Search Results (401)

In this work, we investigate the electrical properties of a metal–insulator–semiconductor (MIS) heterojunction based on porous silicon dioxide (Ag/pSiO₂/Si). The porous silicon (PS) films were elaborated by electrochemical anodization under specific experimental conditions to obtain a porosity of about 55%. Porous silicon (PS) was oxidized by IR-RTP at different oxidation temperatures (Tox) ranging from 200 to 950 °C under an oxygen atmosphere. The morphology of the samples was analyzed using a scanning electron microscope (SEM). Ag/Al and Ag contacts were screen printed on the back and front sides of the heterojunction, respectively. Both the series and shunt resistances were derived from dark current–voltage (I–V) characteristics related to the various Ag/pSiO₂/Si heterojunctions. In this context, the reflectance was also measured at different oxidation temperatures to investigate its correlation with the series resistance (Rs) and shunt resistance (Rsh). The optimum electrical performance was obtained for an oxidation temperature close to 400 °C. Depending on the pSiO₂ thickness, two conduction mechanisms were highlighted within the devices. For a Tox below 200 °C, as well as for the non-oxidized devices, the conduction mechanism is governed by the tunneling current through the pSiO₂ film. However, when the Tox increases and exceeds 200 °C, the pSiO₂ thickness increases, leading to the switching of the conduction mechanism to a thermionic instead of a tunneling effect mechanism. Full article

Diamond is a promising next-generation semiconductor material, offering a wider band gap, higher electron mobility, and superior thermal conductivity compared with silicon. However, its exceptional hardness makes it challenging to fabricate. In this study, we demonstrate a novel approach to realize material removal on hydrogen-terminated diamond surfaces by atomic force microscope (AFM) tip-based local anodic oxidation. By adjusting both the applied voltage and hydrogen plasma etching parameters, the material is removed over an area larger than the AFM tip size. Notably, the hardness of the material surrounding the removal zone is significantly reduced, enabling it to be scratched with a silicon tip. These findings open a promising pathway for improving the machinability of diamonds in future device applications. Full article

In most commercial lithium-ion batteries, graphite remains the primary anode material. However, its theoretical specific capacity is only 372 mAh∙g⁻¹, which falls short of meeting the demands of high-performance electronic devices. Silicon anodes, despite boasting an ultra-high theoretical specific capacity of 4200 mAh∙g⁻¹, suffer from significant volume expansion (>300%) during cycling, leading to severe capacity fade and limiting their commercial viability. Currently, silicon-based polymer-derived ceramics have emerged as a highly promising next-generation anode material for lithium-ion batteries, thanks to their unique nano-cluster structure, tunable composition, and low volume expansion characteristics. The maximum capacity of the ceramics can exceed 1000 mAh∙g⁻¹, and their unique synthesis routes enable customization to align with diverse electrochemical application requirements. In this paper, we present the progress of silicon oxycarbide (SiOC), silicon carbonitride (SiCN), silicon boron carbonitride (SiBCN) and silicon oxycarbonitride (SiOCN) in the field of LIBs, including their synthesis, structural characteristics and electrochemical properties, etc. The mechanisms of lithium-ion storage in the Si-based anode materials are summarized as well, including the key role of free carbon in these materials. Full article

This work aims to clarify whether the individual advantages of the two commonly used silicate- and aluminate-based electrolytes for the plasma electrolytic oxidation (PEO) of steel can be combined in a two-step process. The first PEO step was carried out in an aluminate–phosphate electrolyte with pulsed voltage and anodic amplitudes between 150 V and 200 V. The second PEO step was carried out at an increased anodic voltage amplitude of 400 V in a silicate–phosphate electrolyte. As a reference, PEO was conducted in a single step in the same silicate–phosphate electrolyte at an increased anodic voltage amplitude of up to 400 V. The microstructural layer analysis was carried out using SEM and EDX analyses, Raman spectroscopy and XRD analysis. Heterogeneous layers containing iron oxide and iron phosphate form in the silicate–phosphate electrolyte at anodic voltage amplitudes up to 300 V by electrochemical reactions. Further increasing the anodic voltage amplitude up to 400 V results in heterogeneous layers, too. PEO in the aluminate–phosphate electrolyte at 150 V causes the formation of thin, amorphous layers mainly consisting of aluminum and iron oxides. At 200 V amplitude, a PEO layer with pronounced open porosity is formed, which primarily consists of the crystalline phases corundum and hercynite. During subsequent PEO in the silicate–phosphate electrolyte, the previously formed layers were replaced by a macroscopically homogeneous layer that is mostly nanocrystalline and may contain amorphous iron(-aluminum) phosphates and oxides as well as silicon oxide. It can be concluded that the two-step PEO process is suitable for the production of more homogeneous PEO layers. Full article

Silicon alloy-based materials are widely studied as high-capacity anode materials to replace commercial graphite in lithium-ion batteries (LIBs). Among these, silicon suboxide (SiO_x) offers superior cycling performance compared to pure Si-based materials. However, achieving a high initial Coulombic efficiency (ICE) remains a key challenge. To address this, previous studies have explored Si_xO composites (x ≈ 1, 2), where nano-Si is uniformly dispersed within a Si suboxide matrix to enhance ICE. While this approach improves reversible capacity and ICE compared to conventional SiO, it still falls short of the capacity achieved with pure Si. This study employs a high-energy mechanical milling approach with increased Si content to achieve higher reversible capacity and further enhance the ICE while also examining the effects of trace oxygen uniformly distributed within the Si suboxide matrix. Structural characterization via X-ray diffraction, Raman spectroscopy, and electron microscopy confirm that Si crystallites (<10 nm) are homogeneously embedded within the SiO_x matrix, reducing crystalline Si size and inducing partial amorphization. Electrochemical analysis demonstrates an ICE of 89% and a reversible capacity of 2558 mAh g⁻¹, indicating significant performance improvements. Furthermore, carbon incorporation enhances cycling stability, underscoring the material’s potential for commercial applications. Full article

Silicon-based anodes have emerged as promising candidates for advanced lithium-ion batteries (LIBs) owing to their outstanding lithium storage capacity; however, the commercial implementation of silicon-based anodes is hindered primarily by their significant volumetric changes and the resulting solid electrolyte interphase (SEI) instability during the lithiation/delithiation process. To overcome these issues, electrolyte optimization, particularly through the use of functional additives and solid-state electrolytes, has attracted significant research attention. In this paper, we review the recent developments in electrolyte additives, such as vinylene carbonate, fluoroethylene carbonate, and silane-based additives, and new additives, such as dimethylacetamide, that improve the SEI stability and overall electrochemical performance of silicon-based anodes. We also discuss the role of solid electrolytes, including oxides, sulfides, and polymer-based systems, in mitigating the volume changes in Si and improving safety. Such approaches can effectively enhance both the longevity and capacity retention of silicon-based anodes. Despite significant progress, further studies are essential to optimize electrolyte formulation and solve interfacial problems. Integrating these advances with improved electrode designs and anode materials is critical for realizing the full potential of silicon-based anodes in high-performance LIBs, particularly in electric vehicles and portable electronics. Full article

Silicon oxide–graphite is a promising high-capacity anode material for next-generation lithium-ion batteries (LIBs). However, despite using a small fraction (≤5%) of Si, it suffers from a short cycle life owing to intrinsic swelling and particle pulverization during cycling, making practical application challenging. High-nickel (Ni ≥ 80%) oxide cathodes for high-energy-density LIBs and their operation beyond 4.2 V have been pursued, which requires the anodic stability of the electrolyte. Herein, we report a nonflammable multi-functional fluorinated ester–based liquid electrolyte that stabilizes the interfaces and suppresses the swelling of highly loaded 5 wt% SiO–graphite anode and LiNi_0.88Co_0.08Mn_0.04O₂ cathode simultaneously in a 3.5 mAh cm⁻² full cell, and improves cycle life and battery safety. Surface characterization results reveal that the interfacial stabilization of both the anode and cathode by a robust and uniform solid electrolyte interphase (SEI) layer, enriched with fluorinated ester-derived inorganics, enables 80% capacity retention of the full cell after 250 cycles, even under aggressive conditions of 4.35 V, 1 C and 45 °C. This new electrolyte formulation presents a new opportunity to advance SiO-based high-energy density LIBs for their long operation and safety. Full article

In this study, we systematically analyzed selective lithium plating on graphite (Gr)–silicon (Si) composite anodes for lithium-ion batteries during fast charging, using electrochemical techniques. To achieve this, half-cells were first constructed with single Gr and Si electrodes, and lithium plating on each electrode was examined at different charging rates. It was observed that lithium plating on both electrodes began at a lower state of charge (SoC) as the charge rate increased. Furthermore, at a given charge rate, lithium plating occurred on the Si electrode at a lower SoC than on the Gr electrode. Based on the experimental findings, the lithium plating behavior of Gr and Si as a function of the charge rate was formulated to investigate the plating behavior of hypothetical composite electrodes with varying Gr–Si ratios. The lithium plating behavior observed on the actual composite electrode was consistent with that predicted from the hypothetical composite electrode, which was simulated using the same Gr–Si ratio based on the behaviors of the individual electrodes. By comparing the results from the single and composite electrodes, it is proposed that lithium plating occurs first on Si and then on Gr at low charge rates, whereas, at high charge rates, it proceeds first on Gr and then on Si. We discuss how to extrapolate the preferential plating signals—namely, plating onto Si at low charge rates and onto Gr at high charge rates—that are not directly evident in the signal from the actual composite electrode. Full article

Germanium/tin-containing silicon oxide [SiO–(GeO/SnO)] nanoclusters have been designed with different Si/Ge/Sn particles and characterized as electrodes for magnesium-ion batteries (MIBs) due to forming MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] complexes. In this work, alkaline earth metals of magnesium (Mg), beryllium (Be), and calcium (Ca) have been studied in hybrid Mg-, Be-, and Ca-ion batteries. An expanded investigation on H capture by MgBe [SiO–(GeO/SnO)] or MgCa [SiO–(GeO/SnO)] complexes was probed using computational approaches due to density state analysis of charge density differences (CDD), total density of states (TDOS), and electron localization function (ELF) for hydrogenated hybrid clusters of MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO]. Replacing Si by Ge/Sn content can increase battery capacity through MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] nanoclusters for hydrogen adsorption processes and could improve the rate performances by enhancing electrical conductivity. A small portion of Mg, Be, or Ca entering the Si–Ge or Si–Sn layer to replace the alkaline earth metal sites could improve the structural stability of the electrode material at high multiplicity, thereby improving the capacity retention rate. In fact, the MgBe [SiO–GeO] remarks a small enhancement in charge transfer before and after hydrogen adsorption, confirming the good structural stability. In addition, [SiO–(GeO/SnO)] anode material could augment the capacity owing to higher surface capacitive impacts. Full article

The projected global energy demand for 2050 drives the imperative search for alternative and environmentally friendly energy sources. An emerging and promising alternative is microbial fuel cells assisted with microalgae. This research evaluated the potential of Chlorella sp. biomass in electricity production using microbial fuel cells (MFCs) with a single chamber and activated carbon and zinc electrodes at the laboratory scale over 20 days of operation. Maximum values of voltage (1271 ± 2.52 mV), current (4.77 ± 0.02 mA), power density (247.514 mW/cm²), current density (0.551 mA/cm²), and internal resistance (200.83 ± 0.327 Ω) were obtained. The biomass-maintained pH values of 7.32 ± 0.03–7.74 ± 0.02 and peaks of electrical conductivity of 2450 ± 17.1 µS/cm and oxidation-reduction potential of 952 ± 20 mV were reached. Meanwhile, cell density and absorbance increased to average values of 2.2933 × 10⁷ ± 1.15 × 10⁶ cells/mL and 3.471 ± 0.195 absorbance units (AU), respectively. Scanning electron microscopy micrographs allowed the observation of filamentous structures of the formed biofilm attached to carbon particles, and energy-dispersive X-ray spectroscopy spectra of the anodes determined the predominance of oxygen, carbon, silicon, aluminum, and iron. Finally, this research demonstrates the great potential of Chlorella sp. biomass for sustainable bioelectricity generation in MFCs. Full article

Lithium-ion batteries (LIBs) are widely used in diverse applications, ranging from portable ones to stationary ones. The appropriate handling of the immense amount of spent batteries has, therefore, become significant. Whether recycled or repurposed for second-life applications, knowing their chemistry type can lead to higher efficiency. In this paper, we propose a novel machine learning-based approach for accurate chemistry identification of the electrode materials in LIBs based on their temperature dynamics under constant current cycling using gated recurrent unit (GRU) networks. Three different chemistry types, namely lithium nickel cobalt aluminium oxide cathode with silicon-doped graphite anode (NCA-GS), nickel cobalt aluminium oxide cathode with graphite anode (NCA-G), and lithium nickel manganese cobalt oxide cathode with graphite anode (NMC-G), were examined under four conditions, 0.2 C charge, 0.2 C discharge, 1 C charge, and 1 C discharge. Experimental results showed that the unique characteristics in the surface temperature measurement during the full charge or discharge of the different chemistry types can accurately carry out the classification task in both experimental setups, where the model is trained on data under different cycling conditions separately and jointly. Furthermore, experimental results show that the proposed approach for chemistry type identification based on temperature dynamics appears to be more universal than voltage characteristics. As the proposed approach has proven to be efficient in the chemistry identification of the electrode materials LIBs in most cases, we believe it can greatly benefit the recycling and second-life application of spent LIBs in real-life applications. Full article

To enhance the performance of state-of-the-art lithium-ion batteries, high-capacity silicon is increasingly introduced as active material for anodes. Furthermore, advanced batteries with new electrode architectures—so-called 3D architectures—can provide significantly enhanced electrochemical performance compared to state-of-the-art batteries. To facilitate and speed up the architectural development, the laser-induced forward transfer (LIFT) process was applied as a digital additive manufacturing method. As polyvinylidene fluoride (PVDF), the binder commonly used in the LIFT process, is not a suitable binder for silicon-containing electrodes due to its weak binding forces, polyacrylic acid (PAA) was introduced as a binder for use in printable electrode pastes. Since water as a solvent in such pastes evaporates quickly and the corresponding printing time would be too short, glycerol was added to the solvent mixture in different amounts. The silicon in the printed electrodes reaches a specific capacity of more than 3000 mAh$·{\mathrm{g}}^{–1}$ for most of the printed anodes. To further improve the electrochemical performance of the printed electrodes, as well as the rheology of the slurries, two different conductive additives with different particle sizes were used. Full article

This paper reports the field emission (FE) current stability of a diamond nanowire (DNW) array. Assembled with a silicon anode with a 1.03 μm gap, the FE properties, as well as the current stability of the DNW cathode, were systematically evaluated in a vacuum test system under different vacuum degrees, current densities, and atmospheres. Experiments demonstrate that lower pressure and current density can improve FE properties and current stability. In addition, compared to air and compressed air, DNWs exhibit higher FE properties and current stability in N₂. DNWs achieve a remarkably low turn-on field of 1.65 V/μm and a high current density of 265.38 mA/cm². Notably, they demonstrate merely 0.70% current fluctuation under test conditions of 1.2 × 10⁻⁴ Pa and 0.1 mA/cm². Additionally, based on the Fowler–Nordheim theory, the change in work function after gas adsorption was analyzed, and the noise generation mechanism was derived from the noise power spectrum. The current exponent is determined as 1.94, while the frequency exponent ranges from 0.92 to 1.32, confirming that the dominant noise mechanism in DNWs arises from surface work function fluctuations due to the adsorption and desorption of residual gas. Full article

Prelithiation has been widely accepted as one of the most promising strategies to compensate for the loss of active substance and to improve the initial Coulombic efficiency in silicon-based anodes for advanced high-energy-density batteries. But because of their unstable solid electrolyte interface (SEI) layer and low initial Coulombic efficiency, they expand in volume during prelithiation and react with moisture, which makes commercialization a difficult process. Herein, we have developed a strategy using lithium bis(fluorosulfonyl)imide (LiFSI) treatment to eliminate redundant lithium and generate LiF-based inorganic compounds on the surface of the prelithiated electrode. Such method not only reduces the reactiveness of the prelithiated anode but also enhances the ionic conductivity of the SEI. The rich LiF surface works as an artificial SEI, and according to electrochemical evaluation, the initial Coulombic efficiency of the prelithiated silicon anode treated with LiFSI can reach 92.9%. This technique not only increases the battery’s energy density but also its cycle stability, resulting in superior capacity retention and a longer cycling life. Full article

Integrated light-emitting diodes (LEDs) with waveguides play an important role in applications such as augmented reality (AR) displays, particularly regarding coupling efficiency optimization. Quantum dot light-emitting diodes (QLEDs), an emerging high-performance optoelectronic device, demonstrate substantial potential for next-generation display technologies. This study investigates the influence of microcavity modulation on the output of QLEDs coupled with a silicon nitride (SiNx) waveguide by simulating a white light QLED (W-QLED) with a broad spectrum and mixed RGB QDs (RGB-QLED) with a comparatively narrower spectrum. The microcavity converts both W-QLED and RGB-QLED emissions from broadband white-light emissions into narrowband single-wavelength outputs. Specifically, both of them have demonstrated wavelength tuning and full-width at half-maximum (FWHM) narrowing across the visible spectrum from 400 nm to 750 nm due to the microcavity modulation. The resulting RGB-QLED achieves a FWHM of 11.24 nm and reaches 110.76% of the National Television System Committee 1953 (NTSC 1953) standard color gamut, which is a 20.95% improvement over W-QLED. Meanwhile, due to the Purcell effect of the microcavity, the output efficiency of the QLED coupled with a SiNx waveguide is also significantly improved by optimizing the thickness of the Ag anode and introducing a tilted reflective mirror into the SiNx waveguide. Moreover, the optimal output efficiency of RGB-QLED with the tilted Ag mirror is 10.13%, representing a tenfold increase compared to the sample without the tilted Ag mirror. This design demonstrates an efficient and compact approach for the near-eye full-color display technology. Full article