• 제목/요약/키워드: Electrocatalytic

검색결과 219건 처리시간 0.022초

고체산화물 연료전지의 페로브스카이트와 스피넬 구조를 갖는 Sm-Sr-(Co,Fe,Ni)-O 시스템의 공기극 특성 (Cathode Properties of Sm-Sr-(Co,Fe,Ni)-O System with Perovskite and Spinel Structures for Solid Oxide Fuel Cell)

  • 백승욱;김정현;백승환;배중면
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 춘계학술대회
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    • pp.133-136
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    • 2007
  • Perovskite-structured samarium strontium cobaltite (SSC), which is mixed ionic electronic conductor (MIEC), is considered as a promising cathode material for intermediate temperature-operating solid oxide fuel cell (SOFC) due to its high electrocatalytic property. Cathode material containing cobalt (Co) is unstable at high temperature and has a relatively high thermal expansion property. In this paper, Sm-Sr-(Co,Fe,Ni)-O system with perovskite and spinel structures was investigated in terms of electrochemical property and thermal expansion property, respectively. Area specific resistance (ASR) was measured by ac impedance spectroscopy to investigate the electrochemical property of cathode, and thermal expansion coefficient (TEC) was measured by using dilatometer. Micro structure of cathode was observed by scanning electron microscopy. Perovskite-structured $Sm_{0.5}Sr_{0.5}CoO_{3-\delta}$ showed the ASR of $0.87{\Omega}/cm^{2}$, and $Sm_{0.5}Sr_{0.5}NiO_{3-\delta}$, which actually has a spinel structure, showed the lowest TEC value of $13.3{\times}10^{-6}/K$.

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The Determination of Dopamine in the Presence of Ascorbic Acid at the Modified Glassy Carbon Electrode with Phytic Acid and Single-Walled Carbon Nanotubes

  • Bae, Si-Ra;Jeong, Hae-Sang;Jeon, Seung-Won
    • Bulletin of the Korean Chemical Society
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    • 제28권12호
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    • pp.2363-2368
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    • 2007
  • A glassy carbon electrode (GCE) modified with phytic acid (PA) and single-walled carbon nanotubes (SWNTs) were investigated by voltammetric methods in buffer solution. The PA-SWNTs/GCE-modified electrode demonstrated substantial enhancements in electrochemical sensitivity and selectivity towards dopamine (DA) in the presence of L-ascorbic acid (AA). The PA-SWNTs films promoted the electron transfer reaction of DA, while the PA film, acting as a negatively charged linker, combined with the positively charged DA to induced DA accumulation in the film at pH under 7.4. However, the PA film restrained the electrochemical response of the negatively charged AA due to the electrostatic repulsion. The anodic peak potentials of DA and AA could be separated by electrochemical techniques, and the interferences from AA were effectively eliminated in the DA determination. Linear calibration plots were obtained in the DA concentration range of 0.1-10 μM and the detection limit of the DA oxidation current was determined to be 0.06 μM at a signal-to-noise ratio of 3. The results indicated that the modified electrode is used to determine DA without interference from AA.

메탄올 산화 반응을 위한 PtNi과 PtRuNi 합금 촉매 (PtNi and PtRuNi Alloy catalysts for Methanol Electrooxidation)

  • 박경원;권부길;최종호;성영은
    • 한국전기화학회:학술대회논문집
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    • 한국전기화학회 2001년도 연료전지심포지움 2001논문집
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    • pp.37-42
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    • 2001
  • The electrooxidation of methanol was studied using Pt, PtNi(1.1 and 3:1), PtRuNi and PtRu(1:1) alloy nanoparticles in sulfuric acid solution for application to a direct methanol fuel cell. The PtNi and PtRuNi alloys showed excellent catalytic activities compared to those of pure Pt and PtRu. The role of Ni in the electrocatalytic activity was investigated using cyclic voltammetry (CV), chronoamperometry (CA), X-ray photoelectron spectroscopy (XPS). The XPS data confirm that the chemical states of Pt are exclusively metal as well as the presence of metallic Ni, NiO, $Ni(OH)_2$, NiOOH, metallic Ru, $RuO_2$, and $RuO_3$. Negative shifts of the binding energies of Pt for the PtNi alloy nanoparticles were determined by XPS measurements. This can be explained based by assuming that the enhanced activities of PtNi alloys for methanol electrooxidation were caused by the oxide states of Ni and by the change in the electronic structure of Pt component in the alloys.

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Electrodeposition of Some Selective Metals Belonging to Light, Refractory and Noble Metals from Ionic Liquid Electrolytes

  • Dilasari, Bonita;Kwon, Kyung-Jung;Lee, Churl-Kyoung;Kim, Han-Su
    • 전기화학회지
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    • 제15권3호
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    • pp.135-148
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    • 2012
  • Ionic liquids are steadily attracting interests throughout a recent decade and their application is expanding into various fields including electrochemistry due to their unique properties such as non-volatility, inflammability, low toxicity, good ionic conductivity, wide electrochemical potential window and so on. These features make ionic liquids become an alternative solution for electrodeposition of metals that cannot be electroplated in aqueous electrolytes. In this review, we classify investigated metals into three categories, which are light (Li, Mg), refractory (Ti, Ta) and noble (Pd, Pt, Au) metals, rather than covering the exhaustive list of metals and try to update the recent development in this area. In electrodeposition of light metals, granular fine Li particles were successfully obtained while the passivation of electrodeposited Mg layers is an obstacle to reversible deposition-dissolution process of Mg. In the case of refractory metals, the quality of Ta and Ti deposit particles was effectively improved with addition of LiF and pyrrole, respectively. In noble metal category, EMIM TFSA ionic liquid as an electrolyte for Au electrodeposition was proven to be effective and BMP TFSA ionic liquid developed a smooth Pd deposit. Pt nanoparticle production from ionic liquid droplet in aqueous solution can be cost-effective and display an excellent electrocatalytic activity.

Enhanced Electrocatalytic Activity of Low Ni Content Nano Structured NiPd Electrocatalysts Prepared by Electrodeposition Method for Borohydride Oxidation

  • Zolfaghari, Mahdieh;Arab, Ali;Asghari, Alireza
    • Journal of Electrochemical Science and Technology
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    • 제11권3호
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    • pp.238-247
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    • 2020
  • Some nano structured bimetallic NiPd electrocatalysts were electrodeposited on glassy carbon electrodes using a double potential step chronoamperometry. The morphology of the electrodeposited samples was investigated by field emission-scanning electron microscopy, while their compositions were evaluated using energy dispersive X-ray spectroscopy. It was observed that the electrodeposited samples contained a low Ni content, in the range of 0.80 - 7.10%. The electrodeposited samples were employed as the anode electro-catalysts for the oxidation of sodium borohydride in NaOH solution (1.0 M) using cyclic voltammetry, chronoamperometry, rotating disk electrode, and impedance spectroscopy. The number of exchanged electrons, charge transfer resistances, apparent rate constants, and double layer capacitances were calculated for the oxidation of borohydride on the prepared catalysts. According to the results obtained, the NiPd-2 sample with the lowest Ni content (0.80%), presented the highest catalytic activity for borohydride oxidation compared with the other NiPd samples as well as the pure Pd sample. The anodic peak current density was obtained to be about 1.3 times higher on the NiPd-2 sample compared with that for the Pd sample.

다양한 온도에서 합성한 전기방사 LaCoO3 페롭스카이트 나노섬유의 알칼리용액에서 산소환원 및 발생반응에 대한 전기화학 특성 (Electrochemical Characterization of Electrospun LaCoO3 Perovskite Nanofibers Prepared at Different Temperature for Oxygen Reduction and Evolution in Alkaline Solution)

  • 로페즈 카린;선호정;박경세;엄승욱;심중표
    • 한국수소및신에너지학회논문집
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    • 제26권2호
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    • pp.148-155
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    • 2015
  • Electrospun $LaCoO_3$ perovskite nanofibers were produced for the air electrode in Zn-air rechargeable batteries using electrospinning technique with sequential calcination. The final calcination temperature was varied from 500 to $800^{\circ}C$ in order to determine its effect on the physical and electrochemical properties of the prepared $LaCoO_3$ perovskite nanofibers. The surface area of the electrospun $LaCoO_3$ perovskite nanofibers were observed to decrease with increasing final calcination temperature. Electrospun $LaCoO_3$ perovskite nanofibers calcined with final calcination temperature of $700^{\circ}C$ had the best electrocatalytic activity among the prepared perovskite nanofibers.

Simple Electrochemical Immunosensor for the Determination of Rabbit IgG Using Osmium Redox Polymer Films

  • Choi, Young-Bong;Lee, Seung-Hwa;Tae, Gun-Sik
    • 전기화학회지
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    • 제10권3호
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    • pp.229-232
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    • 2007
  • An amperometric immunosensor for the determination of rabbit IgG is proposed. The immunoassay utilizes a screen-printed carbon electrode on which osmium redox polymer is electrodeposited. This immunoassay detects 0.1 ng/ml of rabbit IgG, which is ${\sim}10^2$ fold higher than the most sensitive enzyme amplified amperometric immunoassay. The assay utilizes a screen-printed carbon electrode which was pre-coated by a co-electrodeposited film of an electron conducting redox hydrogel and a rabbit IgG. The rabbit IgG in the electron conducting film conjugates captures, when present, the anti-rabbit IgG. The captured anti-rabbit-IgG is labeled with horseradish peroxidase (HRP) which catalyzes the two-electron reduction of $H_2O_2$ to water. Because the redox hydrogel electrically connects HRP reaction centers to the electrode, completion of the sandwich converts the film from non-electrocatalytic to electro-catalytic for the reduction of $H_2O_2$ to $H_2O$ when the electrode is poised at 200 mV vs. Ag/AgCl.

Simultaneous Determination of Ranitidine and Metronidazole at Poly(thionine) Modified Anodized Glassy Carbon Electrode

  • Rahman, Md. Mahbubur;Li, Xiao-Bo;Jeon, Young-Deok;Lee, Ho-Joon;Lee, Soo Jae;Lee, Jae-Joon
    • Journal of Electrochemical Science and Technology
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    • 제3권2호
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    • pp.90-94
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    • 2012
  • A simple and sensitive electrochemical sensor for simultaneous and quantitative detection of ranitidine (RT) and metronidazole (MT) was developed, based on a poly(thionine)-modified anodized glassy carbon electrode (PTH/GCE). The modified electrode showed the excellent electrocatalytic activity towards the reduction of both RT and MT in 0.1M phosphate buffer solution (PBS, pH 7.0). The peak-to-peak separations (${\Delta}E_p$) for the simultaneous detection of RT and MT between the two reduction waves in CV and DPV were increased significantly from ca. 100 mV at anodized GCE, to ca. 550 mV at the PTH/GCE. The reduction peak currents of RT and MT were linear over the range from 35 to $500{\mu}M$ in the presence of 200 and $150{\mu}M$ of RT and MT, respectively. The sensor showed the sensitivity of 0.58 and $0.78{\mu}A/cm^2/{\mu}M$ with the detection limits (S/N = 3) of 1.5 and $0.96{\mu}M$, respectively for RT and MT.

Voltammetric Determination of Droxidopa in the Presence of Tryptophan Using a Nanostructured Base Electrochemical Sensor

  • Yaghoubian, Halimeh;Jahani, Shohreh;Beitollahi, Hadi;tajik, Somayeh;Hosseinzadeh, Rahman;Biparva, Pouria
    • Journal of Electrochemical Science and Technology
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    • 제9권2호
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    • pp.109-117
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    • 2018
  • A novel carbon paste electrode modified with $Cu-TiO_2$ nanocomposite, 2-(ferrocenylethynyl)fluoren-9-one (2FF) and ionic liquid (IL) (2FF/$Cu-TiO_2$/IL/CPE) was fabricated and employed to study the electrocatalytic oxidation of droxidopa, using cyclic voltammetry (CV), chronoamperometry (CHA) and differential pulse voltammetry (DPV) as diagnostic techniques. It has been found that the oxidation of droxidopa at the surface of modified electrode occurs at a potential of about 295 mV less positive than that of an unmodified CPE. DPV exhibits a linear dynamic range from $5.0{\times}10^{-8}$ to $4.0{\times}10^{-4}M$ and a detection limit of 30.0 nM for droxidopa. Finally this modified electrode was used for simultaneous determination of droxidopa and tryptophan. Also the 2FF/$Cu-TiO_2$/IL/CPE shows excellent ability to determination of droxidopa and tryptophan in real samples.

도파민으로 수식된 SAMs 전극에서 NADH의 전기촉매에 의한 산화 (Electrocatalytic Oxidation of NADH at Electrodes of Self-assembled Monolayers Modified with Dopamine)

  • 차성극
    • 대한화학회지
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    • 제48권2호
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    • pp.151-155
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    • 2004
  • 금 전극 표면을 시스테인으로 수식한 자기조립 단층막(self-assembled monolayers; SAMs)을 만들고 이를 퀴논 작용기를 갖고 있는 도파민과 반응시킨 수식전극을 제작하였다. 이 전극을 에탄올 내에서 6시간 정도 정치하면 SAMs가 잘 정돈 되어서 보다 개선된 형태의 순환전압전류법(cyclic voltammetry; CV)의 결과를 얻게 되었다. 그 결과 SAMs 말단에 o-퀴논의 산화-환원특성은 0.1 M 인산염 완충용액(pH=7.10)에서 형식전위 값이 0.28 V이고 피크 전위차이가 없는 가역성이 뛰어난 전극이 제작되었다. 이 전극으로 NADH의 정량을 위한 검정선을 제작하였으며, 5.0 ${\times}\;10^{-4}$ M농도까지 정량이 가능한 0.993의 뛰어난 상관관계를 보였다.