• Proceedings of the Materials Research Society of Korea Conference
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• 2011.05a
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• pp.29.1-29.1
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• 2011

ReRAM은 metal-oxide-metal구조로 차세대 비활성 메모리를 대체하기 위하여 연구되어왔다. ReRAM은 낮은 전력 소모와 다른 두 저항상태 사이의 높은 scalability를 갖는 장점이 있지만 높은 reset전류와 일정하지 않은 저항 값을 갖고 있어 실용화에 어려움을 겪고 있다. 저항변화현상의 메커니즘은 일반적으로 일정 전압이 가해 졌을 때, MIM 구조의 산화물 내에서 필라멘트가 형성되었다 파괴되는 것으로 알려져 있다. 저항스위칭 메모리의 작동능력을 증진시키기 위해서는, oxide층의 두께조절, 산화층과 electrode 사이의 계면 특성 연구가 필요하다. 본 연구에서는, 전기화학증착법을 이용하여 Au-NiO-Au segmented 나노와이어 구조를 만들었다. 전기화학증착 방법을 이용하면 에칭 손상없이 간단하게 나노 구조체를 형성 할 수 있고, 나노 사이즈로 제작된 산화층이 전도성 필라멘트가 형성되는 영역을 제한하여 reset전류를 줄일 수 있는 장점이 있다. 또한 열처리 과정에서 Au가 NiO부분에 diffusion되는 현상을 이용하여 doping에 따른 switching 변화 특성도 관찰하였다.

• Journal of the Korean Institute of Telematics and Electronics D
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• v.34D no.4
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• pp.47-53
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• 1997

We fabricated gamma radiation detector using high resistive p-Cd$_{80}$Zn$_{20}$Te grown by high pressure bridgman method and forming au thin film electrode by chemically electroless deposition method. The device of Au/Cd$_{80}$Zn$_{20}$Te/Au is a typical MIM structure. The characteristic of current-voltage showed good linearity to 3kV/cm but it depend on the square of electric field over 3kV/cm. As the results of rutherford backscattering spectroscope(RBS) and auger spectroscope on the Au/Cd$_{80}$Zn$_{20}$Te, Au penetrated to the surface of Cd$_{80}$Zn$_{20}$Te detector absorbed slightly high energy radiation like a few hundred keV and showed good performance to detect low energy gamma ray.mma ray.

• Proceedings of the Korean Vacuum Society Conference
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• 1999.07a
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• pp.110-110
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• 1999

Polyvinylidenefluoride (PVDF) is most used in piezoelectric polymer industry. Electrode effect on the electrical properties of PVDF has been investigated. al has been used due to fair adhesion for PVDF. Work function of metal plays an important role on the electrical properties of ferroelectrics for top and /or bottom electrode. However, Al has much lower work function than Pt or Au and so leakage current of Al/PVDF/Al may be large. Pt or Au has not been used for electrode of PVDF system due to poor adhesion. PVDF irradiated by Ar+ ion beam with O2 environment takes good adhesion to inert metal. Contact angle of PVDF to triple distilled water was reduced from 75$^{\circ}$ to 31$^{\circ}$ at 1$\times$1015 Ar+/cm2. Working pressure was 2.3$\times$10-4 Torr and base pressure was 5$\times$10-6 Torr. Pt was deposited by ion beam sputtering and thickness of pt film was about 1000$\AA$. in previous study, enhancing adhesion of Pt on PVDF was shown. in this study, effect of electrode on PVDF will be represented.

• Bulletin of the Korean Chemical Society
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• v.31 no.1
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• pp.104-111
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• 2010

The heterogeneous electron transfer at $SiMo_{12}O_{40}^{4-}$ monolayers on GC, HOPG, and Au electrode surfaces are investigated using cyclic voltammetric and electrochemical impedance spectroscopic (EIS) methods. The electron transfer of negatively charged $Fe(CN)_6^{3-}$ species is retarded at $SiMo_{12}O_{40}^{4-}$-modified electrode surfaces, while that of positively charged $Ru(NH_3)_6^{3+}$species is accelerated at the modified surfaces. This is due to the electrostatic interactions between $SiMo_{12}O_{40}^{4-}$ layers on surfaces and charged redox species. The electron transfer kinetics of a neutral redox species, 1,1‘-ferrocenedimethanol (FDM), is not affected by the modification of electrode surfaces with $SiMo_{12}O_{40}^{4-}$, indicating the $SiMo_{12}O_{40}^{4-}$ monolayers do not impart barriers to electron transfer of neutral redox species. This is different from the case of thiolate SAMs which always add barriers to electron transfer. The effect of $SiMo_{12}O_{40}^{4-}$ layers on the electron transfer of charged redox species is dependent on the kind of electrodes, where HOPG surfaces exhibit marked effects. Possible mechanisms responsible for different electron transfer behaviors at $SiMo_{12}O_{40}^{4-}$ layers are proposed.

• Journal of Electrochemical Science and Technology
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• v.1 no.1
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• pp.10-18
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• 2010

Controlled electrodeposition of dendritic nano-structured gold-platinum (AuPt) alloy onto an electrochemically pretreated carbon paper substrate was conducted in an attempt to improve catalyst utilization and to secure an electronic percolation network toward formic acid (FA) fuel cell application. The AuPt catalysts were obtained by potentiostatic deposition. AuPt catalysts synthesized as bimetallic alloys with 60% Au content exhibited the highest catalytic activity towards formic acid electro-oxidation. The origin of this high activity and the role of Au were evaluated, in particular, by XPS analysis. Polarization and stability measurements with 1 mg $cm^{-2}$ AuPt catalyst (only 0.4 mg $cm^{-2}$ Pt) showed 52 mW $cm^{-2}$ and sustainable performance using 3M formic acid and dry air at $40^{\circ}C$.

• Journal of the Korean Electrochemical Society
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• v.18 no.3
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• pp.107-114
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• 2015

Electrochemical fabrication of nanostructured Au surfaces has received increased attention. In the present work, electrochemical modification of Au surfaces for fabricating nanostructured Au surfaces in the absence of externally added precursors is presented, which is different to the previous methods utilizing electrochemical deposition of externally added precursors. Application of anodic potential at Au surfaces in phosphate buffers containing $Br^-$ resulted in the anodic dissolution of Au, which produced Au precursors at the electrode surfaces. The resulting Au precursors were further reduced at the surface to produce nanostructured Au structures. The effects of applied potential and time on the morphology of Au nanostructures were systematically examined, from which a unique backbone type Au nanostructures was produced. The backbone type Au nanostructures exhibited high surface-enhanced Raman activity. The present work would give insights into the formation of electrochemical fabrication of nanostructured Au surfaces.

• Bulletin of the Korean Chemical Society
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• v.27 no.3
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• pp.403-406
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• 2006

The surface structure and electrochemical behavior of self-assembled monolayers (SAMs) formed by aromatic thiols on Au(111) were investigated by scanning tunneling microscopy (STM) and cyclic voltammetry. Benzenethiol (BT) forms disordered phases on Au(111) which are composed of many bright domains, while benzyl mercaptan (BM), with a methylene unit between the aromatic group and sulfur atom, forms twodimensional ordered SAMs on Au(111). In addition, two phase-separated domains consisting of disordered and ordered phases were observed in binary SAMs formed from a 1 : 1 mixed ethanol solution of BT and BM. From STM and CV measurements, we found that the blocking efficiency of aromatic thiol SAMs coated on an Au(111) electrode for an electron transfer reaction decreases as the structural order of the SAMs increases. Molecular-scale STM and CV results obtained here will be very useful in designing functional SAMs for further applications, such as the improvement of corrosion passivation of Au(111) on an aromatic thiolmodified Au(111) surface.

• Proceedings of the KIEE Conference
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• 2009.07a
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• pp.1539_1540
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• 2009

본 논문에서는 Porous Au-Pt 전극을 기반으로 연료전극과 공기전극으로 구성된 초소형 메탄올 센서를 설계 및 제작하고 그 특성을 분석해 보았다. 제안된 Porous Au-Pt 전극은 Porous 구조의 금속을 만드는 방법 중 하나인 Templating기법을 적용하여 수백나노 크기의 Pore들을 가진 Porous Au 전극을 제작하였고 그 위에 수 나노 크기의 Pt particles을 전해 도금하여 제작되었다. 고분자 전해질막 층으로서 Nafion film은 전해 도금한 Porous Au-Pt 전극 사이에 삽입하고 hot Pressing 통하여 센서를 구성하였다. Porous Au-Pt 전극을 기반으로한 전기화학 메탄올 센서는 $0.25\;cm^2$ 의 작은 전극 면적에도 불구하고 넓은 온도 범위 ($20^{\circ}C-100^{\circ}C$) 에서 온도에 따른 뛰어난 선형성(Correlation coefficient = 0.986)을 보였으며, 특히, 일정온도 ($60^{\circ}C$)에서 메탄올 농도 0 M에서 2 M 까지의 전류응답 특성을 측정, 분석 결과 메탄올 농도에 따른 9.6 mA/$mM{\cdot}cm^2$ 의 민감도 및 10 초 이내의 응답시간 특성을 보였다.

• Bulletin of the Korean Chemical Society
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• v.35 no.7
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• pp.2072-2076
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• 2014

Sub-micrometer size gold particles were electrodeposited on a transparent fluorine-doped tin oxide (FTO) from acetonitrile solution containing $AuCl_4{^-}$ and tetramethylammonium tetraflouroborate (TMATFB) for detecting $NO_2{^-}$. A series of two-electron ($2e^-$) and one-electron ($1e^-$) reductions of the $AuCl_4{^-}-AuCl_2{^-}-Au$ redox systems were observed at FTO and a highly stable and homogeneous distribution of Au on FTO (Au/FTO) was obtained by stepping the potential from 0 to -0.55 V (vs. Ag/$Ag^+$). The Au/FTO electrode exhibited sufficiently high catalytic activity toward the oxidation of $NO_2{^-}$ with a detection limit (S/N = 3) and sensitivity of 2.95 ${\mu}M$ and 223.4 ${\mu}A{\cdot}cm^{-2}{\cdot}mM^{-1}$, respectively, under optimal conditions. It exhibited an interference-free signal for $NO_2{^-}$ detection with excellent recoveries from real samples.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2016.11a
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• pp.183.1-183.1
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• 2016

Due to the latest research trend toward wearable energy devices, transparent and stretchable supercapacitors which can sustain their performance even under physical deformation have steadily attracted huge attention. Despite the Ag NW is the most promising candidate for fabrication of transparent and stretchable electronics, the electrochemical instability interrupts its application to development of the energy device. Here, we introduce a transparent and highly stretchable supercapacitor made by Au-Ag core shell NW network percolation electrode. The Au-Ag core shell NW synthesized by a simple solution process not only shows excellent electrical conductivity but also greatly enhanced chemical and electrochemical stability compare to pristine Ag NW. These outstanding properties of the Au-Ag core shell NW are attributed both to the core Ag NW and the Au protecting sheath layer. The proposed Au-Ag core shell NW based supercapacitor exhibits optical transmittance with outstanding mechanical stability withstanding 60% strain without any decrease of the performance. The supercapacitors connected in series are charged and discharged stable in 30% strain turning on a red LED. These notable results demonstrate the potential of the Au-Ag core shell NW as a strong candidate for development of wearable energy devices.