Stacked Layer Structure Research Articles

Threshold Switching and Resistive Switching in SnO2-HfO2 Laminated Ultrathin Films

Polycrystalline SnO2-HfO2 nanolaminated thin films were grown by atomic layer deposition (ALD) on SiO2/Si(100) and TiN substrates at 300 °C. The samples, when evaluated electrically, exhibited bipolar resistive switching. The sample object with a stacked oxide layer structure of SnO2 | HfO2 | SnO2 | HfO2 additionally exhibited bidirectional threshold resistive switching properties. The sample with an oxide layer structure of HfO2 | SnO2 | HfO2 displayed bipolar resistive switching with a ratio of high and low resistance states of three orders of magnitude. Endurance tests revealed distinguishable differences between low and high resistance states after 2500 switching cycles.

The influence of divalent ions on the osmotic energy conversion performance of 2D cation exchange membrane in reverse electrodialysis process

As reverse electrodialysis (RED) technology evolves, achieving high-performance osmotic energy conversion (OEC) necessitates porous membranes with exceptional ion selectivity and permeability. Two-dimensional membranes crafted from graphene oxide (GO) or MXene stand out for their immensely high surface charges, which facilitate superb ion selectivity during transport. Their unique layered stacking structure further yields ultra-small nanochannel radii, bolstering ion selectivity while maintaining high permeability. This makes them prime candidates for osmotic energy conversion. However, the presence of divalent ions in natural seawater readily alters the surface charge density and interlayer spacing of these 2D membranes, significantly impacting their OEC performance, resulting in a power density reduction of about 6 % -10 %. Prior research focused on the ionic properties of divalent ions but overlooked their impact on the nanochannel structure, including changes in interlayer spacing and surface charge density. This study thus delves into the OEC performance variations of GO and MXene 2D layered membranes under varying divalent ion concentrations and salt ratios. Starting from the ion properties of divalent ions and their impact on the nanochannel structure, combined with simulation research, explain their mechanism of action. This research offers theoretical foundations for the future design and application of 2D layered membranes, providing novel solutions and insights to tackle critical challenges like enhancing power density and adapting to real seawater conditions.

Alumina fiber/reduced graphene oxide composite films for high-temperature heating and sensing

Reduced graphene oxide (rGO) and its composite films have aroused intense interest in electrical heating and temperature sensing fields, but the working temperature is usually limited because the internal layer-stacked structure is breakable at high temperature. In order to promote structure stability, a series of Al2O3 fiber/rGO composite films were developed. It is found that gaseous products mainly including CO2 and CO during thermal reduction contribute to pores, bulges and intervals in rGO films, while appropriate Al2O3 fiber has an adhesion effect on rGO sheets and tightens them together, in which case defects can hardly form and the layered structure is significantly compacted. Therefore, the degree of stacking order and tensile strength tend to increase, resulting in the improvement of structure stability and decrease of electrical resistivity. However, excess Al2O3 fiber makes the formation of debris and cracks, causing the deterioration of conductivity and mechanical properties. With 20 wt% Al2O3 fiber, the composite films can bear higher heating voltage than pure rGO films and stabilize at 634.65 °C under 36 V, which also keep a good linearity between resistance and temperature from 25 to 600 °C, exhibiting a considerable temperature coefficient of resistance (TCR) with −1.70×10−3 /°C at room temperature.

CO2/N2 and redox dual-responsive organogels based on ferrocenemethanol and octadecylamine

Herein, we report a CO2/N2 and redox dual-responsive organogel using low molecular mass gelators (LMWGs) of octadecylamine (NC18) and ferrocenemethanol (FcOH). The organogels of NC18-FcOH in cyclohexane have a layered stacking structure and the critical gelling concentration (CGC) is 55 mmol/L. The organogel can be reversibly switched between gel and solution states by CO2 trigger, resulting from the reversible protonation of NC18. Moreover, the organogel can be destroyed by a redox reaction after adding Ce(NH4)2(NO3)6, originating from the oxidization of the ferrocene group in FcOH. Compared with other redox-responsive gelators, complex organic synthesis could be avoided since FcOH is a commercially available compound. The dual responsiveness of the organogel allows for the smart control of the “sol-gel” transition, which has potential applications in functional materials and sensors.

Flexible Graphene Film-Based Antenna Sensor for Large Strain Monitoring of Steel Structures.

In the field of wireless strain monitoring, it is difficult for the traditional metal-made antenna sensor to conform well with steel structures and monitor large strain deformation. To solve this problem, this study proposes a flexible antenna strain sensor based on a ductile graphene film, which features a 6.7% elongation at break and flexibility due to the microscopic wrinkle structure and layered stacking structure of the graphene film. Because of the use of eccentric embedding in the feeding form, the sensor can be miniaturized and can simultaneously monitor strain in two directions. The sensing mechanism of the antenna is analyzed using a void model, and an antenna is designed based on operating frequencies of 3 GHz and 3.5 GHz. The embedding size is optimized using a Smith chart and impedance matching principle. Both the simulation and experimental results verify that the resonant frequency and strain magnitude are linearly inversely proportional. The experimental results show that the strain sensitivity is 1.752 kHz/με along the geometric length and 1.780 kHz/με along the width, with correlation coefficients of 0.99173 and 0.99295, respectively.

High-Performance 3D Sand Printing Process Using Interlayer Heating

Sand mold 3D printing technology has been recognized as a digital, high-quality, and promising sand mold forming method. However, sand mold 3D printing technology has drawbacks, such as single molding material and long curing time, which limit its further industrial application. Therefore, this study proposes a method for forming composite sand molds based on a layer-stacking structure and a strengthening method based on interlayer heating. The influence of the process parameters on the properties of traditional and composite sand molds was systematically studied. Experimental results demonstrated that when the heating temperature was 150 °C, the enhancement of the sand mold was obvious, with an increase of approximately 20% compared to untreated sand mold. When the composite sand mold with a laminated thickness of 1.5 mm was heated at this temperature, its tensile strength reached 1.53 MPa, and compressive strength reached 5.80 MPa, which met the casting requirements. The composite sand mold printed by interlayer heating has excellent casting performance and economic advantages, which provide theoretical guidance for the high-performance printing of sand molds.

Construction of High-Performance Anode of Potassium-Ion Batteries by Stripping Covalent Triazine Frameworks with Molten Salt.

Covalent triazine frameworks (CTFs) are promising battery electrodes owing to their designable functional groups, tunable pore sizes, and exceptional stability. However, their practical use is limited because of the difficulty in establishing stable ion adsorption/desorption sites. In this study, a melt-salt-stripping process utilizing molten trichloro iron (FeCl3) is used to delaminate the layer-stacked structure of fluorinated covalent triazine framework (FCTF) and generate iron-based ion storage active sites. This process increases the interlayer spacing and uniformly deposits iron-containing materials, enhancing electron and ion transport. The resultant melt-FeCl3-stripped FCTF (Fe@FCTF) shows excellent performance as a potassium ion battery with a high capacity of 447 mAh g-1 at 0.1 A g-1 and 257 mAh g-1 at 1.6 A g-1 and good cycling stability. Notably, molten-salt stripping is also effective in improving the CTF's Na+ and Li+ storage properties. A stepwise reaction mechanism of K/Na/Li chelation with C═N functional groups is proposed and verified by in situ X-ray diffraction testing (XRD), ex-situ X-ray photoelectron spectroscopy (XPS), and theoretical calculations, illustrating that pyrazines and iron coordination groups play the main roles in reacting with K+/Na+/Li+ cations. These results conclude that the Fe@FCTF is a suitable anode material for potassium-ion batteries (PIBs), sodium-ion batteries (SIBs), and lithium-ion batteries (LIBs).

Concept and simulation of a novel dual-layer linear ion trap mass analyzer for micro-electromechanical systems mass spectrometry.

This paper proposed a dual-layer linear ion trap mass analyzer (dLIT) based on micro-electromechanical systems (MEMS) technology and stacked-layer structure for the development of MEMS mass spectrometry. Its basic performance and potential capabilities were explored by ion trajectory simulations. The theoretical formulas were modified by implementing multipole expansion. The simulation results were confirmed to be highly consistent with theoretical calculations in multiple aspects, including stability diagram, secular frequencies, and mass linearity, with only a deviation of 1-2%. In the boundary ejection mode, close to 100% ejection was achieved in a single dimension by applying extra quadrupole DC voltage. Preliminary simulation results showed that dLIT can achieve a peak width of ∼2 mass units (full width at half maximum, FWHM) for m/z 60 ions even at pressures as high as 50 Pa. Furthermore, the application of AC frequency scanning mode in dLIT was also evaluated, and preliminary simulation results yield a peak width of 0.3-0.4 mass units (FWHM). The dLIT offered several advantages, including high-precision fabrication at the sub-millimeter scale, excellent high-pressure performance, and a clear physical model. It preliminarily proved to be an ideal mass analyzer for MEMS mass spectrometry.

Layer-by-layer Assembly of Nanosheets with Matching Size and Shape for More Stable Membrane Structure than Nanosheet-Polymer Assembly.

Layer-by-layer (LbL) assembly of oppositely charged materials has been widely used as an approach to make two-dimensional (2D) nanosheet-based membranes, which often involves 2D nanosheets being alternately deposited with polymer-based polyelectrolytes to obtain an electrostabilized nanosheet-polymer structure. In this study, we hypothesized that using 2D nanosheets with matching physical properties as both polyanions and polycations may result in a more ordered nanostructure with better stability than a nanosheet-polymer structure. To compare the differences between nanosheet-nanosheet vs nanosheet-polymer structures, we assembled negatively charged molybdenum disulfide nanosheets (MoS2) with either positively charged graphene oxide (PrGO) nanosheets or positively charged polymer (PDDA). Using combined measurements by ellipsometer and quartz crystal microbalance with dissipation, we discovered that the swelling of MoS2-PrGO in ionic solutions was 60% lower than that of MoS2-PDDA membranes. Meanwhile, the MoS2-PrGO membrane retained its permeability upon drying, whereas the permeability of MoS2-PDDA decreased by 40% due to the restacking of MoS2. Overall, the MoS2-PrGO membrane demonstrated a better filtration performance. Additionally, our X-ray photoelectron spectroscopy results and analysis on layer density revealed a clearer transition in material composition during the LbL synthesis of MoS2-PrGO membranes, and the X-ray diffraction pattern suggested its resemblance to an ordered, layer-stacked structure. In conclusion, the MoS2-PrGO membrane made with nanosheets with matching size, shape, and charge density exhibited a much more aligned stacking structure, resulting in reduced membrane swelling under high salinity solutions, controlled restacking, and improved separation performance.

Sulfonate Functional Ultramicroporous Materials with Suitable Pore Size and Layer-Stacked Structure for C4 Olefins Purification.

Selective recognition of 1,3-butadiene from complex olefin isomers is vital for 1,3-butadiene purification, but the lack of porous materials with suitable pore structures results in poor selectivity and low capacity in C4 olefin separation. Herein, two sulfonate-functionalized organic frameworks, ZU-601 and ZU-602, are designed and show impressive separation performance toward C4 olefins. Benefiting from the suitable aperture size caused by the flexibility of coordinated organic ligand, ZU-601, ZU-602 that are pillared with different sulfonate anions could discriminate C4 olefin isomers with high uptake ratio: 1,3-butadiene/1-butene (207), 1,3-butadiene/trans-2-butene (10.1). Meanwhile, their layer-stacked structure enables the utilization of both intra- and interlayer space, enhancing the accommodation of guest molecules. ZU-601 exhibits record high 1,3-butadiene adsorption capacity of 2.90 mmol g-1 (0.5 bar, 298 K) among the reported flexible porous materials with high 1,3-butadiene/1-butene selectivity. The breakthrough experiments confirm their superior separation ability even for all five C4 olefin isomers, and the molecular-level structural change is well elucidated via powder, crystal analysis, and simulation studies. The work provides ideas toward advanced materials design with simultaneous high separation capacity and high separation selectivity for challenging separations.

Simulation study of a planar quadrupole mass filter for MEMS mass spectrometer

Micro-electro-mechanical system (MEMS) based mass spectrometry, MEMS mass spectrometry, emerges a new technique branch of miniature mass spectrometry. One of the main challenges hindering the development of MEMS mass spectrometry is the poor compatibility between the complex electrode structure of traditional ion optics and MEMS processes. This paper proposed a planar quadrupole mass filter utilizing a highly simplified stacked-layer structure and film electrodes, which is easy to fabricate with high precision by MEMS surface micromachining. The ion trajectory simulation model of the MEMS mass spectrometry chip involving all necessary ion optics was elaborated for investigating the preliminary performance of the planar quadrupole mass filter. By optimizing the crucial parameters such as the frequency of radio frequency voltage, the ratio of direct current voltage and radio frequency voltage, pre-pole length, main-pole length, and injection kinetic energy, the preliminary simulation result of planar quadrupole mass filter achieved a 1–2 Da peak width (at 50% of peak height) and 20–80% ion transmission efficiency. Importantly, the planar quadrupole mass filter demonstrated a maximum working pressure of 0.1 Pa (using air as the buffer gas), 100 times higher than that of conventional quadrupole mass filters, while maintaining a 0.7–1.8 Da peak width and ∼5% ion transmission efficiency. Additionally, to modify the theoretical formulas for the non-ideal quadrupolar field of planar quadrupole mass filter, a novel approach based on stability diagrams obtained by simulation was also introduced. The pretty good linearity (R2=1) between ion masses in the range of 10 to 100 Da and the corresponding radio frequency voltages was verified through the simulated mass spectra. Notably, the proportional coefficient of ion mass and radio frequency voltage exhibited a minimal 4% deviation between the simulated value (4.7132 V0P/Da) and the calculated value (4.9036 V0P/Da) through the modified formula. In conclusion, the preliminary simulation results demonstrated that the planar quadrupole mass filter possessed moderate performance, high-pressure tolerance, and excellent theoretical consistency, which proved it a promising technology of MEMS mass spectrometry. It can find applications in the fields of gas detection, including the rapid response to hazardous gas emissions and in situ detection of dissolved gases in the deep sea.

Broadband nonlinear optical response and sub-picosecond carrier dynamics in graphene-SnSe2 van der Waals heterostructures.

The van der Waals (vdWs) heterostructures, with vertical layer stacking structure of various two-dimensional (2D) materials, maintain the reliable photonic characteristics while compensating the shortcomings of the participating individual components. In this work, we combine the less-studied multilayer tin selenide (SnSe2) thin film with one of the traditional 2D materials, graphene, to fabricate the graphene-based vdWs optical switching element (Gr-SnSe2) with superior broadband nonlinear optical response. The transient absorption spectroscopy (TAS) measurement results verify that graphene acts as the recombination channel for the photogenerated carrier in the Gr-SnSe2 sample, and the fast recovery time can be reduced to hundreds of femtoseconds which is beneficial for the optical modulation process. The optical switching properties are characterized by the I-scan measurements, exhibiting a saturable energy intensity of 2.82 mJ·cm-2 (0.425 µJ·cm-2) and a modulation depth of 15.6% (22.5%) at the wavelength of 1030 nm (1980nm). Through integrating Gr-SnSe2 with a cladding waveguide, high-performance picosecond Q-switched operation in the near-infrared (NIR) and mid-infrared (MIR) spectral regions are both achieved. This work experimentally demonstrates the great potential of graphene-based vdWs heterostructures for applications in broadband ultrafast photonics.

Molecular dynamics investigation on the interfacial thermal resistance between annealed pyrolytic graphite and copper.

Modern highly integrated microelectronic products often face the challenge of internal heat dissipation, leading to a significant decrease in their operational efficiency. Annealed Pyrolytic Graphite (APG), due to its superior thermal conductivity, has garnered attention from researchers. The interface thermal resistance between APG and supporting materials like copper significantly affects heat transfer during APG's operation. Existing studies rarely delve into the influence of factors such as the shape of APG material interfaces on thermal resistance from a microscopic perspective. In this paper, utilizing transient thermo-reflectance method and non-equilibrium molecular dynamics simulations, the interface thermal resistance of the APG-Cu structure was investigated under different conditions. The impact of parameters such as copper thickness, interface micro-surface morphology, and APG thickness on the calculated interface thermal resistance was examined. Simulation results revealed that copper thickness had a minor effect on the interface thermal resistance. This is because the phonon participation ratio remains unaffected by changes in the thickness of the copper layer. The interfacial thermal resistance beneath microscopically cylindrical copper surfaces was considerably lower than that of rectangular copper surfaces. This is because beneath the cylindrical surface, the enlarged interface contact area facilitates enhanced thermal transport between the interfaces. The computed results of the radial distribution function in the paper also indirectly validate this viewpoint. The magnitude of interfacial thermal resistance for different APG layers was influenced by the coupling effect of intermolecular forces and the layered stacking structure of APG. The interfacial thermal resistance under the condition of three layers of APG reaches its minimum value, which is 2.2 × 10-9 (K m2 W-1). Furthermore, from the phonon perspective, it is found that the interfacial thermal resistance with different numbers of APG layers is closely related to the localization or delocalization state of phonons. As the number of APG layers increased, the interface thermal resistance showed a trend of initial decrease followed by an increase, this is because the average phonon participation ratio increases and then decreases with the number of APG layers. The average phonon participation ratio reaches its maximum value of 0.45778 under the condition of three layers of APG.

Device parameter to evaluate exciton energy transfer in organic whispering-gallery-mode microresonators and its dependence on the amplified spontaneous emission threshold.

Exciton energy transfer in organic whispering-gallery-mode (WGM) resonators and its effect on the amplified spontaneous emission (ASE) threshold have been investigated using the stilbene-based energy donor 4,4'-bis[(N-carbazole)styryl]biphenyl (BSB-Cz) and the coumarin-based energy acceptor 2,3,6,7-tetrahydro-1,1,7,7,-tetramethyl-1H,5H,11H-10-(2-benzothiazolyl)quinolizino[9,9a,1gh]coumarin (C545T). Using the stacked-layer structure of BSB-Cz/C545T/BSB-Cz, we fabricated bowl-shaped microresonators on silica microspheres with a total thickness of 250 nm fixing the thickness of the C545T layer to 1 nm. The ASE threshold depended on the thicknesses of the top and bottom BSB-Cz layers, which affect the magnitude of the energy transfer. To assess the relationship between the ASE threshold and energy transfer, we developed a device parameter to evaluate the magnitude of the energy transfer by formulating the rate equations. We found that ASE easily occurs under the condition that the C545T molecules become unable to accept energy from the BSB-Cz excitons owing to the high exciton density of C545T, and that the ASE threshold decreases with decreasing device parameter. The device parameter is useful for optimizing microresonator structures in multi-component organic WGM resonators that utilize energy transfer.

Lithography-free polarization insensitive and wide-angle solar absorber operating in wide spectrum

The largest source of renewable energy on Earth is Sun. Metamaterial can convert solar radiation into useful thermal energy. Therefore, it would be valuable for use in several practical applications, such as thermal photovoltaics, sensing, and heat generation. This work investigates a wideband solar absorber using the lithography-free approach to attain high absorption efficiency when operating in the visible and near-infrared spectrum range. The proposed unit cell comprises a stacking layer structure made of MXene/SiO2. As a results, an average absorptivity of 90 % is depicted within the 400-200 nm. Further, the lithography-free planar layered design shows insensitivity to polarized waves and stability to the wide obliquity of the incidence wave. This work shows its potential for utilizing it in light-to-thermal conversion and thermal imaging-based applications.

Electrocatalytic Mechanisms for an Oxygen Evolution Reaction at a Rhombohedral Boron Monosulfide Electrode/Alkaline Medium Interface.

Rhombohedral boron monosulfide (r-BS) with a layer stacking structure is a promising electrocatalyst for an oxygen evolution reaction (OER) within an alkaline solution. We investigated the catalytic mechanisms at the r-BS electrode/alkaline medium interface for an OER using hybrid solvation theory based on the first-principles method combined with classical solution theory. In this study, we elucidate the activities of the OER at the outermost r-BS sheet with and without various surface defects. The Gibbs free energies along the OER path indicate that the boron vacancies at the first and second layers of the r-BS surface (VB1 and VB2) can promote the OER. However, we found that the VB1 is easily occupied by the oxygen atom during the OER, degrading its electrocatalytic performance. In contrast, VB2 is suitable for the active site of the OER due to its structure stability. Next, we applied a bias voltage with the OER potential to the r-BS electrode. The bias voltage incorporates the positive excess surface charge into pristine r-BS and VB2, which can be understood by the relationship between the OER potential and potentials of zero charge at the r-BS electrode. Because the OH- ions are the starting point of the OER, the positively charged surface is kinetically favorable for the electrocatalyst owing to the attractive interaction with the OH- ions. Finally, we qualitatively discuss the flat-band potential at a semiconductor/alkaline solution interface. It suggests that p-type carrier doping could promote the catalytic performance of r-BS. These results explain the previous measurement of the OER performance with the r-BS-based electrode and provide valuable insights into developing a semiconductor electrode/water interface.

Layer-stacked network hybrid aerogels for the adsorption of U(VI): Concentration screening, efficient recovery, and cycle mechanism

Uranium contamination is a key issue in the sustainable development of nuclear energy. In this study, a cellulose/sericite hybrid aerogel with a layer-stacked network structure (MCC/AS-P) was prepared for uranium-contaminated wastewater treatment. Systematic characterization and multiple-batch static adsorption experiments were conducted to analyze the aerogel’s preparation, adsorption, and desorption. The kinetics demonstrated a noticeable transition between mass transfer diffusion control and mass transfer control, approaching adsorption equilibrium within 8 min and 180 min, respectively, wherein polymer layers led to a more stable adsorption process. Adsorption isotherm and thermodynamic studies established that the theoretical adsorption capacity of MCC/AS-P for U(VI) at T = 298 K could reach 374.5 mg·g−1. The adsorption behavior was endothermic and spontaneous, and the DFT calculations demonstrated that the adsorption energy of MCC/AS for UO22+ was − 506.5 kcal/mol. Temperature, U(VI) concentration, and desorption can all lead to a transition of the dominant mechanism between chemisorption and physisorption. After six swelling–deswelling adsorption cycles, the adsorption efficiency remained above 80%, and the structure remained intact. Furthermore, the excellent performance in terms of interference resistance and chemical stability offers potential for practical application.

Group Replacement-Rearrangement-Triggered Linear-Assembly Nonaqueous Precipitation Synthesis of Hydroxyapatite Fibers.

A novel method for hydroxyapatite fiber preparation with highly large-scale production prospects is of paramount importance but remains particularly difficult. Here, group replacement-rearrangement-triggered linear-assembly nonaqueous precipitation synthesis has been proposed for hydroxyapatite fibers under mild conditions. Pure hydroxyapatite fibers can be fabricated taking disodium hydrogen phosphate, calcium acetate, and glycerol as the phosphorus source, calcium source, and solvent, respectively. Single hexagonal crystal structures of hydroxyapatite fibers growing along the c-axis and preferential growth of the (002) crystal plane similar to the layered stacking structure of an adult bone have been confirmed by XRD refinement tests and calculation, TEM electron diffraction calibration, and FE-SEM. Highly active carbonate apatite is further demonstrated by EDS, FT-IR, Raman spectroscopy, and XPS. Unsaturated P-O and O-Ca bonds at both ends of the hexagonal-sheet assembly unit in a high-polarity nonaqueous glycerol environment without strongly coordinated OH- confirm the solution spontaneous linear assembly to form the single hydroxyapatite fibers.

C-doped Bi3O4X nanosheets with self-induced internal electric fields for pyrene degradation: Effects of carbon and halogen element type on photocatalytic activity

A series of C-doped Bi3O4X (X = Cl, Br, I) photocatalysts with layer-stacked structure was synthesized using glucose as carbon source, and the carbon doping and halogen species on harvesting broader solar spectrum and promoting charge carrier separation were systematically investigated. For pyrene photolysis, the photodegradation rate of pristine materials followed the order of Bi3O4I > Bi3O4Br > Bi3O4Cl, which was attributed to the difference in electronegativity of the halogen elements. The doped carbon boosted photocatalytic performance and the optimal C/Bi3O4I achieved 100% pyrene removal within 20 min, which primarily benefited from the dramatic improvement of the internal electric field (IEF). The improved IEF further increased the separation and transfer efficiency of photogenerated charge carriers. XRD and XPS characterizations confirmed that the doped carbon implanted into the lattice of [X] layers, and mainly affected the X np states. The X np orbitals contributed to the valence band (VB) of Bi3O4X, thus the local occupied states induced by doped carbon formed above VB and significantly decreased the VB potential. Meanwhile, the doped carbon narrowed the band gap and greatly improved visible light utilization. The O2−, h+ and OH were identified as dominant active species for pyrene degradation, and the generation rate of O2− and OH was further measured by the probe technique. Moreover, the photodegradation pathways of pyrene were proposed and the ecotoxicity of intermediates was assessed. This study reveals the effect of halogen species on photocatalytic activity and provides guidance for enhancing IEF by doping inorganic element.

Voltage-Mediated Enhances Lithium-Ion Storage in LiTiOPO4 by Combustion Method

Abstract LiTiOPO4 was prepared by solid-phase combustion method using citric acid as fuel. The LiTiOPO4 materials were characterized by X-ray diffraction test (XRD), scanning electron microscope (SEM), and transmission electron microscope (TEM). The XRD test showed that the synthesized samples were pure phases and the addition of different weight fractions of the combustion agent citric acid did not change the phase structure of the LiTiOPO4. The microscopic observations revealed that the LiTiOPO4 prepared after the addition of citric acid as a combustion agent was a sheet-like stacked structure. The electrochemical test results showed that the rate discharge capacity of LiTiOPO4 anode at 5000 mA g−1 maintains 184.7 mAh g−1 in the voltage range of 0.01–3.0 V and keeps at 147.2 mAh g−1 after 500 cycles. The LiTiOPO4 anode exhibits excellent cycling stability and good reversibility, which is attributed to the high crystallinity of LiTiOPO4 prepared by solid-phase combustion and the lamellar stacked layer structure that facilitates lithium-ion insertion/de-insertion.