• Membrane Journal
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• v.20 no.1
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• pp.13-20
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• 2010

Using poly(ethylene oxide) (PEO) as a polymer host, poly(ethylene glycol) (PEG) as a plasticizer, potassium iodide and iodine as sources of $I^-/{I_3}^-$ PEO-PEG-KI/$I_2$ polymer gel electrolytes were prepared. Based on the polymer gel electrolytes, solid-state dye-sensitized solar cell(DSSC)s were fabricated. The content of PEG in the electrolyte was changed from 0 to 85%. The electrolyte showed self-supporting form through whole range of the PEG content. As the PEG content increased, the ionic conductivity and ${I_3}^-$ diffusivity increased and the light-to electrical energy conversion efficiency increased under irradiation of 100 $mWcm^{-2}$ simulated sunlight.

• Membrane Journal
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• v.20 no.1
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• pp.21-28
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• 2010

Organic/inorganic composite electrolyte membranes were prepared for dye sensitized solar cell (DSSC). Poly (ethylene glycol) (PEG)s with various molecular weight (600, 1,500, 2,000 and 3,400) were ethoxysilated to fabricate organic/inorganic composite materials through sol-gel processes. The electrolyte membranes were produced by doping the composite materials with KI and $I_2$, and their ionic conducting behaviors were investigated. The ionic conductivity of the composite membrane was highly affected by PEG molecular weight. The highest conductivity was shown by the composite membrane prepared with PEG with the molecular weight of 2,000. The composite electrolyte membranes showed considerable improvement of ionic conductivity. Compared to PEO electrolyte membranes, the composite electrolyte membrane by PEG, MW 2,000 showed much higher ionic conductivity.

• Membrane Journal
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• v.18 no.4
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• pp.345-353
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• 2008

Organic/inorganic composite electrolyte membranes were prepared for dye sensitized solar cell (DSSC). Polyethylene Glycol (PEG)s with various molecular weight (400, 600, 1,500 and 3,400) was ethoxysilated to fabricate organic/inorganic composite materials through sol-gel processes. The electrolyte membranes were produced by doping the composite materials with NaI and $I_2$, and their ionic conducting behavior was investigated. The ionic conductivity of the composite electrolyte was highly affected by the PEG molecular weight, and the highest conductivity was shown by the composite membrane prepared with PEG with the molecular weight of 1,500. The composite electrolyte membranes showed considerable improvement of ionic conductivity. Compared to PEO electrolyte membranes, the composite electrolyte membrane prepared by PEG, MW 1,500, showed much higher ionic conductivity.

• Membrane Journal
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• v.26 no.2
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• pp.141-145
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• 2016

Polymer electrolyte membranes (PEMs) are key components to determine electrochemical fuel cell performances, in addition to electrode materials. The PEMs need to satisfy selective transport behaviors to small molecules including gases and protons; the PEMs have to transport protons as fast as possible, while they should act as hydrogen barriers, since the permeated gas induces the thermal degradation of cathode catalyst, resulting in rapid electrochemical reduction. To date, limited tools have been used to measure how fast hydrogen gas permeates through PEMs (e.g., Constant volume/variable Pressure (time-lag) method). However, most of the measurements are conducted under vacuum where PEMs are fully dried. Otherwise, the obtained hydrogen permeance is easily changeable, which causes the measurement errors to be large. In this study, hydrogen permeation properties through Nafion212 used as a standard PEM are evaluated using an in-situ measurement system in which both temperature and humidity are controlled at the same time.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.7 no.6
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• pp.1292-1295
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• 2006

Three kinds of electrolyte membranes were prepared by impregnating filter papers with one of the electrolyte solutions fur primary manganese battery ($NH_4Cl$, $ZnCl_2$, and alkaline types) and hygroscopic agent ($CaBr_2$ or $CaCl_2$), respectively. The thickness of them was $250{\sim}300{\mu}m$, and they were very flexible. The electrochemical characteristics greatly depended on the hygroscopic agent to supply water to the cell. The electrolyte membrane containing $CaCl_2$ showed the highest ionic conductivity and the largest discharge capacity.

• Prospectives of Industrial Chemistry
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• v.24 no.3
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• pp.14-27
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• 2021

수소 에너지는 환경 문제를 최소화하고 고갈되는 화석연료를 대체할 수 있는 에너지원으로 각광을 받고 있다. 수소연료전지는 이러한 수소를 에너지원으로 사용하고 수소를 전기에너지로 전환하여 그 부산물로 물을 만드는 대표적인 친환경 전기화학 장치이다. 고분자 전해질막 연료전지는 수소이온교환 특성을 갖는 고분자막을 전해질로 사용하는 연료전지로 막전극집합체의 전극층은 촉매가 포함된 고분자 전해질막 연료전지의 주요 요소 중의 하나이다. 소재개발 측면에서 고분자 전해질막 연료전지 전극층 핵심 소재의 물성 발현 원리 등을 이해하고 최적화된 소재 설계를 위해서는 원자레벨에서의 소재 설계 접근법이 필요하다. 따라서 실험적인 연구가 어려운 부분과 원자단위에서의 물질 현상에 대한 이해 그리고 연구 개발의 효율성 증진을 위해 전산재료과학(computational materials science) 기술이 광범위하게 활용될 수 있다. 본 기고문에서는 고분자 전해질막 연료전지에서의 전극층 소재에 대한 분자동역학 기반의 전산모사 활용과 연구동향에 대하여 소개하고자 한다.

• 한국신재생에너지학회:학술대회논문집
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• 2009.11a
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• pp.197-198
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• 2009

고분자 전해질막으로 사용할 수 있는 소수성/친수성 랜덤 멀티블럭 공중합체를 합성하였다. 공중합체는 수산화기를 각 말단에 가지고 있는 소수성 올리고머, 친수성 올리고머 및 반응성이 좋은 커플링 단량체로 친핵성 치환 반응을 활용하여 합성 하였다. 높은 반응성의 커플링 단량체의 존재로 비교적 낮은 온도에서 합성이 됨으로서 고온에서의 에테르-에테르 교환반응에 의한 랜덤화를 억제할 수 있었으며, 높은 중합도의 공중합체를 합성 할 수 있었다. 각 수산화기로 같은 말단으로 조정된 올리고머는 투입 비율의 조정으로 쉽게 이온교환용량을 조정할 수 있었다. 솔루션 캐스팅 방법으로 강도를 가지고 잘 휘어지며 투명한 전해질막을 제조할 수 있었다. 전해질막은 이온전도도, 물흡수율, 부피 변화율, 연료 투과성 등의 측정이 되었다.

• Proceedings of the Membrane Society of Korea Conference
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• 2004.05b
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• pp.199-202
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• 2004

DMFC 성능을 개선시키기 위한 연구의 큰 영역은 고분자전해질막에 있으며 methanol crossover에 대한 영향을 최소화시킬 수 있는 소재개발이 우선적으로 요구되는 실정이다. 이러한 문제의 해결을 위해 Pivovar와 Cussler [1] 등은 투과증발 막분리공정에서 메탄올 저항체로 잘 알려진 폴리비닐알콜(poly vinyl alcohol, PVA)를 이용한 전해질막 연구를 하였다.(중략)

• Membrane Journal
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• v.18 no.2
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• pp.116-123
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• 2008

Proton conductive hybrid nanocomposite polymer electrolyte membranes comprising polystyrene-5-poly (hydroxyethyl methacrylate) (PS-b-PHEMA), sulfosuccinic acid (SA) and phosphotungstic acid (PWA) were prepared by varying PWA concentrations. The PHEMA block was thermally crosslinked by SA via the esterification reaction between -OH of PHEMA and -COOH of SA. Upon the incorporation of PWA into the diblock copolymer, the symmetric stretching bands of the $SO_3^-$ group at $1187cm^{-1}$ shifted to a lower wavenumber at $1158cm^{-1}$, demonstrating that the PWA particles strongly interact with the sulfonic acid groups of SA. When the concentration of PWA was increased to 30wt%, the proton conductivity of the composite membrane at room temperature increased from 0.045 to 0.062 S/cm, presumably due to the intrinsic conductivity of the PWA particles and the enhanced acidity of the sulfonic acid in the membranes. The membrane containing 30wt% of PWA exhibited a proton conductivity of 0.126 S/cm at $100^{\circ}C$. Thermal stability of the composite membranes was also enhanced by introducing PWA nanoparticles.

• Membrane Journal
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• v.21 no.3
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• pp.213-221
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• 2011

Using poly(ethylene oxide) (PEO) as a polymer host, poly(ethylene glycol) (PEG) as a plasticizer, potassium iodide and iodine as sources of $I^-/I_3^-$, polymer electrolyte membranes were prepared. Based on the polymer electrolytes, solid-state dye-sensitized solar cell (DSSC)s were fabricated. The content of PEG in the electrolyte was controlled to be 95%. The mole number of KI per 1 mole of EO ([KI]/[EO] ratio) in the electrolyte was changed to be 0.022, 0.044, 0.066 and 0.088. The electrolyte membrane showed wax phase in ambient temperature. The ionic conductivity increased with increasing KI content to reach the maximum value at which [KI]/[EO] ratio is 0.066. After the maximum value, the ionic conductivity decreased with increasing KI content. In the case of DSSC, the Voc decreased continuously with increasing KI content in the polymeric electrolyte membrane. The $J_{SC}$ increased with increasing KI content to show maximum value at which [KI]/[EO] ratio is 0.044. In the higher KI content region, $J_{SC}$ value decreased with increasing KI content.