• 제목/요약/키워드: intercalated graphite

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Thermal Analysis of Poly(Sodium 4-Styrenesulfonate) Intercalated Graphite Oxide Composites

  • 정혜경
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.555-555
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    • 2012
  • The thermal stability of poly(sodium 4-styrenesulfonate) intercalated graphite oxide has been investigated using a differential scanning calorimeter. The poly(sodium 4-styrenesulfonate) intercalated graphite oxide composite shows a prominent exothermic reaction near $207^{\circ}C$ and an endothermic reaction near $453^{\circ}C$. Graphite oxide is responsible for the exothermic reaction while the endothermic reaction is caused by the poly(sodium 4-styrenesulfonate) used in the synthesis of poly(sodium 4-styrenesulfonate) intercalated graphite oxide. The onset temperature of the exothermic reaction of poly(sodium 4-styrenesulfonate) intercalated graphite oxide decreased by $92^{\circ}C$ in comparison with that of graphite oxide, indicating the addition of poly(sodium 4-styrenesulfonate) in the composite has diminished the thermal stability of graphite oxide.

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$H_2SO_4$-Intercalated Graphite Fiber의 Deintercalation에 관한 연구 (Study on the Deintercalation of $H_2SO_4$--Intercalated Graphite Fiber)

  • 김인기;최상흘;고영신
    • 한국세라믹학회지
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    • 제30권10호
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    • pp.797-802
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    • 1993
  • Graphite fiber intercalated compound was deintercalated at $25^{\circ}C$, 65% of humidity and its deintercalated compound was discussed, based on the X-ray diffraction analysis, electrical resistivity measurement, and UV/VIS spectrometer measurements. During deintercalation, the structure was changed in orderlongrightarrowdisorderlongrightarroworder, and resistivity was decreased in the disorder state of the structure, which reflectance minimum of the UV/VIS spectrum ranged from 660 to 750nm (1.88~1.65eV).

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리튬 이온 전지 탄소부극용 Sn-GIC의 합성과 그 전기화학적 특성 (Synthesis of Sn-GIC for Carbon Electrode of Lithium Ion Battery and Its Electrochemical Characteristics)

  • 엄의흠;이택영;이철태
    • 공업화학
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    • 제18권5호
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    • pp.449-453
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    • 2007
  • 리튬이온이차전지에 사용되는 탄소부극의 성능 향상을 위하여 새로운 탄소부극물질로서 Sn-GIC (Graphite intercalated compound)를 합성하고 그 전기화학적 특성을 조사하였다. 합성시 $SnCl_2$ 수용액의 농도가 증가할수록, 그리고 수용액에 함침한 후 건조한 시료의 열처리 온도가 증가할수록 흑연에 삽입되는 Sn의 함량이 증가하였으며, 또한 흑연 내부로 삽입된 Sn의 함량이 증가함에 따라 이를 부극활물질로 사용한 cell의 초기 방전용량은 증가하였다. 가장 우수한 특성을 나타내는 1.0M $SnCl_2$ 수용액에 함침한 후 $900^{\circ}C$에서 열처리하여 제조한 Sn-GIC는 346 mA/g의 초기용량과 10 cycle 후 13%의 용량감소를 나타내었다.

Co, Ni 마가다이트 주형을 이용한 다공성 흑연의 합성 (Preparation of Porous Graphite by Using Template of Co- and Ni-Magadiite)

  • 정순용
    • 한국분말재료학회지
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    • 제12권2호
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    • pp.151-158
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    • 2005
  • Porous graphite was synthesized by removal of template in HF after pyrolysis of pyrolyzed fuel oil (PFO) at $900^{\circ}C$ using the template of Co or Ni intercalated magadiite. Porous graphite had a plate structure like template, and d-spacing value of about 0.7 nm. The extent of crystallization of porous graphite was dependent on the contents of Co or Ni intercalated in interlayer. It can be explained that the metal such as Co and Ni acts as a promotion catalyst for graphite formation. Porous graphite shows the surface area of $328\sim477 m^2/g$.

전기 화학적으로 리튬이 층간 삽입된 인조흑연의 구조와 열적 특성 분석 (Structural and thermal analysis of electrochemically Li intercalated synthetic graphite)

  • 오원춘
    • 분석과학
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    • 제14권3호
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    • pp.197-202
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    • 2001
  • 고온에서 만들어진 인조흑연을 음극 재료로 사용하여, 전기화학적으로 완전 충전된 상태에서 형성된 리튬이 층간 삽입된 인조흑연 화합물에 대하여 XRD와 DSC 분석 및 $^7Li-NMR$를 사용하여 특성화하였다. X-선 회절 결과로부터, 음극에 리튬이 충전된 상태의 인조 흑연 층간화합물의 경우, 1 stage가 주요한 회절선으로 강하게 나타났음 알 수 있었다. 리튬의 기저 평면 사이에 열적 안정성과 관련하여, 발열반응과 흡열반응의 변화량으로부터 리튬의 흑연 층간에서의 발산과 상관관계가 있음을 알 수 있다. $^7Li-NMR$ 스펙트럼 결과로부터, 방향족성의 증가와 삽입된 리튬의 거동으로부터 흡수선의 이동과 흡수밴드의 변이가 수반됨을 나타내었다. 이들 결과로부터, 리튬이 흑연층에 이상적으로 채워짐에 따라 높은 파장 쪽에서 이동이 나타남을 알 수 있다. 이러한 현상은 채워지지 않은 전자껍질에 전하이동밀도의 증가때문으로 여겨진다. 또한 리튬이 탄소층 사이에 채워짐과 관련하여 채워진 리튬의 무질서한 전자 스핀 방향과 불균일한 자기차수로 인하여 흡수밴드가 좁아진 것으로 여겨진다.

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X-ray Absorption Spectroscopy of a Poly Sodium 4-Styrensulfonate Intercalated Graphite Oxide Electrode

  • 정혜경;박병규;김재영;노한진
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.393-393
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    • 2011
  • We investigated the electronic structures of a poly sodium 4-styrensulfonate intercalated graphite oxide (PSSGO) electrode and a precursor graphite oxide (GO) electrode using X-ray absorption spectroscopy (XAS). Both electrodes were obtained from electrochemical cells. We found that in the C K-edge XAS spectra the ${\pi}^*$ state intensity originating from the sp2 hybridization of graphite decreases predominantly in the graphite oxide and PSSGO electrodes. This indicates that the negatively charged electrolyte ion (BF4-) is absorbed onto the electrodes and is transferred to the ${\pi}^*$ state of the both electrodes. The analysis of their F K-edge spectra reveals that more BF4- ions were found in the PSSGO electrode than in the graphite oxide electrode. This indicates that more electrolyte ions are absorbed in the PSSGO than in the graphite oxide electrode. We argue that this is the main reason why PSSGO cells have higher capacitance, higher energy density, and higher power density when compared to the graphite oxide cells. We also found that BF4- is the primary working ion that can be inserted into the interlayers of the PSSGO electrode.

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EnhAnced Electric Double Layer Capacitance of New Poly Sodium 4-tyrenesulfonate Intercalated Graphene Oxide Electrodes

  • 정혜경
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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    • pp.287.2-287.2
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    • 2013
  • We synthesized a new composite of poly sodium 4-styrenesulfonate intercalated graphene oxide for energy storage devices by controlling oxidation time in the synthesis of graphite oxide. Specific capacitance was improved from 20 F/g of the previous composites to 88 F/g of the new composite at the current density of 0.3 A/g. The capacitance retention was 94% after 3000 cycles, indicating that the new composites of high cyclic stability, prominent performance as electric double layer capacitor, and even low resistance could be an excellent carbon based electrode for further energy storage devices.

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Oil Adsorption of Exfoliated Graphite Prepared by Direct Reaction between $SO_3$ Gas and Graphite

  • Lee, Beom-Jae;Kwon, Young-Bae
    • Carbon letters
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    • 제2권1호
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    • pp.55-60
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    • 2001
  • Graphite intercalation compounds (GIC) were prepared by direct reaction of $SO_3$ gas with flake graphite. The intercalated $SO_3$ molecules were ejected by rapid heating to $950^{\circ}C$ under an oxidizing atmosphere for about 1 minute, resulting in surprisingly high expansion in the direction of c-axis. The characteristics of the micro-structure and pore size distribution were examined with a SEM and mercury intrusion porosimetry. The XRD analysis and spectroscopic analysis were used for the identification of the graphite and surface chemistry state. The pore size distribution of the exfoliated graphite (EG) was a range of $1{\sim}170{\mu}m$. The higher expanding temperature the higher expanded volume, so oil sorption capacities were 58.8 g of bunker-C oil and 34.7 g of diesel oil per 1 g of the the EG. The sorption equilibrium was achieved very rapidly within several minutes. As the treatment temperature increases, bulk density decreases.

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탄소섬유의 구조가 섬유층간화합물의 구조에 미치는 영향 (The Effect of the Structure of the Carbon Fibers on the Structure of the Fiber Intercalated Compounds)

  • 김인기;최상흘;고영신
    • 한국세라믹학회지
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    • 제30권9호
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    • pp.768-774
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    • 1993
  • Sulphuric acid was intercalated in mesophase pitch based graphite fiber (Thornel P100 of Amoco), PAN based graphite fiber (M40 of Thoray) and PAN based carbon fiber (T300 ofThoray, TZ307 of Taekwang in Korea) by 0.4wt% CrO3/H2SO4 solution. The degree of crystallization of fibers increased P100, M40, TZ307, T300 fiber in order and their d002 values were 3.384, 3.424, 3.470, 3.493$\AA$, respectively. After intercalation P100 fiber formed 1 stage compound whose d002 value was 3.994$\AA$(d001=7.988$\AA$). Other fibers showed (002) reflection belonging to their 1 stage comound and prinstine fiber.

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리튬-흑연 층간 화합물의 합성 및 특성 분석 (Synthesis and Characterization of Lithium-Graphite Intercalation Compounds)

  • 홍승현;김태영;서광석
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2010년도 하계학술대회 논문집
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    • pp.227-227
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    • 2010
  • The intercalation chemistry of graphite presents an attractive route to obtain few-layered graphene platelets based on the expanded interlayer spacing. We report that the lithium can be intercalated into the graphite in a controllable manner by adjusting the variables such as temperature, pressure, and reaction time. From the X-ray diffraction experiments, the lithium-graphite intercalaltion compounds (Li-GICs) can be produced as the first stage compounds ($LiC_6$), the second-stage compounds ($LiC_{12}$), and the mixtures, which is most likely to be dependent on the temperature and reaction time. Since these Li-GICs are expected to facilitate the exfoliation of graphite, we investigated the feasibility of Li-GICs as a effective precursors for the generation of single-or few-layered graphite nano-platelets.

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