• 제목/요약/키워드: Oxidation State

검색결과 586건 처리시간 0.026초

산화공정을 통해 제작 된 전이금속산화물 박막의 저항변화 특성 연구

  • 성용헌;고대홍;김상연;도기훈;서동찬
    • 한국재료학회:학술대회논문집
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    • 한국재료학회 2009년도 추계학술발표대회
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    • pp.30.1-30.1
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    • 2009
  • 정보화가 급속히 진전됨에 따라 보다 많은 양의 정보를 전송, 처리, 저장하게 되면서 이를 위해 대용량, 고속, 비휘발성의 특징을 갖는 차세대 메모리의 개발이 절실히 요구되고있다. 이 중 저항 변화 메모리(ReRAM)는 일반적으로 TiO2, Al2O3, NiO2, HfO2, ZrO2 등의 전이금속산화물을 이용한 MIM 구조로서 적당한 전기 신호를 가하면 저항이 높아서 전도되지 않는 상태(Offstate)에서 저항이 낮아져 전도가 가능한 상태(On state)로 바뀌는 메모리 특성을가진다. ReRAM은 비휘발성 메모리이며 종래의 비휘발성 기억소자인 Flash memory 보다 access time 이105 배 이상 빠르고, 5V 이하의 낮은 전압에서도 동작이 가능하다. 또한 구조가 간단하여 공정 단순화가 가능하고 소자의 집적화도 쉽다는 점 등 많은 장점들이 있어서 Flash memory를 대체할 수 있는 유력한 후보로 여겨지고 있다. 본연구에서는 DC-magnetron Sputtering 방법으로 전이금속 박막을 증착하고, Dry furnace로 산화시켜 전이금속산화물 박막을 제작한 후 저항변화 특성을 연구하였다. 두 개의 전이금속산화물 박막을 dual-layer로 형성시켜 저항변화특성을 관찰하였으며 또한, 전이금속산화물 박막의 조성을 달리 하여 저항변화를 관찰 하였다. 전이금속산화물 박막의 전기적 특성을 알아보기 위해 Si(100) wafer 위에 Pt를 이용 MIM 형태로 capacitor 시편을 제작 하여, probe station으로 I-V 측정을 하였고 조성 및 표면 분석을 위해서는 AES와 AFM을, 미세구조를 분석을 위해서는 TEM과 SEM 을 사용하였다.

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Atomic layer chemical vapor deposition of Zr $O_2$-based dielectric films: Nanostructure and nanochemistry

  • Dey, S.K.
    • E2M - 전기 전자와 첨단 소재
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    • 제16권9호
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    • pp.64.2-65
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    • 2003
  • A 4 nm layer of ZrOx (targeted x-2) was deposited on an interfacial layer(IL) of native oxide (SiO, t∼1.2 nm) surface on 200 mm Si wafers by a manufacturable atomic layer chemical vapor deposition technique at 30$0^{\circ}C$. Some as-deposited layers were subjected to a post-deposition, rapid thermal annealing at $700^{\circ}C$ for 5 min in flowing oxygen at atmospheric pressure. The experimental x-ray diffraction, x-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, and high-resolution parallel electron energy loss spectroscopy results showed that a multiphase and heterogeneous structure evolved, which we call the Zr-O/IL/Si stack. The as-deposited Zr-O layer was amorphous $ZrO_2$-rich Zr silicate containing about 15% by volume of embedded $ZrO_2$ nanocrystals, which transformed to a glass nanoceramic (with over 90% by volume of predominantly tetragonal-$ZrO_2$(t-$ZrO_2$) and monoclinic-$ZrO_2$(m-$ZrO_2$) nanocrystals) upon annealing. The formation of disordered amorphous regions within some of the nanocrystals, as well as crystalline regions with defects, probably gave rise to lattice strains and deformations. The interfacial layer (IL) was partitioned into an upper Si $o_2$-rich Zr silicate and the lower $SiO_{x}$. The latter was sub-toichiometric and the average oxidation state increased from Si0.86$^{+}$ in $SiO_{0.43}$ (as-deposited) to Si1.32$^{+}$ in $SiO_{0.66}$ (annealed). This high oxygen deficiency in $SiO_{x}$ indicative of the low mobility of oxidizing specie in the Zr-O layer. The stacks were characterized for their dielectric properties in the Pt/{Zr-O/IL}/Si metal oxide-semiconductor capacitor(MOSCAP) configuration. The measured equivalent oxide thickness (EOT) was not consistent with the calculated EOT using a bilayer model of $ZrO_2$ and $SiO_2$, and the capacitance in accumulation (and therefore, EOT and kZr-O) was frequency dispersive, trends well documented in literature. This behavior is qualitatively explained in terms of the multi-layer nanostructure and nanochemistry that evolves.ves.ves.

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상황버섯 추출물의 항산화 효과 (Antioxidative Effects of Phellinus linteus Extract)

  • 류동영;김민석;민오진;김동욱
    • 한국자원식물학회지
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    • 제21권1호
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    • pp.91-95
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    • 2008
  • 본 연구에서는 ${O_2}^-,{\cdot}OH$ radical, NO, $ONOO^-$ 자유라디칼을 유발시키는 in vitro assay system과 free radical-induced oxidative stress에 의한 단백질 손상에 대한 진흙버섯속에 속하는 상황버섯 물 추출물의 항산화 효과를 측정하였다. 상황버섯 물 추출물의 ${O_2}^-,{\cdot}OH$ radical, NO, $ONOO^-$ 자유라디칼 억제효과에서는 실험에 사용된 양성 대조물 보다는 낮게 나타났으나 모든 실험계에서 대조군에 비해 뚜렷하게 자유라디칼 소거효과를 나타냈다. 또한 상황버섯 물 추출물은 산화적 스트레스에 의한 단백질 손상 억제효과에서도 대조군에 비해 명확한 저해효과를 나타냈다. 그러므로 상황버섯의 항산화 효과는 상황버섯의 약리학적 효능을 설명하는데 중요한 기초 자료라고 사료된다.

용융탄산염형 연료전지에서 과전압에 미치는 전극두께의 영향 (Effect of Anode Thickness on the Overpotential in a Molten Carbonate Fuel Cell)

  • 이충곤;이성윤;류보현;김도형;임희천
    • 전기화학회지
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    • 제13권1호
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    • pp.34-39
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    • 2010
  • 본 연구에서는 용융탄산염형 연료전지의 연료극 전극두께가 과전압에 미치는 영향을 $100\;cm^2$ 급 단위전지를 사용하여 검토하였다. 용융탄산염형 연료전지에서의 수소 산화속도는 충분히 빨라 전극면적이 성능에 크게 영향을 미치지 않을 수 있어, 본 연구에서는 전극의 기하학적 면적의 크기가 과 전압에 미치는 영향에 대해 연구하였다. 평가는 정상분극법과 비활성가스 계단형 첨가법 (ISA)와 반응물 첨가법 (RA)를 사용하여 연료극 두께 0.77 mm와 0.36 mm에 대해 수행하였다. 평가결과 두 전지에서 연료극 과전압이 거의 동일하게 관찰되어 연료극 두께에 의한 과전압의 차이는 발생하지 않았다.

레늄카보닐에 의한 고활성 메타세시스 촉매제조 및 그의 촉매작용 (Preparation of Highly Active Metathesis Catalyst from Rhenium Carbonyl and its Catalysis)

  • 안호근
    • 공업화학
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    • 제9권1호
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    • pp.115-120
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    • 1998
  • 메타세시스에 높은 활성을 나타내는 고분산 레늄촉매을 제조하기 위한 레늄카보닐 침착의 표면화학 및 활성점 생성에 관하여 연구하였다. 알루미나는 773K(PDA)와 1223K(DA)에서 각각 처리하여 담체로 사용하였고, 메타세시스 활성은 순수한 프로펜을 사용하여 상압하의 298K에서 조사하였다. PDA상의 레늄 산화가는 상당히 높았으나, DA에서는 저산화가의 레늄으로 담지되어 있었다. 제조한 Re/DA촉매를 고온에서 열분해시킨 다음 저온에서 산소로 처리하면 메타세시스 활성이 나타났고, 그 활성은 극히 낮은 담지율에서도 Re/PDA이나 통상의 $Re_2O_7/Al_2O_3$촉매에 비해 높은 활성을 보여, 레늄 카보닐을 출발물질로 하고 DA를 사용하는 것이 효과적이었다. 열분해하여 얻은 Re/DA촉매상의 레늄이온은 알루미나의 산소원자 2개와 결합하여 2가를 가지고, 산소처리에 의하여 4가만큼 증가한 6가의 레늄이온이 되며, 메타세시스는 그 6가이온에 의해 생성된 카르벤착체를 통하여 진행됨을 알았다.

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The Origin and Biogeochemistry of Organic Matter in Surface Sediments of Lake Shihwa and Lake Hwaong

  • Won, Eun-Ji;Cho, Hyen-Goo;Shin, Kyung-Hoon
    • Ocean Science Journal
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    • 제42권4호
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    • pp.223-230
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    • 2007
  • To understand the origin and biogeochemistry of the organic matter in surface sediments of Lake Shihwa and Lake Hwaong, organic nitrogen, inorganic nitrogen, labile organic carbon, and residual organic carbon contents as well as stable isotope ratios for carbon and nitrogen were determined by KOBr-KOH treatment. Ratios of organic carbon to organic nitrogen $(C_{org}/N_{org})$ (mean = 24) were much higher than ratios of organic carbon to total nitrogen $(C_{org}/N_{tot})$ (mean= 12), indicating the presence of significant amounts of inorganic nitrogen in the surface sediments of both lakes. Stable isotope ratios for organic nitrogen were, on average, $5.2\%_{\circ}$ heavier than ratios of inorganic nitrogen in Lake Shihwa, but those same ratios were comparable in Lake Hwaong. This might be due to differences in the origin or the degree of degradation of sedimentary organic matter between the two lakes. In addition, stable isotope ratios for labile organic carbon were, on average, $1.4\%_{\circ}$ heavier than those for residual organic carbon, reflecting the preferential oxidation of $^{13}C$-enriched organic matter. The present study demonstrates that KOBr-KOH treatment of sedimentary organic matter can provide valuable information for understanding the origin and degradation state of organic matter in marine and brackish sediments. This also suggests that the ratio of $(C_{org}/N_{org})$ and stable isotope ratios for organic nitrogen can be used as indexes of the degree of degradation of organic matter.

하수고도처리용 미세조류의 최적회수를 위한 전기응집기술 적용에 있어 전류의 영향 (Effects of electric current on electrocoagulation for optimal harvesting of microalgae for advanced wastewater treatment)

  • 이석민;주성진;최경진;장산;황선진
    • 상하수도학회지
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    • 제28권4호
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    • pp.473-478
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    • 2014
  • Microalgae is known as one alternative energy source of the fossil fuel with the small size of $5{\sim}50{\mu}m$ and negative charge. Currently, the cost of microalgae recovery process take a large part, about 20 - 30% of total operating cost. Thus, the microalgae recovery method with low cost is needed. In this study, the optimum current for Scenedesmus dimorphus recovery process using electrocoagulation techniques was investigated. Under the electrical current, Al metal in anode electrode is oxidized to oxidation state of $Al^{3+}$. In the cathode electrode, the water electrolysis generated $OH^-$ which combine with $Al^{3+}$ to produce $Al(OH)_3$. This hydroxide acts as a coagulant to harvest microalgae. Before applying in 1.5 L capacity electrocoagulation reactor, Scenedesmus dimorphus was cultured in 20 L cylindrical reactor to concentration of 1 OD. The microalgae recovery efficiency of electrocoagulation reactor was evaluated under different current conditions from 0.1 ~ 0.3 A. The results show that, the fastest and highest recovery efficiency were achieved at the current or 0.3 A, which the highest energy efficiency was achieved at 0.15 A.

하이드라진 방법에 의한 ZnO 미분말의 합성 및 에탄올 감응성 (Preparation of ZnO Powders by Hydrazine Method and Its Sensitivity to C2H5OH)

  • 김선중;이종흔
    • 한국재료학회지
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    • 제18권11호
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    • pp.628-633
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    • 2008
  • ZnO nanopowders were synthesized by the sol-gel method using hydrazine reduction, and their gas responses to 6 gases (200 ppm of $C_2H_5OH$, $CH_3COCH_3$, $H_2$, $C_3H_8$, 100 ppm of CO, and 5 ppm of $NO_2$) were measured at $300\;{\sim}\;400^{\circ}C$. The prepared ZnO nanopowders showed high gas responses to $C_2H_5OH$ and $CH_3COCH_3$ at $400^{\circ}C$. The sensing materials prepared at the compositions of [$ZnCl_2$]:[$N_2H_4$]:[NaOH] = 1:1:1 and 1:2:2 showed particularly high gas responses ($S\;=\;R_a/R_g,\;R_a$ : resistance in air, $R_g$ : resistance in gas) to 200 ppm of $C_2H_5OH$($S\;=\;102.8{\sim}160.7$) and 200 ppm of $CH_3COCH_3$($S\;= 72.6{\sim}166.2$), while they showed low gas responses to $H_2$, $C_3H_8$, CO, and $NO_2$. The reason for high sensitivity to these 2 gases was discussed in relation to the reaction mechanism, oxidation state, surface area, and particle morphology of the sensing materials.

수소-알코올연료전지를 위한 금속-산화물 나노구조제어 (Control of Metal-Oxide Nanostructures for $H_{2}-Alcohol$ Fuel Cells)

  • 박경원;송유정;한상범;이종민
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 춘계학술대회
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    • pp.141-145
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    • 2007
  • Due to their excellent catalytic activity with respect to methanol oxidation on platinum at low temperature, platinum nanosized catalysts have been a topic of great interest for use in direct methanol fuel cells (DMFCs). Since pure platinum is readily poisoned by CO, a by-product of methanol electrooxidation, and is extremely expensive, a number of efforts to design and characterize Pt-based alloy nanosized catalysts or Pt nanophase-support composites have been attempted in order to reduce or relieve the CO poisoning effect. In this review paper, we summarize these efforts based upon our recent research results. The Pt-based nanocatalysts were designed by chemical synthesis and thin-film technology, and were characterized by a variety of analyses. According to bifunctional mechanism, it was concluded that good alloy formation with $2^{nd}$ metal (e.g., Ru) as well as the metallic state and optimum portion of Ru element in the anode catalyst contribute to an enhanced catalytic activity for methanol electrooxidation. In addition, we found that the modified electronic properties of platinum in Pt alloy electrodes as well as the surface and bulk structure of Pt alloys with a proper composition could be attributed to a higher catalytic activity for methanol electooxdation. Proton conducting contribution of nanosized electrocatalysts should also be considered to be excellent in methanol electrooxidation (Spillover effect). Finally, we confirmed the ensemble effect, which combined all above effects, in Pt-based nanocatalsyts especially, such as PtRuRhNi and $PtRuWO_{3}$, contribute to an enhanced catalytic activity.

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Morphology-dependent Nanocatalysis: Rod-shaped Oxides

  • Shen, Wenjie
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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    • pp.130-131
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    • 2013
  • Nanostructured oxides are widely used in heterogeneous catalysis where their catalytic properties are closely associated with the size and morphology at nanometer level. The effect of particle size has been well decumented in the past two decades, but the shape of the nanoparticles has rarely been concerned. Here we illustrate that the redox and acidic-basic properties of oxides are largely dependent on their shapes by taking $Co_3O_4$, $Fe_2O_3$, $CeO_2$ and $La_2O_3$ nanorods as typical examples. The catalytic activities of these rod-shaped oxides are mainly governed by the nature of the exposed crystal planes. For instance, the predominant presence of {110} planes which are rich in active $Co^{3+}$ on $Co_3O_4$ nanorods led to a much higher activity for CO oxidation than the nanoparticles that mainly exposed the {111} planes. The simultaneous exposure of iron and oxygen ions on the surface of $Fe_2O_3$ nanorods have significantly enhanced the adsorption and activation of NO and thereby promoted the efficiency of DeNOx process. Moreover, the exposed surface planes of these rod-shaped oxides mediated the reaction performance of the integrated metal-oxide catalysts. Au/$CeO_2$ catalysts exhibited outstanding stability under water-gas shift conditions owing to the strong bonding of gold particle on the $CeO_2$ nanorods where the formed gold-ceria interface was resistant towards sintering. Cu nanoparticles dispersed on $La_2O_3$ nanorods efficiently catalyzed transfer dehydrogenation of primary aliphatic alcohols based on the uniue role of the exposed {110} planes on the support. Morphology control at nanometer level allows preferential exposure of the catalytically active sites, providing a new stragegy for the design of highly efficient nanostructured catalysts.

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