Tuning of Composition and Morphology of LiFePO4 Cathode for Applications in All Solid-State Lithium Metal Batteries

All solid-state rechargeable lithium metal batteries (SS-LMBs) are gaining more and more importance because of their higher safety and higher energy densities in comparison to their liquid-based counterparts. In spite of this potential, their low discharge capacities and poor rate performances limit them to be used as state-of-the-art SS-LMBs. This arise due to the low intrinsic ionic and electronic transport pathways within the solid components in the cathode during the fast charge/discharge processes. Therefore, it is necessary to have a cathode with good electron conducting channels to increase the active material utilization without blocking the movement of lithium ions. Since SS-LMBs require a different morphology and composition of the cathode, we selected LiFePO4 (LFP) as a prototype and, we have systematically studied the influence of the cathode composition by varying the contents of active material LFP, conductive additives (super C65 conductive carbon black and conductive graphite), ion conducting components (PEO and LiTFSI) in order to elucidate the best ion as well as electron conduction morphology in the cathode. In addition, a comparative study on different cathode slurry preparation methods was made, wherein ball milling was found to reduce the particle size and increase the homogeneity of LFP which further aids fast Li ion transport throughout the electrode. The SEM analysis of the resulting calendered electrode shows the formation of non-porous and crack-free structures with the presence of conductive graphite throughout the electrode. As a result, the optimum LFP cathode composition with solid polymer nanocomposite electrolyte (SPNE) delivered higher initial discharge capacities of 114 mAh g-1 at 0.2C rate at 30 ᴼC and 141 mAh g-1 at 1C rate at 70 ᴼC. When the current rate was increased to 2C, the electrode still delivered high discharge capacity of 82 mAh g-1 even after 500 cycle, which indicates that the optimum cathode formulation is one of the important parameters in building high rate and long cycle performing SS-LMBs.

Investigation of Ion and Electron Conduction in the Mixed Ionic-Electronic Conductor- La-Sr-Co-Fe-Oxide (LSCF) Using Alternating Current (AC) and Direct Current (DC) Techniques

Among many mixed ionic electronic conductors (MIECs), lanthanum strontium cobalt iron oxide (LSCF) has been proven as a promising material for use as cathode in SOFCs. The ion and electron conduction in LSCF need to be studied separately. To measure the ionic conductivity of LSCF, YSZ disks were applied to block the electronic current, and multilayered samples were made with YSZ disks in series with an LSCF disk. Both AC and DC techniques were used for the measurements. An LSCF(porous)/LSCF(dense)/LSCF(porous) bar-shaped sample was made to measure the electronic conductivity of LSCF. DC technique was utilized for the measurement. Results show that the ionic conductivity of LSCF is much lower than its electronic conductivity. The ionic conductivity of LSCF increases with increasing temperature (600-900°C), and the electronic conductivity decreases with increasing temperature (600-900°C). Measurements were also made on a foil of silver to investigate oxygen transport through it. From this, oxygen ion conductivity through silver was estimated.

Nickel Foam Electrode with Low Catalyst Loading and High Performance for Alkaline Direct Alcohol Fuel Cells

Nickel foam has a unique three-dimensional (3-D) network structure that helps to effectively utilize catalysts and is often used as an electrode support material for alkaline direct alcohol fuel cells. In this chapter, first, the effect of nickel foam thickness on cell performance is explored. The results show that the thickness affects both mass transfer and electron conduction, and there is an optimal thickness. The thinner the nickel foam is, the better the conductivity is. However, the corresponding three-dimensional space becomes narrower, which results in a partial agglomeration of the catalyst and the hindrance of mass transfer. The cell performance of 0.6 mm nickel foam electrode is better than that of 0.3 and 1.0 mm. Secondly, to fully exert the catalytic function of the catalyst even at a lower loading, a mixed acid-etched nickel foam electrode with lower Pd loading (0.35 mg cm−2) is prepared then by a spontaneous deposition method. The maximum power density of the single alkaline direct ethanol fuel cell (ADEFC) can reach 30 mW cm−2, which is twice the performance of the hydrochloric acid treated nickel foam electrode. The performance improvement is attributed to the micro-holes produced by mixed acids etching, which enhances the roughness of the skeleton and improves the catalyst electrochemical active surface area.

Harnessing Electrostatic Interactions for Enhanced Conductivity in Metal-Organic Frameworks

The poor electrical conductivity of metal-organic frameworks (MOFs) has been a stumbling block for its applications in many important fields. Therefore, exploring a simple and effective strategy to regulate the conductivity of MOFs is highly desired. Herein, anionic guest molecules are incorporated inside the pores of a cationic MOF (PFC-8), which increases its conductivity by five orders of magnitude while maintaining the original porosity. In contrast, the same operation in an isoreticular neutral framework (PFC-9) does not bring such a significant change. Theoretical studies reveal that the guest molecules, stabilized inside pores through electrostatic interaction, play the role of electron donors as do in semiconductors, bringing in an analogous n-type semiconductor mechanism for electron conduction. Therefore, we demonstrate that harnessing electrostatic interaction provides a new way to regulate the conductivity of MOFs without necessarily altering the original porous structure. This strategy would greatly broaden MOFs’ application potential in electronic and optoelectronic technologies.

Chlorosulfonic Acid Stretched Carbon Nanotube Sheet for Flexible and Low-Voltage Heating Applications

The carbon nanotube (CNT) is celebrated for its electrothermal property, which indicates the capability of a material to transform electrical energy into heat due to the Joule effect. The CNT nanostructure itself, as a one-dimensional material, limits the electron conduction path, thereby creating a unique heating phenomenon. In this work, we explore the possible correlation between CNT alignment in sheets and heating performance. The alignment of carbon nanotubes is induced by immersion and stretching in chlorosulfonic acid (CSA) solution. The developed CSA-stretched CNT sheet demonstrated excellent heating performance with a fast response rate of 6.5 °C/s and reached 180 °C in less than 30 s under a low voltage of 2.5 V. The heating profile of the stretched CNT sheet remained stable after bending and twisting movements, making it a suitable heating material for wearable devices, heatable smart windows, and in de-icing or defogging applications. The specific strength and specific conductance of the CSA-stretched CNT sheet also increased five- and two-fold, respectively, in comparison to the pristine CNT sheet.

High-Quality Single-Crystalline β-Ga2O3 Nanowires: Synthesis to Nonvolatile Memory Applications

One of the promising nonvolatile memories of the next generation is resistive random-access memory (ReRAM). It has vast benefits in comparison to other emerging nonvolatile memories. Among different materials, dielectric films have been extensively studied by the scientific research community as a nonvolatile switching material over several decades and have reported many advantages and downsides. However, less attention has been given to low-dimensional materials for resistive memory compared to dielectric films. Particularly, β-Ga2O3 is one of the promising materials for high-power electronics and exhibits the resistive switching phenomenon. However, low-dimensional β-Ga2O3 nanowires have not been explored in resistive memory applications, which hinders further developments. In this article, we studied the resistance switching phenomenon using controlled electron flow in the 1D nanowires and proposed possible resistive switching and electron conduction mechanisms. High-density β-Ga2O3 1D-nanowires on Si (100) substrates were produced via the VLS growth technique using Au nanoparticles as a catalyst. Structural characteristics were analyzed via SEM, TEM, and XRD. Besides, EDS, CL, and XPS binding feature analyses confirmed the composition of individual elements, the possible intermediate absorption sites in the bandgap, and the bonding characteristics, along with the presence of various oxygen species, which is crucial for the ReRAM performances. The forming-free bipolar resistance switching of a single β-Ga2O3 nanowire ReRAM device and performance are discussed in detail. The switching mechanism based on the formation and annihilation of conductive filaments through the oxygen vacancies is proposed, and the possible electron conduction mechanisms in HRS and LRS states are discussed.