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송진훈 ( Jin Hoon Song ),김세훈 ( Sae Hoon Kim ),인병기 ( Byung Ki Ahn ),고재준 ( Jai Joon Ko ),박권필 ( Kwon Pil Park ) 한국화학공학회 2012 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.50 No.5
Until a recent day, degradation of PEMFC MEA (membrane and electrode assembly) has been studied, separated with membrane degradation and electrode degradation, respectively. But membrane and electrode were degraded coincidentally at real PEMFC operation condition. Therefore in this work, AST (Accelerated Stress Test) of MEA degradation was done at the condition that membrane and electrode were degraded simultaneously. There was interaction between membrane degradation and electrode degradation. Membrane degradation reduced the decrease range of catalyst active area by electrode degradation. Electrode degradation reduces increase range of the hydrogen crossover current and FER (Fluoride Emission Rate) by membrane degradation.
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고분자전해질 연료전지에서 기체 크로마토그래프에 의한 수소투과도 측정
정재진 ( Jae Jin Jeong ),정재현 ( Jae Hyeun Jeong ),김세훈 ( Sae Hoon Kim ),안병기 ( Byung Ki Ahn ),고재준 ( Jai Joon Ko ),박권필 ( Kwon Pil Park ) 한국화학공학회 2014 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.52 No.4
최근까지 대부분의 PEMFC MEA(Membrnae and Electrode Assembly) 열화 연구는 전극과 전해질 막 각각 분리되어 연구되었다. 그런데 실제 PEMFC 운전조건에서는 전극과 전해질 막은 동시에 열화된다. 동시열화과정에서 전극열화와 전해질 막 열화는 상호 작용한다. 전해질 막의 열화정도를 측정하는데 수소투과도가 많이 사용되고 있다. 그런데 동시 열화가 발생했을 때 선형 쓸음 전기량 측정법(Linear Sweep Voltammetry, LSV)에 의해 수소투과도를 측정하면 전극열화가 수소투과전류를 감소시키는데, LSV 방법이 전극 촉매의 활성 면적에 의존하기 때문이다. 본 연구에서는 전극과 막 동시 열화과정에서 기체 크로마토그래프에 의한 PEMFC 전해질막의 수소투과도를 측정하였다. 기체 크로마토그래프 측정 방법은 전극 상태와 무관하기 때문에 전극과 막 동시 열화 과정에서 수소투과도가 전극 열화 영향을 받지 않음을 확인하였다. Until a recent day, degradation of PEMFC MEA(membrane and electrode assembly) has been studied, separated with membrane degradation and electrode degradation, respectively. But membrane and electrode were degraded coincidentally at real PEMFC operation condition. During simultaneous degradation, there was interaction between membrane degradation and electrode degradation. Hydrogen permeability was used often to measure degradation of electrolyte membrane in PEMFC. In case of hydrogen permeability measured by LSV(Linear Sweep Voltammetry) method, the degradation of electrode decrease the value of hydrogen crossover current due to LSV method`s dependence on electrode active area. In this study hydrogen permeability was measured by gas chromatograph (GC) when membrane and electrode degraded at the same time. It was showed that degradation of electrode did not affect the hydrogen permeability measured by GC because of GC method`s independence on electrode active area.
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정재진 ( Jae Jin Jeong ),정재현 ( Jae Hyeun Jeong ),김세훈 ( Sae Hoon Kim ),안병기 ( Byung Ki Ahn ),고재준 ( Jai Joon Ko ),박권필 ( Kwon Pil Park ) 한국화학공학회 2015 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.53 No.4
고분자 막 성능 평가 및 내구성 평가에 이용하기 위해 고분자전해질 연료전지(PEMFC) 구동 중에 수소 크로스오버 측정이 필요하다. 수소 크로스오버 측정 시에 불활성 기체 대신에 공기를 cathode에 공급하면서 기체 크로마토그래프로 수소 농도를 cathode 출구에서 분석하였다. PEMFC 구동 중 고분자 막을 통과한 수소는 cathode에서 산소와 반응해 불활성 가스를 공급할 때에 비해 수소 농도가 감소하였다. cathode 공기 공급 유량이 증가하면 수소 농도가 감소했고, 셀의 온도와 습도, 압력이 증가하면 cathode의 수소 농도는 증가했다. 일반적인 PEMFC 구동 조건에서 120 mA/㎠ 전류밀도에서 수소농도는 약 5.0 ppm이었다. To evaluate the performance and durability of membrane, measurement of hydrogen crossover is needed during PEMFC(Proton Exchange Membrane Fuel Cells) operation. In this work, concentration of hydrogen at cathode was analysed by gas chromatograph during operation suppling with air instead of inert gas into the cathode. The hydrogen permeated through membrane reacted with oxygen at cathode and then the concentration of hydrogen was lower than in case inert gas was supplied. Hydrogen concentration decreased as the flow rate of air increased at cathode. Increase of temperature, humidity and pressure of anode gas enhanced the hydrogen concentration at cathode. The hydrogen concentration was about 5.0 ppm at current density of 120 mA/㎠ during general PEMFC operation.
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PEMFC에서 전극 열화가 전해질 막 열화에 미치는 영향
박권필 ( Kwon Pil Park ),송진훈 ( Jin Hoon Song ),김세훈 ( Sae Hoon Kim ),안병기 ( Byung Ki Ahn ),고재준 ( Jai Joon Ko ) 한국화학공학회 2013 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.51 No.1
Until a recent day, degradation of PEMFC MEA (membrane and electrode assembly) has been studied, separated with membrane degradation and electrode degradation, respectively. But membrane and electrode were degraded coincidentally at real PEMFC operation condition. During simultaneous degradation, there was interaction between membrane degradation and electrode degradation. The effect of electrode degradation on membrane degradation was studied in this work. We compared membrane degradation after electrode degradation and membrane degradation without electrode degradation. I-V performance, hydrogen crossover current, fluoride emission rate (FER), impedance and TEM were measured after and before degradation of MEA. Electrode degradation reduced active area of Pt catalyst, and then radical/H2O2 evolution rate decreased on Pt. Decrease of radical/H2O2 reduced the velocity of membrane degradation.
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송진훈 ( Jin Hoon Song ),정재진 ( Jae Jin Jeong ),정재현 ( Jae Hyeun Jeong ),김세훈 ( Sae Hoon Kim ),안병기 ( Byung Ki Ahn ),고재준 ( Jai Joon Ko ),박권필 ( Kwon Pol Park ) 한국화학공학회 2013 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.51 No.3
실제 고분자 전해질 연료전지(PEMFC) 운전조건에서는 전극과 전해질 막은 동시에 열화된다. 그런데 고분자전해질연료전지의 전극 열화와 전해질 열화의 상호 작용에 대해 연구되지 않았다. 본 연구에서는 전해질 막 열화가 전극 열화에 미치는 영향에 대해 연구하였다. 전해질 막 열화 후 전극을 열화시켜 전해질 막 열화없이 전극을 열화시켰을 때와 비교하였다. 열화전후의 I-V 성능, 수소투과전류, 순환 전압측정(CV), 임피던스, TEM 등을 측정하였다. 전해질 막열화에 의해 수소투과도가 증가하고, 이에 따라 백금 입자 성장속도가 감소함으로써 전극 열화속도가 감소함을 보였다. The membrane and electrode were degraded coincidentally at real PEMFC(Proton Exchange Membrane Fuel Cells) operation condition. But the interaction membrane degradation between electrode degradation has not been studied. The effect of membrane degradation on electrode degradation was studied in this work. We compared electrode degradation after membrane degradation and electrode degradation without membrane degradation. I-V performance, hydrogen crossover current, impedance and TEM were measured after and before degradation of MEA. Membrane degradation enhanced hydrogen crossover, and then Pt particle growth rate was reduced. Increase of hydrogen crossover by membrane degradation reduced the electrode degradation rate.
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