微纳结构柔性压力传感器的制备及应用

柔性压力传感器是一种能够感知或监测外界压力变化的柔性电子器件,具备灵敏度高、形变灵活、制备工艺简单等特点,在可穿戴式电子产品、健康医疗、软体机器人、人机交互等新兴领域具有广泛而重要的应用。灵敏度、检测极限、响应时间与循环工作稳定性是柔性压力传感的核心性能指标,微纳结构的引入对提高柔性压力传感器综合性能具有重要作用。本文根据微纳结构的主要类型介绍了基于微纳结构的柔性压力传感器的最新研究进展,包括各种不同形貌微纳结构对柔性压力传感器性能的影响及其在柔性压力传感器中的应用,并对柔性压力传感器未来的发展提出展望。     

基于二维材料的柔性可穿戴传感器件研究进展

柔性可穿戴传感器是附着于人体皮肤或组织上的监测装置,可以持续监测和量化特定微环境变化所产生的电信号或化学信号,在医学诊断和治疗方面具有广泛的应用前景.二维材料具有原子薄层的平面结构、优异的机械柔性和电学性能,非常适合用于构建可穿戴传感器.近年来,基于二维材料的柔性传感器在材料制备、工艺设计和设备集成等方面取得了巨大的进...     

溶液法制备柔性压阻式传感器的研究进展

柔性压阻式传感器具有结构简单、易于制备、检测范围广等优势, 在可穿戴电子器件领域中扮演着非常重要的角色. 在制备柔性压阻式传感器的众多方法中, 溶液法由于操作简单、反应条件温和、材料的适用性广泛、易于规模化制备等优势, 成为极具发展前景的制备工艺. 在此基础上, 如何进一步提高柔性压阻式传感器的力学与电学性能也成为研究者们更加关注的话题. 另外, 制备图案化、微型化、规模化的传感器阵列为柔性压阻式传感器的应用范围拓展了新的道路. 本综述首先介绍了柔性压阻式传感器的工作原理与性能指标, 同时讨论了其性能指标对传感器在实际应用中的影响. 随后, 简单介绍了其构成材料, 并通过梳理近年来溶液法制备柔性传感器的研究成果, 选取了几种典型的溶液法制备方法进行重点介绍, 指出其具备的优势及目前存在的问题. 最后, 对溶液法制备柔性传感器的发展方向进行总结与展望.     

基于微纳结构的高灵敏度柔性压力传感器

近年来,随着互联网和人工智能的发展和普及,轻薄便捷、电子性能优异的柔性压力传感器作为可穿戴电子设备的核心器件,拥有了越来越广阔的市场。柔性压力传感器具有灵活柔韧、可折叠、传感性能优异等优点,因而在电子皮肤、运动检测、医疗监测和人机界面等方面已引起广泛的关注。构筑微纳结构是提高压力传感器灵敏度和传感性能的关键。基于此,本文首先总结了高灵敏度压力传感器的传感机制(压阻式、电容式、压电式和摩擦电式)和关键性能参数(灵敏度、压力检测范围、检测限、响应/恢复时间、循环稳定性和线性度等),然后归纳了利用基材构建表面微纳结构(微凸结构、荆棘结构和褶皱结构)和利用导电材料构建微纳结构(微球结构、海胆状结构、蜂窝状结构)的柔性压力传感器的研究进展及其优缺点,总结了基于微纳结构的高灵敏度柔性压力传感器在脉搏监测、电子皮肤、运动检测和人机界面等方面的应用现状。最后,从今后应用的角度出发,概述了高灵敏度柔性压力传感器即将面临的挑战及未来发展方向。     

石墨烯基气凝胶催化还原特性及其应用

石墨烯基气凝胶(GA)是一种内部连通的三维石墨烯宏观体,其在继承了石墨烯良好的化学稳定性和优良催化性能的同时拥有更高的比表面积和导电性。GA由于其优越的性能和独特的结构在催化、能量存储、吸附等领域得到广泛的应用。本文主要从GA催化还原特性展开,综述了具有不同催化性能的石墨烯基气凝胶的制备方法,将其总结归纳分为GA、掺杂型GA、复合型GA以及掺杂复合型GA四种类型,并详细介绍了制备方法对石墨烯基气凝胶催化性能的影响。石墨烯基气凝胶因具有优良的电化学活性和催化特性,在燃料电池、染料敏化太阳能电池、微生物电解池和电化学传感器等领域具有广泛的应用前景。最后对石墨烯基气凝胶在催化领域的应用前景进行分析和展望。     

纳米碳材料在可穿戴柔性导电材料中的应用研究进展

可穿戴设备的兴起使得对柔性器件的需求日益提高,柔性导电材料作为可穿戴器件的重要组成部分而成为研究的热点。传统的电极材料主要是金属,因金属材料本身不具有柔性,一般通过降低金属层厚度以及设计波纹结构等策略实现其在柔性器件中的应用,其加工程序复杂,成本较高。以碳纳米管和石墨烯为代表的纳米碳材料兼具良好的柔性和优异的导电性,且具有化学稳定、热稳定、光学透明性等优点,在柔性导电材料领域展现了极大的应用潜力。本文简要综述了近年来纳米碳材料在柔性导电材料领域的研究进展,首先介绍了碳纳米管基柔性导电材料,分别包括基于碳纳米管水平阵列、碳纳米管垂直阵列、碳纳米管薄膜、碳纳米管纤维的柔性导电材料;继而介绍了石墨烯基柔性导电材料,包括基于剥离法制备的石墨烯和化学气相沉积法制备的石墨烯以及石墨烯纤维基柔性导电材料;并简述了碳纳米管/石墨烯复合柔性导电材料;最后论述了纳米碳材料基柔性导电材料所面临的挑战并展望了其未来发展方向。     

可穿戴柔性触觉传感器的研究进展

可穿戴柔性触觉传感器是用来模仿人类触觉的器件, 可以感知人体以及外界环境的运动、 形变和压力等信息, 在智慧医疗和智能机器人等领域具有广泛的应用前景. 近年来, 大量柔性触觉传感器的研究使其性能得到了巨大的提升, 并在很多领域得到了应用. 本文首先简述了柔性触觉传感器的结构和基本性能; 然后重点介绍了具有自愈合、 自驱动以及可视化等新型高性能触觉传感器的研究进展; 接下来讨论了柔性触觉传感器在可穿戴电子技术、 医疗保健以及人机交互界面等方面的应用; 最后展望了柔性触觉传感器未来所面临的机遇与挑战.     

石墨烯及其衍生物在离子传感中的应用

离子传感器的检测对象主要是在水中痕量存在的、但对人体健康或生态环境有重大影响的离子。石墨烯独特的热学、电学与机械性质使得其在离子传感领域受到广泛的关注。目前,人们通过对石墨烯进行修饰和功能化,得到了石墨烯的诸多衍生物和相关的复合材料,满足了不同条件下的传感要求。本文主要选取了石墨烯及其衍生物在Hg~(2+)、Pb~(2+)、Cu~(2+)、K~+等传感中的应用进行了简要介绍,对这些石墨烯及其衍生物基离子传感器的传感机理进行了概括性说明,并对石墨烯及其衍生物基离子传感器的发展趋势进行了展望。     

石墨烯/纤维素复合材料的制备及应用

近年来,石墨烯/纤维素复合材料引起了研究者的广泛关注。该材料在透明导电柔性薄膜、电容器、载药、紫外线防护、传感器、吸附等领域有重要的应用价值。本文在收集、归类研究国内外研究者在石墨烯/纤维素复合材料制备方法、性能以及应用工作的基础上,对石墨烯和纤维素复合材料的混合技术、制备方法及应用进行了综述。     

石墨烯基高分子复合材料的研究进展

自2004年石墨烯被发现以来,石墨烯优异的机械、热学、电学及光学性能引起广大学者的浓厚兴趣,许多石墨烯基高分子复合材料被相继合成和表征,研究显示,石墨烯基高分子复合材料有着广泛的应用前景。本文对石墨烯基高分子复合材料的研究进展进行了综述,重点对石墨烯基高分子复合材料的制备方法和性能进行了阐述,并对其在传感器、太阳能电池、超级电容器及其他方面的应用做了相关介绍,并对石墨烯／高分子复合材料的发展前景进行了展望。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

Synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives

Different approaches for the synthesis of 1-benzyloxypyrazin-2(1H)-one derivatives from simple amino acids have been investigated. A library of 33 precursors for the preparation of N-hydroxy pyrazinones was obtained in moderate to good yields.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Chemistry of heterocyclic compounds at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, over 50 years (Review)

The review contains a concise historical account and information on the most significant researches undertaken by the staff at the A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences on the Chemistry of Heterocyclic Compounds. Dedicated to Academician of the Russian Academy of Sciences B. A. Trofimov on his 70th jubilee. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1443–1502, October, 2008.     

A general and convenient synthesis of 4-(tosylmethyl)semicarbazones and their use in amidoalkylation of hydrogen,heteroatom, and carbon nucleophiles

A general synthesis of previously unknown semicarbazone-based α-amidoalkylating reagents, 4-(tosylmethyl)semicarbazones, has been developed. The synthesis involved three-component condensation of semicarbazones of aliphatic or aromatic aldehydes with the same or other aldehydes and p-toluenesulfinic acid. The scope and limitations of this reaction were investigated. The compounds obtained were demonstrated to be an efficient α-(4-semicarbazono)alkylating agents. They were reacted with H- (sodium borohydride), O- (sodium methylate), S- (sodium phenylthiolate), N- (pyrrolidine, sodium succinimide), P- (trialkyl phosphites), and C-nucleophiles (sodium diethyl malonate) to give the corresponding products of the tosyl group substitution, 4-substituted semicarbazones, including analogues of nitrofurazone. Among the prepared compounds tested in vitro for antibacterial and antifungal activity, three nitrofuryl-containing semicarbazones exhibited high biological activities with minimum inhibitory concentration (MIC) values of 8–32 μg/mL.     

Sulfur-directed metal-free and regiospecific methyl C(sp3)–H imidation of thioanisoles

Regiospecific and direct imidation of the methyl C(sp³)–H bond of thioanisoles is realized under mild and metal-free conditions with N-fluorobis(benzenesulfonyl)imide as an oxidant and nitrogen source. Proposed mechanism suggests that thionium ion intermediates and a Pummerer-type reaction are involved. The imidation has advantages such as high step-economy, excellent functionality tolerance, and regiospecificity, giving structurally diverse imidation products.     

Synthesis of novel chiral bidentate hydroxyalkyl-N-heterocyclic carbene ligands and their application in palladium-catalyzed Mizoroki–Heck couplings and asymmetric addition of diethylzinc to benzaldehyde

A small library of new chiral bidentate hydroxyalkyl-imidazolium salts 1 is conveniently synthesized on multi-gram scale from inexpensive and commercially available chiral pool amino acids. The corresponding carbenes, generated by deprotonation of imidazolium salts 1, in combination with palladium(II) chloride were tested in the Mizoroki–Heck coupling reaction. The most significant results in terms of yields and reactivities were achieved with low catalyst loading. The catalytic activities of these imidazolium salts were also investigated in the asymmetric addition of diethylzinc to benzaldehyde. The use of MgO nanoparticles as an additive in conjunction with these ligands played a crucial role in increasing the efficiency of these reactions.