• Journal of the Korean Crystal Growth and Crystal Technology
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• v.19 no.5
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• pp.256-261
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• 2009

Hydrophilic and transparent $TiO_2$ thin film was fabricated by sol-gel method and the properties of contact angle, surface morphology, and transmittance were measured. In addition, surfactant Tween 80 was used for increasing the hydrophilic property of thin film. When the contents of Tween 80 in $TiO_2$ solution was 0, 10, 30, 50wt%, the contact angles of $TiO_2$ thin film were $41.4^{\circ}$, $18.2^{\circ}$, $16.0^{\circ}$, $13.2^{\circ}$, respectively. Fabricated $TiO_2$ thin film showed the photocatalytic property that decomposed methylene blue and decreased the absorbance of solution after UV irradiation. $TiO_2$ thin films fabricated with the solution of 30 wt% Tween 80 were deposited on glass (bare), antimony tin oxide (ATO), fluorine tin oxide (FTO), indium tin oxide (ITO) coated glass substrates, and the contact angle and transmittance of thin film was measured. The contact angles of thin films deposited on four substrates were $16.2\sim27.1^{\circ}$ and was decreased to the range of $13.2\sim17.6^{\circ}$ after UV irradiation, Especially, the thin films coated on ATO and FTO glass substrate showed high transmittance of 74.6% in visible range, respectively, and low transmittance of 54.2% and 40.4% in infrared range, respectively.

• Journal of the Korean Electrochemical Society
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• v.18 no.4
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• pp.161-171
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• 2015

High-yield zinc germanium oxide ($Zn_2GeO_4$) and zinc tin oxide ($Zn_2SnO_4$) nanowires were synthesized using a hydrothermal method. We investigated the electrochemical properties of these $Zn_2GeO_4$ and $Zn_2SnO_4$ nanowires as anode materials of lithium ion battery and sodium ion battery. The $Zn_2GeO_4$ and $Zn_2SnO_4$ nanowires showed excellent cycling performance of the lithium ion battery, with a maximum capacity of 1021 mAh/g and 692 mAh/g after 50 cycles, respectively, with a high Coulomb efficiency of 98 %. For the first time, we examined the cycling performance of $Zn_2GeO_4$ and $Zn_2SnO_4$ nanowires for sodium ion batteries. The maximum capacity is 168 mAh/g and 200 mAh/g after 50 cycles, respectively, with a high Coulomb efficiency of 97%. These nanowires are expected as promising electrode materials for the development of high-performance lithium ion batteries as well as sodium ion batteries.

• Journal of the Korean Electrochemical Society
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• v.3 no.3
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• pp.178-181
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• 2000

In this experiments, tin oxide thin film anode for microbattery was deposited by using RF magnetron sputtering. The RF power and operating pressure during deposition were fixed at $2.5W/cm^2$ and 10mTorr respectively. The partial pressure of oxygen was varied from $0\%\;to\;100\%$ to control oxygen content and metal Sn chips were used further reducing of oxygen content. According to reduction in the oxygen content formation of the irreversible $Li_2O$ was reduced a thin film anode of $SnO_x$ of high capacity was fabricated. The optimum $SnO_x$, thin film was $SnO_{1.43}$ which exhibited a reversible capacity of $ 500{\mu}Ah/cm^2{\mu}m$ and exhibited good reversibility.

• Korean Journal of Materials Research
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• v.17 no.7
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• pp.376-381
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• 2007

Fluorine-doped tin oxide (FTO) thin film was coated on aluminosilicate glass at $450^{\circ}C$ by spray pyrolysis method. In the range of 0-2.7 molar ratio of F/Sn, the variations of electrical conductivity and visible light transmission were investigated. At the F/Sn ratio of 1.765, the film showed the lowest electrical resistivity value of $3.0{\times}10^{-4}{\Omega}\;cm$, the highest carrier concentration of $2.404{\times}10^{21}/cm^3$, and about $8\;cm^2/V{\cdot}sec$ of electronic mobility. The FTO film showed a preferred orientation of (200) plane parallel to the substrate. X-ray photoelectron spectroscopy analysis results indicated that the contents of $Sn^{4+}-O$ bonding are the highest at 1.765 of F/Sn molar ratio.

• Journal of the Korean Electrochemical Society
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• v.17 no.2
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• pp.86-93
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• 2014

Mesoporous tin oxide (meso-$SnO_2$) with 5 nm mesopore and well-aligned $SnO_2$ nanowire-bundles with 5~7 nm diameters were prepared by template synthesis method. In addition to meso-$SnO_2$, meso-$SnO_2$/$SiO_2$, which has almost the same structure as meso-$SnO_2$ including $SiO_2$ used as the template were prepared by the modification of template synthesis. X-ray diffraction, N2 adsorption-desorption isotherms, transmission electron microscopy observed structures of meso-$SnO_2$ and meso-$SnO_2$/$SiO_2$. Although the meso-$SnO_2$/$SiO_2$ showed some positive evidences to suppress the volume change of meso-$SnO_2$ through cyclic voltammogram, electrochemical impedance spectroscopy, and voltage profiles during cycling, its cycle life was not improved highly to address modified structural effects. Thus, further study might be done to control the nanostructure of meso-$SnO_2$/$SiO_2$ for enhanced cycle performance.

• Journal of the Korea Institute of Information and Communication Engineering
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• v.14 no.4
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• pp.935-938
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• 2010

Indium-tin-oxide (ITO) films show a low electrical resistance and high transmittance in the visible range of an optical spectrum. The transparent electrodes have to get resistivity and sheet resistance less than $1{\times}10^{-3}{\Omega}/cm$ and $10^3{\Omega}/sq$ respectively and transmittance over 80% at wavelength of 380nm~780nm. This study establishes DC magnetron sputtering process condition on ITO thin film by measuring electrical and optical properties of the thin film. As results, we obtained $300\;{\mu}{\Omega}cm$ resistivity of ITO films with good transmittance (above 90 %) under 90:10 wt% composition rate of $In_2O_3:SnO_2$. Also, we understood that the ITO thin film by DC magnetron sputtering depends on the deposition condition, especially substrate temperature, and the composition rate of $In_2O_3:SnO_2$ that is one of the most critical parameters was successfully optimized for high qualified transparent electrodes.

• Korean Journal of Materials Research
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• v.25 no.1
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• pp.27-31
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• 2015

This paper proposes a novel way of fabricating aligned porous Sn by freeze-drying of camphene slurry with stannic oxide ($SnO_2$) coated Sn powders. The $SnO_2$ coated Sn powders were prepared by surface oxidation of the initial and ball-milled Sn powders, as well as heat treatment of tin chloride coated Cu powders. Camphene slurries with 10 vol% solid powders were prepared by mixing at $50^{\circ}C$ with a small amount of oligomeric polyester dispersant. Freezing the slurry was done in a Teflon cylinder attached to a copper bottom plate cooled at $-25^{\circ}C$. Improved dispersion stability of camphene slurry and the homogeneous frozen body was achieved using the oxidized Sn powder at $670^{\circ}C$ in air after ball milling. The porous Sn specimen, prepared by freeze-drying of the camphene slurry with oxidized Sn powder from the heat-treated Sn/tin chloride mixture and sintering at $1100^{\circ}C$ for 1 h in a hydrogen atmosphere, showed large pores of about $200{\mu}m$, which were aligned parallel to the camphene growth direction, and small pores in their internal walls. However, $100{\mu}m$ spherical particles were observed in the bottom part of the specimen due to the melting of the Sn powder during sintering of the green compact.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.398-398
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• 2012

SnO2 나노세선은 n-형 전기적 성질과 화학적인 안정성 때문에 가스센서, 투명 전극 및 태양전지와 같은 전자소자와 광소자에 널리 사용되고 있다. 화학 기상 증착, 전자빔 증착과 전기화학증착법을 사용하여 SnO2 나노세선을 제작하고 있다. 여러 가지 증착 방법중에서 전기화학증착방법은 낮은 온도와 진공 공정이 필요하지 않으며 대면적 공정이 가능하고 빠른 성장 속도로 나노구조를 효과적으로 성장할 수 있는 장점을 가지고 있다. 본 연구에서는 전기화학증착법을 이용하여 Indium Tin Oxide (ITO) 기판 위에 SnO2 나노세선 성장하고 성장시간에 따라 형성한 SnO2 나노세선의 구조적 성질을 조사하였다. SnO2 나노세선을 성장하기 위하여 D.I. water와 Entanol을 7:3의 비율로 섞은 용액을 $65^{\circ}C$로 유지하였고, 0.015 M의 Tin chloride pentahydrate ($Cl4{\cdot}Sn{\cdot}5H2O$)를 타겟 물질로 이용하였고, 0.1 M의 Potassium chloride (KCl)를 완충 물질로 사용하였다. 전기화학증착 방법을 사용하여 제작한 ITO 기판위에 성장한 SnO2 나노세선 위에 전극을 제작하고 전류-전압 특성을 측정하였다. SnO2 나노세선이 성장되는 전기화학증착 전압을 1.2 V로 고정하고, 성장시간을 15분, 30분 및 1시간으로 변화하여 SnO2 나노세선의 구조적 특성을 분석하였다. X-선회절 (X-ray diffraction; XRD) 실험 결과는 $31^{\circ}$에서 (101) 성장방향을 갖는 SnO2 나노세선이 성장함을 확인하였고, 성장 시간이 길어짐에 따라(101) 성장방향의 XRD 피크의 intensity가 증가하였다. 전기화학증착 성장 시간이 길어짐에 따라 SnO2 나노세선의 지름이 60 nm에서 150 nm로 변화하는 것을 주사전자현미경으로 관측하였다. 이 실험 결과는 전기화학증착방법을 사용하여 제작한 SnO2 나노세선의 성장 시간에 따른 구조적 특성들을 최적화하여 소자제작에 응용하는데 도움이 된다.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.397-397
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• 2012

에너지갭이 큰 SnO2 반도체는 빛 투과율이 우수하여 투명성이 좋으며 화학적으로 안정된 구조를 가지고 있어 전자소자 및 광소자 응용에 대단히 유용하다. SnO2 박막을 증착하는 방법은 Physical Vapor Deposition과 Chemical Vapor Deposition이 있으나 나노 구조를 가진 SnO2를 형성하기 어렵다. 전기 화학적 증착 (Electrochemical Deposition: ECD)은 낮은 온도에서 진공 공정이 필요하지 않기 때문에 경제적이며 빠른 성장 속도를 가지고 있기 때문에 SnO2 나노 구조를 효과적으로 형성 할 수 있다. 본 연구에서는 Indium Tin Oxide (ITO) 기판 위에 SnO2 나노 구조를 형성시켜 전기적 및 구조적 특성을 관찰하였다. 0.015 M의 Tin chloride pentahydrate(SnCl4 5H2O)를 타켓 물질로 사용하고 0.1 M의 KCl을 완충물질로 사용하여 SnO2 나노구조를 성장하였다. 타겟 물질이 잘 녹지 않으므로 DI water와 ethanol을 7：3의 비율로 용매 사용하였다. 전류-전압 곡선을 분석하여 최적의 성장조건을 확보하고, $65^{\circ}C$ 1기압 하에서 -2.5 V 부터 -1.0 V까지 0.5 V 간격으로 나누어서 SnO2 나노구조를 성장하였다. X-선 회절 분석결과에서 SnO2의 피크의 크기가 큰 전기화적적 성장 전압구간과, 주사전자현미경 분석 결과에서 나노 구조가 가장 잘 나타난 성장 전압구간을 다시 0.1 V 간격으로 세분화하여 최적화 조건을 분석하였다. X-선 회절 실험으로 형성한 SnO2 나노구조의 피크가 (110) (101) (200) (211) (310)로 나타났다. X-선 회절 분석의 intensity의 값이 (101)방향이 가장 크게 나타났으므로 우선적으로 (101) 방향으로 SnO2 나노구조가 성장됨을 알 수 있었다. 주사전자현미경상은 grain size가 50~100 nm 사이의 SnO2 나노구조가 형성되며, grain size가 전기화학적 증착 장치의 성장전압이 저 전압 구간에서 커지는 것을 알 수 있었다.

• Korean Journal of Materials Research
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• v.18 no.3
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• pp.123-127
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• 2008

The production of tin oxide ($SnO_2$) microrods on iridium (Ir)-coated substrates was achieved through the thermal evaporation of Sn powders in which a sufficiently high $O_2$ partial pressure was employed. Scanning electron microscopy revealed that the product consisted of microrods with diameters that ranged from 0.9 to $40\;{\mu}m$. X-ray diffraction, high-resolution transmission electron microscopy, and selected area electron diffraction indicated that the microrods were $SnO_2$ with a rutile structure. As the microrod tips were free of metal particles, it was determined that the growth of $SnO_2$ microrods via the present route was dominated by a vapor-solid mechanism. The thickening of rod-like structures was related to the utilization of sufficiently high $O_2$ partial pressure during the synthesis process, whereas low $O_2$ partial pressure facilitated the production of thin rods.