited on a porous carbon electrode. The first strategy of this study is to produce the ZVI via the electrochemical reduction of iron (II) on a porous carbon electrode coated with a conducting polymer, instead of employing expensive $NaBH_4$. The present method produced well distributed ZVI on conducting polymer (polypyrrole thin film) and increased surface area. ZVI surface can be regenerated easily for successive reduction. The second strategy is to apply a mild reducing condition (-0.3 V) to enhance the efficiency of the degradation of perchlorate with ZVI without the evolution of hydrogen. The electrochemically generated ZVI nanoparticles may offer an alternative means for the complete destruction perchlorate without evolution of hydrogen in water with high efficiency and at low cost.

COMPUTATIONAL STUDY FOR PERFORMANCE EVALUATION OF FLOW CHANNELS INSIDE CDI UNIT CELL (수치모사를 이용한 CDI Unit Cell 내부의 유로성능 평가)

  • Sohn, D.Y.;Choi, Y.H.;Park, D.W.;Jung, C.H.
    • Journal of computational fluids engineering
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    • v.15 no.1
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    • pp.31-36
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    • 2010
  • In the present study, computations for flow fields inside the CDI unit cells with electrodes and spacers have been made to evaluate their performance. Three types of unit cells that include a planar type, a serpentine channel type, and a spiral wound type were considered and their flow characteristics were compared. From the computational results, it is found that the serpentine channel type has a large flow resistance and can not guarantee the outflow flux for industrial applications. On the other hand, the planar type can sustain a large enough outflow flux but it's efficiency is low for the electrode-use because of the non-uniform velocity distribution inside the cell and dead zones in every corner. Finally, The spiral wound type has not only a large outflow flux as much as the planar type has, but also a high efficiency for the electrode-use because of uniform velocity distribution. From this comparison, we can expect that the spiral wound type of CDI unit cell would have a high performance deionization capability.

Porous Nickel-Tin Nano-Dendritic Electrode for Rechargeable Lithium Battery (리튬 이차 전지를 위한 다공성 니켈-주석 나노 수지상 전극)

  • Jung, Hye-Ran;Shin, Heon-Cheol
    • Korean Journal of Materials Research
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    • v.20 no.11
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    • pp.592-599
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    • 2010
  • A porous nickel-tin nano-dendritic electrode, for use as the anode in a rechargeable lithium battery, has been prepared by using an electrochemical deposition process. The adjustment of the complexing agent content in the deposition bath enabled the nickel-tin alloys to have specific stoichiometries while the amount of acid, as a dynamic template for micro-porous structure, was limited to a certain amount to prevent its undesirable side reaction with the complexing agent. The ratios of nickel to tin in the electro-deposits were nearly identical to the ratios of nickel ion to tin ion in the deposition bath; the particle changed from spherical to dendritic shape according to the tin content in the deposits. The nickel to tin ratio and the dendritic structure were quite uniform throughout the thickness of the deposits. The resulting nickel-tin alloy was reversibly lithiated and delithiated as an anode in rechargeable lithium battery. Furthermore, the resulting anode showed much more stable cycling performance up to 50 cycles, as compared to that resulting from dense electro-deposit with the same atomic composition and from tin electrodeposit with a similar porous structure. From the results, it is expected that highly-porous nickel-tin alloys presented in this work could provide a promising option for the high performance anode materials for rechargeable lithium batteries.

The diffusion model on the electrodes with nano-porous surfaces (나노 다공성 표면 전극 위의 확산 모델)

  • Park, Jin-Hyoung;Park, Sae-Jin;Chung, Taek-Dong;Kim, Hee-Chan
    • Proceedings of the KSME Conference
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    • 2003.04a
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    • pp.1100-1103
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    • 2003
  • One of the good ways to raise the rate of the electrochemical reaction is to broaden the effective surface area of the electrode by developing cylindrical nano-pores on the surfaces. The numerous pores of several nanometer in diameter can be used to enhance a specific faradaic reaction so that the nano-porous structure attract keen attention in terms of implication of new bio/chemical sensors, in which no chemical modification is involved. Amperometric glucose sensor is a representative example that needs the selective enhancement of glucose oxidation over the current due to physiological interferents such as ascorbic acid. The present paper reports how the ascorbic acid and glucose diffuse around the nano-porous surface by simulation study, for which 2D-FDM (Finite Difference Method) was adopted. The results of the simulation not only consist with those from electrochemical experiments but also reveal valuable potential for more advanced application of the nano-porous electrode.

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A Study on the Performance Analysis and Design of Cathode in Fuel Cells (연료전지 전극(Cathode)의 성능해석 및 설계에 관한 연구)

  • Kim, H.G.;Kang, S.S.;Song, H.Y.;Kang, Y.W.;Kwac, L.K.
    • Transactions of the Korean Society of Machine Tool Engineers
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    • v.16 no.1
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    • pp.75-79
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    • 2007
  • The cathode design is one of the most important parts in order to enhance the performance of fuel cells. A 3-D model of the porous oxygen reducing cathode with perforated current collectors is analysed for the enhanced design in fuel cells. Simulation is performed using equations of electric potential balance, momentum balance, and mass balance. The gas concentrations are quite large and are significantly affected by the reactions that take place. The weight fraction of oxygen, velocity field for the gas phase, and local overvoltage are illustrated in the porous reactive cathode layer. The current density is also analysed and the result shows the distribution and variation are stated in a wide range. It is found that the rate of reaction and the current production is higher beneath the orifice, and decreases as the distance to the gas inlet increases. The significance of the results is discussed in the viewpoint of the mass transportation phenomena, which is inferred that the mass transport of reactants dictates the efficiency of the electrode in this design and at these conditions.

The Development of Buried Type Reference Electrode Using Porous Ceramic(${\alpha}-Al_{2}O_{3}$) (다공성 세라믹(${\alpha}-Al_{2}O_{3}$)를 이용한 지중 매설형 기준전극)

  • Bae, Jeong-Hyo;Ha, Yoon-Cheol;Ha, Tae-Hyun;Lee, Hyun-Goo;Kim, Dae-Kyeong
    • Proceedings of the KIEE Conference
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    • 2005.11a
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    • pp.145-147
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    • 2005
  • In present, most of metallic structures(gas pipeline, oil pipeline, water pipeline, etc) are running parallel with subway and power line in seoul. Moreover subway system and power line make a stray current due to electrical corrosion on metallic structures. The owner of metallic structures has a burden of responsibility for the protection of corrosion and the prevention against big accident such as gas explosion or soil pollution and so on. So, they have to measure and analyze the data about P/S(Pipe to Soil) potential due to stray current of subway system. So, we have developed the Real-time Wireless Remote Monitoring System for Stray Current of Subway System. In this system, the permanent buried type reference electrode is necessary. In this paper, results of development of buried type reference electrode using porous ceramic$({\alpha}-Al_{2}O_{3})$ are presented.

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저온에서 Hydropolymer를 이용한 ZnO 나노입자 염료감응형 태양전지

  • Gwon, Byeong-Uk;Son, Dong-Ik;Park, Dong-Hui;Hong, Tae-U;Choe, Heon-Jin;Choe, Won-Guk
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.02a
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    • pp.439-439
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    • 2011
  • 기존의 고온에서 제작되는 TiO2 나노 입자를 이용한 염료감응형 태양전지를 저온에서 제작하기 위해 전자 이동층으로 ZnO 나노 입자를 사용하여, 저온($200^{\circ}C$)에서 염료감응태양전지(DSSC)를 제작하였다[1,2]. 상대전극(counter electrode)으로는 RF magnetron sputtering을 사용하여 ITO/glass위에 Pt를 증착하여 태양전지의 특성을 측정하였다. $180^{\circ}C$ 이상에서 hydropolymer가 증발되는 것을 이용하여, ZnO 나노입자와 hydropolymer 혼합한 paste 제작하여 소결 후 ZnO 나노입자 사이에 다공성을 생성시켜 Dye가 잘 침투하여 ZnO 나노입자 표면에 잘 흡착 되도록 하였다[3]. 20 nm 및 60 nm 크기의 ZnO 나노 입자를 사용하여 실험 해본 결과, 20 nm에 비하여 60 nm ZnO 나노입자의 경우 IPCE 값이 약 7% 정도로 높은 전환효율 값을 보였다. 60 nm ZnO 나노입자를 전자 수송층으로 사용한 DSSC 소자에서 단위면적당 흐르는 전류(Jsc), 전압 (Voc), fill factor (ff), 그리고 효율(${\eta}$)의 최대값은 4.93 mA/$cm^2$, 0.56V, 0.40, and 1.12%, 로 보였다.

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Development of CdSe/CdS Quantum Dot Co-sensitized ZnO Nanowire Solar Cell

  • Seol, Min-Su;Kim, Hui-Jin;Kim, U-Seok;Yong, Gi-Jung
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.08a
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    • pp.369-369
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    • 2011
  • 양자점 감응형 태양전지는 가시광 영역을 흡수, 이용할 수 있는 광감응 물질로 무기물 양자점을 사용하며, 이 경우 나노미터 크기의 무기물 양자점으로 인한 양자제한 효과 (quantum confinement effect)에 의해 양자점의 사이즈 조절 만으로 밴드갭을 조절할 수 있어 광학적 특성 조절이 용이하며, 하나의 광자를 흡수하여 두개 이상의 전자-정공쌍을 만들 수 있는 (multiple exciton generation) 가능성이 있어 기존 태양전지가 가지는 이론적 한계효율(Shockley-Queisser limit)을 뛰어넘을 수 있다. 본 연구에서는 양자점 및 염료 감응형 태양전지분야에서 가장 많이 사용되고 있는 TiO2 다공성 필름이 아닌, ZnO 나노선 구조를 이용하여 양자점 감응형 태양전지를 제작하였다. ZnO의 경우 TiO2보다 높은 전자이동도를 가지며, 나노선 구조가 바닥전극까지 수직 연결된 1차원의 전자전달경로를 제공하여 결과적으로 광전자 포집에 유리하다. 또한, CdS, CdSe 양자점을 동시에 사용하여 광흡수 범위를 가시광 전 영역으로 확장하였으며, 계단형 밴드구조를 통해 광전자-정공 분리 및 포집을 용이하게 하였다. 더 나아가 전해질의 조성, 나노선의 길이 등 다양한 부분을 조절하면서 각 변수가 소자의 효율에 미치는 영향을 관찰하였다.

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Perfluorinated Sulfonic Acid Ionomer-PTFE Pore-filling Membranes for Polymer Electrolyte Membrane Fuel Cells (고분자전해질연료전지용 과불소계 술폰화 이오노머-PTFE 강화막)

  • Kang, Seong Eun;Lee, Chang Hyun
    • Membrane Journal
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    • v.25 no.2
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    • pp.171-179
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    • 2015
  • Perfluorinated sulfonic acid ionomers (PFSAs) have been widely as solid electrolyte materials for polymer electrolyte membrane fuel cells, since they exhibit excellent chemical durability under their harsh application conditions as well as good proton conductivity. Even PFSA materials, however, suffer from physical failures associated with repeated membrane swelling and deswelling, resulting in fairly reduced electrochemical lifetime. In this study, pore-filling membranes are prepared by impregnating a Nafion ionomer into the pore of a porous PTFE support film and their fundamental characteristics are evaluated. The developed pore-filling membranes exhibit extremely high proton conductivity of about $0.5S\;cm^{-1}@90^{\circ}C$ in liquid water.