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Development of Porous Polyacrylonitrile Composite Fibers: New Precursor Fibers with High Thermal Stability 多孔聚丙烯腈复合纤维的开发:新型高热稳定性前驱纤维
Pub Date : 2021-10-08 DOI: 10.3390/electronicmat2040031
Ehsan Samimi-Sohrforozani, S. Azimi, A. Abolhasani, S. Malekian, S. Arbab, M. Zendehdel, M. M. Abolhasani, N. Yaghoobi Nia
Polyacrylonitrile (PAN) fibers with unique properties are becoming increasingly important as precursors for the fabrication of carbon fibers. Here, we suggest the preparation of porous PAN composite fibers to increase the homogeneity and thermal stability of the fibers. Based on the thermodynamics of polymer solutions, the ternary phase diagram of the PAN/H2O/Dimethylformamide (DMF) system has been modeled to introduce porosity in the fibers. Adding a conscious amount of water (4.1 wt.%) as a non-solvent to the PAN solution containing 1 wt.% of graphene oxide (GO), followed by wet spinning, has led to the preparation of porous composite fibers with high thermal stability and unique physicochemical properties. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results elucidate that PAN/GO/H2O porous composite fibers have a higher thermal decomposition temperature, increased residual weight, reduced heat release rate, and higher crystallinity in comparison with the pristine PAN fibers, being a promising precursor for the development of high-performance carbon fibers. The results show a promising application window of the synthesized PAN fibers in electronic and electrochemical devices.
聚丙烯腈(PAN)纤维以其独特的性能作为碳纤维的前驱体正变得越来越重要。在此,我们建议制备多孔PAN复合纤维,以提高纤维的均匀性和热稳定性。基于聚合物溶液的热力学,建立了PAN/H2O/二甲基甲酰胺(DMF)体系的三元相图,以引入纤维中的孔隙率。在含有1 wt.%氧化石墨烯(GO)的PAN溶液中加入一定量的水(4.1 wt.%)作为非溶剂,然后进行湿纺丝,可以制备出具有高热稳定性和独特物理化学性能的多孔复合纤维。差示扫描量热法(DSC)和热重分析(TGA)结果表明,与原始PAN纤维相比,PAN/GO/H2O多孔复合纤维具有更高的热分解温度、更大的残余重量、更低的放热速率和更高的结晶度,是开发高性能碳纤维的良好前驱体。结果表明,合成的聚丙烯腈纤维在电子和电化学器件中具有广阔的应用前景。
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引用次数: 8
High Rectification Ratio in Polymer Diode Rectifier through Interface Engineering with Self-Assembled Monolayer 基于自组装单层界面工程的高整流率聚合物二极管整流器
Pub Date : 2021-10-01 DOI: 10.3390/electronicmat2040030
Khaoula Ferchichi, Sébastien Pecqueur, D. Guérin, R. Bourguiga, K. Lmimouni
In this work, we demonstrate P3HT (poly 3-hexylthiophene) organic rectifier diode both in rigid and flexible substrate with a rectification ratio up to 106. This performance has been achieved through tuning the work function of gold with a self-assembled monolayer of 2,3,4,5,6-pentafluorobenzenethiol (PFBT). The diode fabricated on flexible paper substrate shows a very good electrical stability under bending tests and the frequency response is estimated at more than 20 MHz which is sufficient for radio frequency identification (RFID) applications. It is also shown that the low operating voltage of this diode can be a real advantage for use in a rectenna for energy harvesting systems. Simulations of the diode structure show that it can be used at GSM and Wi-Fi frequencies if the diode capacitance is reduced to a few pF and its series resistance to a few hundred ohms. Under these conditions, the DC voltages generated by the rectenna can reach a value up to 1 V.
在这项工作中,我们在刚性和柔性衬底上展示了P3HT(聚3-己基噻吩)有机整流二极管,整流比高达106。这种性能是通过自组装的2,3,4,5,6-五氟苯乙醇(PFBT)单层调节金的功函数来实现的。在柔性纸衬底上制造的二极管在弯曲测试中显示出非常好的电稳定性,频率响应估计在20 MHz以上,足以用于射频识别(RFID)应用。这也表明,这种二极管的低工作电压可以是一个真正的优势,用于整流天线的能量收集系统。仿真结果表明,将二极管电容减小到几个pF,串联电阻减小到几百欧姆,可以在GSM和Wi-Fi频率下使用。在这种情况下,整流天线产生的直流电压最高可达1v。
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引用次数: 5
Effect of synthesis conditions and composition on structural and phase states and electrical properties of nanogranular (FeCoZr)x (PZT)100-x films (30 ≤ x ≤ 85 at.%) 合成条件和组成对纳米颗粒(FeCoZr)x (PZT)100-x薄膜(30≤x≤85 at.%)结构、相态和电学性能的影响
Pub Date : 2021-09-30 DOI: 10.3897/j.moem.7.3.76277
J. Fedotova
Granular films containing Fe50Co50Zr10 alloy nanoparticles inside Pb0,81Sr0,04(Na0,5Bi0,5)0,15(Zr0,575Ti0,425)O3 (PZT) ferroelectric matrix possess a combination of functional magnetic and electrical properties which can be efficiently controlled by means of external electric or magnetic fields. The formation of the required granular structure in PZT matrix is only possible if synthesis is carried out in an oxygen-containing atmosphere leading to substantial oxidation of metallic nanoparticles. Thus an important task is to study the oxidation degree of metallic nanoparticles depending on synthesis conditions and the effect of forming phases on the electrical properties of the films. The relationship between the structural and phase state and electrical properties of granular FeCoZr)x (PZT)100-x films (30 ≤ x ≤ 85 at.%) synthesized in an oxygen-containing atmosphere at the oxygen pressure PO in a range of (2.4–5.0) · 10–3 Pa has been studied using X-ray diffraction, EXAFS and four-probe electrical resistivity measurement. Integrated comparative analysis of the structural and phase composition and local atomic order in (FeCoZr)x (PZT)100-x films has for the first time shown the fundamental role of oxygen pressure PO during synthesis on nanoparticle oxidation and phase composition. We show that the oxygen pressure being within PO = 3.2 · 10–3 Pa an increase in x leads to a transition from nanoparticles of Fe(Co,Zr)O complex oxides to a superposition of complex oxides and a-FeCo(Zr,O) ferromagnetic nanoparticles (or their agglomerations). At higher oxygen pressures РО = 5.0 · 10–3 Pa the nanoparticles undergo complete oxidation with the formation of the (FexCo1-x)1-δO complex oxide having a Wurtzite structure. The forming structural and phase composition allows one to explain the observed temperature dependences of the electrical resistivity of granular films. These dependences are distinguished by a negative temperature coefficient of electrical resistivity over the whole range of film compositions at a high oxygen pressure (РО = 5.0 · 10–3 Pa) and a transition to a positive temperature coefficient of electrical resistivity at a lower oxygen pressure (РО = 3.2 · 10–3 Pa) in the synthesis atmosphere and x > 69 at.% in the films. The transition from a negative to a positive temperature coefficient of electrical resistivity which suggests the presence of a metallic contribution to the conductivity is in full agreement with the X-ray diffraction and EXAFS data indicating the persistence of unoxidized a-FeCo(Zr,O) ferromagnetic nanoparticles or their agglomerations.
在pb0,81sr0,04 (na0,5bi0,5)0,15(Zr0,575Ti0,425)O3 (PZT)铁电基体中含有Fe50Co50Zr10合金纳米颗粒的颗粒膜具有功能磁性和电学性质,可以通过外加电场或磁场有效地控制。PZT基体中所需颗粒结构的形成只有在含氧大气中进行合成才能导致金属纳米颗粒的大量氧化。因此,研究金属纳米颗粒在不同合成条件下的氧化程度以及形成相对薄膜电性能的影响是一项重要的任务。采用x射线衍射、EXAFS和四探针电阻率测量等方法,研究了在含氧气氛下,在(2.4-5.0)·10-3 Pa的氧压PO范围内合成的FeCoZr (PZT)100-x颗粒状薄膜(30≤x≤85 at.%)的结构、相态和电学性能之间的关系。通过对(FeCoZr)x (PZT)100-x薄膜结构、相组成和局部原子序的综合对比分析,首次揭示了合成过程中氧压PO对纳米颗粒氧化和相组成的影响。我们发现,当氧压在PO = 3.2·10-3 Pa范围内时,x的增加会导致Fe(Co,Zr)O络合物氧化物纳米粒子向复合氧化物和a- feco (Zr,O)铁磁性纳米粒子(或它们的团块)的叠加转变。在较高的氧压РО = 5.0·10-3 Pa下,纳米颗粒完全氧化,形成具有纤锌矿结构的(FexCo1-x)1-δO络合物氧化物。形成结构和相组成允许人们解释观察到的颗粒膜电阻率的温度依赖性。在高氧压(РО = 5.0·10-3 Pa)下,薄膜组成的整个范围内的电阻率温度系数为负,而在合成气氛中,在低氧压(РО = 3.2·10-3 Pa)下,电阻率温度系数转变为正,且x > 69。在电影中。从负到正的电阻率温度系数的转变表明存在金属对电导率的贡献,这与x射线衍射和EXAFS数据完全一致,表明未氧化的a- feco (Zr,O)铁磁性纳米颗粒或它们的团块的存在。
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引用次数: 0
Comparison between results of optical and electrical measurements of free electron concentration in n-InAs specimens n-InAs样品中自由电子浓度的光学与电学测量结果比较
Pub Date : 2021-09-30 DOI: 10.3897/j.moem.7.3.76700
T. G. Yugova, A. Belov, V. E. Kanevskii, E. I. Kladova, S. Knyazev, I. B. Parfent'eva
A theoretical model has been developed for determining the free electron concentration in n-InAs specimens from characteristic points in far IR reflection spectra. We show that this determination requires plasmon-phonon coupling be taken into account, otherwise the measured electron concentration proves to be overestimated. A correlation between the electron concentration Nopt and the characteristic wavenumber ν+ has been calculated and proves to be well fit by a third order polynomial. The test specimens have been obtained by tin or sulfur doping of indium arsenide. The electron concentration in the specimens has been measured at room temperature using two methods: the optical method developed by the Authors (Nopt) and the conventional four-probe Hall method (the Van der Pau method, NHall). The reflecting surfaces of the specimens have been chemically polished or fine abrasive ground. The condition Nopt > NHall has been shown to hold for all the test specimens. The difference between the optical and the Hall electron concentrations is greater for specimens having polished reflecting surfaces. The experimental data have been compared with earlier data for n-GaAs. A qualitative model explaining the experimental data has been suggested.
建立了从远红外反射光谱特征点测定n-InAs样品中自由电子浓度的理论模型。我们表明,这种测定需要考虑等离子体-声子耦合,否则测量的电子浓度被证明是高估的。计算了电子浓度Nopt与特征波数ν+之间的关系,并用三阶多项式很好地拟合。试样是用锡或硫掺杂砷化铟制成的。在室温下,用两种方法测量了样品中的电子浓度:由作者(Nopt)开发的光学方法和传统的四探针霍尔方法(Van der Pau法,NHall)。样品的反射表面已经过化学抛光或精细研磨。情况Nopt > NHall已被证明适用于所有的测试样本。对于具有抛光反射表面的样品,光学电子浓度和霍尔电子浓度之间的差异更大。实验数据与n-GaAs的早期数据进行了比较。提出了一个定性模型来解释实验数据。
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引用次数: 4
Magnetization of magnetically inhomogeneous Sr2FeMoO6-δ nanoparticles 磁不均匀Sr2FeMoO6-δ纳米颗粒的磁化研究
Pub Date : 2021-09-30 DOI: 10.3897/j.moem.7.3.75786
Gunnar Suchaneck
Magnetization is a key property of magnetic materials. Nevertheless, a satisfactory, analytical description of the temperature dependence of magnetization in double perovskites such as strontium ferromolybdate is still missing. In this work, we develop, for the very first time, a model of the magnetization of nanosized, magnetically inhomogeneous Sr2FeMoO6-δ nanoparticles. The temperature dependence of magnetization was approximated by an equation consisting of a Bloch-law spin wave term, a higher order spin wave correction, both taking into account the temperature dependence of the spin-wave stiffness, and a superparamagnetic term including the Langevin function. In the limit of pure ferromagnetic behavior, the model is applicable also to SFMO ceramics. In the vicinity of the Curie temperature (T/TC > 0.85), the model fails.
磁化是磁性材料的一个重要特性。然而,对双钙钛矿(如钼铁酸锶)磁化的温度依赖性的令人满意的分析描述仍然缺失。在这项工作中,我们首次建立了纳米级,磁性不均匀的Sr2FeMoO6-δ纳米颗粒的磁化模型。磁化的温度依赖性由一个布洛赫定律自旋波项、一个考虑了自旋波刚度的温度依赖性的高阶自旋波修正和一个包含朗之万函数的超顺磁项组成的方程近似。在纯铁磁行为的极限下,该模型也适用于SFMO陶瓷。在居里温度(T/TC > 0.85)附近,模型失效。
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引用次数: 0
Two-dimensional WSe2 flakes under high power optical excitation 高功率光激发下的二维WSe2薄片
Pub Date : 2021-09-30 DOI: 10.3897/j.moem.7.3.74274
K. Brekhov, S. Lavrov, A. Kudryavtsev, N. Ilyin
Quasi-2D layers of transition metal dichalcogenides are promising candidates for creating saturable absorbers for pulsed lasers. However, the peculiarities of intense electromagnetic radiation’s influence on such structures have not been thoroughly studied. This paper explores the dynamics of photoexcited carriers in WSe2 flakes through experimental studies. These studies found that WSe2 flakes significantly change their optical properties under the influence of a high-power optical pump, allowed estimating the thermalization time of these structures (about 2 ps), and found that full relaxation takes more than 10 ps. The concentration of carriers in the semiconductor surface layer was estimated to be about 1028 m–3. It was found that standard description models of the optical response based on exciton resonances and absorption by free carriers could not adequately describe the experiments’ results. Thus, for an accurate description of the optical response, it was necessary to consider the effects associated with Coulomb screening that are caused by the high concentration of photo-excited carriers of the optical pumping densities used in this experiment.
准二维过渡金属二硫族化合物层是制造脉冲激光可饱和吸收剂的有希望的候选者。然而,强电磁辐射对此类结构影响的特性尚未得到深入研究。本文通过实验研究探讨了WSe2薄片中光激发载流子的动力学。这些研究发现,在高功率光泵的影响下,WSe2薄片的光学性质发生了明显的变化,可以估计这些结构的热化时间(约2 ps),并发现完全弛豫需要10 ps以上。半导体表层载流子的浓度估计约为1028 m-3。发现基于激子共振和自由载流子吸收的光学响应的标准描述模型不能充分描述实验结果。因此,为了准确地描述光响应,有必要考虑与库仑屏蔽相关的效应,这是由本实验中使用的光泵浦密度的高浓度光激发载流子引起的。
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引用次数: 0
Synthesis, structure and electromagnetic properties of FeCoAl/C nanocomposites FeCoAl/C纳米复合材料的合成、结构和电磁性能
Pub Date : 2021-09-30 DOI: 10.3897/j.moem.7.3.77105
D. Muratov, L. Kozhitov, E. Yakushko, A. Vasilev, A. Popkova, V. Tarala, E. Korovin
Magnetic nanoparticles play an important role in rapidly developing advanced branches of science and industry, e.g. fabrication of magnetic storage media, synthesis of ferromagnetic liquids, medicine and chemistry. One problem faced in the usage of magnetic nanoparticles is their high chemical activity leading to oxidation in air and agglomeration. The chemical activity of magnetic nanoparticles stems from the contribution of their large specific surface to volume ratio. Carbon coating of nanoparticles reduces the interaction between nanoparticles. FeCoAl/C metal-carbon nanocomposites have been synthesized using IR pyrolysis of polymer/metal salt precursors. The effect of synthesis temperature (IR heating) in the range from 500 to 700 °C on the structure and composition of the nanomaterials has been studied. We show that the forming particles are the FeCoAl ternary solid solution with a FeCo based bcc lattice. An increase in the synthesis temperature from 500 to 700 °C leads to an increase in the coherent scattering region of three-component nanoparticles from 5 to 19 nm. An increase in the aluminum content from 20 to 30% relative to Fe and Co results in an increase in the size of the nanoparticles to 15 nm but this also entails the formation of a Co based solid solution having an fcc lattice. An increase in the nanocomposite synthesis temperature and a growth of the relative Al content as a result of a more complete carbonization and the structure-building effect of metals reduce the degree of amorphousness of the nanocomposite carbon matrix and lead to the formation of graphite-like phase crystallites having an ordered structure. The effect of synthesis temperature and relative content of metals on the electromagnetic properties (complex permittivity and permeability) of the synthesized nanocomposites has been studied. Synthesis conditions affect the radio absorption properties of the nanocomposites, e.g. reflection loss (RL) in the 3–13 GHz range.
磁性纳米颗粒在磁性存储介质的制造、铁磁液体的合成、医学和化学等快速发展的先进科学和工业领域发挥着重要作用。磁性纳米颗粒在使用中面临的一个问题是它们的高化学活性导致在空气中氧化和团聚。磁性纳米颗粒的化学活性源于其较大的比表面积与体积比。纳米颗粒的碳涂层减少了纳米颗粒之间的相互作用。采用聚合物/金属盐前驱体红外热解法合成了FeCoAl/C金属碳纳米复合材料。研究了合成温度(红外加热)在500 ~ 700℃范围内对纳米材料结构和组成的影响。结果表明,形成颗粒为feocal三元固溶体,具有feoco基bcc晶格。当合成温度从500℃增加到700℃时,三组分纳米粒子的相干散射区域从5 nm增加到19 nm。相对于Fe和Co,铝的含量从20%增加到30%,导致纳米颗粒的尺寸增加到15 nm,但这也需要形成具有fcc晶格的Co基固溶体。随着纳米复合材料合成温度的升高和相对Al含量的增加,炭化过程更加彻底,金属的结构构建作用降低了纳米复合碳基体的非晶化程度,形成了结构有序的类石墨相晶。研究了合成温度和金属相对含量对所合成纳米复合材料电磁性能(复介电常数和磁导率)的影响。合成条件影响了纳米复合材料的无线电吸收性能,如反射损耗(RL)在3-13 GHz范围内。
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引用次数: 2
Metal–Insulator Transition in Doped Barium Plumbates 掺杂铅酸钡的金属-绝缘体跃迁
Pub Date : 2021-09-16 DOI: 10.3390/electronicmat2030029
Andreza Eufrasio, I. Pegg, Amrit Kafle, W. Wong-Ng, Qingzhen Huang, Biprodas Dutta
Solid solutions in the Ba(Pb1−xSrx)O3−z system were prepared by aliovalent substitution of Pb4+ by Sr2+ ions to investigate the effect of cation stoichiometry on thermal and electrical properties as x was varied between 0 and 0.4, in the temperature range 300–523 K. The starting compound, barium plumbate (BaPbO3), has a perovskite structure and is known to exhibit metallic conductivity due to an overlap of the O2p nonbonding and the Pb–O spσ antibonding band, which is partially filled by the available electrons. The large difference in the ionic radii between the Pb4+ and Sr2+ ions introduces significant strain into the (Pb/Sr)O6 octahedra of the perovskite structure. Additionally, charged defects are created on account of the different oxidation states of the Pb4+ and Sr2+ ions. Evidence of a metal to insulator transition (MIT) of the Mott–Hubbard type has been observed at a critical concentration of Sr2+ ions.
用Sr2+离子取代Pb4+,制备了Ba(Pb1−xSrx)O3−z体系的固溶体,研究了在300-523 K温度范围内,当x在0 ~ 0.4范围内变化时,阳离子化学计量对热学和电学性能的影响。起始化合物铅酸钡(BaPbO3)具有钙钛矿结构,由于O2p非键带和Pb-O spσ反键带重叠,其中部分被可用电子填充,因此已知其具有金属导电性。Pb4+和Sr2+离子半径的巨大差异使钙钛矿结构的(Pb/Sr)O6八面体产生了明显的应变。此外,由于Pb4+和Sr2+离子的氧化态不同,产生了带电缺陷。在Sr2+离子的临界浓度下,已经观察到莫特-哈伯德型金属到绝缘体转变(MIT)的证据。
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引用次数: 0
Sterically Stabilized Multilayer Graphene Nanoshells for Inkjet Printed Resistors 用于喷墨印刷电阻器的立体稳定多层石墨烯纳米壳
Pub Date : 2021-09-14 DOI: 10.3390/electronicmat2030027
M. Orrill, Dustin T. Abele, M. Wagner, S. LeBlanc
In the field of printed electronics, there is a pressing need for printable resistors, particularly ones where the resistance can be varied without changing the size of the resistor. This work presents ink synthesis and printing results for variable resistance, inkjet-printed patterns of a novel and sustainable carbon nanomaterial—multilayer graphene nanoshells. Dispersed multilayer graphene nanospheres are sterically stabilized by a surfactant (Triton X100), and no post-process is required to achieve the resistive functionality. A surface tension-based adsorption analysis technique is used to determine the optimal surfactant dosage, and a geometric model explains the conformation of adsorbed surfactant molecules. The energetic interparticle potentials between approaching particles are modeled to assess and compare the stability of sterically and electrostatically stabilized multilayer graphene nanoshells. The multilayer graphene nanoshell inks presented here show a promising new pathway toward sustainable and practical printed resistors that achieve variable resistances within a constant areal footprint without post-processing.
在印刷电子领域,迫切需要可印刷的电阻,特别是那些可以在不改变电阻尺寸的情况下改变电阻的电阻。本文介绍了一种新型可持续碳纳米材料——多层石墨烯纳米壳的油墨合成和可变电阻喷墨打印结果。分散的多层石墨烯纳米球被表面活性剂(Triton X100)立体稳定,不需要后处理就能实现电阻功能。采用基于表面张力的吸附分析技术确定了表面活性剂的最佳用量,并用几何模型解释了吸附表面活性剂分子的构象。模拟了接近粒子之间的高能粒子间势,以评估和比较空间稳定和静电稳定多层石墨烯纳米壳的稳定性。本文提出的多层石墨烯纳米壳油墨为可持续和实用的印刷电阻器提供了一条有前途的新途径,可以在恒定的面积范围内实现可变电阻,而无需后处理。
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引用次数: 0
Highly Flexible Polyaniline-Based Implantable Electrode Materials for Neural Sensing/Stimulation Applications 用于神经传感/刺激应用的高柔性聚苯胺基植入式电极材料
Pub Date : 2021-09-14 DOI: 10.3390/electronicmat2030028
N. Almufleh, A. Al-Othman, Zaid Alani, M. Al-Sayah, H. Al-Nashash
Implantable bioelectrodes have the potential to advance neural sensing and muscle stimulation, mainly in patients with peripheral nerve injuries. They function as the transducer at the interface between the damaged nerve and the muscle which is controlled by that nerve. This work reports the fabrication and characterization of novel, low-cost, flexible bioelectrodes based on polyaniline (PANI) and supported with silicone polymer. The fabricated electrodes were evaluated for their electrical and mechanical characteristics. PANI was used as the main transducer component in this fabrication. The characterization methods included electrical conductivity, capacitive behavior, long-term electrical impedance, and mechanical evaluation. The results of the fabricated PANI-silicone-based samples displayed a bulk impedance of 0.6 kΩ with an impedance of 1.6 kΩ at the frequency of 1 kHz. Furthermore, the bioelectrodes showed a charge storage capacity range from 0.0730 to 4.3124 C/cm2. The samples were stable when subjected to cyclic voltammetry tests. The bioelectrodes revealed very flexible mechanical properties as observed from the value of Young’s modulus (in the order of MPa) which was less than that of skin. Hence, the PANI-based bioelectrodes reported herein showed promising electrochemical characteristics with high flexibility.
植入式生物电极具有促进神经传感和肌肉刺激的潜力,主要用于周围神经损伤患者。它们在受损神经和由神经控制的肌肉之间起到换能器的作用。本文报道了一种新型的、低成本的、基于聚苯胺(PANI)和硅酮聚合物支撑的柔性生物电极的制造和表征。对所制备电极的电学和力学特性进行了评价。聚苯胺被用作主要的换能器元件。表征方法包括电导率、电容行为、长期电阻抗和力学评价。制备的聚苯胺硅基样品在1 kHz频率下阻抗为1.6 kΩ,体阻抗为0.6 kΩ。此外,生物电极的电荷存储容量范围为0.0730 ~ 4.3124 C/cm2。经循环伏安试验,样品稳定。从杨氏模量(MPa数量级)来看,生物电极显示出非常灵活的力学性能,比皮肤的力学性能要小。因此,本文报道的聚苯胺基生物电极具有良好的电化学特性和高柔韧性。
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引用次数: 5
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Modern Electronic Materials
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