• Korean Chemical Engineering Research
• /
• 제60권2호
• /
• pp.202-207
• /
• 2022

고분자 전해질 연료전지(PEMFC)의 전극 열화에 대한 연구는 전극상에서 Pt의 입자 성장 및 활성면적 감소에 대한 연구가 대부분이다. 고분자막과 접해 있는 전극촉매 Pt의 열화는 고분자막 열화에 영향을 주는데, 이와 관련된 연구는 많지 않다. 본 연구에서는 전극촉매 열화 가속 시험 과정에서 열화된 Pt가 고분자막 내부에 석출되는 현상과 그 영향에 대해서 연구하였다. 백금 열화 속도를 가속화시키기 위해 전압 변화(0.6 V ↔ 0.9 V)를 30,000 사이클까지 반복했다. Cathode에 산소를 유입하면서 전압 변화 사이클을 반복했을 때 질소를 유입했을 때 보다 막 내부에 석출된 Pt의 양이 더 많았다. 전압 변화 사이클 횟수가 증가할수록 막 내부에 석출된 Pt의 양이 증가하였고, cathode에서 용해된 Pt가 anode 쪽으로 이동해 20,000 사이클에서는 막 내부에 전체적으로 균일한 분포를 보였다. 이와 같은 전극촉매 열화 가속 시험과정에서 고분자막의 수소투과 전류밀도는 거의 변하지 않아서, 석출된 Pt가 고분자막의 내구성에는 영향을 주지 않음을 확인하였다.

• 한국수소및신에너지학회논문집
• /
• 제25권3호
• /
• pp.311-318
• /
• 2014

Performance degradation of a battery in 20 kWh energy storage system (ESS) under various operating conditions was studied. And energy saving of the ESS was also monitored by connecting with 20 kW photovoltaic (PV). PV-connected ESS saved 5~7% of energy consumption in 2013 compared to that without such system in 2012. As charge-discharge cycle increased, capacity decreased and the performance degradation was glaringly obvious after 40 cycles. And as charge and discharge rate increased, the performance degradation was more serious. After 50 charge-discharge cycles, a lot of degraded product was deposited on the surface of anode and cathode electrodes, and the cathode side was more contaminated. Therefore, in order to maintain the cell performance, it was more important to protect the degradation of the cathode side.

• Journal of Electrochemical Science and Technology
• /
• 제15권1호
• /
• pp.190-197
• /
• 2024

A commercial PbO₂ mesh cylinder electrode was utilized as the anode for the electrochemical degradation of the textile effluent after the biological treatment with the titanium cylinder as the cathode in a self-made tube electrolyzer. The electrochemical performances of the PbO₂ electrode in tube electrolyzer under different initial pH, electrolyte flow rates, current densities and times of the electrochemical degradation were investigated. The experimental results illustrated that the PbO₂ electrode can reduce the chemical oxygen demand (COD) of the textile effluent from 94.0 mg L^-1 to 65.0 mg L^-1 with the current efficiency of 88.3%, the energy consumption of 27.7 kWh kg^-1 (per kilogram of degraded COD) and the carbon emissions of 18.0 kg CO₂ kg^-1 (per kilogram of degraded COD) under the optimal operating conditions. In addition, the COD of the textile effluent could be reduced from 94.0 mg L^-1 to 22.0 mg L^-1 after the fifth electrochemical degradation. Therefore, PbO₂ mesh cylinder electrode in the tube cylinder was promising for the electrochemical degradation of the textile effluent.

• 한국세라믹학회지
• /
• 제45권12호
• /
• pp.788-795
• /
• 2008

An electrolyte supported SOFC cell was tested at $800^{\circ}C$ in air for 3600 h with an applied current density of $200\;mA/cm^2$ to examine possible cathode degradation issues. A scandium- stabilized zirconia (ScSZ) with additional manganese doping (ScSZ: Mn) was used as electrolyte. A strontium and copper-doped lanthanum ferrite (LaSrCuFe) and platinum were used as cathode and quasi-anode material, respectively. The DC resistance was logged over the complete testing period. Additionally, impedance spectroscopy was used from time to time to track changes of the cell in-situ. Post-test analysis of the cell using methods like scanning electron microscopy imaging and other electrochemical testing methods allow the identification of different degradation sources. The results indicate a promising combination of electrolyte and cathode material in terms of chemical compatibility and electrical performance.

• Journal of Electrochemical Science and Technology
• /
• 제13권2호
• /
• pp.269-278
• /
• 2022

Utilization of high-voltage electrolyte additive(s) at a small fraction is a cost-effective strategy for a good solid electrolyte interphase (SEI) formation and performance improvement of a lithium-rich layered oxide-based high-energy lithium-ion cell by avoiding the occurrence of metal-dissolution that is one of the failure modes. To mitigate metal-dissolution, we explored fluorinated dual-additives of fluoroethylene carbonate (FEC) and di(2,2,2-trifluoroethyl)carbonate (DFDEC) for building-up of a good SEI in a 4.7 V full-cell that consists of high-capacity silicon-graphite composite (15 wt% Si/C/CF/C-graphite) anode and Li_1.13Mn_0.463Ni_0.203Co_0.203O₂ (LMNC) cathode. The full-cell including optimum fractions of dual-additives shows increased capacity to 228 mAhg^-1 at 0.2C and improved performance from the one in the base electrolyte. Surface analysis results find that the SEI stabilization of LMNC cathode induced by dual-additives leads to a suppression of soluble Mn²⁺-O formation at cathode surface, mitigating metal-dissolution event and crack formation as well as structural degradation. The SEI and structure of Si/C/CF/C-graphite anode is also stabilized by the effects of dual-additives, contributing to performance improvement. The data give insight into a basic understanding of cathode-electrolyte and anode-electrolyte interfacial processes and cathode-anode interaction that are critical factors affecting full-cell performance.

• Korean Chemical Engineering Research
• /
• 제49권6호
• /
• pp.775-780
• /
• 2011

50 $cm^2$의 활성면적을 가진 셀을 이용하여 5-셀 DMFC 스택을 제작하고 4 A의 부하로 4,000 시간 운전한 후 성능감소 및 성능 감소 원인을 분석하였다. 4,000 시간 운전 후 10 A에서 스택의 전력 밀도가 28.7% 감소하였으며 다섯개의 셀 중 두 개는 거의 성능저하가 일어나지 않았고 두 개는 약 40%의 성능 저하, 한 개는 약 60%의 성능 저하를 보였으며 각 셀별 성능저하의 정도의 차이는 스택 내에서의 위치와 상관관계가 없었다. 스택 내의 다섯 셀 중 가장 성능감소가 심하였던 셀의 경우 연료극 촉매층의 Pt 입자 크기가 증가하였으며 연료가 들어가는 쪽의 Pt 입자의 크기 증가가 더 심하였다. 그러나 4,000 시간 장기운전 후 공기극 촉매층에서는 Pt 입자 크기의 변화는 거의 없었다. 스택 내의 모든 셀에서 4,000 시간 운전 후 연료극 촉매에서 공기극 촉매로의 루테늄의 크로스오버가 SEM-EDX로 관찰되었으며 특히 성능감소가 심하였던 셀의 경우 공기극 촉매층에서 Ru/Pt의 비율이 가장 컸다.

• 한국수소및신에너지학회논문집
• /
• 제18권2호
• /
• pp.157-163
• /
• 2007

During PEMFC operation, low current and low humidity conditions accelerate the degradation of perfluorosulfonic acid membrane. But, there have been no studies that clearly explain why these conditions accelerate the membrane degradation. In this study, the hydrogen permeability through the membrane, I-V polarization of MEA, fluoride emission rate(FER) in effluent water were measured during cell operation under low current densities and low relative humidity(RH). The experimental results were evaluated with oxygen radical mechanism the most commonly known for membrane degradation. It seems that low RH of anode is a good condition for $H{\cdot}$ radical formation on the Pt catalyst and the low current condition accelerates the $H{\cdot}$ to form $HO_2{\cdot}$ radical attacking the polymer membrane.

• 한국정보디스플레이학회:학술대회논문집
• /
• 한국정보디스플레이학회 2002년도 International Meeting on Information Display
• /
• pp.685-688
• /
• 2002

In this paper, it is reported that the anode current changes at the constantly applied gate voltages and the current-voltage (I-V) characteristics of Si, Co silicide and Mo silicide field emitter arrays (FEAs) depending on vacuum level from a $10^{-9}$ torr to a $10^{-6}$ torr. The mechanism of the robustness of anode current degradation of Mo silicide FEAs under poor vacuum conditions can be explained by the model of tolerance for the oxygen adsorption and oxidation at the silicide surface. Also, we present the changes of emitting area and work function of the emitters according to vacuum level.

• Journal of Industrial and Engineering Chemistry
• /
• 제67권
• /
• pp.266-275
• /
• 2018

Herein, a novel operating life (OL) test method was evaluated with 200 mAh pouch-type lithium-ion batteries. By combining the calendar life (CL) test with intermediate pulse power cycling, more realistic life prediction was possible, which encompassed real operation of batteries accompanying with thermal acceleration. Larger capacity decrease and resistance increase of pouch cell were observed in the OL test, which was well explained using the SEI film growth model. After dissemble of pouch cell, capacity loss and resistance increase mostly occurred within anode, reflecting that SEI film growth on anode surface was highly attributable to cell degradation.

• 한국환경보건학회지
• /
• 제40권2호
• /
• pp.137-146
• /
• 2014

Objectives: Feasibility of electrochemical oxidation of the aqueous non-biodegradable wastewater such as cationic dye Rhodamine B (RhB) has been investigated in an electrochemical reactor with solid polymer electrolyte (SPE). Methods: Nafion 117 cationic exchange membrane as SPE has been used. Anode/Nafion/cathode sandwiches were constructed by sandwiching Nafion between two dimensionally stable anodes (JP202 electrode). Experiments were conducted to examine the effects of applied current (0.5~2.0 A), supporting electrolyte type (0.2 N NaCl, $Na_2SO_4$, and 1.0 g/L NaCl), initial RhB concentration (2.5~30.0 mg/L) on RhB and COD degradation and $UV_{254}$ absorbance. Results: Experimental results showed that an increase of applied current in electrolysis reaction with solid polymer electrolyte has resulted in the increase of RhB and $UV_{254}$ degradation. Performance for RhB degradation by electrolyte type was best with NaCl 0.2 N followed by SPE, and $Na_2SO_4$. However, the decrease of $UV_{254}$ absorbance of RhB was different from RhB degradation: SPE > NaCl 0.2 N > $Na_2SO_4$. RhB and $UV_{254}$ absorbance decreased linearly with time regardless of the initial concentration. The initial RhB and COD degradation in electrolysis reaction using SPE showed a pseudo-first order kinetics and rate constants were 0.0617 ($R^2=0.9843$) and 0.0216 ($R^2=0.9776$), respectively. Conclusions: Degradation of RhB in the electrochemical reactor with SPE can be achieved applying electrochemical oxidation. Supporting electrolyte has no positive effect on the final $UV_{254}$ absorbance and COD degradation. Mineralization of COD may take a relatively longer time than that of the RhB degradation.