Opto-Electronic Advances (光电进展)•2026•DOI: 10.29026/oea.2026.250150
This study presents the first demonstration of a fast step heterodyne light-induced thermoelastic spectroscopy (SH-LITES) sensor utilizing a high-frequency quartz tuning fork (QTF) with a resonant frequency of approximately 100 kHz. The theoretical basis of heterodyne LITES (H-LITES) signal generation is analyzed, and an acetylene (C2H2) H-LITES sensor is constructed to evaluate performance. Comparative experiments between the high-frequency QTF and a standard commercial QTF (resonant frequency ~32.768 kHz) reveal that the high-frequency QTF achieves a tenfold faster response time, with a measurement cycle of 33 ms—90% shorter than commercial counterparts. The proposed SH-LITES technique further reduces the scanning time to 15 ms, representing the shortest LITES measurement time reported to date. To validate dynamic gas detection capabilities, an H2O-LITES system integrating both QTF types is employed for real-time monitoring of H2O concentration during various respiration patterns. Results demonstrate that SH-LITES more accurately captures rapid H2O concentration fluctuations during respiration, outperforming the commercial QTF-based H-LITES sensor in fast-response scenarios. These findings establish a new benchmark for high-speed trace gas sensing with potential applications in combustion diagnostics, healthcare monitoring, and environmental surveillance.
Journal of Semiconductors (半导体学报 - 中国科学院半导体研究所)•2026•DOI: 10.1088/1674-4926/26020013
Polarization is a defining lever of wurtzite (WZ) III-nitrides, enabling two-dimensional electron and hole gases, polarization doping, and electrostatic control in GaN-based power, RF, and optoelectronic devices. Recent advances, especially ferroelectric nitrides, have pushed polarization to unprecedented magnitudes, elevating it from a static constant to an engineering knob. However, the field has long suffered from ambiguity in polarization magnitude, orientation, and mapping to crystal polarity due to inconsistent sign conventions and reference choices. This mini-review highlights recent progress that rethinks and unifies polarization in wurtzite III-nitrides. It discusses how experimental re-benchmarking of giant polarization is reshaping understanding and enabling predictive polarization engineering. Key issues include the dependence of polarization sign on coordinate choice and magnitude on reference structure, as exemplified by Bernardini et al.'s 1997 predictions (values below 0.1 C/m², downward orientation for metal-polar) and Dreyer et al.'s 2016 refinements. The review emphasizes that consistent benchmarking under a unified convention makes interface bound charge density a quantitative design knob rather than an adjustable fitting parameter, benefiting classical HEMTs, N-polar stacks, polarization-doped structures, and ferroelectric nitride integration. A pragmatic roadmap is proposed: reports should state polarity, sign convention, and reference explicitly to ensure portability and falsifiability.
China Foundry•2026•DOI: 10.1007/s41230-026-5182-6
Abstract: In recent years, Al-Ti-Nb-B grain refiners have attracted increasing attention due to their grain refinement performance and anti-Si poisoning ability. This study investigates the influence of the introduction sequence of Ti and Nb during the synthesis of Al-4Ti-1Nb-1B refiners on their refinement performance on CP-Al and a series of Al-Si alloys (Al-3.5Si, Al-7Si, and Al-10.5Si). It is found that Al-4Ti-1Nb-1B prepared by introducing Ti prior to Nb exhibits the best grain refinement and anti-Si poisoning compared to samples where Nb is introduced before Ti or where both are added simultaneously. This Ti-first approach demonstrates superior grain refinement performance across CP-Al, Al-3.5S1, Ai-7Si, and Al-10.5Si alloys, especially at higher Si contents. It refines the grain size of Al-7Si to 150.1±27.5 μm from over 1,500 μm for the unrefined alloy. This superior performance is attributed to the variation in ground-state energy ΔE for the Ti prior to Nb sequence is lower than that of other sequences, thereby facilitating Nb adsorption on the TiB2 surface. TEM observations corroborate these findings, showing that TiB2 prepared by this sequence has the highest average Nb content of 3.80at.%. First-principles calculations reveal that this unique Nb adsorption enhances the TiB2/Al interfacial adhesion energy Wad and suppresses the segregation tendency of Si atoms at the interface, κSi(cSi). The higher the Nb adsorption at the TiB2/Al interface, the stronger the resistance to Si poisoning. These findings underscore the pivotal role of Nb-modified TiB2 in improving grain refinement and offer a novel strategy for advancing grain refiner technologies in Al-Si alloys.
Nano-Micro Letters•2026•DOI: 10.1007/s40820-025-01997-6
Single-atom catalysts (SACs) have demonstrated excellent performance in heterogeneous catalytic reactions owing to their maximized atomic efficiency, distinctive geometric, and electronic configurations. However, the efficacy of SACs remains limited for certain reactions requiring simultaneous activation of multiple reactants over metallic active sites. Herein, we report an atomically dispersed Pt1Ru1 dual-atom pair site anchored on nanodiamond@graphene (ND@G) for CO oxidation. The Pt1Ru1 dual-atom catalyst shows an exceptional turnover frequency (TOF) of 17.6 × 10−2 s−1 at significantly lower temperature (30 °C), achieving a tenfold increase in TOF compared to single-atom Pt1/ND@G catalyst (1.5 × 10−2 s−1) and surpassing to previously reported Pt-based catalysts under similar conditions. Moreover, the catalyst demonstrates excellent stability, maintaining its activity for 40 h at 80 °C without significant deactivation. The superior catalytic performance of Pt-Ru dual-atom catalysts is attributed to the synergistic effect between Pt and Ru atoms with enhanced metallicity for improving simultaneous adsorption and activation of CO and O2, and the tuning of conventional competitive reactant adsorption into a non-competitive pathway over dual-atom pair sites. The present work manifests the advantages of dual-atom pair sites in heterogeneous catalysis and paves the way for precise design of catalysts at the atomic scale.
Nano-Micro Letters•2025•DOI: 10.1007/s40820-025-01792-3
Currently, perovskite solar cells have achieved commendable progresses in power conversion efficiency (PCE) and operational stability. However, some conventional laboratory-scale fabrication methods become challenging when scaling up material syntheses or device production. Particularly, the prolonged high-temperature annealing process for the crystallization of perovskites requires a substantial amount of energy consumption and impact the modules’ throughput. Here, we report a modified near-infrared annealing (NIRA) process, which involves the excess PbI2 engineered crystallization, efficiently reduces the preparation time for perovskite active layer to within 20 s compared to dozens of min in conventional hot plate annealing (HPA) process. The study showed that the incorporated PbI2 promoted the consistent nucleation of the perovskite film, leading to the subsequent rapid and homogeneous crystallization at the NIRA stage. Thus, highly crystalized perovskite film was realized with even better crystallization performance than conventional HPA-based film. Ultimately, efficient perovskite solar modules of 36 and 100 cm2 were readily fabricated with the optimal PCEs of 22.03% and 20.18%, respectively. This study demonstrates, for the first time, the successful achievement of homogeneous and high-quality crystallization in large-area perovskite films through rapid NIRA processing. This approach not only significantly reduces energy consumption during production, but also substantially shortens the manufacturing cycle, paving a new path toward the commercial-scale application of perovskite solar modules.
Nano-Micro Letters•2025•DOI: 10.1007/s40820-024-01632-w
Alkali metal batteries (AMBs) have undergone substantial development in portable devices due to their high energy density and durable cycle performance. However, with the rising demand for smart wearable electronic devices, a growing focus on safety and durability becomes increasingly apparent. An effective strategy to address these increased requirements involves employing the quasi-solid gel electrolytes (QSGEs). This review focuses on the application of QSGEs in AMBs, emphasizing four types of gel electrolytes and their influence on battery performance and stability. First, self-healing gels are discussed to prolong battery life and enhance safety through self-repair mechanisms. Then, flexible gels are explored for their mechanical flexibility, making them suitable for wearable devices and flexible electronics. In addition, biomimetic gels inspired by natural designs are introduced for high-performance AMBs. Furthermore, biomass materials gels are presented, derived from natural biomaterials, offering environmental friendliness and biocompatibility. Finally, the perspectives and challenges for future developments are discussed in terms of enhancing the ionic conductivity, mechanical strength, and environmental stability of novel gel materials. The review underscores the significant contributions of these QSGEs in enhancing AMBs performance, including increased lifespan, safety, and adaptability, providing new insights and directions for future research and applications in the field.
Chinese Journal of Mechanical Engineering•2025•DOI: 10.1186/s10033-024-01172-9
Tracking control of tendon-driven manipulators has become a prevalent research area. However, the existence of flexible elastic tendons generates substantial residual vibrations, resulting in difficulties for trajectory tracking control of the manipulator. This paper proposes the radial basis function neural network adaptive hierarchical sliding mode control (RBFNNA-HSMC) method, which combines the dynamic model of the elastic tendon-driven manipulator (ETDM) with radial basis neural network adaptive control and hierarchical sliding mode control technology. The aim is to achieve trajectory tracking control of ETDM even under conditions of model inaccuracy and disturbance. The Lyapunov stability theory demonstrates the stability of the proposed RBFNNA-HSM controller. In order to assess the effectiveness and adaptability of the proposed control method, simulations and experiments were performed on a two-DOF ETDM. The RBFNNA-HSM method shows superior tracking accuracy compared to traditional model-based HSM control. The experiment shows that the maximum tracking error for ETDM double-joint trajectory tracking is below 2.593×10-3 rad and 1.624×10-3 rad, respectively.
Int. Journal of Minerals, Metallurgy and Materials (矿物冶金与材料学报)•2025•DOI: 10.1007/s12613-024-3011-8
Amino acids have emerged as promising green alternatives to replace toxic inhibitors in corrosion protection applications. In this study, we present a one-step synthetic approach to get 4-(tert-butyl)benzoyl)methionine (P-Meth) and 4-(tert-butyl)benzoyl)cysteine (P-Cys) through the acylation reactions between methionine or cysteine and p-tert-butylbenzoic acid, respectively, which exhibit a super protective performance toward metals against corrosion. The corrosion rates of Q235 steel in 1 M HCl were reduced from 4.542 to 0.202 and 0.312 mg·h−1·cm−2 in the presence of 100 mg·L−1 P-Meth and P-Cys, respectively. The surface structures of Q235 steel remained unbroken after 12 h in 1 M HCl medium. The charge transfer resistances of corrosion reactions were enhanced by 12 and 9 times in the presence of P-Meth and P-Cys, respectively. P-Meth and P-Cys were adsorbed onto the Q235 steel via chemical actions, which were accompanied by minimal physical action. Molecular dynamic simulations demonstrate the higher binding energy of P-Meth onto Q235 steel than P-Cys. The study contributes to the corrosion protection of metals with green and environmentally friendly methods.
Int. Journal of Mining Science and Technology (采矿与安全工程)•2024•DOI: 10.1016/j.ijmst.2024.12.011
As mining activities expand deeper, deep high-temperature formations seriously threaten the future safe exploitation, while deep geothermal energy has great potential for development. Combining the formation cooling and geothermal mining in mines to establish a thermos-hydraulic coupling numerical model for fractured formation. The study investigates the formation heat transfer behaviour, heat recovery performance and thermal economic benefits influenced during the life cycle. The results show that the accumulation of cold energy during the cold storage phase induces a decline in formation temperature. The heat recovery phase is determined by the extent of the initial cold domain, which contracts inward from the edge and decelerates the heat recovery rate gradually. With groundwater velocity increases, the thermal regulation efficiency gradually increases, the production temperature decreases, while the effective radius and thermal power increase first and then decrease. The injected volume and temperature significantly affect, with higher injection temperatures slowing thermal recovery, and the thermal regulation efficiency is more sensitive to changes in formation permeability and thermal conductivity. The heat extraction performance is positively correlated with all factors. The levelized cost of electricity is estimated at 0.1203 $/(kW h) during the cold storage. During the heat recovery, annual profit is primarily driven by cooling benefits.