Search Results (451)

The reliability of the characteristics of high-voltage (HV) thyristors is related to the operational safety of the entire HVDC project. In order to investigate the degradation mode of thyristors in HVDC projects more realistically, aging experiments were conducted on HV thyristors under the combined action of sinusoidal half-wave voltage and current in a simulated operating environment. Experimental results show that the on-state voltage, reverse recovery characteristics, and reverse leakage current of thyristors have all degraded to varying degrees during the aging process. The main failure mode of thyristors can be summarized as the failure of the reverse blocking characteristic. Microstructural characterization of failed HV thyristors is conducted to explain the degradation mechanisms, including device surface morphology and elemental composition analysis. Observations have shown that the failed thyristor silicon wafer has been burned and hollowed out, accompanied by copper impurities, and significant thermal breakdown has occurred at the edge of the anode surface of the chip. Defects in chip structure and the invasion of impurities can lead to a decrease in the minority carrier lifetime of materials, which is an important factor in the characteristics of semiconductor devices. On this basis, further simulation research is carried out to conclude that the shortening of the minority carrier lifetime of the thyristor will distort the carrier space distribution, resulting in the rise in the on-state voltage. Meanwhile, the carrier transport capability decreases, leading to a decrease in the reverse recovery speed. The energy released during the rapid generation and recombination of carriers is one of the main reasons for the failure of blocking characteristics. This work provides comprehensive insights into the failure modes and mechanisms of HV thyristors. Full article

The valorization of biomass waste into advanced electrode materials presents a promising pathway toward sustainable electrochemical energy storage. Herein, a silicon-doped carbon material (Si-CTS-Carbon) is synthesized from chitosan via an in situ reaction with silicon tetrachloride (SiCl₄) and subsequent controlled pyrolysis. When evaluated as an anode for lithium-ion batteries (LIBs), Si-CTS-Carbon exhibits a high reversible capacity of 509.2 mAh g⁻¹ with 99% capacity retention after 100 cycles at 0.05 A g⁻¹. For sodium-ion battery (SIB) applications, it achieves a stable reversible capacity of 155.4 mAh g⁻¹ under identical conditions. Structural and electrochemical analyses reveal that the robust C–O–Si covalent network effectively accommodates volume variation of silicon and enhances structural integrity during cycling. Furthermore, the hierarchically porous architecture shortens ion diffusion pathways, leading to improved Li⁺/Na⁺ transport kinetics. This work demonstrates a viable strategy for fabricating high-performance battery anodes by synergistically doping silicon into biomass-derived carbon, enabling practical biowaste valorization for energy storage. Full article

The oxygen evolution reaction (OER), serving as the anodic bottleneck in electrochemical water splitting for hydrogen production, severely limits the overall energy conversion efficiency due to its sluggish kinetics. Developing efficient and stable electrocatalysts based on earth-abundant elements is a critical challenge for advancing clean energy technologies. In recent years, silicate materials have demonstrated significant potential in alkaline OER catalysis owing to their unique stable silicon-oxygen tetrahedral framework and flexibly tunable metal-oxygen-silicon electronic coordination environments. This review systematically summarizes recent progress in silicate-based materials, including natural clay mineral supports such as halloysite, for OER electrocatalysis. It focuses on controllable synthesis strategies for silicate materials and provides an in-depth analysis of the regulation mechanisms for their electronic structure and surface properties through defect engineering, anion vacancy construction, and bimetallic/non-metallic heteroatom doping. Particular emphasis is placed on research pathways that utilize natural silicate clay minerals as both supports and silicon sources to construct high-performance composite catalytic materials via innovative structural design and interface engineering. Systematic studies indicate that precisely modulated silicate-based catalysts exhibit excellent electrochemical activity and long-term stability in the alkaline OER process. This review offers perspectives on the future development of efficient and stable silicate-based catalytic systems for renewable energy conversion. Full article

Micro-electro-mechanical systems (MEMS) sensors offer the benefits of compact size, lightweight design, and low cost, which has led to widespread use in consumer electronics, vehicles, healthcare, defense, and communications. As their performance has improved, MEMS sensors have also found applications in oil exploration and geophysical studies. Pressure and temperature measurements during hydraulic fracturing have long been employed to improve downhole conductivity during oil and gas extraction. Nevertheless, the development of high-precision MEMS sensors for oil exploration remains an active area of research. This paper presents the design, fabrication, packaging, and characterization of a silicon-on-insulator (SOI) MEMS piezoresistive pressure sensor integrated with a temperature sensor. It also describes the design of a chamber intended to emulate conditions at the bottom of oil exploration wells. The sensors were successfully designed and fabricated on the basis of physics-based simulations, deep reactive ion etching and anodic bonding. The pressure sensors, together with the signal-conditioning system, exhibited a linear response with a sensitivity of 0.0268 mV/V/MPa and maximum hysteresis of 5.3%. Full article

Trace amounts of H₂O are inevitably introduced during lithium battery manufacturing processes, which induces the hydrolysis of LiPF₆, leading to HF formation, which triggers a cascade of deleterious reactions that degrade the solid electrolyte interphase (SEI) and corrode electrode materials. In this work, a water-scavenging electrolyte was constructed by employing a boroxine-linked covalent organic framework (COF) as the suspended phase. The ring-opening reaction of the boroxine ring units in COFs can effectively capture H₂O, thereby suppressing the hydrolysis of PF₆⁻ and mitigating electrode corrosion caused by HF. Consequently, a Li-metal battery with a high-nickel cathode retained 73% of its initial capacity after 500 cycles at 1 C, and a silicon-based lithium-ion battery with a high-nickel cathode sustained stable cycling over 500 cycles at a high rate of 10 C. This suspension strategy, leveraging a boroxine-linked COF with dual H₂O-scavenging capability, offers a scalable and versatile platform for electrolyte engineering toward practical next-generation lithium batteries. Full article

Aqueous zinc-ion batteries have emerged as a research hotspot due to their advantages of safety, environmental friendliness, low cost, and high capacity. At the same time, there are some problems with anode materials, such as zinc dendrite growth and corrosion reactions. In this work, silica fume, a byproduct of industrial silicon smelting, was selected as a coating material for the Zn anode (SF@Zn). This material is not only cost-effective and widely available but also exhibits superior hydrophilicity, enhancing the electrolyte’s wettability on the anode. Additionally, it serves as an ion shunt, preventing uneven deposition of Zn²⁺, and it was demonstrated that the symmetrical cell achieved a cycle life of up to 1800 h at 0.5 mA·cm⁻². The full cell delivered a capacity of 246.2 mAh·g⁻¹ at 1 mA·cm⁻² and retained a capacity of 100.4 mAh·g⁻¹ after 1800 cycles. Full article

Silicon-based materials offer exceptional theoretical capacity for lithium-ion batteries (LIBs), but their practical application remains severely hindered by large volume expansion, low electrical conductivity, and unstable solid electrolyte interphase (SEI) formation during cycling. Herein, a binder-free silicon-containing carbon composite anode (denoted as CP-Si@C-4, where CP represents the conductive carbon paper substrate) is designed: carbon constitutes the structural and conductive framework, while silicon nanoparticles serve as a functional alloying component contributing characteristic lithiation/delithiation behavior. This framework comprises a conductive carbon paper (CP) scaffold, a resin-derived carbon matrix for homogeneous silicon dispersion, an interconnected carbon nanotube (CNT) network enabling long-range electron transport, and a conformal chemical vapor deposition (CVD) carbon layer for interfacial stabilization. Rather than simply increasing the overall carbon content, a series of control electrodes with distinct carbon configurations are deliberately designed to decouple the respective roles of bulk stress buffering and particle-level interfacial stabilization during cycling. The results indicate that functionally differentiating and coordinately regulating these two functions is critical for achieving durable binder-free silicon-containing carbon composite anodes. Benefiting from this cooperative multidimensional carbon architecture, the optimized CP-Si@C-4 anode delivers an initial Coulombic efficiency (ICE) of 86.3% and maintains a reversible capacity of ~990 mA h g⁻¹ at 2 A g⁻¹ after 1000 cycles. This work provides a structural design concept for improving long-term stability in binder-free silicon-containing carbon composite anodes. Full article

The photovoltaic industry generates a substantial amount of high-purity waste silicon powder during the diamond-wire saw cutting process, which can serve as an environmentally friendly and cost-effective resource for lithium-ion battery recycling. However, its commercial application is hindered by the surface attachment of silicon dioxide, organic substances, metal impurities, as well as its intrinsic drawbacks such as significant volume expansion (>300%) during lithium (de)intercalation and low electronic conductivity. To address these issues, this study first purifies the waste silicon powder and then designs the structure of the composites. Using a simple ball-milling combined with sol-gel method, a core-shell composite material with a carbon-coated two-dimensional conductive network (FVW-Si/G₅₀₀@C) was synthesized. The two-dimensional conductive network provides sufficient space to accommodate the volume expansion of silicon, while the mesoporous structure on the carbon shell offers a fast transport pathway for Li⁺, thereby enhancing the electrode kinetics. The prepared FVW-Si/G₅₀₀@C electrode maintained a high reversible capacity of 951.8 mAh g⁻¹ after 100 cycles at a current density of 0.2 A g⁻¹. Even at a high current density of 1 A g⁻¹, it retained a reversible capacity of 230.4 mAh g⁻¹. The results indicated that the synergistic effect between graphite sheets and the mesoporous carbon shell significantly improved the rate performance and cycling stability of the FVW-Si/G₅₀₀@C electrode. This study provided a theoretical foundation for the scalable, green, and high-value utilization of waste silicon powder in the photovoltaic industry and offered technical support for sustainable energy development. Full article

Silicon (Si) has attracted extensive attention as a promising anode material for next-generation lithium-ion batteries (LIBs) due to its ultra-high theoretical capacity, low lithiation potential, and economic advantages. However, drastic volume expansion during cycling and slow reaction kinetics severely compromise its structural stability and practical application. Recently, two-dimensional (2D) MXenes have been explored as effective functional components in Si-based electrodes because of their excellent electrical conductivity, high specific surface area, adjustable surface terminations, and mechanical robustness. When integrated with Si, MXenes serve as conductive matrices that alleviate volumetric stress, enhance charge transport, and accelerate electron/ion diffusion. Consequently, Si/MXene nanocomposites (NCs) exhibit significantly improved lithium (Li) storage performance. This review outlines recent advances in Si/MXene NCs, covering fabrication strategies, structural engineering, and various configurations, including particulate materials, three-dimensional (3D) architectures, films, and fibrous systems, and establishes the relationship between structural design and electrochemical behavior. Remaining challenges and prospective research directions are also discussed to guide the development of high-energy-density LIB anodes. Full article

This study presents a high-performance MEMS accelerometer employing a symmetrical differential ‘sandwich’ capacitive structure. An orthogonal rectangular compensation method was integrated with wet anisotropic etching to achieve high structural symmetry. An innovative glass–silicon composite cover plate was adopted, and the upper and lower plates were encapsulated by a sensitive structure via anodic bonding, which effectively reduced the parasitic capacitance. Simulations confirmed sufficient separation between the sensitive-axis (Z-axis) resonant frequency and orthogonal/torsional modes, ensuring low cross-axis coupling. The fabricated device exhibits high sensitivity (0.2216 V/g) and excellent linearity (99.842%) within a 0–8 g range. Furthermore, it demonstrates outstanding noise (7.88 µg/√Hz) and bias-instability (6.39 µg) performance, positioning it competitively against commercial counterparts. The proposed design and process offer a viable technical route for high-precision inertial sensing applications. Full article

The Probe Of Extreme Multi-Messenger Astrophysics (POEMMA) is a proposed dual-satellite mission to observe Ultra-High-Energy Cosmic Rays (UHECRs), increase the statistics at the highest energies, and observe Very-High-Energy Neutrinos (VHENs) following multi-messenger alerts of astrophysical transient events, such as gamma-ray bursts and gravitational wave events, throughout the universe. POEMMA–Balloon with radio (PBR) is a small-scale version of the POEMMA design, adapted to be flown as a payload on one of NASA’s suborbital Super Pressure Balloons (SPBs) circling over the Southern Ocean for more than 20 days after a launch from Wanaka, New Zealand. The main science objectives of PBR are: (1) to observe UHECRs via the fluorescence technique from suborbital space; (2) to observe horizontal high-altitude air showers (HAHAs) with energies above the cosmic ray knee (E > 3PeV) using optical and radio detection for the first time; and (3) to follow astrophysical event alerts in the search of VHENs. The PBR instrument consists of a 1.1 m aperture Schmidt telescope similar to the POEMMA design, with two cameras on its focal surface: a Fluorescence Camera (FC) and a Cherenkov Camera (CC). In addition, PBR has a Radio Instrument (RI) optimized for detecting EASs (covering the 60–660 Mhz range). The FC observes UHECR-induced EASs in the ultraviolet (UV) spectrum using an array of 9216-pixel Multi-Anode Photo-Multiplier Tubes (MAPMTs) imaged every 1 $\mathsf{\mu }$s. The CC uses a 2048-pixel Silicon Photo-Multiplier (SiPM) imager to observe cosmic-ray-induced HAHAs and search for neutrino-induced upward-going EASs. The CC covers a spectral range of 320–900 nm, with an integration time of 10 ns. This contribution provides an overview of PBR instruments and their current status. Full article

Porous silicon (PSi), characterized by its high specific surface area and highly tunable morphology, presents significant potential across optoelectronics, energy storage, and biomedical applications. This review provides a systematic analysis of the synthesis methodologies, interfacial chemical engineering, and diverse applications of PSi. Initially, fabrication techniques are examined, contrasting the pore formation mechanisms of electrochemical anodization, metal-assisted chemical etching (MACE), and emerging vapor-phase etching methods, while elucidating the control of geometric parameters from microporous to macroporous scales. To address the thermodynamic instability of the hydride-terminated surface, this review systematically evaluates modification strategies such as thermal oxidation, hydrosilylation, carbonization, and atomic layer deposition (ALD). We critically analyze their efficacy in mitigating oxidative drift and enabling specific functionalization. Subsequently, the review summarizes current applications in sensing (refractive index and photoluminescence modulation), energy storage (lithium-ion battery anodes and supercapacitors), and microsystem technologies (radio frequency (RF) isolation, gettering, and micro-electro-mechanical systems (MEMS) sacrificial layers), emphasizing the critical role of structure–property relationships. Finally, an objective assessment is provided regarding the challenges in translating PSi technology to industrial scales, specifically addressing the trade-offs between biodegradability and stability, wafer-scale process uniformity, and the compatibility of wet-chemical processing with standard complementary metal–oxide–semiconductor (CMOS) integration flows. Full article

Lithium-ion batteries (LIBs) power devices from portable electronics to electric vehicles and grid storage, yet their reliable operation requires real-time monitoring of battery state, particularly at the anode where complex reactions and structural changes occur. Sensor technologies capable of capturing dynamic physical and chemical signals have therefore gained increasing attention for probing internal battery processes. This review summarizes recent operando and in situ monitoring strategies for carbon-based and silicon-based anodes, highlighting advances in electrical, optical, and acoustic sensing. These methods reveal degradation mechanisms and morphological evolution in real time. Multimodal sensing strategies that integrate multiple signals for improved battery state estimation are also discussed. Finally, future directions are outlined, focusing on real-time anode monitoring and the integration of sensing technologies with next-generation battery designs. This review aims to guide the development of smart battery sensing for artificial-intelligence-assisted and multimodal sensing, providing solutions for battery management system that enable accurate synchronous detection of mechanical, thermal, and electrical signals. Full article

Silicon is a well-known anode material for lithium-ion batteries that has attracted a lot of interests because of its high theoretical specific capacity (4200 mAh g⁻¹). However, its severe volume expansion during cycling leads to structural degradation and rapid capacity fading. The design of porous silicon architectures has emerged as a fundamental and effective strategy to mitigate these issues by accommodating mechanical stress and preserving electrode integrity. Concurrently, the development of advanced in situ/operando characterization techniques has shifted the research paradigm, enabling direct observation of dynamic structural and interfacial evolution under operating conditions. This review systematically summarizes recent progress in the rational design of porous Si-based anodes and critically examines how state-of-the-art in situ methods provide direct mechanistic validation of these designs. The work highlights the synergistic interplay between targeted material engineering and in situ/operando characterization, offering a roadmap for the development of high-performance porous silicon anodes. Full article

In silicon–carbon (Si-C) anode materials fabricated via chemical vapor deposition (CVD), the pore size distribution of porous carbon is a critical parameter that strongly affects the overall electrochemical performance. In this study, biomass-derived hard carbon was employed as the precursor, and porous carbon materials with distinct pore size characteristics were prepared via fluidized bed porosimetry after carbonization at different temperatures. Based on these porous carbon substrates, three types of Si-C anodes corresponding to low-, medium-, and high-temperature treatments were synthesized through a combination of SiH₄ deposition and carbon coating processes. Electrochemical evaluation demonstrated that all three Si-C anodes exhibited favorable electrochemical performance and suppressed volume expansion. Among them, the Si-C anode prepared at a medium temperature of 1100 °C, denoted as NT-P-SC, delivered the most balanced performance, achieving an initial coulombic efficiency of 94.47% together with excellent rate capability. Furthermore, when Si-C anodes derived from different porous carbon matrices were blended with graphite to achieve a composite capacity of 500 mAh/g and evaluated in full-cell configurations, the NT-P-SC silicon-based composite exhibited superior cycling stability. The composite delivered an initial discharge capacity of 3.53 mAh and maintained a capacity of 2.74 mAh after 1628 cycles, corresponding to a capacity retention of 77.62%. The improved electrochemical performance of the Si-C anode is primarily attributed to the optimized pore structure of the porous carbon matrix synergistically combined with the carbon coating process. Full article