• 대한화학회지
• /
• 제41권1호
• /
• pp.1-11
• /
• 1997

0.5 M $K_2SO_4$ 용액에서 여러 가지 세 탄소전극(glassy carbon, 인조흑연, graphite foil)에 대하여 양극분극에 따른 전극표면반응에 대한 연구를 임피던스 스펙트로스코피를 통하여 실시했다. Graphite foil 전극의 경우 이중츨 capacotance는 다른 두 전극재료에 비하여 높게 나타났으며, 양극분극시 glassy carbon과 인조 흑연(PVDF 혼합 graphite)은 전극계면에서 흡착현상에 의한 capacitance C의 영향이 현저하게 나타남을 알 수 있었다. 3종류 전극재료의 전기화학적 거동은 전극표면 조직의 차이에 의해 glassy carbon의 경우는 분극시 파라데이 임피던스의 영향을 받으며, graphite foil의 경우는 field transport의 지배를 받아 전압의 변화에 의한 임피던스 파라미터의 변화는 거의 나타나지 않았다.

• 한국결정성장학회지
• /
• 제24권5호
• /
• pp.207-212
• /
• 2014

2차원 흑연구조를 갖는 카본나노시트는 큰 비표면적과 우수한 전기적, 화학적 및 기계적 물성으로 인하여 미래소재로 각광받고 있다. 경제적이고 쉬운 카본나노시트의 양산공정개발을 위해 본 연구에서는 메테인($CH_4$)과 프로페인($C_3H_8$) 가스를 이용한 유도 열플라즈마 공정을 통해 기상 합성하여 카본나노시트 분말을 합성하였다. 유도 열플라즈마를 이용한 카본나노시트 합성은 촉매나 증착공정 없이 진행되었으며, 합성된 카본나노시트의 물성을 TEM, Raman, XRD, BET로 분석하였다. 메테인과 프로페인으로부터 합성된 카본 나노시트는 각각 5~6개의 그래핀 층과 15~16개의 그래핀 층으로 이루어진 분말로 합성되었으며 분말의 크기는 약 100 nm임을 확인할 수 있었다.

• 한국결정성장학회지
• /
• 제3권2호
• /
• pp.167-175
• /
• 1993

여러 가지 탄소물질을 사용하여 변형된 스테인레스 금속재 Two-bulbs를 사용하여 Li-CIC를 합성하였다. 합성한 결과 출발물질의 구조적 특성에 따라 여러 가지 색깔의 층간화합물이 각각 형성되었다. 합성된 Li-CIC들은 X-선 회절법을 이용하여 출발물질의 결정화도에 따라 stage 형성과정을 확인하였다. 이들 결과에서 출발물질의 결정화도가 좋은 천연흑연과 흑연섬유는 낮은 stage(1 stage, 2 stage)가 형성되었고, 결정화도가 나쁜 탄소섬유와 석유계 코크스는 높은 stage(3 stage, 4 stage, 5 stage)가 얻어졌다. 또한 (hkl)회절선의 이값을 계산된 값과 비교하였을 때 이들 값들은 거의 일치하였다. 그러나 결정화도가 나쁜 경우 다소의 차이가 있음을 보이고 있다. 이들 Li-CIC에 대하여 UV/VIS 분광기를 사용하여 stage 안정성과 에너지 상태를 알수 있었다. X-선 회절법에 의한 결과와 UV/VIS 분광학적 데이터는 결정화도가 좋은 탄소물질은 에너지와 반사율의 관계곡선이 뚜렷하게 나타났음을 제시하였다. 이들 결과는 타소층과 층사이에 전하운반자와 관계가 있으며, 이들 성질이 삽입물질의 농도와 관계있음을 알수 있었다. 뿐만 아니라 본 연구는 Li-CIC의 삽입과정에서 고성능 에너지 저장제에 대한 정보를 역시 제공하여 준다.

• Bulletin of the Korean Chemical Society
• /
• 제26권1호
• /
• pp.103-106
• /
• 2005

In order to investigate the catalytic mechanism for the growth of carbon nanotubes (CNTs), a comprehensive study was conducted using carbon materials synthesized at 680 ${^{\circ}C}$ with a gas mixture of CO-H$_2$ after reduction at 800 ${^{\circ}C}$ by H$_2$ gas from iron oxide, and metal Pt. The resulting material was observed by scanning electron microscopy (SEM) and X-ray diffraction patterns (XRD) after a variety of reaction times. The carbon materials synthesized by metal Pt were little affected by reaction time and the sintered particles did not form CNTs. Xray analysis revealed that metal Fe was completely converted to iron carbide (Fe$_3$C) without Fe peaks in the early stage. After 5 min, iron carbide (Fe$_3$C) and carbon (C) phases were observed at the beginning of CNTs growth. It was found that the intensity of the carbon(C) peak gradually increased with the continuous growth of CNTs as reaction time increases. It was also found that the catalyst of growth of CNTs was metal carbide.

• 공업화학
• /
• 제29권4호
• /
• pp.405-412
• /
• 2018

알칸디올로부터 유래된 주사슬의 탄소수가 6, 9, 11인 bis[3-(dialkyloxylphosphorothionyl)thio-2-methylpropanyloxy]alkane (BAPA)를 합성하였으며, 이를 zinc dialkyl dithiophosphates (ZDDP)와 비교하여 마모억제성능을 살펴보았다. 탄소 주사슬의 길이에 따른 BAPA의 내마모성능을 확인하기 위하여 4-ball 시험을 하였다. 기유무게의 1% 농도로 첨가제를 넣고 WSD (wear scar diameter)를 측정하였고, 각 0.472, 0.459, 0.480 mm로 나타났다. 또한 BAPA 화합물 중 bis[methacryloyloxy]nonane (BMOO9)의 곁사슬인 dialkyl dithiophosphoric acid (DDP)의 탄소수를 4, 8, 12로 변화시켜 합성하여, 4-ball 시험을 하였다. 그 결과로 WSD의 값은 각각 0.537, 0.459, 0.531 mm로 측정되었다. 곁사슬이 짧으면 필름이 얇게 형성되고, 길면 필름형성을 방해하여 탄소수가 8개일 때의 값이 제일 좋게 나타났다. ZDDP의 경우 동일한 조건에서 WSD의 값이 0.563 mm로 측정되었고, 합성한 BAPA의 화합물이 마모억제용 첨가제로 더 우수한 성능을 갖는다는 것을 확인하였다.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
• /
• pp.488.2-488.2
• /
• 2014

Carbon-based materials such as carbon nanotubes and graphene have emerged as promising building blocks in applications for nanoelectronics and energy devices due to electrical property, ease of processability, and relatively inert electrochemistry. In recent years, there has been considerable interest in core-shell nanomaterials, in which inorganic nanowires are surrounded by inorganic or organic layers. Especially, carbon encapsulated semiconductor nanowires have been actively investigated by researchers in lithium ion batteries. We report a method to synthesize silicon nanowire (SiNW) core/carbon shell structures by chemical vapor deposition (CVD), using methane (CH4) as a precursor at growth temperature of $1000{\sim}1100^{\circ}C$. Unlike carbon-based materials synthesized via conventional routes, this method is of advantage of metal-catalyst free growth. We characterized these materials with FE-SEM, FE-TEM, and Raman spectroscopy. This would allow us to use these materials for applications ranging from optoelectronics to energy devices such as solar cells and lithium ion batteries.

• 한국신재생에너지학회:학술대회논문집
• /
• 한국신재생에너지학회 2009년도 추계학술대회 논문집
• /
• pp.305-305
• /
• 2009

The carbon nano-structured materials could be applied to the fields of advanced fillers, templates, electrode materials, sensor, storage, and absorption materials. The polyacrylonitrile (PAN) based carbon nano-particles provide the remarkable properties of high specific surface area, large pore volume, chemical inertness, and good mechanical stability. In this study, well-defined carbon nano-particles were obtained through pyrolysis of polyacrylonitrile based particles. The precursor nano-particles were prepared by modified aqueous dispersion polymerization using hydrophilic poly(vinyl alcohol) in a water/ N,N-dimethylformamide mixture media. Synthesized precursor nanoparticles have relatively monodisperse particles ranging 80 ~ 250nm. Stable spherical particles are obtained without coagulum or secondary particles in our system. The characteristic of the carbon nanoparticles were investigated in terms of surface area, morphology, and size distribution.

• 한국표면공학회:학술대회논문집
• /
• 한국표면공학회 2012년도 추계총회 및 학술대회 논문집
• /
• pp.163-164
• /
• 2012

Carbon coils could be synthesized using $C_2H_2/H_2$ as source gases and $SF_6$ as an incorporated additive gas under thermal chemical vapor deposition system. The substrate with oxygen incorporation and the substrate without oxygen incorporation were employed to elucidate the effect of substrate on the formation of carbon coils. The characteristics (formation densities, morphologies, and geometries) of the deposited carbon coils on the substrate were investigated. In case of Si substrate, the microsized carbon coils were dominant on the substrate surface. While, in case of oxygen incorporated substrate, the nanosized carbon coils were prevail on the substrate surface. The cause for the different geometry formation of carbon coils according to the different substrates was discussed in association with the different thermal expansion coefficient values between the substrate with oxygen incorporation and the substrate without oxygen incorporation.

• 한국전기전자재료학회:학술대회논문집
• /
• 한국전기전자재료학회 1996년도 추계학술대회 논문집
• /
• pp.373-377
• /
• 1996

Carbon materials have become a major interestings of research directed toward the development for anode of lithium batteries of enhanced cell capacity. The purpose of this study is to research and develop poly(p-phenylene)(PPP)-based carbon as a anode of lithium secondary batteries. We have synthesized PPP from benzen by chemical reaction. And then disordered carbon materials were obtained by heat-treating PPP in a nitrogen atmosphere at 40$0^{\circ}C$ to 100$0^{\circ}C$ for 1 hour. The carbon prepared by heat treatment showed a broad x-ray diffraction peak around 2$\theta$=23$^{\circ}$. Electrodes were charged and discharged at a current density of 0.1㎃/$\textrm{cm}^2$. Excellent reversible capacity of 275㎃h/g and 97% of charge/discharge efficiency were observed heat treated PPP-based carbon a $700^{\circ}C$.

• Carbon letters
• /
• 제8권1호
• /
• pp.17-24
• /
• 2007

Microporous carbons with narrow pore size distribution have been successfully synthesized by using hydrolyzed and calcined silica as templates and phenol formaldehyde (pf) resin as carbon precursor. Phenol formaldehyde-silica micro composites were prepared by solution route. Subsesequently, silica templates were removed by HF leaching. Resulting carbons were steam activated. The porous carbons were characterized by nitrogen adsorption-desorption isotherm, SEM, FTIR analysis, iodine adsorption, thermogravimetry analysis, etc. Adsorption isotherms show that the porous carbon prepared from calcined silica as templates are microporous with 88% pores of size <2 nm porosity and are of type I isotherm, while porous carbon prepared by using hydrolyzed silica are microporous with 89% microporosity, shows hysteresis loop at high relative pressure indicating the presence of some mesoporosity in samples. The microporosity in porous carbon materials has a bearing on the nature of silica templates used for pore formation.