• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.131-131
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• 2012

We present our recent temperature-programmed desorption (TPD) study on catalytic reductions of $NO_x$ such as NO, $NO_2$, and $N_2O$ over rutile $TiO_2$(110) surfaces. Our results indicate that $NO_2$/NO readily reacts to give NO/$N_2O$ desorption at the substrate temperature as low as 100 K/70 K. Interestingly, $N_2O$, however, does not dissociate into $N_2$ and $O_{BBO}$ over the oxygen vacancy on the $TiO_2$(110) surface. Successive reduction of NO and $NO_2$ into $N_2O$ and NO, respectively, leaves oxygen atoms on the $TiO_2$(110) surface in a form of $O_{ad}$, which can induce additional reductive channels of NO and $NO_2$ at higher temperatures up to 400 K. During the repeated TPD cycles of $NO_x$, our x-ray photoelectron spectroscopy (XPS) analysis indicates that no N atom accumulates on the $TiO_2$ surface.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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• pp.265-265
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• 2012

The adsorption of molecular $NH_3$ on rutile $TiO_2(110)-1{\times}1$ surfaces was investigated using a temperature-programmed desorption (TPD) technique combined with a molecular beam apparatus. A quantitative investigation into the TPD spectra of $NH_3$ was made for $NH_3$ adsorbed on two kinds of rutile $TiO_2(110)-1{\times}1$ surfaces with the oxygen vacancy ($V_O$) concentration of ~0% (p-$TiO_2(110)$) and ~5% (r-$TiO_2(110)$), respectively. On both surfaces, non-dissociative adsorption of $NH_3$ was inferred from a quantitative analysis on the amount of adsorbed $NH_3$ and those desorbed. With increasing coverage, the monolayer desorption feature shifted from 400 K toward lower temperatures until it saturates at 160 K, suggesting a repulsive nature in the interaction between $NH_3$ molecules. At the very low coverage regime, the desorption features were found to extend up to 430 K and 400 K on p-$TiO_2(110)$ and p-TiO(110), respectively. As a result, the saturation coverage of monolayer of $NH_3$ was higher on the p-$TiO_2(110)$ surface than on the p-TiO(110) by about 10%. The desorption energy ($E_d$) of $NH_3$ obtained by inversion of the Polanyi-Wigner equation indicated that the difference between the $E_d$'s of $NH_3$ (that is, $E_d(on\;p-TiO_2(110)$) - $E_d$(on p-TiO(110)) was 14 kJ/mol at ${\theta}(NH_3)=0$ and decreased to 0 as the coverage approached to a monolayer. The observed adsorption behavior of $NH_3$ was interpreted using an interaction model between $NH_3$ and surface defects on $TiO_2$ such as VO's and $Ti^{3+}$ interstitials.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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• pp.196-196
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• 2011

Molecular $N_2O$ has bee known to react over oxygen vacancy on a reduced rutile $TiO_2$(110)-1${\times}$1 surface to desorb as molecular $N_2$ leaving oxygen atom behind. In the present study, we investigated the reaction of $N_2O$ on rutile $TiO_2$(110) using temperature-programmed desorption (TPD). Our results indicate that $N_2O$ does not react over the oxygen vacancy under a typical UHV experimental condition. On a rutile $TiO_2$(110)-1${\times}$1 with a well-defined oxygen vacancy concentration of 5% ($2.6{\times}10^{13}/cm^2$), $N_2O$ desorption features show a monolayer peak maximum at 135 K followed by a small peak maximum at 170 K. When the oxygen vacancy is blocked with $H_2O$, the $N_2O$ peak at 170 K disappears completely, indicating that the peak is due to molecular $N_2O$ interacting with oxygen vacancy. The integrated amount of desorbed $N_2O$ plotted against the amount of adsorbed $N_2O$ however shows a straight line with no offset indicating no loss of $N_2O$ during our cycles of TPD measurements. In addition, our $N_2O$ uptake measurements at 70~100 K showed no $N_2$ (as a reaction product) desorption except contaminant $N_2$. Also, $H_2O$ TPD taken after $N_2O$ scattering up to 350 K indicates no change in the vacancy-related $H_2O$ desorption peak at 500 K showing no change in the oxygen vacancy concentration after the interaction with $N_2O$.

• International Journal of Oral Biology
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• 제46권3호
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• pp.105-110
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• 2021

The physicochemical properties of crystalline titanium dioxide nanoparticles (TiO₂ NPs) were investigated by comparing amorphous (amTiO₂), anatase (aTiO₂), metaphase of anatase-rutile (arTiO₂), and rutile (rTiO₂) NPs, which were prepared at various calcination temperatures (100℃, 400℃, 600℃, and 900℃). X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses confirmed that the phase-transformed TiO₂ had the characteristic features of crystallinity and average size. The surface chemical properties of the crystalline phases were different in the spectral analysis. As anatase transformed to the rutile phase, the band of the hydroxyl group at 3,600-3,100 cm^-1 decreased gradually, as assessed using Fourier transform infrared spectroscopy (FT-IR). For ultraviolet-visible (UV-Vis) spectra, the maximum absorbance of anatase TiO₂ NPs at 309 nm was blue-shifted to 290 nm at the rutile phase with reduced absorbance. Under the electric field of capillary electrophoresis (CE), TiO₂ NPs in anatase migrated and detected as a broaden peak, whereas the rutile NPs did not. In addition, anatase showed the highest photocatalytic activity in an UV-irradiated dye degradation assay in the following order: aTiO₂ > arTiO₂ > rTiO₂. Overall, the phases of TiO₂ NPs showed characteristic physicochemical properties regarding size, surface chemical properties, UV absorbance, CE migration, and photocatalytic activity.

• 한국세라믹학회지
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• 제27권8호
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• pp.1050-1054
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• 1990

Rutile(TiO2) single crystals were grown by FZ method. Feed rod was sintered in the longitudinal tube-shaped furnace at 135$0^{\circ}C$ and optimum growth condition was growth rate 5-8mm/hr, rotation rate 30-40rpm. When crystal was growing, atomosphere was oxidized condition, and grown single crystal was annealed at 110$0^{\circ}C$. The rutile single crystals were oriented to [001] direction and color change of single crystals were related to atmosphere, and difference of electric conductivity and resistance was due to the fact above.

• 한국분말재료학회지
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• 제9권2호
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• pp.110-115
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• 2002

In order to obtain the nano size $10wt%Cu-TiO_2$composite powders by mechanical alloying method for useful composite catalysis, the effects of mechanical alloying time on the formationof $10wt%Cu-TiO_2$ composite powders were analyzed. The phase transformation behaviors were experimented as the heat treating temperature increased. Homogeneous 10wt% Cu-rutile type $TiO_2$composite powders were synthesized in 40 hours by mechanical alloying. After 60 hours mechanical alloying 50 nm size $TiO_2$powders were obtained. Both the phase of mechanically alloyed 10 wt% $Cu-TiO_2$ and pure $TiO_2$ powders were not transformed to anatase after annealing at the temperature range between 350 to 500 $^{\circ}C$. The intermetallic compound of $Cu_2Ti_4$O was formed after 10 hours mechanical alloying, however it could be considered that this intemetallic phase dose not prevent the transformation of rutile $TiO_2$ to the anatase phase after heat treatment at the temperature between 350 and $550^{\circ}C$.

• 한국진공학회지
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• 제11권4호
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• pp.240-248
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• 2002

결정성이 좋을 것으로 기대되는 Fe이 도핑된 $Fe_{x}Ti_{l-x}O_2$박막 (x=0.07과 0.16)을 rutile $TiO_2$(110) 기판위에 산소 플라즈마 적층 성장 방법으로 성장시켰다. 도핑되는 Fe의 함량에 따른 표면 특성을 규명하기 위하여 박막 성장은 같은 조건에서 이루어졌다. 여러 가지의 표면분석법을 이용하여 성장된 박막의 표면 특성을 규명하였다. $Fe_{x}Ti_{l-x}O_2$박막에 존재하는 Ti의 산화상태는 +4 이었고 Fe의 경우는 +2와 +3의 산화상태가 섞여있었으며 Fe의 함량이 높은 $Fe_{0.16}Ti_{0.84}O_2$박막에서 $Fe^{3+}$ 이온의 함량이 더 높은 것으로 나타났다. $Fe_{0.07}Ti_{0.93}O_2$박막은 기판과 유사한 평탄한 표면에 막대형과 원통형의 높은 island 형태로 성장되었다. $Fe_{0.16}Ti_{0.84}O_2$박막은 $Fe_{0.07}Ti_{0.93}O_2$ 박막보다는 평탄하지만 적은 island들이 뭉쳐있는 다소 거칠은 표면을 한 다결정성 형태로 성장되어 Fe의 함량에 따라 morphology가 다르게 나타났다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.126-126
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• 2016

Understanding adsorption behavior organic molecules at oxide surfaces is very important for the application of organic-inorganic hybrid materials. Recently, monoethanolamine (MEA) adsorbed on $TiO_2$ surface has received great interests because it can lower the work function of $TiO_2$ in photo-electronic devices such as OLED and solar cells. In this study, we investigated the role of surface defects in adsorption behaviors of MEA at the rutile $TiO_2$ (110) surface by combined study of scanning tunneling microscopy and density functional theory calculations. Our results revealed that oxygen vacancy is the most stable adsorption site for MEA on $TiO_2$ (110) surface at low coverage. As coverage increases, the oxygen vacancies are occupied with the molecules and MEA molecules start to adsorb at Ti rows at higher coverages. Our results show that the defects at oxide surfaces and the intermolecular interactions are important factors for determining stable adsorption structure of MEA at $TiO_2$ (110) surfaces.

• 한국건축시공학회:학술대회논문집
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• 한국건축시공학회 2006년도 춘계학술논문 발표대회 제6권1호
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• pp.147-153
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• 2006

Photocatalyst reaction has limit of its usage because application range mostly centered on atmosphere purification area. Thus, it is true that an alternative plans are necessary to increase usage of $TiO_2$ as photocatalyst material. (1) The result of flow felt according to $TiO_2$ replacement rate has shown that both of anatase type and rutile type over 12% deviated from desired flow, $110{\pm}5mm$. Consequently, the range below 9% will be suitable when the anatase type $TiO_2$ if used for functional additives if workability is considered. (2) After compressive strength test, replacement rate 6-9% is estimated as suitable range if $TiO_2$ is used as compressive strength material. Rutile type and anatase type are suitable for in early-age strength and long-age strength respectively. (3) It was revealed that bending strength was dramatically decreased when replacement rate was increased. The main reason were the increase of $TiO_2$ doesn't influence hydration reaction and the decrease of bending strength. (4) The result from the water purification properties test using ion-chromatograhpy has shown that the condition with anatase type $TiO_2$ was normally better than rutile type on the same replacement rate.

• 분석과학
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• 제22권6호
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• pp.464-470
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• 2009

온도에 따른 티타늄금속의 산화거동을 조사하기 위하여 금속시편을 각각의 온도($300{\sim}1000^{\circ}C$)에서 2시간 동안 가열한 후, 생성된 산화시편의 표면에 대하여 X-선 회절(XRD)분석, 주사전자현미경 (SEM)/energy dispersive spectroscopy (EDS) 분석과 감쇠된 전반사(ATR) Fourier 변환 적외선(FT-IR) 분광 분석을 수행하였다. $300^{\circ}C$에서 대기 중의 산소가 티타늄 금속(hexagonal) 표면층으로 확산되어 적외선 흡수띠가 검출되었으며 온도가 높아짐에 따라 확산되는 산소 양이 증가하여 적외선 흡수띠와 X-선 회절 피크의 이동(shift) 현상이 나타났고 $700^{\circ}C$에서 XRD에 의해 $Ti_3O$ (hexagonal)의 생성이 확인되었다. 티타늄 금속 표면에 $TiO_2$ (rutile, tetragonal) 산화층이 생성되기 시작한 온도는 $600^{\circ}C$ 이었으며 이때 두께가 $1{\mu}m$ 이하 수준이었으나 $700^{\circ}C$에서는 약 $2{\mu}m$로 두꺼워졌고 $1000^{\circ}C$에서는 약 $110{\mu}m$ 두께에 달했다. 또한 $900^{\circ}C$ 이상의 온도에서 $TiO_2$ (rutile) 산화층 표면은 (110) 면의 방향으로 결정이 성장하였다.