Modified Sol Gel Synthesis Research Articles

In-situ carbon integration on atomically dispersed platinum metal oxide nanocomposites for hydrogen evolution reaction

In this study, a novel in-situ carbon growth technique by a modified sol gel synthesis method is presented. The carbon support developed on a transition metal oxide composite transforms the electronic conductivity and is engineered for hydrogen evolution reaction by a dispersion of unit atomic concentration of platinum. Through two different synthesis techniques, platinum dispersion is implemented on the metal oxide-carbon system, one by direct sol-gel technique and another by chemical reduction technique, whereby a homogeneous dispersion of the noble metal on the composite is achieved. Carbon-based cerium oxide and titanium oxide composites are used as the base material, and one atomic percentage of platinum metal is ensured while synthesizing each of the carbon composites. The functionality of these catalysts towards hydrogen evolution reaction in a 0.5 M H2SO4 acidic media revealed the synthesis technique's uniqueness and the effect of metal support interaction that plays a vital role in the electrocatalytic activity. The intrinsic activity of the titania system, along with enhanced metal support interaction due to highly enriched platinum availability on the surface of the substrate, provides for strong electrochemical activity. The titanium oxide carbon composite with platinum dispersed by hydrazine reduction exhibited the finest activity with an overpotential of just 44 mV at j = 10 mA/cm2 and a tafel slope of 118 mV/dec. The gas chromatographic analysis on platinum supported titania catalyst showcased better performance by a margin of four times than the commercial three weight percentage platinum supported carbon.

Halide solid-state electrolyte achieving high ionic conductivity by engineering nanocrystals

Lithium-ion battery (LIB) technologies utilize liquid electrolytes, which can cause safety issues due to electrolyte leakage, uncontrolled side reactions between the liquid electrolyte and electrode, dendrite formation, and flammability of the liquid components with air. These problems can be minimized using solid-state electrolytes (SSEs) containing the functionality of an electrolyte. Our research discovery meets the urgent requirement of developing rapid ionic conductive solid-state electrolytes for lithium metal battery applications, emphasizing safe operation and high energy density. The breakthrough lies in the functionalization and tunability of monoclinic doped Li3InCl6-based solid electrolytes to achieve desirable structural and high ionic conductivity (> 0.15 S cm−1). We report four formulations of solid-state electrolytes obtained using modified sol–gel synthesis and used to assemble symmetrical half cells for electrochemical impedance spectroscopic (EIS) analyses in the frequency ranging from 10–2 to 106 Hz under five different temperatures (15–55 °C). The EIS data of non-doped, F-, Ce-, and Mo-doped electrolytes showed R1 (solid-electrolyte) ranging from 0.05 to 0.10 Ohm and R2 (interfacial) resistance varying from 0.05 to 1.25 Ohm, resulting in superionic conductivity (0.15–0.45 S cm−1), equivalent to the commercially available liquid electrolyte and evidenced two magnitudes increase compared to the published data.Graphical abstract

Boosting LiMn2O4 Diffusion Coefficients and Stability via Fe/Mg Doping and MWCNT Synergistically Modulating Microstructure

The dissolution of manganese and its deposition on the anode surface cause poor cycling stability in lithium-ion batteries. To alleviate these issues, this study probes the electrochemical activity of highly crystalline and cation-adjusted lithium manganese oxide (LMO) carbon spinel composite obtained via a modified sol-gel synthesis procedure. The pristine LMO cathode was functionalized with a Fe and Mg alloy and fused with purified multiwalled carbon nanotubes (MWCNTs) to form a catalytically stabilized LiMn1.98Fe0.01Mg0.01O4/MWCNT (LMO-FeMg/MWCNT) framework. High-resolution SEM analysis showed well-dispersed particles in the nanometer size range. The electrochemical characteristics of the novel composite materials yielded favourable electrochemical results with diffusion coefficients of 1.91 × 10−9 cm2·s−1 and 5.83 × 10−10 cm2·s−1 for LMO-FeMg and LMO-FeMg/MWCNT, respectively. This improvement was supported by impedance studies which showed a considerable Rct reduction of 0.27 Ω and 0.71 Ω. The cation stabilized system outperformed the pristine LMO material with specific capacities around 145 mAh·g−1, due to an enhancement in electrochemical activity and structural stability.

Stabilization of the cubic, fast-ion conducting phase of Li7La3Sn2O12 garnet by gallium doping.

All-solid-state batteries present promising high-energy-density alternatives to conventional Li-ion chemistries, and Li-stuffed garnets based on Li7La3Zr2O12 (LLZO) remain a forerunner for candidate solid-electrolytes. One route to access fast-ion conduction in LLZO phases is to stabilize the cubic LLZO phase by doping on the Li sites with aliovalent ions such as Al3+ or Ga3+. Despite prior attempts, the stabilization of the cubic phase of isostructural Li7La3Sn2O12 (LLSO) by doping on the Li sites has up to now not been realised. Here, we report a novel cubic fast-ion conducting Li7La3Sn2O12-type phase stabilized by doping Ga3+ in place of Li. 0.3 mole of gallium per formula unit of LLSO were needed to fully stabilize the cubic garnet, allowing structural and electrochemical characterizations of the new material. A modified sol-gel synthesis approach is introduced in this study to realise Ga-doping in LLSO, which offers a viable route to preparing new Sn-based candidate solid-electrolytes for all-solid-state battery applications.

Luminescent thermometry with YVO4:Er/Nd: Achieving high sensitivities within the 1st and 2nd biological windows

YVO4:Er3+, Nd3+ powders were prepared by the modified sol gel synthesis route using glucose as chelating agent and characterized by X-ray powder diffraction (XRD) and scanning electron microscope (SEM). Under 660 nm excitation, four infrared emission bands located between 790 and 845 nm, 870 and 930 nm, 950 and 1030 nm, and between 1050 and 1100 nm were observed, and were assigned the transitions 4F5/2 – 4I9/2 (Nd) and 4I9/2 – 4I15/2 (Er), 4F3/2 – 4I9/2 (Nd), 4I11/2 – 4I15/2 (Er), and 4F3/2 – 4I11/2 (Nd), respectively. The performance of these powders as optical temperature sensors using the luminescence intensity ratio (LIR) technique between thermally coupled levels (TCLs) and non-thermally coupled levels (non-TCLs) was studied within the temperature range of 293–373 K. Using different combinations of the emission intensities at 809, 880, 914 and 1003 nm, three distinct (LIR) temperature sensors schemes were built, with both excitation and emission within the first and second biological window. These LIRs relative sensitivity (Sr) and temperature uncertainties (δT) were investigated for samples with different Er and Nd concentrations. Sr values up to 2.08 ± 0.03%. K−1 and δT smaller than 1 K, were obtained. Repeatability and reproducibility tests demonstrated the reliability of the proposed LIRs.

A Modified Sol-Gel Synthesis of Anatase {001}-TiO2/Au Hybrid Nanocomposites for Enhanced Photodegradation of Organic Contaminants.

A sol-gel synthesis technique was employed for the preparation of anatase phase {001}-TiO2/Au hybrid nanocomposites (NCs). The scalable, schematic, and cost-efficient method was successfully modified using HF and NH4OH capping agents. The photocatalytic activity of the as-synthesized {001}-TiO2/Au NCs were tested over 2-cycle degradation of methylene blue (MB) dye and pharmaceutical active compounds (PhACs) of ibuprofen and naproxen under direct sunlight illumination at 35 °C and 44,000 lx. Transmission electron microscopy (TEM), high resolution transmission electron microscopy (HR-TEM), fast Fourier transform (FFT), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) were employed for the characterization of the as-prepared sample. The characterization results from the TEM, XPS, and XRD studies established both the distribution of Au colloids on the surface of TiO2 material, and the presence of the highly crystalline structure of anatase {001}-TiO2/Au NCs. Photodegradation results from the visible light irradiation of MB indicate an enhanced photocatalytic performance of Au/TiO2 NCs over TiO2. The results from the photocatalytic activity test performed under direct sunlight exposure exhibited promising photodegradation efficiencies. In the first cycle, the sol-gel synthesized material exhibited relatively better efficiencies (91%) with the MB dye and ibuprofen, while the highest degradation efficiency for the second cycle was 79% for the MB dye. Pseudo first-order photodegradation rates from the first cycle were determined to be comparatively slower than those from the second degradation cycle.

Analyzing the role of copper in the soot oxidation performance of BaMnO3-perovskite-based catalyst obtained by modified sol-gel synthesis

• Carbon black decreases the calcination temperature to obtain perovskite structure. • The distribution of copper depends on the calcination temperature. • The insertion of copper into the structure is promoted with calcination temperature. • BMC3-C600 shows the most stable performance during cyclic experiments. • The presence of copper on surface and of oxygen vacancies are promoted for BMC3-C600. A series of BaMn 0.7 Cu 0.3 O 3 solids were prepared by a modified sol-gel method in which carbon black (VULCAN XC-72R), and different calcination temperatures (BMC3-CX, where X indicates the calcination temperature) have been used. The fresh and used catalysts were characterized by ICP-OES, XRD, XPS, FESEM, TEM, O 2 -TPD and H 2 -TPR. The presence of a carbon black during sol-gel synthesis of BMC3 mixed oxide allows diminishing the calcination temperature needed to achieve the perovskite structure, but it hinders the formation of the BaMnO 3 polytype. The use of low calcination temperatures during synthesis reduces the sintering effects, and the mixed oxides present lower particle size, slightly higher BET surface areas and macropores with lower diameter than BMC3. The distribution of copper in BMC3-CX catalysts depends on the calcination temperature and copper insertion into the perovskite structure is promoted as the calcination temperature increases. All BMC3-CX catalysts are active for NO to NO 2 and NO x -assisted soot oxidation processes, but only BMC3-C600 and BMC3-C700 show higher catalytic activity than BMC3 reference catalyst. BMC3-C600 presents the best performance as it features a high amount of surface copper and oxygen vacancies that increase during reaction. The comparison between the performance of the two best catalysts of the BM-CX series (BM-C700) and the BMC3-CX series (BMC3-C600) suggests that the unique advantage of using copper in the modified sol-gel synthesis is an additional decrease of 100 °C in the calcination temperature used for the synthesis of the best catalyst, which is 700 °C for BM-CX and 600 °C for BMC3-CX.

Synthesis of vacancy-rich titania particles suitable for the additive manufacturing of ceramics

In the last decades, titania (or TiO2) particles played a crucial role in the development of photo-catalysis and better environmentally-friendly energy-harvesting techniques. In this work, we engineer a new generation of TiO2 particles rich in oxygen vacancies using a modified sol–gel synthesis. By design, these vacancy-rich particles efficiently absorb visible light to allow carefully-controlled light-induced conversion to the anatase or rutile crystalline phases. FTIR and micro-Raman spectroscopy reveal the formation of oxygen vacancies during conversion and explain this unique laser-assisted crystallization mechanism. We achieve low-energy laser-assisted crystallization in ambient environment using a modified filament 3D printer equipped with a low-power laser printhead. Since the established high-temperature treatment necessary to convert to crystalline TiO2 is ill-suited to additive manufacturing platforms, this work removes a major fundamental hurdle and opens whole new vistas of possibilities towards the additive manufacturing of ceramics, including carefully-engineered crystalline TiO2 substrates with potential applications for new and better photo-catalysis, fuel cells and energy-harvesting technologies.

Modified Sol-Gel Synthesis of Mesoporous Borate Bioactive Glasses for Potential Use in Wound Healing.

In this study, we successfully utilized nitrate precursors for the synthesis of silver (Ag)-doped borate-based mesoporous bioactive glass (MBGs) based on the 1393B3 glass formulation in the presence of a polymeric substrate (polyvinyl alcohol (PVA)) as a stabilizer of boric acid. The X-ray diffraction (XRD) analysis confirmed the glassy state of all the MBGs. The incorporation of 7.5 mol% Ag into the glass composition led to a decrease in the glass transition temperature (Tg). Improvements in the particle size, zeta potential, surface roughness, and surface area values were observed in the Ag-doped MBGs. The MBGs (1 mg/mL) had no adverse effect on the viability of fibroblasts. In addition, Ag-doped MBGs exhibited potent antibacterial activity against gram-positive and gram-negative species. In summary, a modified sol–gel method was confirmed for producing the Ag-doped 1393B3 glasses, and the primary in vitro outcomes hold promise for conducting in vivo studies for managing burns.

Modified sol-gel synthesis of lithium ternary oxide

Lithium-ion batteries currently equip portable electronic devices, such as smartphones and laptops, and are the choice to power electric vehicles. The scarcity of raw materials in nature, however, has required the development of new technologies and the ternary lithium compound LiNi1/3Mn1/3Co1/3O2 has stood out as an alternative for replacing part of the cobalt in LiCoO2 by nickel and manganese, which are more abundant, reducing the electrode’s cost. The sol-gel route for synthesis of ternary electrode materials has been widely used, but it faces problems of volumetric expansion due to the decomposition of organic material during calcination. To improve the synthesis of the ternary compound, a modified sol-gel route with control of the heating kinetics in the pre-calcination step and without pH control was investigated in this study. The compound was analyzed by X-ray diffraction, Rietveld refinement, Fourier transform infrared absorption spectroscopy, and Raman that showed the purification of the ternary phase with appropriate crystallinity for application as electrode in batteries from 700 ºC. In conclusion, ternary synthesis with rate control during heat treatment may be a useful alternative for industrial scale-up production.

Analyzing the Role of Copper in the Soot Oxidation Performance of Bamno3-Perovskite-Based Catalyst Obtained by Modified Sol-Gel Synthesis

Analyzing the Role of Copper in the Soot Oxidation Performance of Bamno3-Perovskite-Based Catalyst Obtained by Modified Sol-Gel Synthesis

Investigation on the formation, structural and photocatalytic properties of mixed Mn-Zn ferrites nanoparticles embedded in SiO2 matrix

The structure, morphology and photocatalytic features of the Mn-Zn ferrite nanoparticles embedded in SiO2 matrix produced by a modified sol-gel synthesis were investigated. The synthesis consists of mixing the metal nitrates, 1,4-butanediol and tetraethylorthosilicate, formation of the SiO2 matrix by gelation, formation of the metallic succinate precursors by heating the gel up to 200 °C and formation of the ferrite system by thermal treatment at higher temperatures. The formation of Mn-, Zn- and Fe-succinate precursors up to 200 °C and their decomposition into ferrites up to 400 °C was confirmed both by thermal analysis and Fourier-transform infrared spectroscopy. The X-ray diffraction provided information on the crystalline phases, crystallite size and lattice constant, while the morphology of the samples was investigated by transmission electron microscopy. The crystallite size increased (30.5–53.4 nm), while the energy band gap of the samples decreased (2.09−1.33 eV) with the increase of the Mn content in the ferrite; thus, the amount of manganese nitrate used in the synthesis could be an easy tailoring approach of the mixed Mn-Zn ferrites. All samples showed sonophotocatalytic activity, being able to degrade Rhodamine B under visible light irradiation, Mn0.3Zn0.7Fe2O4@SiO2 sample having the best sonophotocatalytic performance.

Nanostructured mesoporous g-Fe2O3: a novel photocatalyst for degradation of organic pollutants

The modified sol-gel synthesis technique was used to created of nanostructured maghemite (γ-Fe2O3). It has been shown that the molar concentration of the original precursors during synthesis affects on the average particle sizes, specific surface area, pore size distributions, optical and conductivity properties. The XPS metod allowed to establish features of electronic structure of the synthesized materials. Optimal conditions for the synthesis of nanostructured maghemite with mesoporous structure were selected. The mechanism of electrical conductivity formation for synthesized mesoporous materials was established. The width of the band gap is determined and its dependence on the molar concentration of precursors is established. The positive correlation between the specific surface area of γ-Fe2O3 samples and photocatalytic activity was installed - the photocatalytic activity of synthesized γ-Fe2O3 increase with growth of specific surface area of γ-Fe2O3 samples.

Modified sol gel synthesis of MoO3 NPs using organic template: synthesis, characterization and electrochemical investigations

Over the past numerous decades, unrelenting attention has been dedicated for sustainable design and synthesis of electrochemical metal oxide with controlled morphology and nano scale structural complexity to enhance their electrochemical properties. Here in, we reported the sol–gel synthesis of molybdenum trioxide NPs using bioactive compounds of Euphorbia cgnata Boiss as fuel. The current study demonstrated the stabilization of molybdenum trioxide nanoparticles by Benzeneethanamine and Benzenemethanol. The chemical and structural intrinsic features with low band gap energy of 2.02 eV rendered the MoO3 NPs suitable for electrochemical applications. On this account, we fabricated MoO3 nickel foam electrode to investigate its supercapacitor properties. MoO3 electrode revealed the moderate capacitance of 63.5 F/g at 2 mV/s with energy density of 1.8 Wh/kg and high power density of 4551.3 W/kg. Therefore, the overall results are proposing the potential of fabricated electrode toward energy storage device like supercapacitor.

A modified sol-gel synthesis to yield a stable Fe3+/ZnO photocatalyst: Degradation of water pollutants and mechanistic insights under UV and visible light

Abstract We synthesized pristine and Fe3+ doped ZnO photocatalysts with a modified sol-gel method, which included a peptization step. X-ray diffraction, scanning and transmission microscopy identified the crystalline nature of pure and doped ZnO having wurtzite (hexagonal) structure. UV–vis diffuse spectroscopy detected a red shift towards longer wavelengths upon incorporation of Fe3+ in ZnO, revealing that the Fe3+ ions replaced some of the crystal lattice Zn2+ ions. X-ray photoelectron spectroscopy demonstrated the coexistence of Fe2+ and Fe4+ ions in addition to the presence of Zn vacancies. Fe doping also reduces the dissolution of ZnO in acidic or alkaline solution, as well as its photocorrosion through self-oxidation. Moreover, the nano-oxides were stable at a pH of 7.5. The photocatalytic activity was tested to degrade methylene blue (MB, 12 mg/L, reaction volume of 2 L)) under UV and 4-chlorophenol (4-CP, 0.6 mg/L, reaction volume of 0.8 L) under Vis light. Fe0.8-ZnO had the highest activity, degrading 93 % MB (UV, 2 h) and 73 % 4-CP (Vis, 1 h), respectively. The increased activity ascribes to higher BET surface area (136 m2 g−1 vs 42 m2 g−1 for the control ZnO), surface hydroxyl groups, increased photons absorption at longer wavelength and decreased electron-hole recombination. Hydroxyl radicals (OH ) and superoxide anions (O2 -) were the key species responsible for the pollutant decomposition as the scavenging tests demonstrated. In the light of the observed characterization data and ROS (reactive oxidizing species) experiments, we propose a photocatalytic mechanism.

Mesoporous Bioactive Glass Combined with Graphene Oxide Quantum Dot as a New Material for a New Treatment Option for Dentin Hypersensitivity.

Dentin hypersensitivity is one of the most common clinical conditions usually associated with exposed dentinal tubules. The purpose of this study was to identify the potential of a graphene oxide quantum dot coating for mesoporous bioactive glass nanoparticles as a new material for the treatment of dentin hypersensitivity by investigating its mineralization activity and dentinal tubules sealing. Mesoporous bioactive glass nanoparticle was fabricated by modified sol-gel synthesis. X-ray diffraction was performed to characterize the synthesized nanoparticle Fourier transform infra-red spectroscopy investigated the functionalized surfaces. The distribution of the specific surface area and the pore size was measure by Pore size analysis. The morphology of sample was observed by Field Emission Scanning Electron Microscope (FESEM) and Field Emission Transmission Electron Microscope (FETEM). After disk-shaped specimens of mesoporous bioactive glass nanoparticles and graphene oxide quantum dot coated mesoporous bioactive glass nanoparticles (n = 3) were soaked in the simulated body fluid for 0, 1, 5, 10,and 30 days, the amount of ions released was observed to confirm the ionic elution for mineralization. Sensitive tooth model discs (n = 20) were applied with two samples and evaluated the dentinal tubule sealing ability. The spherical mesoporous bioactive glass nanoparticles and graphene oxide quantum dot coated mesoporous bioactive glass nanoparticles with a diameter of about 500 nm were identified through FESEM and FETEM. The ion release capacity of both samples appeared to be very similar. The amount of ion released and in vitro mineralization tests confirmed that graphene oxide quantum dot coating of mesoporous bioactive glass nanoparticles did not inhibit the release of calcium, silicon and phosphate ions, but rather that graphene oxide quantum dot promoted hydroxyapatite formation. In the FESEM image of the sensitive tooth disc surface, it was observed that graphene oxide quantum dot coated mesoporous bioactive glass nanoparticles sealed tightly the dentinal tubules. The graphene oxide quantum dot coating of mesoporous bioactive glass nanoparticles not only showed the excellent dentinal sealing ability but also rapidly promoted mineralization while minimizing the size increase by coating the mesoporous bioactive glass nanoparticles.

Sol-gel synthesis and determination of optimal sintering conditions of the Li6.75La3Zr1.75Nb0.25O12 solid electrolyte

Solid electrolytes are widely used in electrochemical devices. Among these materials, electrolytes with the lithium-ion conductivity can be used in high-energy lithium and lithium-ion power sources. The perspective Li6.75La3Zr1.75Nb0.25O12 solid electrolyte was synthesized by modified sol-gel synthesis method using the sparingly soluble Nb2O5 as one of the initial compounds. The influence of pressure and final sintering temperature on phase composition, density and lithium-ion conductivity was studied. Solid electrolyte obtained at 1150°C was single phase and had a cubic structure with the space group Ia-3d. Thus in the presented work, the cubic modification of Li6.75La3Zr1.75Nb0.25O12 was obtained by thermal treatment for 1 h at 1150°C (versus 36 h at 1200°C in the literature). Moreover at this temperature the samples had the highest density and total lithium-ion conductivity (3.9·10–5 Scm–1 at 25°C). According to the SEM study ceramic samples have a dense structure with a particle size ∼1-3 μm. Solid electrolyte was also obtained by isostatic pressing at a pressure of 500 MPa but the values of density and total lithium-ion conductivity were comparable with that of the samples compressed statically.

Surface modification using silver nanoparticles for Y4Al2O9:Nd – Synthesis and their selected studies

Abstract A modified sol-gel synthesis was used to produce powders of yttrium aluminum monoclinic Y4Al2O9 (YAM) doped with 1 at% of Nd3+ ions. This was followed by surface modification using dispersed Ag metallic nanoparticles (AgNPs) in a concentration of n = 1, 2 and 3 wt%. The structure of the prepared composites was characterized using X-ray diffraction patterns (XRD), scanning electron microscopy (SEM), absorption, Raman and emission measurements. To the best of our knowledge, we present for the first time far IR spectrum of the family of RE4Al2O9 (RE: rare earth ions) compounds. The measurements confirm the purity of the obtained polycrystals.

Enhanced Power Performance of Highly Mesoporous Sol-Gel TiC Derived Carbons in Ionic Liquid and Non-Aqueous Electrolyte Based Capacitors

The electrical double layer capacitors (EDLC) based on hierarchical micro-mesoporous sol-gel TiC derived carbon (SgTiC-CDC) electrodes and 1-ethyl-3-methylimidazolium tetrafluoroborate (EtMeImBF4) and 1M Et3MeNBF4 + acetonitrile (AN) as the electrolytes were tested to establish the electrochemical characteristics and region of ideal polarizability. The precursors for the micro-mesoporous carbon electrodes were synthesized via modified sol-gel synthesis process. Compared to traditional titanium carbide derived carbons, where precursor carbide is commercially available, the sol-gel TiC derived hierarchical carbon materials exhibit larger specific density functional theory (DFT) surface areas (up to 1700 m2 g−1) and an unique pore size distribution with more mesopores between 2 and 10 nm. The electrochemical properties of the EDLCs were investigated using the cyclic voltammetry, electrochemical impedance spectroscopy, galvanostatic charge/discharge and constant power discharge methods. The EDLCs demonstrated nearly ideal capacitive behavior even at very high charging/discharging currents (10 A g−1) and cell potential scan rates (500 mV s−1). The EDLCs completed from SgTiC-CDC materials and EtMeImBF4 and Et3MeNBF4 + AN show good energy efficiencies (varying from 93% to 95% at current 1 A g−1) and coulombic efficiency values exceeded 99%. Thus, the EDLCs completed are very promising devices for extremely high power/energy density applications.

Preparation of a Li7La3Zr1.5Nb0.5O12 Garnet Solid Electrolyte Ceramic by using Sol-gel Powder Synthesis and Hot Pressing and Its Characterization

In this study, we prepared and characterized Nb-doped Li7La3Zr2−xO12 (LLZNO) powder and pellets with a cubic garnet structure by using a modified sol-gel synthesis and hot pressing. LLZNO powder with a very small grain size and cubic structure without secondary phases could be obtained by using a synthesis method in which Li and La sources in a propanol solvent were mixed together with Zr and Nb sources in 2-methoxy ethanol. A pure cubic phase LLZNO pellet could be fabricated from the prepared LLZNO and an additional 6-wt% of Li2CO3 powder by hot pressing at 1050 °C and 15.8 MPa. The hot-pressed LLZNO pellet with a relative density of 99% exhibited a very dense surface morphology. The total Li ionic conductivity of the hot-pressed LLZNO was 7.4×10 −4 S/cm at room temperature, which is very high level compared to other reported values. The activation energy for ionic conduction was estimated to be 0.40 eV.