• 제목/요약/키워드: Solid-State Electrolyte

검색결과 204건 처리시간 0.029초

Resistive Switching Characteristics of Ag Doped Ge0.5Se0.5 Solid Electrolyte

  • Kim, Jang-Han;Nam, Ki-Hyun;Chung, Hong-Bay
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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    • pp.478-478
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    • 2013
  • Resistance-change Random Access Memory (ReRAM) memory, which utilizes electrochemical control of metal in thin films of solid electrolyte, shows great promise as a future solid state memory. The technology utilizes the electrochemical formation and removal of metallic pathways in thin films of solid electrolyte. Key attributes are low voltage and current operation, excellent scalability, and a simple fabrication sequence. In this work, we investigated the nature of thin films formed by photo doping of Ag+ ions into chalcogenide materials for use in solid electrolyte of Resistance-change RAM devices and switching characteristics.

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Field-induced Resistive Switching in Ge25Se75 Based ReRAM

  • 김장한;남기현;정홍배
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제42회 동계 정기 학술대회 초록집
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    • pp.413-414
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    • 2012
  • Programmable Metallization Cell (PMC) memory, which utilizes electrochemical control of nanoscale quantities of metal in thin films of solid electrolyte, shows great promise as a future solid state memory. The technology utilizes the electrochemical formation and removal of metallic pathways in thin films of solid electrolyte. Key attributes are low voltage and current operation, excellent scalability, and a simple fabrication sequence. In this study, we investigated the nature of thin films formed by photo doping of Ag+ ions into chalcogenide materials for use in solid electrolyte of programmable metallization cell devices. We measured the I-V characteristics by field-effect of the device. The results imply that a Ag-rich phase separates owing to the reaction of Ag with free atoms from chalcogenide materials.

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Ge25Se75-based ReRAM 소자의 전계에 의한 저항 변화에 대한 연구 (Field-induced Resistive Switching in Ge25Se75-based ReRAM Device)

  • 김장한;남기현;정홍배
    • 한국전기전자재료학회논문지
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    • 제25권3호
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    • pp.182-186
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    • 2012
  • Resistance-change Random Access Memory(ReRAM) memory, which utilizes electrochemical control of metal in thin films of solid electrolyte, shows great promise as a future solid state memory. The technology utilizes the electrochemical formation and removal of metallic pathways in thin films of solid electrolyte. Key attributes are low voltage and current operation, excellent scalability, and a simple fabrication sequence. In this work, we investigated the nature of thin films formed by photo doping of $Ag^+$ ions into chalcogenide materials for use in solid electrolyte of Resistance-change RAM devices and switching characteristics according to field-effect.

전고체형 에너지 저장 매체 제조를 위한 이온성 액체 기반의 고체 전해질과 탄소나노복합체 기반의 전극소재 개발 (Development of ionic liquid based solid state electrolyte and nanocarbon composite for all solid-state energy storage device)

  • 김용렬;강혜주;정현택
    • 한국응용과학기술학회지
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    • 제36권4호
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    • pp.1253-1258
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    • 2019
  • 고분자를 기반으로 하는 고체 전해질은 수퍼커패시터, 배터리, 센서, 액추에이터 등 다양한 전기화학 소자에 응용이 가능한 소재로써, 기존 고분자 전해질의 낮은 이온전도도를 향상시키기 위해서 다양한 이온성 액체 기반의 고체 전해질에 관한 연구가 활발히 진행 중에 있다. 이온성 액체의 높은 전기적 특성 및 전기화학적, 열적 안정성과 고분자의 우수한 기계적인 강도를 활용한 젤 상태의 고체 전해질인 이온젤은 차세대 웨어러블 및 플렉시블 전자소자에 응용되어 연구되고 있다. 따라서 본 연구에서는 이러한 이온성 액체와 고분자 기반의 고체 전해질을 제조하고 특성을 분석하여 탄소나노복합체 기반의 전극에 적용하여 다양한 전자소자에 응용이 가능한 이온전도도 및 안정성이 향상된 이온성 액체 기반의 고체 전해질을 개발하고자 한다. 제조된 고체전해질은 전기화학적 임피던스법을 이용하여 이온 전도도를 측정하여 보았으며 이온성 액체를 첨가하여 제조한 고체전해질의 이온 전도도가 1.26 × 10-1 S/cm 로 확인되었다. 또한 제조된 고체 전해질을 이용하여 전고체형 수퍼커패시터를 제조하여 전기화학적 특성을 비교하여 보았으며, 수퍼커패시터의 전기화학적 특성 역시 이온성 액체를 첨가하여 제조된 고체 전해질을 사용하였을 때 향상된 전기화학적 특성을 나타내었다.

UV-cured Polymer Solid Electrolyte Reinforced using a Ceramic-Polymer Composite Layer for Stable Solid-State Li Metal Batteries

  • Hye Min Choi;Su Jin Jun;Jinhong Lee;Myung-Hyun Ryu;Hyeyoung Shin;Kyu-Nam Jung
    • Journal of Electrochemical Science and Technology
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    • 제14권1호
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    • pp.85-95
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    • 2023
  • In recent years, solid-state Li metal batteries (SSLBs) have attracted significant attention as the next-generation batteries with high energy and power densities. However, uncontrolled dendrite growth and the resulting pulverization of Li during repeated plating/stripping processes must be addressed for practical applications. Herein, we report a plastic-crystal-based polymer/ceramic composite solid electrolyte (PCCE) to resolve these issues. To fabricate the one-side ceramic-incorporated PCCE (CI-PCCE) film, a mixed precursor solution comprising plastic-crystal-based polymer (succinonitrile, SN) with garnet-structured ceramic (Li7La3Zr2O12, LLZO) particles was infused into a thin cellulose membrane, which was used as a mechanical framework, and subsequently solidified by using UV-irradiation. The CI-PCCE exhibited good flexibility and a high room-temperature ionic conductivity of over 10-3 S cm-1. The Li symmetric cell assembled with CI-PCCE provided enhanced durability against Li dendrite penetration through the solid electrolyte (SE) layer than those with LLZO-free PCCEs and exhibited long-term cycling stability (over 200 h) for Li plating/stripping. The enhanced Li+ transference number and lower interfacial resistance of CI-PCCE indicate that the ceramic-polymer composite layer in contact with the Li anode enabled the uniform distribution of Li+ flux at the interface between the Li metal and CI-PCCE, thereby promoting uniform Li plating/stripping. Consequently, the Li//LiFePO4 (LFP) full cell constructed with CI-PCCE demonstrated superior rate capability (~120 mAh g-1 at 2 C) and stable cycle performance (80% after 100 cycles) than those with ceramic-free PCCE.

Quasi-Solid-State Polymer Electrolytes Based on a Polymeric Ionic Liquid with High Ionic Conductivity and Enhanced Stability

  • Jeon, Nawon;Jo, Sung-Geun;Kim, Sang-Hyung;Park, Myung-Soo;Kim, Dong-Won
    • Journal of Electrochemical Science and Technology
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    • 제8권3호
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    • pp.257-264
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    • 2017
  • A polymeric ionic liquid, poly(1-methyl 3-(2-acryloyloxypropyl) imidazolium iodide) (PMAPII), was synthesized as a single-iodide-ion-conducting polymer and employed in a gel polymer electrolyte. Gel polymer electrolytes prepared from iodine, 4-tert-butylpyridine, ${\gamma}$-butyrolactone, and PMAPII were applied in quasi-solid-state dye-sensitized solar cells (DSSCs). The addition of 16 wt.% PMAPII provided the most favorable environment, striking a compromise between the iodide ion concentration and the ionic mobility, which resulted in the highest conversion efficiency of the resulting DSSCs. The quasi-solid-state DSSC assembled with the optimized gel polymer electrolyte exhibited a relatively high conversion efficiency of 7.67% under AM 1.5 illumination at $100mA\;cm^{-2}$ and better stability than that of the DSSC with a liquid electrolyte.

금속염을 이용한 염료감응 태양전지의 고체전해질의 전기화학적 특성 (Electrochemical properties of metal salts polymer electrolyte for DSSC)

  • ;;구할본
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 추계학술대회 초록집
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    • pp.55.1-55.1
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    • 2011
  • Dye-sensitized solar cell(DSSC) have been considered one of the promising alternatives to conventional solar cells, because of their low cost, easy fabrication and relatively high energy conversion efficiency. However, although the cell offers reasonable efficiency at least 11%, the use of a liquid electrolyte placed technological challenges for achieving the desired durability and operational stability of the cell. In order to prevent or reduce electrolyte leakage considerable efforts have been made, such as p-type semiconductor or organic hole-transport material that better mechanical properties and simple fabrication processes. In this work, we synthesized solid-state electrolyte containing LiI and KI metal salt with starting materials of poly ethylene oxide to substitute liquid electrolyte enhance the ionic conductivity and solar conversion efficiency. Li+ leads to faster diffusion and higher efficiency and K+ leading to higher ionic conductivity. The efficiency of poly ethylene oxide/LiI system electrolyte is 1.47% and poly ethylene oxide/potassium electrolyte is 1.21%. An efficiency of 3.24% is achieved using solid-state electrolyte containing LiI and KI concentrations. The increased solar conversion efficiency is attributed to decreased crystallinity in the polymer that leads to enhanced charge transfer.

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고분자 전해질을 이용한 고체형 염료감응 태양전지 (New Polymer Electrolytes for Solid State Dye-Sensitized Solar Cells)

  • 강용수;이용건;강문성;김종학;차국헌
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2007년도 춘계학술대회
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    • pp.231-234
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    • 2007
  • The solid state dye-sensitized saolrc cells (DSSCs) employing polymer electrolytes show high overall energy conversion efficiency as high as 4.5% at 1 sun conditions. The improved efficiency may be primarily due to the enlarged interfacial contact area between the electrolyte and dyes in addition to the increased ionic conductivity, which were done by utilizing liquid oligomers, followed by in situ self-solidification, to form the solid DSSCs "Oligomer Approach". The effect of the charge transfer resistance at the counter electrode side on the effciency has also been investigated.

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Novel P(VDF-TrFE) Polymer Electrolytes: Their Use in High-Efficiency, All-Solid-State Electrochemical Capacitors Using ZnO Nanowires

  • Park, Young Jun;Bae, Joonho
    • Journal of Electrochemical Science and Technology
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    • 제9권2호
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    • pp.126-132
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    • 2018
  • For the first time, an innovative approach using P(VDF-TrFE) as a polymer electrolyte for high efficiency, all-solid-state supercapacitors is presented. The polymer electrolyte was successfully achieved by dissolving P(VDF-TrFE) copolymers in dimethylformamide (DMF). Thermal analysis and infrared spectroscopy revealed excellent thermal stability up to $400^{\circ}C$ and copolymer's interaction with DMF. Electrochemical capacitors fabricated using P(VDF-TrFE) in DMF and ZnO NWs demonstrated high capacitive performance. Furthermore, the gel electrolyte-based supercapacitors demonstrated excellent mechanical durability up to a bend angle of $120^{\circ}$. Novel P(VDF-TrFE) electrolytes could be a promising approach for applications in flexible, fabric-based, and high-efficiency energy devices.