• Journal of Electrochemical Science and Technology
• /
• 제13권1호
• /
• pp.78-89
• /
• 2022

ANODE-free Li-metal batteries (AFLMBs) operating with Li of cathode material have attracted enormous attention due to their exceptional energy density originating from anode-free structure in the confined cell volume. However, uncontrolled dendritic growth of lithium on a copper current collector can limit its practical application as it causes fatal issues for stable cycling such as dead Li formation, unstable solid electrolyte interphase, electrolyte exhaustion, and internal short-circuit. To overcome this limitation, here, we report a novel dual-salt electrolyte comprising of 0.2 M LiPF₆ + 3.8 M lithium bis(fluorosulfonyl)imide in a carbonate/ester co-solvent with 5 wt% fluoroethylene carbonate, 2 wt% vinylene carbonate, and 0.2 wt% LiNO₃ additives. Because the dual-salt electrolyte facilitates uniform/dense Li deposition on the current collector and can form robust/ionic conductive LiF-based SEI layer on the deposited Li, a Li/Li symmetrical cell exhibits improved cycling performance and low polarization for over 200 h operation. Furthermore, the anode-free LiFePO₄/Cu cells in the carbonate electrolyte shows significantly enhanced cycling stability compared to the counterparts consisting of different salt ratios. This study shows an importance of electrolyte design guiding uniform Li deposition and forming stable SEI layer for AFLMBs.

• Journal of Electrochemical Science and Technology
• /
• 제12권2호
• /
• pp.246-256
• /
• 2021

Mo,Cu-doped CeO₂ (CMCuO) nanopowders were synthesized by the nitrate-fuel combustion method aiming to improve the electrical and electrochemical properties of its Mo-doped CeO₂ (CMO) parent by the addition of copper. An electrical conductivity of ca. 1.22·10^-2 S cm^-1 was measured in air at 800℃ for CMCuO, which is nearly 10 times higher than that reported for CMO. This increase was associated with the inclusion of copper into the crystal lattice of ceria and the presence of Cu and Cu₂O as secondary phases in the CMCuO structure, which also could explain the increase in the charge transfer activities of the CMCuO based anode for the hydrogen and carbon monoxide electro-oxidation processes compared to the CMO based anode. A maximum power density of ca. 120 mW cm^-2 was measured using a CMCuO based anode in a solid oxide fuel cell (SOFC) with YSZ electrolyte and LSM-YSZ cathode operating at 800℃ with humidified syngas as fuel, which is comparable to the power output reported for other SOFCs with anodes containing copper. An increase in the area specific resistance of the SOFC was observed after ca. 10 hours of operation under cycling open circuit voltage and polarization conditions, which was attributed to the anode delamination caused by the reduction of the Cu₂O secondary phase contained in its microstructure. Therefore, the addition of a more electroactive phase for hydrogen oxidation is suggested to confer long-term stability to the CMCuO based anode.

• 한국입자에어로졸학회지
• /
• 제20권3호
• /
• pp.95-102
• /
• 2024

Enhancing the oxygen surface exchange reaction by increasing the specific surface area of the electrode is a promising structural approach to lowering the operating temperature of solid oxide fuel cells (SOFCs). Nanowire structures, due to their high specific surface area and lower tortuosity of ion and electron conduction pathways, play a vital role in enhancing SOFC electrode performance. In this study, we synthesized La_0.6Sr_0.4CoO_3-𝛿 (LSC) nanowires using a polycarbonate membrane filter as a nanotemplate and applied them to the cathode for intermediate-temperature SOFC fabrication. The fabricated cell exhibited a 10% increase in peak power density at 650℃, achieving 0.506 W·cm^-2, compared to cell using only commercial LSC powder. Furthermore, distribution of relaxation times analysis revealed a 15% reduction in area-specific polarization resistance in the mid-frequency range. These findings demonstrated that the electrode with LSC nanowires fabricated through electrospray deposition can significantly improve electrochemical performance of intermediate-temperature SOFC.

• 한국수소및신에너지학회논문집
• /
• 제6권2호
• /
• pp.53-63
• /
• 1995

차세대의 새로운 발전방식인 용융탄산염형 연료전지 시스템개발 사업중 실용 스택개발을 위하여 전극유효연적이 $100cm^2$ 인 단위전지를 10단 적층한 Cross Flow형 MCFC스택을 제작하고 2성능측정설비를 구성하여 장기운전시험을 실시하였다 연료로는 $H_2/CO_2/H_2O$의 비율을 72%/18%/10% 로 조성한 가스를 이용하고 산화제가스로는 $O_2/CO_2$ 및 $Air/CO_2$ 비율이 33%/67%, 70%/30%가 되는 가스를 이용하여 운전할때의 초기성능 및 15A($150mA/cm^2$) 정부하 상태에서의 장기운전시험시의 전압 강하율을 조사하였다. 운전시간 310시간이 경과된 후의 스택전압은 8.39V이었고 이때의 출력은 125.8W를 보여주었다. 한편 1845시간이 경과한후 공기를 산화제로 이용하는 경우 전압은 6.95V로서 출력 104W를 나타내고 있다. 초기성능치에 의한 에너지 변환효율은 이용율이 40%인 경우 29.65%이었고 80%로 증가하는 경우 약 51.5%가 된다. 1840시간의 경과한때 까지의 전압 강하율은 약 52.4mV/1000hr로서 이전의 스택보다는 전압강하율이 감소되고 있으며 스택의 성능 저하의 주요한 요인은 개회로 전압의 저하로 내부단락동에서 기인하는 것으로 여겨진다. 또한 장기운전사 스택내부에서의 단위전지 전압분포가 균일하지 않음을 알 수 있어 이에 대한 개선을 필요로 한다.

• 한국세라믹학회지
• /
• 제41권6호
• /
• pp.456-463
• /
• 2004

음극지지형 SOFC의 성능을 향상시키기 위해 단전지 제조공정을 개선하고 그 출력특성을 평가하였다. 액상응결 공정(Liquid Condensation Process : LCP)과 일축가압성형공정을 통하여 NiO/YSZ 복합체 음극기판을 제조하고 위에 YSZ 전해질을 스크린 인쇄한 후 140$0^{\circ}C$에서 3시간동안 동시소결하여 음극/전해질 기판을 제조하였다. 또한 LSM/YSZ 양극층은 임피던스 분석을 통해 분극저항이 최소가 되는 조성 및 열처리 조건을 선택하여 스크린 인쇄법을 이용해 구성하였고 이러한 적층공정을 거쳐 최종적으로 5${\times}$5와 l0${\times}$10 $\textrm{cm}^2$ 크기의 단전지를 제조하였다. 제조된 단전지의 출력특성을 측정한 결과 5${\times}$5와 10${\times}$10 단전지는 80$0^{\circ}C$에서 약 0.45W/$\textrm{cm}^2$ 와 0.22 W/$\textrm{cm}^2$의 최대출력밀도를 각각 나타내어 선행연구에서 기존공정으로 제조된 단전지에 비해 2배 이상 향상된 좋은 성능을 나타내었다.

• 대한기계학회논문집B
• /
• 제36권9호
• /
• pp.931-935
• /
• 2012

본 연구에서는 저온형 연료전지와 고온형 연료전지의 작동 및 구성 요소 측면 단점들을 보완하기 위해 중온 영역에서 작동하는 박막 연료전지를 제작하였다. 박막 연료전지는 이트륨이 도핑된 바륨 지르코네이트(BYZ) 전해질과 백금 수소극/공기극으로 이루어져 있으며, 성능은 $350^{\circ}C$에서 측정하였다. 350nm의 두께를 가지는 백금 수소극은 다공성 기판 위에 스퍼터링 기법을 이용하여 증착하였다. BYZ전해질은 펄스레이저 기법을 이용하여 $1{\mu}m$ 증착하였고, 상부에 스퍼터링 기법을 이용하여 200nm의 두께를 가지는 백금 공기극을 증착하였다. 개회로 전압은 약 0.81V이었고, 최대 출력 성능은 11.9mW/$cm^2$이었다.

• 유기물자원화
• /
• 제18권1호
• /
• pp.57-65
• /
• 2010

양성자 교환막 미생물연료전지(PEM-MFC)의 경우 양극의 표면적을 기준으로 유기물 제거능력을 산출하면 유기물 부하에 관계없이 $3.0gCOD/m^2$ 수준으로 나타났다. 또 안정적인 전압이 관찰된 시기의 쿨롱 효율은 22.4~23.4 %로 높지 않은 수준이었다. 양성자 교환막은 양성자뿐만 아니라 초산도 통과시키는 것으로 확인되었다. 양성자 교환막을 사용하지 않은 상향류식 미생물연료전지(ML-MFC)의 경우 다공성 RVC 전극을 사용한 관계로 전극의 외부면적당 유기물 제거능력은 $9.3{\sim}10.1gCOD/m^2{\cdot}d$로 나타났다. 이는 양성자 교환막을 사용한 경우에 비하여 3배 정도 높은 수준이다. 그러나 RVC 양극의 비표면적 차이에 따른 유기물 제거 능력 차이는 크지 않았다. ML-MFC의 경우 전기 발생이 안정적이지 못하였으며, 쿨롱 효율도 3.6~3.7 %로 매우 낮은 수준이었다. 전기 발생량이 안정적이지 못한 것은 음극에 성장한 미생물의 영향으로 판단된다. 이를 해결하기 위해 음극부의 공기주입량을 증가시키면 일시적으로 전기 발생이 증가하였으나 오래 지속되지 못하였다.

• 대한치과보철학회지
• /
• 제33권3호
• /
• pp.584-609
• /
• 1995

The purpose of this study was to evaluate the difference of the galvanic corrosion behaviour of the titanium in contact with gold alloy, silva-palladium alloy, and nickel-chromium alloy using the immersion and electrochemical method. And the effects of galvallit couples between titanium and the dental alloys were assessed for their usefulness as materials for superstructure. The immersion method was performed by measuring the amount of metal elementsreleased by Inductivey coupled plasma emission spectroscopy(ICPES) The specimen of fifteen titanium plates, the five gold alloy, five silver-palladium, five nickel-chromium plates, and twenty acrylic resin plates ware fabricated, and also the specimen of sixty titanium plugs, the thirty gold alloy, thirty silver-palladium, and nickelc-hromium plugs were made. Thereafter, each plug of gold alloy, silver-palladium, and nickel-chromium inserted into the the titanium and acrylic resin plate, and also titanium plug inserted into the acrylic resin plate. The combination specimens uf galvanic couples immersed in 70m1 artificial saliva solution, and also specimens of four type alloy(that is, titanium, gold, silver-palladium and nickel-chromium alloy) plugs were immersed solely in 70m1 artificial sativa solution. The amount of metal elements released was observed during 21 weeks in the interval of each seven week. The electrochemical method was performed using computer-controlled potentiosta(Autostat 251. Sycopel Sicentific Ltd., U.K). The wax patterns(diameter 11.0mm, thickness,in 1.5mm) of four dental casting alloys were casted by centrifugal method and embedded in self-curing acrylic resin to be about $1.0cm^2$ of exposed surface area. Embedded specimens were polished with silicone carbide paper to #2,000, and ultrasonically cleaned. The working electrode is the specimen of four dental casting alloys, the reference electrode is a saturated calmel electrode(SCE) and the ounter electrode is made of platinum plate. In the artificial saliva solution, the potential scanning was carried out starting from-700mV(SCE) TO +1,000mV(SCE) and the scan rate was 75mV/min. Each polarization curve of alloy was recorded automatically on a logrithmic graphic paper by XY recorder. From the polarization curves of each galvanic couple, corrosion potential and corrosion rates, that is, corrosion density were compared and order of corrosion tendency was determined. From the experiments, the following results were obtained : 1. In the case of immersing titanium, gold alloy, silver-palladium alloy, and nickel-chromium alloysolely in the artificial saliva solution(group 1, 2, 3, and 4), the total amount of metal elements released was that group 4 was greater about 2, 3 times than group 3, and about 7.8 times than group 2. In the case of group 1, the amount of titanium released was not found after 8 week(p<0.001). 2. In the case of galvanic couples of titanium in contact with alloy(group 5, 6), the total amount of metal elements released of group 5 and 6 was less than that of group 7, 8, 9, and 10(p<0.05). 3. In the case of galvanic couples of titanium in contact with silver-palladium alloy(group 7, 8), the total amount of metal elements released of group 7 was greater about twice than that of group 5, and that of group 8 was about 14 times than that of group 6(p<0.05). 4. In the case of galvanic couples of titanium in contact with nickel-chromium alloy(group 9, 10), the total amount of metal elements released of group 9 and 10 was greater about 1.8-3.2 times than that of group 7 and 8, and was greater about 4.3~25 times than that of group 5 and 6(p<0.05). 5. In the effect of galvanic corrosion according to the difference of the area ratio of cathode and anode, the total amount of metal elements released was that group 5 was greater about 4 times than group 6, group 8 was greater about twice than group 7, and group 10 was greater about 1.5 times than group 9(p<0.05). 6. In the effect of galvanic corrosion according to the elasped time during 21 week in the interval of each 7 week, the amount of metal elements released was decreased markedly in the case of galvanic couples of the titanium in contact with gold alloy and silver-palladium alloy but the total amount of nickel and beryllium released was not decreased markedly in the case of galvanic couples of the titanium in contact with nickel-chromium alloy(p<0.05). 7. In the case of galvanic couples of titanium in contact with gold alloy, galvanic current was lower than any other galvanic couple. 8. In the case of galvanic couples of titanium in contact with nickel-chromium alloy, galvanic current was highest among other galvanic couples.

• Korean Chemical Engineering Research
• /
• 제60권4호
• /
• pp.588-593
• /
• 2022

본 논문에서는 hemin, 폴리에틸렌이민(PEI) 및 탄소나노튜브(CNT)를 이용하여 제조 CNT/PEI/hemin/PEI 복합재에 가교제인 테레프탈알데하이드(TPA)를 첨가하여 전자전달이 개선된 과산화수소 환원 반응(HPRR) 촉매를 합성하였다. 합성된 촉매(CNT/PEI/hemin/PEI/TPA)를 과산화수소 10 mM 농도에서 HPRR 반응성을 확인한 결과, 0.2 V (vs. Ag/AgCl)에서 0.2813 mA cm^-2의 전류 밀도로 나타났으며, 이는 가교하지 않은 촉매(CNT/PEI/hemin/PEI)와 범용 가교제인 글루타르알데하이드(GA)에 의해 가교된 촉매(CNT/PEI/hemin/PEI/GA)에 비해 각각 2.43 및 1.87배 증가하였다. CNT/PEI/hemin/PEI/TPA의 HPRR 개시전위는 0.544 V로서 CNT/PEI/hemin/PEI와 CNT/PEI/hemin/PEI/GA의 0.511 및 0.471 V에 비하여 원활한 전자전달에 의해 개선되었음을 확인할 수 있었다. 이는 전기화학 임피던스 분광법(EIS)을 이용한 분석 결과에서도 확인되었는데, CNT/PEI/hemin/PEI/GA의 경우, 전자전달을 방해하는 가교제의 도입에 따라 CNT/PEI/hemin/PEI에 비하여 높은 전자전달저항을 나타낸 반면, CNT/PEI/hemin/PEI/TPA는 6.2% 감소하여, 가장 낮은 전자전달저항을 나타냈다. 막이 없는 흐름형 과산화수소 연료전지를 이용한 평가에서도, CNT/PEI/hemin/PEI/TPA를 환원극으로 활용한 전지의 최대 출력 밀도가 36.34±1.41 μWcm^-2로, CNT/PEI/hemin/PEI (27.87±0.95 μWcm^-2)와 CNT/PEI/hemin/PEI/GA(25.57±1.32 μWcm^-2) 보다 높게 측정되어, TPA는 전자전달을 개선 성능을 확인할 수 있었다.