掺杂8-羟基喹啉铝薄膜的电致发光特性研究

在具有电致发光(EL)的有机整合染料8-羟基喹啉铝(Alq3)中接以染料罗丹明6G(R6G),用真空热蒸发的方法制备器件,获得了峰值波长575nm的黄色直流薄膜电致发光,从而通过掺杂改变了发光颜色.并在Alq3发光层不同区域插入一掺杂薄层(Alq3:R6G),利用其发光波长与未掺杂部分(Alq3)的不同,以此作为“探测层”,通过对器件光谱及电学特性的测量与分析,探讨了有关发光区域,发光机理,界面对发光影响等基本问题.     

铝合金蒙皮激光除漆后新漆层的耐高温性能研究

在实际飞行环境中温度是引起漆层失效的重要因素之一,飞机在长时间服役后需去除老化漆层以便喷涂新漆层,确保飞机运行的安全性和可靠性。本文采用波长为1064 nm的平顶脉冲激光对铝合金蒙皮表面漆层进行清洗,并对铝合金蒙皮激光除漆后新漆层进行高温加速老化,模拟飞机停场时铝合金漆层系统的耐高温性。采用扫描电子显微镜、激光共聚焦显微镜、附着力测试仪以及电化学工作站,综合评价了激光除漆效果及新漆层表面形貌、漆层与铝合金的附着力、电化学阻抗特性等耐温性指标。结果表明：激光功率500 W、扫描速度4000mm/s、扫描间距0.1 mm时可将铝合金表面漆层去除且不损伤铝合金,重新喷涂后的附着力达到0级且附着力时效性能较好;150℃加速老化48 h的漆层附着力为1级,漆层表面微观形貌无明显变化、漆层光滑平整、无缺陷且低频区域电化学阻抗模值>10⁹Ω·cm²。     

基于双摄像头的心率测量系统的设计与改进

针对在外部干扰或昏暗环境下利用图像光电容积描记(image Photoplethysmography,iPPG)技术进行心率测量时准确度较差,提出了一种自适应心率提取算法,并在嵌入式硬件平台上进行了验证。算法根据图像中人脸与背景区域的色度关系来识别不同的场景并启动合适的摄像头进行图像采集及自适应映射,接着对提取出的信号进行滤波,在信号质量评估后输出结果。上述方法在Zynq平台上进行了验证,使用双摄像头实现实时心率测量,并对结果进行可视化输出。实验结果表明:优化后的算法在光照及运动的双重干扰下的测量误差从3.36BPM降至2.78BPM,准确率提升了17.3%。另外,所设计的系统能够实现在极端黑暗条件下的心率采集,平均误差约为2.39BPM。     

基于衍射色散原理的光谱共焦位移测量技术综述

位移检测技术是几何量精密测量的基础,在当代精密制造领域应用广泛。光谱共焦位移测量技术具有对环境杂散光、被测物倾斜、材料类型不敏感,测量频率高以及分辨率高等优点,可以检测位移量、表面粗糙度、三维形貌以及单层或多层透明材料的厚度,在精密位移测量领域中占据重要地位。近年来,利用衍射光学元件提高光学系统性能的光谱共焦测量技术被广泛研究。文章综述了基于衍射色散原理的光谱共焦位移测量技术的研究进展。首先,介绍了光谱共焦位移测量原理和衍射光学元件的色散特性;其次,阐述了基于衍射色散原理的光谱共焦位移测量技术的发展历史及研究进展;最后展望了该技术的发展趋势。     

基于拓扑绝缘体异质结的宽带太赫兹探测器

二维材料中的新量子态对凝聚态物理和现代光电器件的发展具有重要意义。然而具有宽带、室温和快速响应能力的太赫兹光电探测技术,由于缺乏暗电流和光吸收之间的最佳平衡,仍然面临着巨大的挑战。在这项研究中,作者合成了新型拓扑绝缘体材料GeBi₄Te₇,并搭建了其与Bi₂Te₃的范德华异质结,以实现高灵敏度的太赫兹光电探测器。在平面金属-材料-金属结构中实现了在室温下将低光子能量太赫兹波段直接转化为光电流。结果表明,基于Bi₂Te₃-GeBi₄Te₇的太赫兹光电探测器能够实现0.02～0.54 THz的宽谱探测,且具有很高的光响应率(在0.112、0.27、0.5 THz下分别为592 V·W^-1、203 V·W^-1、40 V·W^-1),响应时间小于6μs。值得注意的是,它被用于高频太赫兹的成像应用演示。这些结果为Bi₂Te₃     

Electrochemically Induced Crystalline-to-Amorphous Transition of Dinuclear Polyoxovanadate for High-Rate Lithium-Ion Batteries

Polyoxometalates are intriguing high-capacity anode materials for alkali-metal-ion storage due to their multi-electron redox capabilities and flexible structure. However, their poor electrical conductivity and high working voltage severely restrict their practical application. Herein, the dinuclear polyoxovanadate Sr₂V₂O₇·H₂O with unusually high electrical conductivity is reported as a promising anode material for lithium-ion batteries. During the initial lithiation process, the Sr₂V₂O₇·H₂O anode experiences an electrochemically induced crystalline-to-amorphous transition. The resulting amorphous structure provides high redox activity and fast reaction kinetics via reversible V^4.9+/V^2.8+ redox couple through the intercalation mechanism. Furthermore, when coupled with the LiFePO₄ cathode, the strong V O bonds of the amorphous anode provide excellent structural stability, with the full-cell capable of performing >12 000 cycles with a capacity retention of 72%. Another advantage of Sr_2xV₂O_7-δ·yH₂O (0.5 ≤ x ≤ 1.0) is its composition adjustability, which enables delicately regulating the Sr vacancy content without destroying the structure. The defect Sr_2xV₂O_7-δ·yH₂O (x = 0.5) electrodes show significantly improved specific capacity and rate capability without sacrificing other key properties, delivering a high specific capacity of 479 mAh g^-1 at 0.1 mA cm^-2 and 41.9% of its capacity in 2 min. Overall, the preliminary study points the way forward for the facile preparation of high-quality polyoxometalates for advanced energy storage applications and beyond.     

Versatile Hypoxic Extracellular Vesicles Laden in an Injectable and Bioactive Hydrogel for Accelerated Bone Regeneration

Extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) have emerged as an appealing alternative to cell therapy in regenerative medicine. Unlike bone marrow MSCs (BMSCs) cultured in vitro with normoxia, bone marrow in vivo is exposed to a hypoxic environment. To date, it remains unclear whether hypoxia preconditioning can improve the function of BMSC-derived EVs and be more conducive to bone repair. Herein, it is found that hypoxia preconditioned BMSCs secrete more biglycan (Bgn)-rich EVs via proteomics analysis, and these hypoxic EVs (Hypo-EVs) significantly promote osteoblast proliferation, migration, differentiation, and mineralization by activating the phosphatidylinositide 3-kinase/protein kinase B pathway. Subsequently, an injectable bioactive hydrogel composed of poly(ethylene glycol)/polypeptide copolymers is developed to improve the stability and retention of Hypo-EVs in vivo. The Hypo-EVs-laden hydrogel shows continuous liberation of Hypo-EVs for 3 weeks and substantially accelerates bone regeneration in 5-mm rat cranial defects. Finally, it is confirmed that Bgn in EVs is a pivotal protein regulating osteoblast differentiation and mineralization and exerts its effects through paracrine mechanisms. Therefore, this study shows that hypoxia stimulation is an effective approach to optimize the therapeutic effects of BMSC-derived EVs and that injectable hydrogel-based EVs delivery is a promising strategy for tissue regeneration.     

Nanocellulose-Carboxymethylcellulose Electrolyte for Stable,High-Rate Zinc-Ion Batteries

Aqueous Zn ion batteries (ZIBs) are one of the most promising battery chemistries for grid-scale renewable energy storage. However, their application is limited by issues such as Zn dendrite formation and undesirable side reactions that can occur in the presence of excess free water molecules and ions. In this study, a nanocellulose-carboxymethylcellulose (CMC) hydrogel electrolyte is demonstrated that features stable cycling performance and high Zn²⁺ conductivity (26 mS cm⁻¹), which is attributed to the material's strong mechanical strength (≈70 MPa) and water-bonding ability. With this electrolyte, the Zn-metal anode shows exceptional cycling stability at an ultra-high rate, with the ability to sustain a current density as high as 80 mA cm⁻² for more than 3500 cycles and a cumulative capacity of 17.6 Ah cm⁻² (40 mA cm⁻²). Additionally, side reactions, such as hydrogen evolution and surface passivation, are substantially reduced due to the strong water-bonding capacity of the CMC. Full Zn||MnO₂ batteries fabricated with this electrolyte demonstrate excellent high-rate performance and long-term cycling stability (>500 cycles at 8C). These results suggest the cellulose-CMC electrolyte as a promising low-cost, easy-to-fabricate, and sustainable aqueous-based electrolyte for ZIBs with excellent electrochemical performance that can help pave the way toward grid-scale energy storage for renewable energy sources.