• Membrane Journal
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• v.25 no.1
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• pp.60-66
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• 2015

To investigate the performance of the composite carbon electrodes which the ion exchange polymers were directly casted onto porous carbon electrode surfaces, the adsorption/desorption experiments were carried out by varying the feed concentration, feed flow rate, and desorption voltages for the NaCl solution. When the feed concentration was 100 mg/L, the increase of the adsorption time led to the increase of the salt removal due to the increase of the residence time inside the cell while the increase of the feed flow rate from 15 mL/min to 23 mL/min gave the decrease of the salt removal efficiency, 12% because of the short residence time. When the feed concentration was 200 mg/L, the salt removal was shown 10~15% low because of the incomplete desorption within the desorption intervals.

• Journal of the Korean Electrochemical Society
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• v.11 no.4
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• pp.242-255
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• 2008

In lithium-ion batteries(LIB), the development of electrolytes had mainly focused on the characteristics of lithium cobalt oxide($LiCoO_2$) cathode and graphite anode materials since the commercialization in 1991. Various studies on compatibility between electrode and electrolytes had been actively developed on their interface. Since then, as they try to adopt silicon and tin as anode materials and three components(Ni, Mn, Co), spinel, olivine as cathode materials for advanced lithium batteries, conventional electrolyte materials are facing a lot of challenges. In particular, requirements for electrolytes performance become harsh and complicated as safety problems are seriously emphasized. In this report, we summarized the research trend of electrolyte materials for the electrode materials of lithium rechargeable batteries.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.462-462
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• 2011

그래핀은 탄소원자로 구성된 원자단위 두께의 매우 얇은 2차원의 나노재료로서 높은 투광도 뿐만 아니라 우수한 기계적, 전기적 특성을 지니며 구조적 화학적 으로도 매우 안정한 것으로 알려져 있다. 이러한 그래핀을 얻는 방법에는 물리·화학적 박리법, 탄화규소의 흑연화, 열화학기 상증착법(thermal chemical vapor deposition; TCVD)등 많은 방법들이 존재한다. 이중 TCVD방법이 대면적으로 두께균일도가 높은 그래핀을 얻는데 가장 적합한 방법으로 알려져 있다. 한편 그래핀은 우수한 특성들을 기반으로 센서나 메모리와 같은 기능성 소자로 응용이 가능할 뿐 아니라 투명고분자 기판으로 전사함으로서 유연성 투명전극을 제작 가능하여 기존의 인듐산화물(indium tin oxide; ITO) 투명전극을 대체하여 디스플레이, 터치스크린, 전·자기 차폐재 등의 다양한 분야로의 응용이 가능하다고 예측되고 있다. 본 연구에서는 TCVD법을 이용하여 대면적으로 두께균일도가 높은 그래핀을 합성하여 투명 고분자 기판(polyethylene terephthalate; PET) 위에 전사하여 투명전도막을 제작한 후, 압축변형률(compressive strain)의 변화에 따른 전기적 특성 변화를 측정하였다. 그래핀은 300 nm 두께의 니켈박막이 증착된 산화물 실리콘 기판위에 원료가스로 메탄(CH4)을 사용하여 합성하였다. 합성 결과 단층 그래핀의 면적은 약 80% 이상이었으며, 합성된 그래핀은 분석의 용이함 및 향후 다양한 응용을 위하여 식각공정을 통해 산화막 실리콘 기판과 PET기판으로 전사하였다. PET기판 위로 전사하여 제작한 그래핀 투명전도막의 strain 인가에 따른 전기적 특성을 관찰한 결과, 약 20%의 비교적 높은 strain하에서도 전기적특성이 크게 변화하지 않는 것을 확인하였다. 그래핀의 특성분석을 위해서는 광학현미경, 라만 분광기, 투과전자현미경, 자외 및 가시선 분광광도계, 4탐침측정기 등을 이용하였다.

• Membrane Journal
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• v.24 no.4
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• pp.332-339
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• 2014

In this study, an anion-exchange ionomer solution was developed by employing poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) as the base material for the improvement of the capacitive deionization (CDI) performances. It was found that prepared quaternized PPO (QPPO) exhibited excellent ion conductivity superior to that of a commercial anion-exchange membrane (AMX, Astom Corp., Japan) and also the electrochemical properties were shown to be comparable with each other. The CDI tests were conducted by employing the porous carbon electrode coated with the ionomer solution and the result showed the high salt removal efficiency of about 94.9%. By comparing the desalination efficiencies in conventional CDI, membrane CDI (MCDI) with a commercial anion-exchange membrane, and coated CDI (CCDI) employing the porous carbon electrode coated with QPPO, it was confirmed that CCDI shows the high salt removal performance improved by 52.1% and 18.3% compared with those of conventional CDI and MCDI, respectively.

• Transactions of the Korean hydrogen and new energy society
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• v.30 no.6
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• pp.531-539
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• 2019

The development of cost-effective electrocatalysts with high durability is one of the most important challenges for the commercialization of polymer electrolyte fuel cells (PEFCs). The durability of the electrocatalyst has been studied in terms of structural change in the active metal and the support. In particular, in fuel cell vehicles, degradation of the carbon-based support is known to have a significant effect on the electrocatalyst deterioration since the start-up/shut-down cycle is frequently repeated. The requirements for the support of the electrocatalyst include high surface area, electrical conductivity, chemical stability, and so on. In this study, we propose the evaluation methods for choosing better support materials and present the physicochemical properties that promising carbon supports should have. Three kinds of carbon materials with different crystallinity are compared. From in-depth study using X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, and accelerated stress test, it is clearly confirmed that the durability of carbon-supported electrocatalysts is closely related to the physicochemical properties of the carbon supports.

• Proceedings of the Korean Vacuum Society Conference
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• 2013.08a
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• pp.290.2-290.2
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• 2013

X-선 튜브는 의료 영상 및 치료, 산업용 제전 장치, 비파괴 X-선 영상 장치 등에서 사용되는데 기존의 열전자원을 이용한 X-선 튜브와는 달리, 냉음극형 X-선 튜브는 빠른 속도의 디지털 구동이 가능하며 전력 소비가 낮은 장점이 있다. 따라서, 최근 많은 연구자들에 의해서 냉음극형 X-선 튜브에 관한 연구가 활발하게 진행되고 있다. 냉음극형 X-선 튜브는 전계 방출을 이용한 전자원을 사용하며, 탄소나노튜브 (CNT), Si, 다양한 종류의 나노선 등이 대표적이다. 그 중에서 CNT는 높은 종횡비로 인해 전계 방출 특성이 우수하여 가장 대표적인 물질이다. CNT를 이용한 전자원을 제작하기 위해서는 직접 성장법, 전기영동법, 스크린 프린팅법, 디핑법 등 다양한 방법이 존재한다. 직접 성장법을 제외한 방법들은 모재료인 CNT와 용매, 금속재료들을 섞어 페이스트나 수용액의 상태를 제작하여야 한다. 이 때, 금속 재료는 기판과 CNT간의 접착 및 전자 전도 통로의 역할을 하는 무기 충전제이며 일반적으로 나노 혹은 수 마이크로미터 크기의 상태로 존재하는 것을 주로 사용한다. X-선 튜브 제작은 일반적으로 외벽을 유리 혹은 세라믹을 주로 사용하는데 아노드 전극 및 캐소드 전극 등과 결합하여 진공 밀봉된 형태가 되어야 한다. 브레이징 방법은 금속과 세라믹을 결합하는데 매우 유용한 방법이며, 그 중에서도 진공 브레이징 방법은 다량의 부품을 한 번에 결합시킬 수 있다. 하지만 진공 브레이징 공정의 온도는 약 $700{\sim}1,000^{\circ}C$이며 이는 금속 재료가 충분히 증발할 수 있는 온도가 된다. 본 발표에서는 고온 진공 상태에서의 무기 충전제의 증발에 대한 현상을 관찰하고 고온진공 상태에서 증발없이 무기 충전제로의 역할을 할 수 있도록 다양한 금속 및 합금에 대한 연구를 수행하였다. 또한, 이 연구를 통해 선택된 무기 충전제를 포함하여 CNT 페이스트를 볼밀링 방법을 이용하여 제작하였으며, 이를 이용한 CNT 에미터가 X-선 튜브의 전자원으로 사용될 수 있는지 확인하기 위해 전계 방출 실험을 함께 실시하였다. 제작된 CNT 에미터가 우수한 전계 방출 특성을 가지고 있음을 확인하였으며, 이는 본 연구를 통해 선택된 금속 및 합금 재료가 무기 충전제로의 역할을 잘 수행하고 있음을 보여준다.

• Applied Chemistry for Engineering
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• v.27 no.2
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• pp.145-152
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• 2016

In this study, CuO was introduced on MWCNTs dispersed with Au nanoparticles to improve the glucose sensing capability of electrochemical biosensors. Nano-cluster shaped CuO was synthesized due to the presence of Au nanoparticle, which affects glucose sensing performance. The biosensor featuring CuO/Au@MWCNTs nanocomposite as an electrode material when 0.1 mole of CuO was synthesized showed the highest sensitivity of $504.1{\mu}A\;mM^{-1}cm^{-2}$, which is 4 times better than that of MWCNTs based biosensors. In addition, it shows a wider linear range from 0 to 10 mM and lower limit of detection (LOD) of 0.008 mM. These results demonstrate that CuO/Au@MWCNTs nanocomposite sensors are superior to other CuO based biosensors which are attributed that the nano-cluster shaped CuO is favorable for the electrochemical reaction with glucose molecules.

• Membrane Journal
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• v.29 no.1
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• pp.30-36
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• 2019

In this study, we reported a solid-state supercapacitor consisting of titanium nitride (TiN) nanofiber and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT-PSS) conducting polymer electrode and poly(vinyl alcohol) (PVA)-based polymer electrolyte membrane. The TiN nanofiber was selected as electrode materials due to high electron conductivity and 2-dimensional structure which is beneficial for scaffold effect. PEDOT-PSS is suitable for organic/inorganic composites due to good redox reaction with hydrogen ions in electrolyte and good dispersion in solution. By synergetic effect of TiN nanofiber and PEDOT-PSS, the PEDOT-PSS/TiN electrode showed higher surface area than the flat Ti foil substrate. The PVA-based polymer electrolyte membrane could prevent leakage and explosion problem of conventional liquid electrolyte and possess high specific capacitance due to the fast ion diffusion of small $H^+$ ions. The specific capacitance of PEDOT-PSS/TiN supercapacitor reached 75 F/g, which was much higher than that of conventional carbon-based supercapacitors.

• Applied Chemistry for Engineering
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• v.17 no.2
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• pp.223-228
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• 2006

Pore-size controlled porous carbons for the catalyst supports of the direct methanol fuel cell were prepared from the mesophase pitch by using the silica spheres with different sizes. Pitch solution in THF and spheres were mixed, carbonized and etched by 5 M NaOH to make porous carbon. Specific surface area of the porous carbons was $14.7{\sim}87.7m^2/g$ and average pore diameter was 50~550 nm which were dependent on the size of silica spheres. Aqueous reduction method was used to load 60 wt% PtRu on the prepared porous carbon supports. The electro-oxidation activity of the supported 60 wt% Pt-Ru catalysts was measured by cyclic voltammetry and unit cell test. For the 60 wt% Pt-Ru/porous carbon synthesized by 50 nm silica, current density value in the cyclic voltammetry test was $123mA/cm^2$ at 0.4 V and peak power density in the unit cell test were 105 and $162mW/cm^2$ under oxygen at 60 and $80^{\circ}C$, respectively.

• Journal of the Korean Electrochemical Society
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• v.5 no.3
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• pp.117-124
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• 2002

Poly(acrylonitrile)(PAN) solutions in dimethylformamide(DMF) were electrospun to prepare webs consisting of 400nm ultra-fine fibers. The webs were oxidatively stabilized, activated by steam and resulted to be activated carbon fibers(ACFs). The specific surface area was $800\~1230 m^2/g$, which showed a trend of a decrease of the surface area with an increase in activation temperature, showing opposite behavior to the other ACFs. The activation energy of the stabilized fibers for the steam activation was determined as 29.2 kJ/mol to be relatively low indicating the easier activation than that of other carbonized fibers. The ACF webs were characterized by pore size and specific surface uea which would be related to the specific capacitance of the electrical double layer capacitor (EDLC). The specific capacitances measured were 27 F/g, 25 F/g, 22 F/g at the respective activation temperature of $700^{circ}C,\;750^{\circ}C\;800^{\circ}C$, showing similar trend with the specific surface area i.e., the higher activation temperature was, the lower specific capacitance resulted.