• Proceedings of the Korean Society Of Semiconductor Equipment Technology
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• 2003.12a
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• pp.99-104
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• 2003

본 연구에서는 고분자 전해질 연료전지의 촉매 슬러리 함침 도구와 전극 촉매층 형성 방법이 전극 성능에 미치는 영향을 조사하였다. 촉매 슬러리 함침 도구는 브러쉬, 스프레이 건, 스크린 프린터를 이용하였으며, 전극 촉매층 형성 방법은 스크린 프린터를 이용하여 고분자 전해질 막 위에 전극 촉매층을 형성하는 방법, 카본 페이퍼 위에 전극 촉매층을 형성하는 방법과 위의 두 방법을 결합하여 전극 촉매층을 형성하는 방법으로 구분하였다. 스크린 프린터로 제조된 전극은 브러쉬와 스프레이 건으로 제조된 전극들과 비교하여 백금 함침량을 50% 이상 줄일 수 있었으며, 고분자 전해질 막 위에 전극 촉매층을 형성하는 방법과 카본 페이퍼에 전극 촉매층을 형성하는 방법을 결합한 전극이 $1A/\textrm{cm}^2$에서 0.6V로 가장 좋은 I-V 특성을 나타내었다.

• 한국신재생에너지학회:학술대회논문집
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• 2010.11a
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• pp.71.1-71.1
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• 2010

고분자 전해질 연료전지(PEMFC) 내의 기체확산층(GDL)은 셀 내의 물 관리에 중요한 역할을 수행한다. 일반적으로 다공성 기제(GDBL) 위에 미세기공층(MPL)을 코팅한 2층 구조의 기체확산층이 사용되는데, 이 미세기공층은 카본파우더와 테프론의 혼합물로 이루어져 있으며 촉매층에서 발생한 물을 셀 밖으로 빠르게 배출하는 역할을 수행한다. 본 연구에서는 다양한 기공분포를 갖는 미세기공층을 제조하여 고분자 전해질 연료전지 성능에 미치는 영향을 분석하였다. 미세기공층 슬러리내에 암모늄염 계열의 기공형성제를 혼합하여 다공성 기제 위에 코팅한 후 다양한 온도조건에서 건조함에 따라 기공분포가 다른 미세기공층을 제조하였다. 이렇게 제조된 미세기공층의 물성은 수은기공도계, FE-SEM, 자체적으로 제조한 기체투과도 측정 장치를 사용하여 측정하였으며, 단위 전지 성능 측정은 두 개의 가습조건(RH100%, RH50%)에서 실시하였다. 기공분포 측정결과 건조온도가 높은 미세기공층은 건조온도가 낮은 미세기공층에 비해 직경이 1,000 - 20,000 nm 인 대공극(macropore)의 수가 많지만, 직경이 100 nm 이하의 미세공 (micropore)의 수가 적은 것을 확인하였다. 전지성능 측정 결과 고가습 조건 (RH100%)에서는 미세공 (micropore)이 발달한 미세기공층을 포함한 기체확산층을 사용한 경우 가장 우수한 성능을 보여고, 저가습 조건 (RH50%)에서는 대공극 (macropore)이 발달한 미세기공층을 포함한 기체확산층을 사용한 경우 가장 우수한 성능을 나타내었다. 이는 물배출에 유리한 미세공 (micropore)의 성질과 원료 기체의 이동에 유리한 대공극(macropore)의 성질에 의한 것으로 판단된다. 따라서 셀 운전 가습조건에 따라 최적화된 기공구조를 갖는 미세기공층을 사용함으로써 셀 운전 성능을 향상 시킬 수 있을 것으로 예상된다.

• KSBB Journal
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• v.4 no.2
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• pp.150-156
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• 1989

The chaacterisitics of a commercial membrance-coverd electrode in air-saturated saline solution were investigated in terms of a steadystate one-dimensional model. The electrode system miiersed in an aqueous medium consists of three layers: an external concentration boundary layer, a membrance, and an inner electrolyte layer. The membrance can be permeabld to the water and impermeable to the ionic species. In stationary midium, the water migrates from the external medium to the inner electrolyte layer until a thermodynamic equilibrium is reached. In a following midium, however, there is a reverse direction of water movement due to the hyrodynamic pressure differential until both thickness of the electrolyte layer and the membrance are equal.

• Membrane Journal
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• v.19 no.4
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• pp.291-301
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• 2009

Double-layered polymer electrolyte membranes were prepared from two different sulfonated poly(aryl ether sulfone) copolymers by the two-step solution casting method for direct methanol fuel cells (DMFC). Sulfonation degrees were adjusted 10% (SPAES-10) and 50% (SPAES-50) by controlling monomer ratios, and the weight ratios of SPAES-10 copolymer were varied in the range of 5~20% to investigate the effect of thickness of coating layers on the membranes. Proton conducting layers were fabricated from SPAES-50 solutions of N-methyl-2-pyrrolidone (NMP) by a solution casting technique, and coating layers formed on the semiliquid surface of the conducting layer by pouring of SPAES-10-NMP solutions onto. It was found that double-layered polymer electrolyte membrane could significantly reduce the methanol crossover through the membrane and maintain high proton conductivities being comparable to single-layered SPAES-50 membrane. The maximum power density of membrane-electrolyte assembly (MEA) at the condition of $60^{\circ}C$ and 2 M methanol-air was $134.01\;mW/cm^2$ for the membrane prepared in the 5 wt-% of SPAES-10 copolymer, and it was corresponding to the 105.5% of the performance of the commercial Nafion 115 membrane.

• Journal of IKEEE
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• v.27 no.1
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• pp.25-29
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• 2023

Effect of the processes of polysilazane solid electrolyte layer and silver (Ag) active electrode on the electrical characteristics of memristor was investigated. The memristor with the solid electrolyte annealed at higher temperature exhibited the higher set voltage and better memory retention characteristics than that annealed at lower temperature. The increase in the set voltage and the improvement of the memory retention characteristic at high annealing temperature were attributed to a reduction in the void density and an increase in the void uniformity inside the solid electrolyte, respectively. In the case where the polysilazane solution's concentration is high, the memristor exhibited rapid degradation of low resistive state even annealed at high temperature. Lastly, it was shown that the memristor with the solution-processed Ag active electrode showed WORM property unlike that with the vacuum-processed Ag active electrode. The WORM property was possibly due to morphological defects present in the solution-processed Ag active electrode.

• Journal of the Microelectronics and Packaging Society
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• v.23 no.3
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• pp.31-35
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• 2016

This paper demonstrates the successful application of yttria-stabilized zirconia thin films deposited by atomic layer deposition to the anode-side interlayer for cerium oxide electrolyte based solid oxide fuel cell. At the operating temperature over $500^{\circ}C$, the electrical conductivity of cerium oxide electrolyte is known to dramatically increase and, therefore, the open circuit voltage of the cell decreases leading to the decrease of the performance. Ultra-thin (60 nm) atomic layer deposited yttria-stabilized zirconia thin film in this study conformally coated the anode-side surface of the cerium oxide electrolyte and efficiently blocked the electrical conduction through the electrolyte. Accordingly, the open circuit voltage increased by up to 20%, and the maximum power density increased by 52% at $500^{\circ}C$

• Journal of the Korea Academia-Industrial cooperation Society
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• v.15 no.6
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• pp.4013-4018
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• 2014

A 0.45 $cm^2$ DSSC device with a glass/FTO/blocking layer/$TiO_2$/N719(dye)/electrolyte/50 nm-Pt/50 nm-Au/FTO/glass was prepared to examine the stability of the Au/Pt bilayered counter electrode (CE) with electrolyte and the energy conversion efficiency (ECE) of dye-sensitized solar cells (DSSCs). For comparison, a 100 nm-thick Pt only CE DSSC was also prepared using the same method. The photovoltaic properties, such as the short circuit current density ($J_{sc}$), open circuit voltage ($V_{oc}$), fill factor (FF), and ECE, were checked using a solar simulator and potentiostat with time after assembling the DSSC. The microstructure of the Au/Pt bilayer was examined by optical microscopy after 0~25 minutes. The ECE of the Pt only CE-employed DSSC was 4.60 %, which did not show time dependence. On the other hand, for the Au/Pt CE DSSC, the ECEs after 0, 5 and 15 minutes were 5.28 %, 3.64 % and 2.09 %, respectively. The corrosion areas of the Au/Pt CE determined by optical microscopy after 0, 5, and 25 minutes were 0, 21.92 and 34.06 %. These results confirmed that the ECE and catalytic activity of Au/Pt CE decreased drastically with time. Therefore, a Au/Pt CE-employed DSSC may be superior to the Pt only CE-employed one immediately after integration of the device, but it would degrade drastically with time.

• Journal of the Korean Electrochemical Society
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• v.25 no.4
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• pp.174-183
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• 2022

Polymer electrolyte fuel cells and water electrolysis are attracting attention in terms of high energy density and high purity hydrogen production. The catalyst layer for the polymer electrolyte fuel cell and water electrolysis is a porous electrode composed of a precious metal-based electrocatalyst and an ionomer binder. Among them, the ionomer binder plays an important role in the formation of a three-dimensional network for ion conduction in the catalyst layer and the formation of pores for the movement of materials required or generated for the electrode reaction. In terms of the use of commercial perfluorinated ionomers, the content of the ionomer, the physical properties of the ionomer, and the type of the dispersing solvent system greatly determine the performance and durability of the catalyst layer. Until now, many studies have been reported on the method of using an ionomer for the catalyst layer for polymer electrolyte fuel cells. This review summarizes the research results on the use of ionomer binders in the fuel cell aspect reported so far, and aims to provide useful information for the research on the ionomer binder for the catalyst layer, which is one of the key elements of polymer electrolyte water electrolysis to accelerate the hydrogen economy era.

• Journal of the Korean Electrochemical Society
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• v.8 no.1
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• pp.1-5
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• 2005

Electric double layer capacitors(EDLCS) based on the charge stored at the interface between a hi팀 surface area carbon electrode and an organic electrolyte solution are widely used as a maintenance-free power source for IC memories and microcomputers. The achievement of the excellent performance of the capacitor requires an electrolyte solution which provides high conductivities over a wide temperature range and good electrochemical stabilities to allow the capacitor to be operated at high voltage. The electrochemical capacitor using a carbon material as electrodes and using an organic electrolyte with $1M-LiPF_6$ in PC-GBL-DEC(volume ratio 1:1:2) has specific capacitance of 64F/g.

• Transactions of the Korean Society of Mechanical Engineers B
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• v.35 no.5
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• pp.487-490
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• 2011

We used X-ray tomography to carry out an experimental study to visualize the effect of freeze and thaw cycles on the gas diffusion layer (GDL) in a polymer electrolyte membrane fuel cell (PEMFC). A PEMFC has freeze and thaw cycles if the fuel cell is operating at a below-freezing ambient temperature. The cycle permanently deforms the fuel-cell capillary structures and reduces the ability of the cell to generate electric power and also reduces its service life. The GDL is the thickest capillary layer in the fuel cell, so it experiences the most deformation. The X-ray tomography facility at the Pohang Accelerator Laboratory was used to observe the structural changes in GDLs induced by a freeze and thaw cycle. We discuss the effects of these structural changes on the power production and service life of PEMFCs.