Temperature Ionic(온도 이온)란 무엇입니까?
Temperature Ionic 온도 이온 - Experimental studies have reported the possibility of affecting the growth/dissolution of amyloid fibres by the addition of organic salts of the room-temperature ionic-liquid family, raising the tantalizing prospect of controlling these processes under physiological conditions. [1]실험 연구는 실온 이온-액체 계열의 유기 염을 첨가하여 아밀로이드 섬유의 성장/용해에 영향을 미칠 가능성을 보고하여 생리학적 조건에서 이러한 과정을 제어할 수 있는 가능성을 높였습니다. [1]
1 butyl 3 1 부틸 3
The liquid–liquid coexistence curves for the room temperature ionic liquid (RTIL) solutions of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C4mim][NTf2]) in 1-butanol and 2-methyl-1-propanol have been precisely measured. [1] An extraction chromatography (XC) material containing N,N,N',N'-tetra-n-butyl diglycolamide (TBDGA) and 1-butyl-3-methylimidazolium bis(trifluoromethanesulphonyl) imide (C4mim∙NTf2), a room temperature ionic liquid, was used for the uptake of the tetravalent actinide ions Th(IV), Np(IV), and Pu(IV) from nitric acid feed solutions. [2] Two room temperature ionic liquids (RTILs) having the same cation (1-butyl-3-methylimidazolium [ BMIM ] + ) and different anions (tetrafluoroborate [ BF 4 ] − or trifluoromethanesulfonate [ TfO ] − ) have been investigated by ATR-FTIR, NMR, TGA/DTA, UV–vis spectroscopy, agar-disk diffusion, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) assay. [3] Low molecular weight diglycolamide (DGA) extractants were tested for the extraction of europium(III) and americium(III) from nitric acid solutions in n-dodecane, a molecular diluent and 1-butyl-3-methylimidazolium bis(trifluoromethanesulphonyl) imide (C4mim⋅NTf2), a room temperature ionic liquid, as the diluents. [4] 1 M H2SO4 and 1-butyl-3-methyl imidazolium tetrafluoroborate room temperature ionic liquid (BmimBF4 RTIL) as electrolyte. [5] Herein, we describe an amino-functionalized room temperature ionic liquid, 1-butyl-3-methylimidazolium 3-amino-1H-1,2,4-triazolate ([Bmim][ATZ]) with unusual ultrafast physical CO2 capture at room temperature and atmospheric pressure. [6] The graphene device is fabricated with electrolyte comprising of 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4) room temperature ionic liquid and LiClO4 dopant entrapped within polymer matrix formulated as a gel. [7]1-부탄올과 2-메틸-1-프로판올에서 1-부틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([C4mim][NTf2])의 실온 이온성 액체(RTIL) 용액에 대한 액체-액체 공존 곡선은 다음과 같습니다. 정확하게 측정되었습니다. [1] N,N,N',N'-테트라-n-부틸디글리콜아미드(TBDGA) 및 1-부틸-3-메틸이미다졸륨비스(트리플루오로메탄술포닐)이미드(C4mim·NTf2)를 포함하는 추출 크로마토그래피(XC) 물질, 상온 이온성 액체는 질산 공급 용액에서 4가 악티늄 이온 Th(IV), Np(IV) 및 Pu(IV)의 흡수에 사용되었습니다. [2] nan [3] nan [4] nan [5] nan [6] nan [7]
1 ethyl 3 1 에틸 3
A one-step synthesis of room temperature ionic liquid with low viscosity 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][NTf2]) (with reaction yields of 87. [1] The microscopic structures of room-temperature ionic liquids 1-ethyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide ([Emmim]TFSI) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([Emim]TFSI) were studied on a flat Au(111) surface using molecular dynamics simulations. [2] It is noted that SnSe, as a novel positive electrode material of aluminum-ion battery based on aluminium chloride/1-ethyl-3-methylimidazolium chloride (AlCl3/[EMIm]Cl) room temperature ionic liquid electrolyte for the first time, exhibits well-defined discharge voltage plateaus near 1. [3] The rotational and translational diffusion of negatively charged and uncharged spin probes in five imidazolium-based room-temperature ionic liquids (RTILs), 1-ethyl-3-methylimidazolium tetrafluoroborate, emimBF4, 1-butyl-3-methylimidazolium tetrafluoroborate, bmimBF4, 1-octyl-3-methylimidazolium tetrafluoroborate, omimBF4, 1-octyl-3-methylimidazolium hexafluorophosphate, omimPF6, and 1-octyl-3-methylimidazolium chloride, omimCl, has been studied by means of electron paramagnetic resonance spectroscopy. [4] An evaluation of the characteristics of the electrolytes prepared by single and two-step procedures is done by comparing membranes prepared by both methods using PEO as a polymeric scaffold and a solution of the room-temperature ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl) imide (EMI TFSI) and the bis(trifluoromethanesulfonyl) imide lithium salt (Li TFSI) as liquid phase. [5] Molecular dynamics (MD) simulations and X-ray absorption spectroscopy (XAS) were employed to study the solvation of Zn2+ ion in dry [Cnmim][Tf2N] (n = 2, 4; 1-ethyl-3-methylimidazolium and 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide) room temperature ionic liquids (RTILs). [6]저점도 1-에틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([EMIm][NTf2])를 갖는 실온 이온성 액체의 1단계 합성(반응 수율 87. [1] 실온 이온성 액체 1-에틸-2,3-디메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([Emmim]TFSI) 및 1-에틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([Emim]TFSI)의 미세 구조를 연구했습니다. 분자 역학 시뮬레이션을 사용하여 평평한 Au(111) 표면에서 [2] nan [3] nan [4] nan [5] nan [6]
solid state lithium 고체 리튬
The application of flexible, robust, and low-cost solid polymer electrolytes in next-generation all-solid-state lithium metal batteries has been hindered by the low room-temperature ionic conductivity of these electrolytes and the small critical current density of the batteries. [1] Solid-state electrolytes with high room temperature ionic conductivity, broad electrochemical window, and favorable thermal stability are crucial for the practical application of all-solid-state lithium-metal batteries. [2] Poly(ethylene oxide) (PEO)-based solid polymer electrolytes (SPEs) with nonflammability, shape flexibility, and high SPE/Li interfacial stability are poised to be an enabler for solid-state lithium batteries, but their application is restricted by low room-temperature ionic conductivity and poor mechanical strength at elevated temperatures. [3]차세대 전고체 리튬 금속 배터리에 유연하고 견고하며 저렴한 고체 고분자 전해질을 적용하는 것은 이러한 전해질의 낮은 실온 이온 전도도와 배터리의 작은 임계 전류 밀도로 인해 어려움을 겪고 있습니다. [1] 높은 실온 이온 전도성, 넓은 전기화학적 창 및 유리한 열 안정성을 갖는 고체 전해질은 전고체 리튬 금속 배터리의 실제 적용에 중요합니다. [2] nan [3]
1 butyl 1 1 부틸 1
This paper discusses the feasibility of tantalum electrodeposition carried out under potential control from 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide [BMPyr][TFSI] room temperature ionic liquid electrolyte containing tantalum pentafluoride (TaF5). [1] In this work, the charge storage mechanism and the electrochemical performance of α-Co(OH)2 in a room-temperature ionic liquid (IL) namely 1-butyl-1-methyl-pyrrolidinium dicyanamide ionic liquid ([BMPyr+][DCA−] IL) were investigated and compared with those in 6 M KOH. [2] The radiolytic stability of a series of room temperature ionic liquids (ILs) composed of bis(trifluoromethylsulfonyl)imide anion (Tf2N-) and triethylammonium, 1-butyl-1-methylpyrrolidinium, trihexyl(tetradecyl)phosphonium, 1-hexyl-3-methylpyridinium and 1-hexyl-3-methylimidazolium (hmim) cations was studied using spin-trap EPR spectroscopy with a spin trap α-(4-Pyridyl-1-oxide)-N-tert-butylnitrone (POBN). [3]이 논문은 1-부틸-1-메틸피롤리디늄 비스(트리플루오로메틸술포닐)이미드[BMPyr][TFSI] 5불화탄탈(TaF5)을 포함하는 실온 이온성 액체 전해질로부터 전위 제어하에 수행되는 탄탈륨 전착의 가능성에 대해 논의합니다. [1] nan [2] nan [3]
3 methylimidazolium tetrafluoroborate 3 메틸이미다졸륨 테트라플루오로보레이트
X-band electron paramagnetic resonance spectroscopy has been used to investigate the rotational diffusion of a stable, positively charged nitroxide 4-trimethylammonium-2,2,6,6-tetramethylpiperidine-1-oxyl iodide (Cat-1) in a series of 1-alkyl-3-methylimidazolium tetrafluoroborate room-temperature ionic liquids (RTILs) having alkyl chain lengths from two to eight carbons. [1]X-밴드 전자 상자성 공명 분광법은 안정하고 양으로 하전된 니트록사이드 4-트리메틸암모늄-2,2,6,6-테트라메틸피페리딘-1-옥실 요오다이드(Cat-1)의 회전 확산을 조사하는 데 사용되었습니다. -알킬-3-메틸이미다졸륨 테트라플루오로보레이트 실온 이온성 액체(RTIL)는 탄소수 2 내지 8의 알킬 사슬 길이를 갖는다. [1]
preferential solvation parameter 우선적인 용매화 매개변수
Aabbreviations: αCT, solute-centric solvent HBA-acidity parameter; βCT, solute-centric solvent HBA-basicity parameter; πSC*, solute-centric polarity parameter; βSC, solute-centric basicity parameter; αSC, solute-centric acidity parameter; e - dielectric constant; ν ∼ A,F n , maxima of absorption (A) and fluorescence (F) spectra in neat less polar (nonpolar) and polar solvents; ν ∼ A,F n + p , maxima of absorption (A) and fluorescence (F) spectra in binary mixtures ( ν ∼ A,F n + p ) of solvents; δ s 2 , preferential solvation parameter; π*, solvent polarity; AHM, 2-amino-3-((E)-((2-hydroxynaphthalen-1-yl)methylene)amino) maleonitrile; BBIQ-T, benzo[g]indolo[2,3-b]quinoxaline; DR19, disperse red 19 dye; DPTB, dipyren-1-yl(2,4,6-triisopropylphenyl)borane; DSSCs, dye sensitized solar cells; ET(30), Reichardt’s solvent polarity scale; f, volume fraction of each solvent; f12/1 , preferential solvation parameter measuring the tendency of the probe/solute to be solvated by the solvent complex S12 (Bosch and Roses model); f2/1, preferential solvation parameter measuring the tendency of the probe to be solvated by solvent S2 (Bosch and Roses model); ICT, intermolecular charge transfer; TFA, trifluoroacetic acid; HCl, hydrochloric acid; H3PO4, phosphoric acid; ILs, ionic liquids; % LMPC, local mole of the polar cosolvent; L1, azo-based pyridyl ligand; nPSs, non-polar solvents; Nm, solvation number; NIPAM -N-Isopropylacrylamide; PS, polar solvents; pKa, acidity values; PSs, polar solvents; RTILs, room temperature ionic liquids; SMs, solute molecules; SSnonpolar, Stokes shifts (cm-1) in the pure nonpolar solvents; SSpolar, Stokes shifts (cm-1) in the pure polar solvents; SSmixture, Stokes shifts (cm-1) in binary solvent mixture; WS, aqueous environment; SA, solvent acidity; SB, solvent acidity, basicity, SP, polarizability properties; SdP -dipolarity properties; X2, mole fraction of solvent 2 in the bulk solvent mixture; X 2 L , local mole fraction of solvent 2; Y, physicochemical property. [1]약어: αCT, 용질 중심 용매 HBA-산도 매개변수; βCT, 용질 중심 용매 HBA-염기성 매개변수; πSC*, 용질 중심 극성 매개변수; βSC, 용질 중심 염기도 매개변수; αSC, 용질 중심 산도 매개변수; e - 유전 상수; ν ~ A,F n , 순도가 낮은 극성(무극성) 및 극성 용매에서의 최대 흡수(A) 및 형광(F) 스펙트럼; ν ∼ A,F n + p , 용매의 이원 혼합물( ν ∼ A,F n + p )에서 흡수(A) 및 형광(F) 스펙트럼의 최대값; δ s 2 , 우선적 용매화 매개변수; π*, 용매 극성; AHM, 2-아미노-3-((E)-((2-히드록시나프탈렌-1-일)메틸렌)아미노)말레오니트릴; BBIQ-T, 벤조[g]인돌로[2,3-b]퀴녹살린; DR19, 분산 레드 19 염료; DPTB, 디피렌-1-일(2,4,6-트리이소프로필페닐)보란; DSSC, 염료감응 태양전지; ET(30), Reichardt의 용매 극성 척도; f, 각 용매의 부피 분율; f12/1, 용매 복합체 S12(Bosch and Roses 모델)에 의해 용매화되는 프로브/용질의 경향을 측정하는 우선 용매화 매개변수; f2/1, 프로브가 용매 S2에 의해 용매화되는 경향을 측정하는 우선 용매화 매개변수(Bosch and Roses 모델); ICT, 분자간 전하 이동; TFA, 트리플루오로아세트산; HCl, 염산; H3PO4, 인산; IL, 이온성 액체; % LMPC, 극성 공용매의 국부적 몰; L1, 아조계 피리딜 리간드; nPS, 비극성 용매; Nm, 용매화 수; NIPAM -N-이소프로필아크릴아미드; PS, 극성 용매; pKa, 산도 값; PS, 극성 용매; RTIL, 실온 이온성 액체; SM, 용질 분자; SSnonpolar, 순수한 비극성 용매에서 Stokes 이동(cm-1); SSpolar, 순수한 극성 용매에서 Stokes 이동(cm-1); SS혼합물, 2원 용매 혼합물에서 스톡 시프트(cm-1); WS, 수성 환경; SA, 용매 산도; SB, 용매 산도, 염기도, SP, 분극성 특성; SdP -쌍극성 특성; X2, 벌크 용매 혼합물에서 용매 2의 몰 분율; X 2 L, 용매 2의 국부적 몰분율; Y, 물리화학적 특성. [1]
Room Temperature Ionic 실온 이온
A green route for the oxidation of alcohols to corresponding carbonyl compounds in room temperature ionic liquid ([CEMIM]BH4) was developed by using hydrogen peroxide as the oxygen source. [1] room temperature ionic liquid (RTIL) and supercritical carbon dioxide (SC CO2) were studied. [2] Photoexcitation of (neat) room temperature ionic liquids (RTILs) leads to the observation of transient species that are reminiscent of the composition of the RTILs themselves. [3] % LiI recorded the highest room temperature ionic conductivity of 4. [4] Room Temperature Ionic Liquids (RTILs) attract significant interest in nanotribology. [5] The electrodeposition of nanocomposite coatings has been widely investigated in aqueous solutions and room temperature ionic liquids, but there are no literature reports of that in inorganic molten salts. [6] In this research work, a straightforward strategy for the development of carbon-based electrodes is presented using nanoclay as a modifier, and a room temperature ionic liquid was employed as a binder for the simultaneous determination of dopamine (DP) and uric acid (UA) in the presence of ascorbic acid (AA) in real samples in the form of serum and urine. [7] Moreover, in the past few decades, room temperature ionic liquids (RTILs) have been utilized in electrochemical sensors due to their attractive properties. [8] This work aims to study the extraction of Pb(II) from contaminated aqueous solutions using imidazolium-based room temperature ionic liquids as sole extracting agent, i. [9] The liquid–liquid coexistence curves for the room temperature ionic liquid (RTIL) solutions of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C4mim][NTf2]) in 1-butanol and 2-methyl-1-propanol have been precisely measured. [10] Room temperature ionic liquids (RTILs) are known to be green solvents and having fascinating properties suitable for various industrial applications, including the capture of pollutants, like CO2, SO2, etc. [11] In the present study, an amperometric gas sensor based on room temperature ionic liquid (RTIL) electrolyte and screen-printed electrodes (SPE) was fabricated. [12] An extraction chromatography (XC) material containing N,N,N',N'-tetra-n-butyl diglycolamide (TBDGA) and 1-butyl-3-methylimidazolium bis(trifluoromethanesulphonyl) imide (C4mim∙NTf2), a room temperature ionic liquid, was used for the uptake of the tetravalent actinide ions Th(IV), Np(IV), and Pu(IV) from nitric acid feed solutions. [13] Compared to electrolytes prepared with linear PEO of equivalent molecular weight, the HB PEO electrolytes increase the room temperature ionic conductivity from ∼2. [14] In this work, we have successfully synthesized a series of multiclaw-shaped octasilsesquioxanes functionalized ionic liquids and then used it developing novel hybrid solid polymer electrolytes (SPEs) with high room temperature ionic conductivity. [15] The highest room temperature ionic conductivity of 3. [16] A one-step synthesis of room temperature ionic liquid with low viscosity 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][NTf2]) (with reaction yields of 87. [17] % Al2O3 exhibits the highest room temperature ionic conductivity of (6. [18] Further, various new classes of membranes developed for gas separations, including thermally rearranged polymers, polymers of intrinsic microporosity, room temperature ionic liquids, perfluoro polymers, and mixed matrix membranes, that has high separation performance has also been discussed. [19] In this study, we have examined the modeling of gas solubility in twenty room temperature ionic liquids based on the van der Waals and generic Redlich–Kwong equations of state and have also compared the obtained deviations with each other. [20] Those having melting point below room temperature are termed as room temperature ionic liquid. [21] The developed electrolytes show an improved room temperature ionic conductivity (1. [22] In addition to alkali metal salts, room temperature ionic liquids [EMIm][ROB(CN)3] (R = CH3, C2H5, CH2CF3) have been prepared. [23] Measurements of ionic conductivity of the compounds showed room temperature ionic conductivities of 1. [24] Room temperature ionic liquids (RTILs) have been considered an interesting alternative to stabilizers in platinum (Pt) nanoparticle synthesis because they can prevent agglomeration of nanoparticles and act as a reaction medium. [25] %)’ demonstrated more than three orders of magnitude in the room temperature ionic conductivity, as measured by EIS. [26] Room temperature ionic liquids (RTILs) have a wide range of current and potential applications, in areas ranging from supercapacitor energy storage to sequestration of toxic gas phase species and use as reusable solvents for selected organic reactions. [27] Ionic conductivity analysis showed that PVdF-HFP-[Bmim][PF6] samples reached a maximum room temperature ionic conductivity value of 2. [28] The modified microarrays were then used for the sensing of a model analyte (oxygen) in a room temperature ionic liquid, with the larger deposits (with larger surface areas) giving higher current responses. [29] The physicochemical properties of room temperature ionic liquids (RTILs) consisting of bis(trifluoromethanesulfonyl)amide (TFSA - ) combined with 1-hexyl-1-methylpyrrolidinium (Pyr 1,6 + ), 1-(butoxymethyl)-1-methylpyrrolidinium (Pyr 1,1O4 + ), 1-(4-methoxybutyl)-1-methyl pyrrolidinium (Pyr 1,4O1 + ), and 1-((2-methoxyethoxy)methyl)-1-methylpyrrolidinium (Pyr 1,1O2O1 + ) were investigated using both experimental and computational approaches. [30] The prepared DN ion gels present outstanding tensile properties (breaking strain over 1000%), high transparency (>90%), good room temperature ionic conductivity (0. [31] The theoretical principle of choosing suitable room temperature ionic liquids (RTILs) for liquid phase exfoliation of graphene sheet remains a challenge. [32] The locations of hydrophobic and hydrophilic probes in room temperature ionic liquids (RTILs) containing microemulsions have been investigated using femtosecond solvation dynamics study, as the time correlated single photon counting (TCSPC) measurement has limitation in terms of detecting the ultrafast component of relaxation time less than 100 ps. [33] “Association–disassociation” with the carbonyl groups and rapid ion exchange with the ionic liquids are the two migration modes that synergistically increase the room temperature ionic conductivity of the SPE-IL. [34] Room temperature ionic liquids (RTILs)-containing Pickering emulsions exhibit promising application potentials because of the integration of the “green” quality and the tunable applications of RTILs with the advantages of Pickering emulsions, such as the high stability and adjustable droplet size. [35] The optimized membrane displays maximum room temperature ionic conductivity as ~0. [36] Two room temperature ionic liquids (RTILs) having the same cation (1-butyl-3-methylimidazolium [ BMIM ] + ) and different anions (tetrafluoroborate [ BF 4 ] − or trifluoromethanesulfonate [ TfO ] − ) have been investigated by ATR-FTIR, NMR, TGA/DTA, UV–vis spectroscopy, agar-disk diffusion, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) assay. [37] Imidazole-based zwitterionic-type molten salts are a new type of organocatalysts with high catalytic application in various organic transformations with added advantage of room temperature ionic liquid (RTIL) property. [38] In this work the fabrication of fluorescent microstructures through the e-beam induced solidification of two types of room temperature ionic liquids (RTILs) with fluorescent organic dyes is reported. [39] The knowledge of molecular interactions of room temperature ionic liquids is highly relevant to understand and to predict their behavior in many applications. [40] On account of HNTs, the composite solid electrolyte (CSE) exhibits significantly improved room temperature ionic conductivity (6. [41] Over the years room temperature ionic liquids have gained attention as solvents with favorable environmental and technical features. [42] In this work, the main advantages and disadvantages of SPEs are discussed, together with the critical issues to be addressed in the near future, namely the low room temperature ionic conductivity and the interfacial compatibility issues. [43] The frequency-dependent impedance of a metal/oxide/room temperature ionic liquid (RTIL) interface was separated into oxide layer (Cox) and double layer (Cdl) capacitances using electrochemical impedance spectroscopy (EIS). [44] The maximum room temperature ionic conductivity for the optimized system was found to be of the order of 8. [45] This synthesized nanocomposite offers advantages for gas sensing applications as it possesses unique properties such as an electrochemically active Room Temperature Ionic Liquid (RTIL) and a crosslinking Metal Organic Framework (MOF) that provides increased surface area for gas absorption. [46] 8O12 electrolyte has superior room temperature ionic conductivity of 3. [47] H 2 O 2 is a versatile chemical and can be generated by the oxygen reduction reaction in proton donor solution in molecular solvents or room temperature ionic liquids (IL). [48] Low molecular weight diglycolamide (DGA) extractants were tested for the extraction of europium(III) and americium(III) from nitric acid solutions in n-dodecane, a molecular diluent and 1-butyl-3-methylimidazolium bis(trifluoromethanesulphonyl) imide (C4mim⋅NTf2), a room temperature ionic liquid, as the diluents. [49] However, the lower room temperature ionic conductivity and poor mechanical properties greatly hinder. [50]실온 이온성 액체([CEMIM]BH4)에서 알코올을 해당 카르보닐 화합물로 산화시키는 친환경 경로는 산소 공급원으로 과산화수소를 사용하여 개발되었습니다. [1] 실온 이온성 액체(RTIL) 및 초임계 이산화탄소(SC CO2)를 연구했습니다. [2] nan [3] % LiI는 4의 가장 높은 실온 이온 전도도를 기록했습니다. [4] nan [5] nan [6] nan [7] nan [8] nan [9] 1-부탄올과 2-메틸-1-프로판올에서 1-부틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([C4mim][NTf2])의 실온 이온성 액체(RTIL) 용액에 대한 액체-액체 공존 곡선은 다음과 같습니다. 정확하게 측정되었습니다. [10] nan [11] nan [12] N,N,N',N'-테트라-n-부틸디글리콜아미드(TBDGA) 및 1-부틸-3-메틸이미다졸륨비스(트리플루오로메탄술포닐)이미드(C4mim·NTf2)를 포함하는 추출 크로마토그래피(XC) 물질, 상온 이온성 액체는 질산 공급 용액에서 4가 악티늄 이온 Th(IV), Np(IV) 및 Pu(IV)의 흡수에 사용되었습니다. [13] nan [14] nan [15] nan [16] 저점도 1-에틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([EMIm][NTf2])를 갖는 실온 이온성 액체의 1단계 합성(반응 수율 87. [17] nan [18] nan [19] nan [20] nan [21] nan [22] nan [23] nan [24] nan [25] nan [26] nan [27] nan [28] nan [29] nan [30] nan [31] nan [32] nan [33] nan [34] nan [35] nan [36] nan [37] nan [38] nan [39] nan [40] nan [41] nan [42] nan [43] nan [44] nan [45] nan [46] nan [47] nan [48] nan [49] nan [50]
Ambient Temperature Ionic 주변 온도 이온
An ambient temperature ionic conductivity of 1. [1] Among six different GPE samples investigated by Electrochemical Impedance Spectroscopic and Raman Spectroscopic techniques, the best ambient temperature ionic conductivity of 4. [2] It has an ambient temperature ionic conductivity of 1. [3]1의 주변 온도 이온 전도도. [1] Electrochemical Impedance Spectroscopic 및 Raman Spectroscopic 기술로 조사한 6개의 다른 GPE 샘플 중에서 가장 좋은 주변 온도 이온 전도도는 4입니다. [2] nan [3]
temperature ionic liquid 온도 이온성 액체
A green route for the oxidation of alcohols to corresponding carbonyl compounds in room temperature ionic liquid ([CEMIM]BH4) was developed by using hydrogen peroxide as the oxygen source. [1] room temperature ionic liquid (RTIL) and supercritical carbon dioxide (SC CO2) were studied. [2] Photoexcitation of (neat) room temperature ionic liquids (RTILs) leads to the observation of transient species that are reminiscent of the composition of the RTILs themselves. [3] Room Temperature Ionic Liquids (RTILs) attract significant interest in nanotribology. [4] The CPM has been used to study the capacitance of room-temperature ionic liquid supercapacitors and the relationship with electrolyte layering near charged electrodes, the mechanisms and kinetics of charging and discharging, and the utility of nanoporous electrodes in achieving ionic nanoconfinement and superionic states. [5] The electrodeposition of nanocomposite coatings has been widely investigated in aqueous solutions and room temperature ionic liquids, but there are no literature reports of that in inorganic molten salts. [6] In this study, an amperometric electrochemical H2 gas sensor based on room-temperature ionic liquid was developed, which was expected to be applicable to monitoring of H2 concentration in the hydrogen fuel cell ship. [7] In this research work, a straightforward strategy for the development of carbon-based electrodes is presented using nanoclay as a modifier, and a room temperature ionic liquid was employed as a binder for the simultaneous determination of dopamine (DP) and uric acid (UA) in the presence of ascorbic acid (AA) in real samples in the form of serum and urine. [8] Moreover, in the past few decades, room temperature ionic liquids (RTILs) have been utilized in electrochemical sensors due to their attractive properties. [9] The low melting point of KMPSA makes it interesting for low-temperature ionic liquids. [10] This work aims to study the extraction of Pb(II) from contaminated aqueous solutions using imidazolium-based room temperature ionic liquids as sole extracting agent, i. [11] Here, we have successfully synthesized single-phase ZnWO4 nanoparticles using a highly effective low-temperature ionic liquid-assisted hydrothermal method at 180 °C for 24 h. [12] The electrochemical behaviour of a protic quaternary amine cation based room-temperature ionic liquid (RTIL), diethylmethylammonium trifluoromethanesulfonate [N2210(OTf)], has been investigated at negatively and positively polarized molybdenum carbide derived micro-mesoporous carbon [mmp-C(Mo2C)] electrodes by in situ X-ray photoelectron spectroscopy (XPS), in situ mass-spectroscopy (MS), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) methods. [13] The liquid–liquid coexistence curves for the room temperature ionic liquid (RTIL) solutions of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([C4mim][NTf2]) in 1-butanol and 2-methyl-1-propanol have been precisely measured. [14] Room temperature ionic liquids (RTILs) are known to be green solvents and having fascinating properties suitable for various industrial applications, including the capture of pollutants, like CO2, SO2, etc. [15] Various CNT functionalization and graphenation processes can enhance carbon nanotube charge densities, while room-temperature ionic liquids can enhance supercapacitor performance. [16] We have reported previously on the existence of a surface charge-induced free charge density gradient (ρf) in room-temperature ionic liquids (RTILs) with a characteristic persistence length of ca. [17] In the present study, an amperometric gas sensor based on room temperature ionic liquid (RTIL) electrolyte and screen-printed electrodes (SPE) was fabricated. [18] An extraction chromatography (XC) material containing N,N,N',N'-tetra-n-butyl diglycolamide (TBDGA) and 1-butyl-3-methylimidazolium bis(trifluoromethanesulphonyl) imide (C4mim∙NTf2), a room temperature ionic liquid, was used for the uptake of the tetravalent actinide ions Th(IV), Np(IV), and Pu(IV) from nitric acid feed solutions. [19] A one-step synthesis of room temperature ionic liquid with low viscosity 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][NTf2]) (with reaction yields of 87. [20] It is a room-temperature ionic liquid with a glass transition temperature of 237. [21] The room-temperature ionic liquids have unique chemical, electrochemical, and physical properties and they have wide range of applications. [22] Further, various new classes of membranes developed for gas separations, including thermally rearranged polymers, polymers of intrinsic microporosity, room temperature ionic liquids, perfluoro polymers, and mixed matrix membranes, that has high separation performance has also been discussed. [23] In this study, we have examined the modeling of gas solubility in twenty room temperature ionic liquids based on the van der Waals and generic Redlich–Kwong equations of state and have also compared the obtained deviations with each other. [24] Those having melting point below room temperature are termed as room temperature ionic liquid. [25] The reduction of [Fe(OEP)(NO)] has been studied in the presence of aprotic room-temperature ionic liquids (RTIL) and protic (PIL) ionic liquids dissolved within a molecular solvent (MS). [26] In this study, the surface wetting behavior of room-temperature ionic liquids (RTILs) treated steel surfaces is investigated. [27] In addition to alkali metal salts, room temperature ionic liquids [EMIm][ROB(CN)3] (R = CH3, C2H5, CH2CF3) have been prepared. [28] Room temperature ionic liquids (RTILs) have been considered an interesting alternative to stabilizers in platinum (Pt) nanoparticle synthesis because they can prevent agglomeration of nanoparticles and act as a reaction medium. [29] Room temperature ionic liquids (RTILs) have a wide range of current and potential applications, in areas ranging from supercapacitor energy storage to sequestration of toxic gas phase species and use as reusable solvents for selected organic reactions. [30] The modified microarrays were then used for the sensing of a model analyte (oxygen) in a room temperature ionic liquid, with the larger deposits (with larger surface areas) giving higher current responses. [31] The physicochemical properties of room temperature ionic liquids (RTILs) consisting of bis(trifluoromethanesulfonyl)amide (TFSA - ) combined with 1-hexyl-1-methylpyrrolidinium (Pyr 1,6 + ), 1-(butoxymethyl)-1-methylpyrrolidinium (Pyr 1,1O4 + ), 1-(4-methoxybutyl)-1-methyl pyrrolidinium (Pyr 1,4O1 + ), and 1-((2-methoxyethoxy)methyl)-1-methylpyrrolidinium (Pyr 1,1O2O1 + ) were investigated using both experimental and computational approaches. [32] X-band electron paramagnetic resonance spectroscopy has been used to investigate the rotational diffusion of a stable, positively charged nitroxide 4-trimethylammonium-2,2,6,6-tetramethylpiperidine-1-oxyl iodide (Cat-1) in a series of 1-alkyl-3-methylimidazolium tetrafluoroborate room-temperature ionic liquids (RTILs) having alkyl chain lengths from two to eight carbons. [33] Room-temperature ionic liquids (RTILs) stand out among molecular liquids for their rich physicochemical characteristics, including structural and dynamic heterogeneity. [34] The theoretical principle of choosing suitable room temperature ionic liquids (RTILs) for liquid phase exfoliation of graphene sheet remains a challenge. [35] The locations of hydrophobic and hydrophilic probes in room temperature ionic liquids (RTILs) containing microemulsions have been investigated using femtosecond solvation dynamics study, as the time correlated single photon counting (TCSPC) measurement has limitation in terms of detecting the ultrafast component of relaxation time less than 100 ps. [36] We investigate the effects of pore size and ion adsorption on the room-temperature ionic liquid capacitor with nanoporous electrodes, with a focus on optimizing the capacitance and energy storage. [37] Low vapor pressure and several other outstanding properties make room-temperature ionic liquids attractive candidates as lubricants for machine elements in space applications. [38] Promising alternative propellant candidates are combinations of hydrogen peroxide and suitable hypergolic room-temperature ionic liquids. [39] Room temperature ionic liquids (RTILs)-containing Pickering emulsions exhibit promising application potentials because of the integration of the “green” quality and the tunable applications of RTILs with the advantages of Pickering emulsions, such as the high stability and adjustable droplet size. [40] Encapsulated room-temperature ionic liquids (RTILs) can be potentially employed in CO2 capture. [41] Two room temperature ionic liquids (RTILs) having the same cation (1-butyl-3-methylimidazolium [ BMIM ] + ) and different anions (tetrafluoroborate [ BF 4 ] − or trifluoromethanesulfonate [ TfO ] − ) have been investigated by ATR-FTIR, NMR, TGA/DTA, UV–vis spectroscopy, agar-disk diffusion, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) assay. [42] A new protic room-temperature ionic liquid (Tc = 14 ± 1 °C) – pyridinium hydrogen dinitrate – was obtained from a solution of pyridinium nitrate in anhydrous nitric acid in a desiccator with P2O5. [43] Imidazole-based zwitterionic-type molten salts are a new type of organocatalysts with high catalytic application in various organic transformations with added advantage of room temperature ionic liquid (RTIL) property. [44] Electric-field-driven ion emission from the free surface of a planar room-temperature ionic liquid (RTIL) film was studied by using molecular dynamics simulations. [45] In this work the fabrication of fluorescent microstructures through the e-beam induced solidification of two types of room temperature ionic liquids (RTILs) with fluorescent organic dyes is reported. [46] The knowledge of molecular interactions of room temperature ionic liquids is highly relevant to understand and to predict their behavior in many applications. [47] Over the years room temperature ionic liquids have gained attention as solvents with favorable environmental and technical features. [48] The frequency-dependent impedance of a metal/oxide/room temperature ionic liquid (RTIL) interface was separated into oxide layer (Cox) and double layer (Cdl) capacitances using electrochemical impedance spectroscopy (EIS). [49] This synthesized nanocomposite offers advantages for gas sensing applications as it possesses unique properties such as an electrochemically active Room Temperature Ionic Liquid (RTIL) and a crosslinking Metal Organic Framework (MOF) that provides increased surface area for gas absorption. [50]실온 이온성 액체([CEMIM]BH4)에서 알코올을 해당 카르보닐 화합물로 산화시키는 친환경 경로는 산소 공급원으로 과산화수소를 사용하여 개발되었습니다. [1] 실온 이온성 액체(RTIL) 및 초임계 이산화탄소(SC CO2)를 연구했습니다. [2] nan [3] nan [4] CPM은 실온 이온성 액체 슈퍼커패시터의 커패시턴스와 전하를 띤 전극 근처의 전해질 층과의 관계, 충전 및 방전의 메커니즘 및 역학, 이온성 나노 가둠 및 초이온성 상태를 달성하기 위한 나노다공성 전극의 유용성을 연구하는 데 사용되었습니다. [5] nan [6] 본 연구에서는 상온의 이온성 액체를 기반으로 하는 전류계 전기화학적 H2 가스 센서를 개발하였으며, 이는 수소연료전지선박의 H2 농도 모니터링에 적용될 수 있을 것으로 기대된다. [7] nan [8] nan [9] KMPSA의 낮은 융점은 저온 이온성 액체에 흥미롭습니다. [10] nan [11] 여기에서 우리는 180°C에서 24시간 동안 매우 효과적인 저온 이온성 액체 보조 열수법을 사용하여 단상 ZnWO4 나노 입자를 성공적으로 합성했습니다. [12] 양성자성 4차 아민 양이온 기반 실온 이온성 액체(RTIL), 디에틸메틸암모늄 트리플루오로메탄설포네이트[N2210(OTf)]의 전기화학적 거동이 음 및 양으로 극성화된 몰리브덴 카바이드 유래 마이크로 메조포러스 탄소[mmp-C(Mo2C)에서 조사되었습니다. ] 현장 X선 광전자 분광법(XPS), 현장 질량 분광법(MS), 순환 전압전류법(CV) 및 전기화학적 임피던스 분광법(EIS) 방법에 의한 전극. [13] 1-부탄올과 2-메틸-1-프로판올에서 1-부틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([C4mim][NTf2])의 실온 이온성 액체(RTIL) 용액에 대한 액체-액체 공존 곡선은 다음과 같습니다. 정확하게 측정되었습니다. [14] nan [15] 다양한 CNT 기능화 및 그래핀화 공정은 탄소 나노튜브 전하 밀도를 향상시킬 수 있는 반면 실온 이온성 액체는 슈퍼커패시터 성능을 향상시킬 수 있습니다. [16] 우리는 ca의 특성 지속 길이를 갖는 실온 이온성 액체(RTIL)에서 표면 전하 유도 자유 전하 밀도 구배(ρf)의 존재에 대해 이전에 보고했습니다. [17] nan [18] N,N,N',N'-테트라-n-부틸디글리콜아미드(TBDGA) 및 1-부틸-3-메틸이미다졸륨비스(트리플루오로메탄술포닐)이미드(C4mim·NTf2)를 포함하는 추출 크로마토그래피(XC) 물질, 상온 이온성 액체는 질산 공급 용액에서 4가 악티늄 이온 Th(IV), Np(IV) 및 Pu(IV)의 흡수에 사용되었습니다. [19] 저점도 1-에틸-3-메틸이미다졸륨 비스(트리플루오로메틸술포닐)이미드([EMIm][NTf2])를 갖는 실온 이온성 액체의 1단계 합성(반응 수율 87. [20] 유리전이온도가 237℃인 상온의 이온성 액체이다. [21] 상온의 이온성 액체는 독특한 화학적, 전기화학적, 물리적 성질을 가지고 있으며 응용 범위가 넓습니다. [22] nan [23] nan [24] nan [25] [Fe(OEP)(NO)]의 환원은 분자 용매(MS) 내에 용해된 비양성자성 실온 이온성 액체(RTIL) 및 양성자성(PIL) 이온성 액체의 존재하에 연구되었습니다. [26] 이 연구에서는 실온 이온성 액체(RTIL) 처리된 강철 표면의 표면 습윤 거동을 조사했습니다. [27] nan [28] nan [29] nan [30] nan [31] nan [32] X-밴드 전자 상자성 공명 분광법은 안정하고 양으로 하전된 니트록사이드 4-트리메틸암모늄-2,2,6,6-테트라메틸피페리딘-1-옥실 요오다이드(Cat-1)의 회전 확산을 조사하는 데 사용되었습니다. -알킬-3-메틸이미다졸륨 테트라플루오로보레이트 실온 이온성 액체(RTIL)는 탄소수 2 내지 8의 알킬 사슬 길이를 갖는다. [33] 실온 이온성 액체(RTIL)는 구조적 및 동적 불균일성을 포함한 풍부한 물리화학적 특성으로 인해 분자 액체 중에서 두드러집니다. [34] nan [35] nan [36] 우리는 캐패시턴스와 에너지 저장을 최적화하는 데 중점을 두고 나노다공성 전극이 있는 실온 이온성 액체 축전기에 대한 기공 크기와 이온 흡착의 영향을 조사합니다. [37] 낮은 증기압 및 기타 여러 뛰어난 특성으로 인해 실온 이온성 액체는 우주 응용 분야의 기계 요소용 윤활제로 매력적인 후보가 됩니다. [38] 유망한 대체 추진제 후보는 과산화수소와 적절한 하이퍼골릭 실온 이온성 액체의 조합입니다. [39] nan [40] 캡슐화된 실온 이온성 액체(RTIL)는 잠재적으로 CO2 포집에 사용될 수 있습니다. [41] nan [42] 새로운 양성자성 실온 이온성 액체(Tc = 14 ± 1 °C)인 이질산피리디늄 수소는 P2O5가 포함된 건조기의 무수 질산에 있는 질산피리디늄 용액에서 얻어졌습니다. [43] nan [44] 분자 역학 시뮬레이션을 사용하여 평면 RTIL(실온 이온 액체) 필름의 자유 표면에서 전기장 구동 이온 방출을 연구했습니다. [45] nan [46] nan [47] nan [48] nan [49] nan [50]
temperature ionic conductivity 온도 이온 전도도
% LiI recorded the highest room temperature ionic conductivity of 4. [1] Many efforts have focused on the thin solid-state-electrolyte (SSE) films with high room-temperature ionic conductivity, flexibility, and mechanical strength. [2] An ambient temperature ionic conductivity of 1. [3] 3 reached the room-temperature ionic conductivity of 25 mS cm−1, which even exceeds that of liquid electrolytes. [4] The as-prepared SPE membrane demonstrates a high room-temperature ionic conductivity of 2. [5] Poor room-temperature ionic conductivity and lithium dendrite formation are the main issues of solid electrolytes. [6] Compared to electrolytes prepared with linear PEO of equivalent molecular weight, the HB PEO electrolytes increase the room temperature ionic conductivity from ∼2. [7] In this work, we have successfully synthesized a series of multiclaw-shaped octasilsesquioxanes functionalized ionic liquids and then used it developing novel hybrid solid polymer electrolytes (SPEs) with high room temperature ionic conductivity. [8] The highest room temperature ionic conductivity of 3. [9] % Al2O3 exhibits the highest room temperature ionic conductivity of (6. [10] PCPCEs with an ideal ambient-temperature ionic conductivity can drastically reduce the interfacial resistance between the LATP and solid electrodes and effectively avoid a direct reaction and contact between them. [11] Surprisingly, the CMP/MMT delivers a high room-temperature ionic conductivity (~1. [12] The developed electrolytes show an improved room temperature ionic conductivity (1. [13] Measurements of ionic conductivity of the compounds showed room temperature ionic conductivities of 1. [14] %)’ demonstrated more than three orders of magnitude in the room temperature ionic conductivity, as measured by EIS. [15] Ionic conductivity analysis showed that PVdF-HFP-[Bmim][PF6] samples reached a maximum room temperature ionic conductivity value of 2. [16] The prepared DN ion gels present outstanding tensile properties (breaking strain over 1000%), high transparency (>90%), good room temperature ionic conductivity (0. [17] This self-formed polymer electrolyte exhibits excellent properties, including high room-temperature ionic conductivity (2. [18] The cubic iodine-doped Li3FSe has a room-temperature ionic conductivity of 5 × 10-5 S/cm with a bulk activation energy of 0. [19] The Double cross-linked network of PIL-PEI reveals satisfactory flexibility, thermal stability and remarkable electrochemical performances (room-temperature ionic conductivity, 1. [20] “Association–disassociation” with the carbonyl groups and rapid ion exchange with the ionic liquids are the two migration modes that synergistically increase the room temperature ionic conductivity of the SPE-IL. [21] The optimized membrane displays maximum room temperature ionic conductivity as ~0. [22] However, poor room-temperature ionic conductivity and low density of SSEs induced by conventional preparation routes limit their potential future applications. [23] On account of HNTs, the composite solid electrolyte (CSE) exhibits significantly improved room temperature ionic conductivity (6. [24] From the EIS study, it has been observed that 30 wt % TPeAIcontaining GPE has the lowest bulk impedance, Rb (32 ohm) and highest room-temperature ionic conductivity (2. [25] The polymer electrolytes with high safety and high ambient-temperature ionic conductivity developed in this work are potentially useful in solid lithium-ion batteries. [26] The ionogels consist of a special cross-linking network constructed by poly(ionic liquid) and hyperbranched polymer (macro-cross-linkers) that exhibits high stretchability (>1000%), superior room-temperature ionic conductivity (up to 5. [27] In this work, the main advantages and disadvantages of SPEs are discussed, together with the critical issues to be addressed in the near future, namely the low room temperature ionic conductivity and the interfacial compatibility issues. [28] The maximum room temperature ionic conductivity for the optimized system was found to be of the order of 8. [29] 8O12 electrolyte has superior room temperature ionic conductivity of 3. [30] Herein, we propose a new kind of hexagonal Na5YSi4O12 with a high room-temperature ionic conductivity of 1. [31] The application of flexible, robust, and low-cost solid polymer electrolytes in next-generation all-solid-state lithium metal batteries has been hindered by the low room-temperature ionic conductivity of these electrolytes and the small critical current density of the batteries. [32] Thin solid polymer electrolytes (SPEs) with good processability, improved room-temperature ionic conductivity, and better interfacial compatibility are urgently needed to develop solid-state batteries without safety and leakage issues. [33] Among six different GPE samples investigated by Electrochemical Impedance Spectroscopic and Raman Spectroscopic techniques, the best ambient temperature ionic conductivity of 4. [34] Preliminary results show that a room-temperature ionic conductivity as high as 6. [35] However, the lower room temperature ionic conductivity and poor mechanical properties greatly hinder. [36] Among the various types of SEs, including those based on oxides, sulfides, polymers, and hybrids thereof, sulfide-based SEs have gained discernible attention owing to their exceptional room temperature ionic conductivity comparable even to those of their liquid electrolyte counterparts. [37] However, most PEO-based solid-state batteries need to operate at high temperature due to low room temperature ionic conductivity. [38] A small amount of ZnO-NPs was found to enhance the proton-conduction significantly; the highest obtainable room-temperature ionic conductivity was 4. [39] Solid-state electrolytes with high room temperature ionic conductivity, broad electrochemical window, and favorable thermal stability are crucial for the practical application of all-solid-state lithium-metal batteries. [40] Herein, we design a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP)-based polymer-in-salt solid electrolyte (PISSE) with high room-temperature ionic conductivity (1. [41] High room-temperature ionic conductivity and mechanical property are essential for the application of solid electrolyte. [42] Their XRD patterns show that only the crystalline phase β-Li3PS4 is detected for x = 0, 1, 2, 3, 5 mol% and the highest room-temperature ionic conductivity of 2. [43] Poor room-temperature ionic conductivities and narrow electrochemical stable windows severely hinder the application of conventional poly(ethylene oxide)-based (PEO-based) solid polymer electrolytes (SPEs) for high-energy-density lithium metal batteries (LMBs). [44] However, the interfacial and high-temperature instability of GPEs, and the low room-temperature ionic conductivity of SPEs still limit their practical implementation. [45] In contrast, polymer electrolytes are pliable and easy to process but suffer from low room-temperature ionic conductivities (≈10−6-10−7 S cm−1). [46] Therein, chalcogenide-based inorganic sodium solid electrolytes (ISSEs) stand out owing to their decent room temperature ionic conductivity and lower mechanical stiffness. [47] The polymer electrolyte exhibits a room-temperature ionic conductivity as high as 4. [48] The fiber membrane exhibits a high room-temperature ionic conductivity of 1. [49] While supervalent doping is predicted to be effective at increasing ionic conductivity, particularly under Li-poor synthesis conditions, subvalent doping is predicted to decrease room-temperature ionic conductivities at low-to-moderate doping levels. [50]% LiI는 4의 가장 높은 실온 이온 전도도를 기록했습니다. [1] 많은 노력이 높은 실온 이온 전도성, 유연성 및 기계적 강도를 갖는 얇은 고체 전해질(SSE) 필름에 초점을 맞추었습니다. [2] 1의 주변 온도 이온 전도도. [3] 3은 액체 전해질을 능가하는 25mS cm-1의 실온 이온 전도도에 도달했습니다. [4] 준비된 SPE 멤브레인은 2의 높은 실온 이온 전도도를 나타냅니다. [5] 열악한 실온 이온 전도도와 리튬 수지상 형성은 고체 전해질의 주요 문제입니다. [6] nan [7] nan [8] nan [9] nan [10] 이상적인 주변 온도 이온 전도성을 가진 PCPCE는 LATP와 고체 전극 사이의 계면 저항을 크게 감소시키고 이들 사이의 직접적인 반응 및 접촉을 효과적으로 방지할 수 있습니다. [11] 놀랍게도 CMP/MMT는 높은 실온 이온 전도도(~1. [12] nan [13] nan [14] nan [15] nan [16] nan [17] 이 자체 형성 고분자 전해질은 높은 실온 이온 전도도를 포함하여 우수한 특성을 나타냅니다(2. [18] 입방체 요오드 도핑 Li3FSe는 0의 벌크 활성화 에너지와 함께 5 × 10-5 S/cm의 실온 이온 전도도를 갖는다. [19] PIL-PEI의 이중 가교 네트워크는 만족스러운 유연성, 열 안정성 및 놀라운 전기화학적 성능(실온 이온 전도도, 1. [20] nan [21] nan [22] 그러나, 기존의 제조 경로에 의해 유도된 열악한 실온 이온 전도도 및 낮은 밀도의 SSE는 잠재적인 미래 응용을 제한합니다. [23] nan [24] EIS 연구에서 GPE를 함유한 30wt% TPeAI가 가장 낮은 벌크 임피던스, Rb(32옴) 및 가장 높은 실온 이온 전도도(2. [25] 이 연구에서 개발된 높은 안전성과 높은 주변 온도 이온 전도성을 가진 고분자 전해질은 고체 리튬 이온 배터리에 잠재적으로 유용합니다. [26] 이오노겔은 높은 신축성(>1000%), 우수한 실온 이온 전도도(최대 5.5%)를 나타내는 폴리(이온성 액체) 및 하이퍼브랜치 폴리머(거대 가교제)로 구성된 특수 가교 네트워크로 구성됩니다. [27] nan [28] nan [29] nan [30] 여기에서 우리는 1의 높은 실온 이온 전도도를 갖는 새로운 종류의 육각형 Na5YSi4O12를 제안합니다. [31] 차세대 전고체 리튬 금속 배터리에 유연하고 견고하며 저렴한 고체 고분자 전해질을 적용하는 것은 이러한 전해질의 낮은 실온 이온 전도도와 배터리의 작은 임계 전류 밀도로 인해 어려움을 겪고 있습니다. [32] 안전성과 누수 문제가 없는 전고체 전지를 개발하기 위해서는 가공성이 좋고, 상온 이온 전도성이 향상되고, 계면 상용성이 향상된 얇은 고체 고분자 전해질(SPE)이 시급하다. [33] Electrochemical Impedance Spectroscopic 및 Raman Spectroscopic 기술로 조사한 6개의 다른 GPE 샘플 중에서 가장 좋은 주변 온도 이온 전도도는 4입니다. [34] 예비 결과는 실온에서 이온 전도도가 6만큼 높다는 것을 보여줍니다. [35] nan [36] nan [37] nan [38] 소량의 ZnO-NPs가 양성자 전도를 크게 향상시키는 것으로 밝혀졌습니다. 얻을 수 있는 가장 높은 실온 이온 전도도는 4였습니다. [39] 높은 실온 이온 전도성, 넓은 전기화학적 창 및 유리한 열 안정성을 갖는 고체 전해질은 전고체 리튬 금속 배터리의 실제 적용에 중요합니다. [40] 여기에서 우리는 높은 실온 이온 전도도를 갖는 폴리(비닐리덴 플루오라이드-코-헥사플루오로프로필렌)(PVDF-HFP) 기반 염 고분자 고체 전해질(PISSE)을 설계합니다(1. [41] 고체 전해질의 응용에는 높은 상온 이온 전도도와 기계적 물성이 필수적입니다. [42] 그들의 XRD 패턴은 x = 0, 1, 2, 3, 5 mol% 및 2의 가장 높은 실온 이온 전도도에 대해 결정상 β-Li3PS4만이 검출된다는 것을 보여줍니다. [43] 열악한 실온 이온 전도도와 좁은 전기화학적 안정 창은 고에너지 밀도 리튬 금속 배터리(LMB)를 위한 기존의 폴리(에틸렌 옥사이드) 기반(PEO 기반) 고체 고분자 전해질(SPE)의 적용을 심각하게 방해합니다. [44] 그러나 GPE의 계면 및 고온 불안정성과 SPE의 낮은 실온 이온 전도도는 여전히 실제 구현을 제한합니다. [45] nan [46] nan [47] nan [48] nan [49] nan [50]