• 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).

• 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.

• 한국세라믹학회지
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• 제25권4호
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• pp.408-414
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• 1988

This thesis is 2nd thesis from "Mechanism of Intercalation Compounds in Graphite with Hydrogen sulfate(J. Korea Cer. Soc. Vol. 22. No.6, 1985). We have oxidized natural Graphite flakes(0.1~0.2mm., Kropfm hl passau in Deutchland. S40) with a solution of CrO3 in H2SO4. Whilst persulfate ions were intercalated, too, below 7$^{\circ}C$, no evidence for intercalation of a peroxo compound was found at 22$^{\circ}C$. The reaction was interrupted after various times by filtering and washing with concentrated H2SO4. X-ray diffraction showed that the 2nd stage compound had already been formed after 2 minutes. We could only follow further oxidation to the blue stage compound which was completed after 35 minutes. We have found six distinct intermediate stage between 2nd stage and 1 stage. Experiments are described on the formation of intermediate stage color and X-ray diffraction analysis.ysis.

• 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.

• 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.

• Progress in Superconductivity
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• 제12권1호
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• pp.51-56
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• 2010

$^{13}C$ NMR (nuclear magnetic resonance) measurements have been performed to investigate the local electronic structure of a superconducting graphite intercalation compound $CaC_6$ ($T_c$ = 11.4 K). A large number of single crystals were stacked and sealed in a quartz tube for naturally abundant $^{13}C$ NMR. The spectrum, Knight shift, linewidth, and spin-lattice relaxation time $T_1$ were measured in the normal state as a function of temperature down to 80 K at 8.0 T perpendicular to the c-axis. The $^{13}C$ NMR spectrum shows a single narrow peak with a very small Knight shift. The Knight shift and the linewidth of the $^{13}C$ NMR are temperature-independent around, respectively, +0.012% and 1.2 kHz. The spin-lattice relaxation rate, $1/T_1$, is proportional to temperature confirming a Korringa behavior as for non-magnetic metals. The Korringa product is measured to be $T_1T\;=\;210\;s{\cdot}K$. From this value, the Korringa ratio is deduced to be $\xi$ = 0.73, close to unity, which suggests that the independent-electron description works well for $CaC_6$, without complications arising from correlation and many-body effects.

• 분석과학
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• 제7권3호
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• pp.315-320
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• 1994

고성능 에너지 저장제로 사용되는 Li-GICs(Lithium-Graphite Intercalation Compounds)를 혼합 가압법에 의하여 Li의 함유량에 따라 합성하였다. 이들 합성된 화합물을 X-선 회절법, UV/VIS 분광학적 분석법 및 CHN 분석법을 이용하여 화합물의 특성을 알아 보았다. X-선 회절 분석 결과에 의하며 리튬의 함유량이 증가함에 따라 낮은 stage가 관찰되었으나, 이들 화합물이 혼재된 stage를 가지고 있음을 알 수 있었다. $Li_{40wt%}$의 경우 지배적으로 stage 1의 구조가 나타났지만 순수한 stage 1의 화합물은 얻을 수가 없었다. stage 1의 화합물이 가지는 $d_{001}$값은 약 $3.70{\AA}$을 나타내었다. 분광학적 분석결과에 의하면 각각의 화합물들은 뚜렷한 에너지 스펙트럼을 나타내었고, 이들 곡선으로부터 $R_{min}$에 최저값의 형성이 리튬의 함량이 증가함에 따라 높은 에너지쪽에서 형성되었음을 알 수 있다. 이러한 결과는 안정한 stage의 형성을 나타내 주고 있다. 원소분석기에 의한 결과를 이용하여 Li-GICs의 화학적인 구성과 관련하여 혼합된 상태를 알 수 있었으며, 혼합 가압법의 우수성을 알 수 있었다. 이들 결과로부터 $Li_{10wt%}$-GIC와 $Li_{20wt%}$-GIC의 경우는 2차 전지의 양극에서의 이용 가능성을 제시하여 주고 있다.