• 제목/요약/키워드: Electrochemical Efficiency

검색결과 685건 처리시간 0.022초

리튬이차전지 음극용 석유계 피치로 코팅된 천연 흑연의 전기화학적 특성 (Electrochemical Properties of Natural Graphite coated with PFO-based Pitch for Lithium-ion Battery Anode)

  • 김근중;조윤지;이종대
    • Korean Chemical Engineering Research
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    • 제57권5호
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    • pp.672-678
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    • 2019
  • 리튬이차전지용 음극재로서 피치로 코팅된 천연흑연의 전기화학적 특성이 조사되었다. 천연흑연과 피치의 혼합물을 $1000^{\circ}C$에서 소성하여 음극재를 제조하였다. 다양한 연화점의 피치가 탄소전구체로 사용되었다. 제조된 음극재의 물리적 특성은 TGA, SEM, PSA 및 BET로 분석하였다. 피치의 연화점이 증가할수록 코팅 층의 두께가 증가하였고, 비표면적이 감소하였다. 초기 충 방전 효율, 사이클, 순환전압전류, 속도 특성 및 임피던스 테스트를 통해 전기화학적 성능을 조사하였다. 연화점 $250^{\circ}C$의 피치로 탄소 코팅된 천연흑연은 초기 방전용량 361 mAh/g과 쿨롱 효율 92.6%을 보였다. 또한 출력 특성(5 C/0.2 C)은 코팅되지 않은 천연흑연에 비해 1.6배 향상되었으며, 0.5 C로 진행된 사이클 테스트에서 50 사이클 후 90%의 용량 유지율을 나타내었다.

Combined Effect of Catholyte Gap and Cell Voltage on Syngas Ratio in Continuous CO2/H2O Co-electrolysis

  • Ha, Min Gwan;Na, Youngseung;Park, Hee Young;Kim, Hyoung-Juhn;Song, Juhun;Yoo, Sung Jong;Kim, Yong-Tae;Park, Hyun S.;Jang, Jong Hyun
    • Journal of Electrochemical Science and Technology
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    • 제12권4호
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    • pp.406-414
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    • 2021
  • Electrochemical devices are constructed for continuous syngas (CO + H2) production with controlled selectivity between CO2 and proton reduction reactions. The ratio of CO to H2, or the faradaic efficiency toward CO generation, was mechanically manipulated by adjusting the space volume between the cathode and the polymer gas separator in the device. In particular, the area added between the cathode and the ion-conducting polymer using 0.5 M KHCO3 catholyte regulated the solution acidity and proton reduction kinetics in the flow cell. The faradaic efficiency of CO production was controlled as a function of the distance between the polymer separator and cathode in addition to that manipulated by the electrode potential. Further, the electrochemical CO2 reduction device using Au NPs presented a stable operation for more than 23 h at different H2:CO production levels, demonstrating the functional stability of the flow cell utilizing the mechanical variable as an important operational factor.

Corrosion Inhibition Performance of Two Ketene Dithioacetal Derivatives for Stainless Steel in Hydrochloric Acid Solution

  • Lemallem, Salah Eddine;Fiala, Abdelali;Ladouani, Hayet Brahim;Allal, Hamza
    • Journal of Electrochemical Science and Technology
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    • 제13권2호
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    • pp.237-253
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    • 2022
  • The methyl 2-(1,3-dithietan -2- ylidene)-3-oxobutanoate (MDYO) and 2-(1,3-dithietan-2-ylidene) cyclohexane -1,3-dione (DYCD) were synthesized and tested at various concentrations as corrosion inhibitors for 316L stainless steel in 1 M HCl using weight loss, electrochemical impedance spectroscopy (EIS), potentiodynamic polarization (PDP), surface analysis techniques (SEM / EDX and Raman spectroscopy) and Functional Density Theory (DFT) was also used to calculate quantum parameters. The obtained results indicated that the inhibition efficiency of MDYO and DYCD increases with their concentration, and the highest value of corrosion inhibition efficiency was determined in the range of concentrations investigated (0.01 × 10-3 - 10-3 M). Polarization curves (Tafel extrapolation) showed that both compounds act as mixed-type inhibitors in 1M HCl solutions. Electrochemical impedance spectra (Nyquist plots) are characterized by a capacitive loop observed at high frequencies, and another small inductive loop near low frequencies. The thermodynamic data of adsorption of the two compounds on the stainless steel surface and the activation energies were determined and then discussed. Analysis of experimental results shows that MDYO and DYCD inhibitors adsorb to the metal surface according to the Langmuir model and the mechanism of adsorption of both inhibitors involves physisorption. SEM-EDX results confirm the existence of an inhibitor protective film on the stainless steel surface. The results derived from theoretical calculations supported the experimental observation.

Effects of Ag and Cu Additions on the Electrochemical Migration Susceptibility of Pb-free Solders in Na2SO4 Solution

  • Yoo, Y.R.;Nam, H.S.;Jung, J.Y.;Lee, S.B.;Park, Y.B.;Joo, Y.C.;Kim, Y.S.
    • Corrosion Science and Technology
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    • 제6권2호
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    • pp.50-55
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    • 2007
  • The smaller size and higher integration of advanced electronic package systems result in severe electrochemical reliability issues in microelectronic packaging due to higher electric field under high temperature and humidity conditions. Under these harsh conditions, electronic components respond to applied voltages by electrochemical ionization of metal and the formation of a filament, which leads to short-circuit failure of an electronic component, which is termed electrochemical migration. This work aims to evaluate electrochemical migration susceptibility of the pure Sn, Sn-3.5Ag, Sn-3.0Ag-0.5Cu solder alloys in $Na_{2}SO_{4}$. The water drop test was performed to understand the failure mechanism in a pad patterned solder alloy. The polarization test and anodic dissolution test were performed, and ionic species and concentration were analyzed. Ag and Cu additions increased the time to failure of Pb-free solder in 0.001 wt% $Na_{2}SO_{4}$ solution at room temperature and the dendrite was mainly composed of Sn regardless of the solders. In the case of SnAg solders, when Ag and Cu added to the solders, Ag and Cu improved the passivation behavior and pitting corrosion resistance and formed inert intermetallic compounds and thus the dissolution of Ag and Cu was suppressed; only Sn was dissolved. If ionic species is mainly Sn ion, dissolution content than cathodic deposition efficiency will affect the composition of the dendrite. Therefore, Ag and Cu additions improve the electrochemical migration resistance of SnAg and SnAgCu solders.

Co(III)/Co(II) 및 Fe(III)/Fe(II) 산화환원계에 의한 에텔렌글리콜의 연속 매개전해 산화 (Continuous Mediated Electrochemical Oxidation of Ethylene Glycol by Co(III)/Co(II) and Fe(III)/Fe(II) Redox Systems)

  • 김익성;박승조
    • 공업화학
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    • 제16권5호
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    • pp.635-640
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    • 2005
  • 매개전해산화는 저온과 저압 분위기에서 수용액 중에 존재하는 유기물을 전기화학적으로 산화하는 과정이다. 이 공정은 유해 유기물을 함유한 폐물처리에 사용할 수 있는 좋은 공법중의 하나이다. 이 논문은 Fe(III)/Fe(II)나 Co(III)/Co(II) 산화환원계를 이용하여 질산용액 중에서 에틸렌글리콜의 매개전해 산화에 관한 연구를 하였다. 이 논문에서는 에틸렌글리콜을 매개전해 산화시 전류밀도, 지지전해질 농도, 체류시간, 제거효율 등을 검토하였다. 매개전해산화시 에틸렌글리콜의 제거효율은 Fe(III)/Fe(II) 산화환원계보다 Co(III)/Co(II) 산화환원계가 우수하였고 매개전해산화 제거효율은 100%이었다. 에틸렌글리콜을 시료로 하였을 경우 좋은 수율로 탄산가스가 생성됨을 관찰할 수 있었다.

Synthesis and Electrochemical Properties of Li3V2(PO4)3-LiMnPO4 Composite Cathode Material for Lithium-ion Batteries

  • Yun, Jin-Shik;Kim, Soo;Cho, Byung-Won;Lee, Kwan-Young;Chung, Kyung Yoon;Chang, Wonyoung
    • Bulletin of the Korean Chemical Society
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    • 제34권2호
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    • pp.433-436
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    • 2013
  • Carbon-coated $Li_3V_2(PO_4)_3-LiMnPO_4$ composite cathode materials are first reported in this work, prepared by the mechanochemical process with a complex metal oxide as the precursor and sucrose as the carbon source. X-ray diffraction pattern of the composite material indicates that both olivine $LiMnPO_4$ and monoclinic $Li_3V_2(PO_4)_3$ co-exist. We further investigated the electrochemical properties of our $Li_3V_2(PO_4)_3-LiMnPO_4$ composite cathode materials using galvanostatic charging/discharging tests, where our $Li_3V_2(PO_4)_3-LiMnPO_4$ composite electrode materials exhibit the charge/discharge efficiency of 91.9%, while $Li_3V_2(PO_4)_3$ and $LiMnPO_4$ exhibit the efficiency of 87.7 and 86.7% in the first cycle. The composites display unique electrochemical performances in terms of overvoltage and cycle stability, displaying a reduced gap of 141.6 mV between charge and discharge voltage and 95.0% capacity efficiency after $15^{th}$ cycles.

Studying Thermochemical Conversion of Sm2O3 to SmCl3 using AlCl3 in LiCl-KCl Eutectic Melt

  • Samanta, Nibedita;Chandra, Manish;Maji, S.;Venkatesh, P.;Annapoorani, S.;Jain, Ashish
    • Journal of Electrochemical Science and Technology
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    • 제13권2호
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    • pp.279-291
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    • 2022
  • In this report the thermochemical conversion of Sm2O3 to SmCl3 using AlCl3 in LiCl-KCl melt at 773 K is discussed. The final product was a mixture of SmCl3, Al2O3, unreacted Sm2O3 and AlCl3 in the chloride melt. The electrochemical attributes of the mixture was analyzed with cyclic voltammetry (CV) and square wave voltammetry (SWV). The crystallographic phases of the mixture were studied with X-ray diffraction (XRD) technique. The major chemical conversion was optimized by varying the effective parameters, such as concentrations of AlCl3, duration of reaction and the amount of LiCl-KCl salt. The extent of conversion and qualitative assessment of efficiency of the present protocol were evaluated with fluorescence spectroscopy, UV-Vis spectrophotometry and inductively coupled plasma atomic emission spectroscopy (ICP-AES) studies of the mixture. Thus, a critical assessment of the thermochemical conversion efficiency was accomplished by analysing the amount of SmCl3 in LiCl-KCl melt. In the process, a conversion efficiency of 95% was achieved by doubling the stoichiometric requirement of AlCl3 in 50 g of LiCl-KCl salt. The conversion reaction was found to be very fast as the reaction reached equilibrium in 15 min.

Lornoxicam & Tenoxicam Drugs as Green Corrosion Inhibitors for Carbon Steel in 1 M H2SO4 Solution

  • Fouda, A.S.;El-Defrawy, A.M.;El-Sherbeni, M.W.
    • Journal of Electrochemical Science and Technology
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    • 제4권2호
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    • pp.47-56
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    • 2013
  • Inhibition performance of Lornoxicam & Tenoxicam against corrosion of carbon steel in 1M $H_2SO_4$ solutions was investigated by weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) measurements. The inhibition efficiency increased with increasing inhibitor's concentration, but decreased with increase in temperature. Potentiodynamic polarization curves showed that, the inhibitors were of mixed type. The apparent activation energy ($E^*_a$) and other thermodynamic parameters for the corrosion process have also been calculated and discussed. The inhibition of carbon steel corrosion is due to the adsorption of the inhibitor molecules on the surface, which follows Temkin adsorption isotherm. The mechanism of inhibition was discussed in the light of the chemical structure of the undertaken inhibitors.

Electrochemical Properties of Carbon Composites Prepared by Using Graphite Ball-milled in Argon and Air Atmosphere

  • Lee, Kyoung-Muk;Oh, Seh-Min;Lee, Sung-Man
    • Bulletin of the Korean Chemical Society
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    • 제29권6호
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    • pp.1121-1124
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    • 2008
  • A carbon composite was synthesized by mechanical mixing of ball-milled graphite and PVC powders, followed by pyrolysis reaction of PVC. Natural graphite ball milled under atmosphere of argon or air leads to a disordered structure. It appears that the electrochemical lithium intercalation reaction is dependent on the atmosphere in which the graphite is ball milled. The carbon composite obtained using air-milled graphite shows a high reversible capacity and high initial coulombic efficiency compared to argon-milled graphite. This is attributed to the enhanced thermal stability of a disordered structure in the air milled sample. For the one with air-milled graphite, the disordered structure is maintained during heat treatment, while argon-milled graphite is partially crystallized.

COD Removal of Rhodamine B from Aqueous Solution by Electrochemical Treatment

  • Kim, Dong-Seog;Park, Young-Seek
    • 한국환경과학회지
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    • 제21권6호
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    • pp.655-659
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    • 2012
  • This study elucidates the COD removal of dye (Rhodamine B) through electrochemical reaction. Effects of current density (7.2 to 43.3 $mA/cm^2$), electrolyte type (NaCl, KCl, $Na_2SO_4$, HCl), electrolyte concentration (0.5 to 2.0 g/L), air flow rate (0 to 4 L/min) and pH (3 to 11) on the COD removal of Rhodamine B were investigated. The observed results showed that the increase of pH decrease the COD removal efficiency. Whereas, the increase of current density;NaCl concentration and air flow rate caused the increase of the COD removal of Rhodamine B.