• 한국재료학회지
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• 제1권4호
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• pp.184-190
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• 1991

고분해능 전자에너지손실과 자외선광전자분광법을 사용하여 단결정 ZrC(111)면의 산소흡착을 연구하였다. 산소는 낮은 산소노출량에서 $(\sqrt{3}{\times}\sqrt{3})R30^{\circ}$ 구조로 흡착된다. 노출량이 승가하면 $1{\times}1$ 구조로 바뀌는데 이때 흡착하는 산소원자는 $(\sqrt{3}{\times}\sqrt{3})R30^{\circ}$ 구조에서보다 흡착높이가 낮으며 3-fold hollow site의 중심에 놓이지 않고 bridge site에 가까와진다. 서로 다른 산소흡착 거동은 개끗한 ZrC(111) 표면에서 두개의 표면전자상태에 기인한다.

• 한국물환경학회지
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• 제31권4호
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• pp.392-398
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• 2015

The aim of this study was to investigate the bio-adsorption using modified zeolite with Mg (Mg-zeolite) in the dyeing wastewater treatment. Mg-zeolite adsorbed successfully 100% of the color, suspended solid (SS). chemical oxygen demand (COD), biological oxygen demand (BOD), total nitrogen (TN) and total phosphorus (TP) in the dyeing wastewater at the following optimal Mg-zeolite loading: 20 mg/L for colour, SS, TN and TP, 30 mg/L for BOD and COD. These results indicated that the amount of 1 mg/L Mg-zeolite adsorbed 11.6 mg/L for color, 9.5 mg/L for SS, 45.0 mg/L for COD, 12.7 mg/L for BOD, 0.91 mg/L for TP and 2.25 mg/L for TN. The bio-adsorbent, Mg-zeolite, can be a promising adsorption due to its high efficiency and low dose requirements.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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• pp.212-212
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• 2012

The Coverage dependent attachment of multifunctional groups included in threonine molecules adsorbed to Ge (100)$-2{\times}1$ surface was investigated using core-level photoemission spectroscopy (CLPES) and density functional theory (DFT) calculations. The core-level spectra at a low coverage indicated that the both carboxyl and amine groups participated in the bonding with the Ge (100) surface by "O-H dissociated and N-dative bonded structure". However, at high coverage level, additional adsorption geometry of "O-H dissociation bonded structure" appeared possibly to minimize the steric hindrance between adsorbed molecules. Moreover, the C 1s, N 1s, and O 1s core level spectra confirmed that the carboxyl oxygen is more competitive against the hydroxymethyl oxygen in the adsorption reaction. The adsorption energies calculated using DFT methods suggested that four of six adsorption structures were plausible. These structures were the "O-H dissociated-N dative bonded structure", the "O-H dissociation bonded structure", the "Om-H dissociated-N dative bonded structure", and the "Om-H dissociation bonded structure" (where Om indicates the hydroxymethyl oxygen). These structures are equally likely, according to the adsorption energies alone. Conclusively, we investigate in threonine on Ge (100) surface system that the "O-H dissociated-N dative bonded structure" and the "O-H dissociation bonded structure" are preferred at low coverage and high coverage.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2012년도 춘계학술발표대회
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• pp.70.1-70.1
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• 2012

In-situ X-ray photoelectron spectroscopy (XPS) and infrared (IR) spectroscopy studies of SOFC cathode materials will be discussed in this presentation. The mixed conducting perovskites (ABO3) containing rare and alkaline earth metals on the A-site and a transition metal on the B-site are commonly used as cathodes for solid oxide fuel cells (SOFC). However, the details of the oxygen reduction reaction are still not clearly understood. The information about the type of adsorbed oxygen species and their concentration is important for a mechanistic understanding of the oxygen incorporation into these cathode materials. XPS has been widely used for the analysis of adsorbed species and surface structure. However, the conventional XPS experiments have the severe drawback to operate at room temperature and with the sample under ultrahigh vacuum (UHV) conditions, which is far from the relevant conditions of SOFC operation. The disadvantages of conventional XPS can be overcome to a large extent with a "high pressure" XPS setup installed at the BESSY II synchrotron. It allows sample depth profiling over 2 nm without sputtering by variation of the excitation energy, and most importantly measurements under a residual gas pressure in the mbar range. It is also well known that the catalytic activity for the oxygen reduction is very sensitive to their electrical conductivity and oxygen nonstoichiometry. Although the electrical conductivity of perovskite oxides has been intensively studied as a function of temperature or oxygen partial pressure (Po2), in-situ measurements of the conductivity of these materials in contact with the electrolyte as a SOFC configuration have little been reported. In order to measure the in-plane conductivity of an electrode film on the electrolyte, a substrate with high resistance is required for excluding the leakage current of the substrate. It is also hardly possible to measure the conductivity of cracked thin film by electrical methods. In this study, we report the electrical conductivity of perovskite $La_{0.6}Sr_{0.4}CoO_{3-{\delta}}$ (LSC) thin films on yttria-stabilized zirconia (YSZ) electrolyte quantitatively obtained by in-situ IR spectroscopy. This method enables a reliable measurement of the electronic conductivity of the electrodes as part of the SOFC configuration regardless of leakage current to the substrate and cracks in the film.

• 한국진공학회지
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• 제6권2호
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• pp.159-164
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• 1997

X-선 광전자 분광법 (x-ray photoelectron spectroscopy: SPS)과 반사 고에너지 전 자 회절법(reflection high energy electron diffraction: RHEED)을 이용하여 상온과 고온(약 300~$500^{\circ}C$)에서 알칼리금속(AM)/Si(111)7$\times$7표면에 1 monolayer(ML)의 AM을 흡착시키면 Si(111)7$\times$7표면에 비해 산소의 초기 부착 계수(initial sticking coefficient)와 산소의 포화량 은 증가하지 않았다. Si(111)7$\times$7-AM표면에 산소의 주입량을 증가시키면서 측정한 O ls 스 펙트럼으로부터 AM이 흡착된 Si(111)7$\times$7표면에 흡착되는 산소원자는 Si-O, AM-O 두 종 류의 결합형태를 가지는 것으로 생각되며 이중에서 AM-O 결합의 산화과정상에서의 역할 에 대하여 논의하였다. 상온과는 달리 고온에서는, Si(111)3$\times$1-AM표면으로 구조가 변화하 면서 산소의 흡착이 급격히 떨어지는 것을 관측할 수 있었다. 이때 3$\times$1-AM표면을 형성시 키는 AM종류의 산화에 대한 의존성을 살펴보았다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제10권2호
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• pp.44-51
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• 2005

옥동천 퇴적물을 대상으로 중금속의 존재형태 및 이동성에 관하여 조사하였다. 퇴적물내의 중금속의 존재형태는 adsorbed fraction, carbonate fraction, reducible fraction, organic fraction, and residual fraction 다섯 가지 형태로 분류하였으며, 존재형태 중 제일 많은 부분을 차지하는 부분은 reducible fraction이며 다음으로 organic fraction라 residual fraction으로 나타났다. Adsorbed fraction은 중금속의 존재형태 미미한 부분으로 나타났다. 옥동천 퇴적물내 의 총 카드뮴 중 수체로 이동 가능한 부분은 $19.8{\sim}56.7%$이며, 구리, 납의 경우 대부분이 organic fraction으로 나타났다. 구리와 납의 경우 이동 가능한 형태는 납의 경우 총 납의 농도 중 $2.6{\sim}48.1%$, 구리는 $0.2{\sim}36.9%$로 나타났으며, 아연은 $0.5{\sim}48.5%$로 나타났다. 카드뮴, 아연, 구리의 경우 이동 가능한 부분 중 대부분이 reducible fraction이며, 납과 니켈의 경우 adsorbed fraction으로 나타났다. 구리와 아연의 이동이 기능한 경우는 수중의 산소의 유무에 의해 결정되며, 납이나 니켈의 경우 수중에서의 물리적 영향, 수소이온의 농도가 증가, 산소의 고갈 등에 의해 수층으로 이동할 가능성이 높다.

• Bulletin of the Korean Chemical Society
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• 제15권11호
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• pp.933-939
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• 1994

Using an atom superposition and electron delocalization molecular orbital (ASED-MO) method, we have investigated the vibrational and chemisorptive properties of adsorbates on a Pt(100) surface during CO oxidation. The calculated vibrational stretching frequency for a predicted structure of $[CO{\cdot}{\cdot}{\cdot}O]^*$ complex is 1642 $cm^{-1}$. The CO bond stretches by 0.05 ${\AA}$ when adsorbed on one-fold site, and is tilted by 30 ${\AA}$ from the surface normal. We find the decrease in CO vibrational frequency on going from the one-fold to the high coordination sites. Binding at the two-fold site is predicted to be favored for $Pt_{18}(100)$ and at the 1-fold site for $Pt_{23}(100)$. From the calculations of the steric interactions, we have found that pre-adsorbed oxygen modifies the surface so that CO is adsorbed on the one-fold site ordered in a $(\sqrt{2}{\times}{\sqrt}{2})R45^{\circ}$. Our results are in good agreement with recent experimental findings of Hong et al. [J.Phys. Chem. 1993, 97, 1258].

• Bulletin of the Korean Chemical Society
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• 제13권1호
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• pp.30-32
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• 1992

The apparent depth of space charge region on the ZnO $(10{\bar{1}}0)$ surface in chemisorption of oxygen has been estimated from the capacitance of two contacting faces. When the sample (donor concentration: $2.4{\times}10^{22}\;m^{-3}$) was evacuated at 773 K for 1 hr the depth reached to 40-100 ${\AA}$ depending on sample assembly. Admission of oxygen to the sample resulted in an increase of the depth to 3600 ${\AA}$ where the increment was greater at higher oxygen pressure between 6.6-1600 $N/m^2$. Admission of CO to the sample previously exposed to oxygen yields a decrease in the depth. The results of the measurement support that oxygen is adsorbed as an acceptor on ZnO $(10{\bar{1}}0)$.

• Journal of Ceramic Processing Research
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• 제20권1호
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• pp.18-23
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• 2019

Chemical looping combustion (CLC) is a promising carbon capture and storage (CCS) technology whose efficiency and cost primarily relies on the oxygen carrier materials used. In this paper, gadolinium-doped ceria (GDC, Ce0.9Gd0.1O1.95) was added as a promoter to improve the oxygen transfer rate of MgMnO3-δ oxygen carrier materials. Increasing GDC content significantly increased the oxygen transfer rate of MgMnO3-δ-GDC composites for the reduction reaction due to an increase in the surface adsorption of CH4 via oxygen vacancies formed on the surface of the GDC. On the other hand, the oxygen transfer rate for the oxidation reaction decreased linearly with increasing GDC content due to the oxygen storage ability of GDC. Adsorbed oxygen molecules preferentially insert themselves into oxygen vacancies of the GDC lattice rather than reacting with (Mg,Mn)O to form MgMnO3-δ during the oxidation reaction.

• Journal of Photoscience
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• 제9권2호
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• pp.403-405
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• 2002

To study photocatalytic mechanism of metal doped $Ti0_2$, we investigated photodecomposition effect, photocurrent effect and antibacterial effect. When aluminium content was 2 wt %, photodecomposition effect was better than the others. Silver doped thin films had high photocurrent efficiency and antibacterial effect. This reactions were caused by dissolved oxygen in solution and oxygen adsorbed on surface of thin films.