注压成型纳米结构PP/POE共混物表面的液滴低温冲击行为

以制备的阳极氧化不锈钢模板为模具嵌件, 采用注射压缩成型(ICM)工艺快速成型表面具有纳米丝结构的柔性聚丙烯/乙烯-辛烯共聚物(PP/POE, PP与POE质量比为3∶1)共混物复制物和准刚性PP复制物, 研究常温液滴冲击?10 ℃复制物表面的动态行为. 结果表明, 致密的纳米丝使复制物表面呈现超疏水、 极低黏附的润湿状态. 在低冲击速度范围内, 共混物复制物表面上液滴的接触时间比PP复制物上的短, 可归因于液滴铺展阶段柔性纳米丝储存的弹性势能在回缩阶段转换为液滴的动能; 在高冲击速度范围内, 共混物复制物基板和纳米丝储存的弹性势能被转换为液滴的动能, 进一步缩短了液滴的接触时间. 此结果表明, 共混物复制物的柔性和表面超疏水性使其具有优异的防冻黏性能. 共混物复制物表面上水滴(50 μL)的结冰时间得到明显延长、 冰黏附强度明显降低. 研究结果表明, 可采用ICM快速成型具有优异防冻黏和防冰性能的柔性超疏水高分子材料表面.     

聚二甲基硅氧烷封装石墨烯基柔性红外探测器的制备及其应用

采用热还原法在不同退火温度（从100到1200℃）下制备了一系列还原氧化石墨烯（rGO）薄膜，并通过X射线粉末衍射（XRD）、傅里叶变换红外光谱（FTIR）、拉曼光谱、四探针电阻仪和扫描电镜（SEM）对其进行了表征和分析.随后利用旋涂封装法制备了聚二甲基硅氧烷（PDMS）封装的石墨烯基柔性红外探测器（P-rGO-P），并成功用于红外激光、人体红外辐射、弯曲变化和压力探测.实验结果表明，采用不同温度还原的rGO薄膜封装得到的P-rGO-P柔性红外探测器在近红外（1064 nm）激光照射下均有响应，其中最高的光响应可达2.78 mA/W.此外，P-rGO-P柔性探测器对人体红外辐射和弯曲变化也具有快速、灵敏的响应，并且经过反复弯折仍能保持完整性与响应能力.     

具有较高回弹性的乙烯-辛烯共聚物基微孔复合材料的传感性能

通过熔体混炼制备乙烯-辛烯共聚物/多壁碳纳米管/碳纤(POE/MWCNTs/CF,90/5/5,W/W/W)复合材料,采用超临界二氧化碳发泡法对其进行釜压发泡,分析3种发泡温度(55、60和65℃)下制备的微孔样品的泡孔结构,着重研究其对微孔样品压缩性能和传感器压阻响应(灵敏度和线性响应范围等)的影响.结果表明,55℃下制备的微孔样品呈现较均匀的泡孔结构、较窄的泡孔直径分布(主要在10～30μm范围内)和厚度适中、连续性高的泡孔壁,这使其具有较高的回弹性、压缩强度、压缩模量和电导率.采用这种微孔圆片封装成的传感器具有较宽的线性响应范围(0～30%压缩应变)和较高的灵敏度(应变因子为1.67),根据泡孔结构对此进行了分析.该传感器具有较快速的压阻响应和恢复性能以及良好的重复性,在1000次循环压缩/释放测试中表现出较高的稳定性和耐久性,且能检测手指按压、肘部弯曲、深蹲和脚踩等人体运动(对应较宽的压缩应变范围).研究表明,采用超临界流体发泡法制备泡孔结构较均匀、泡孔壁厚度适中且连续的微孔导电复合材料具有良好的传感性能.     

聚合物加工中微纳导电网络构筑及其传感器应用研究进展

设计和构筑有序微纳结构导电网络是聚合物基导电复合材料(CPC)加工中的关键问题,对于降低复合材料的逾渗阈值,提高其电导率和电阻响应灵敏性具有重要意义。本文综述了近年来CPC材料加工中利用双逾渗网络构筑法、隔离结构构筑法、气凝胶模板法、乳液模板法、3D打印法在聚合物基体中构建微纳导电网络及其在柔性传感器中的应用研究进展,并对未来CPC材料及其柔性传感器制备的加工新方法进行了展望。     

Mb/AuNPs/MWCNTs/GC电极对H2O2电催化性能的研究

采用还原法制备了AuNPs/MWCNTs复合材料,并构建了氧化还原蛋白质的固定化和生物传感界面AuNPs/MWCNTs/GC电极.以肌红蛋白(Myoglobin,Mb)为例,研究了固定化蛋白质在AuNPs/MWCNTs/GC电极上的直接电化学.结果表明,AuNPs/MWCNTs复合材料不仅能有效地促进Mb与电极表面的直接电子转移,而且能很好地保持固定化Mb的生物催化活性.Mb/AuNPs/MWCNTs/GC电极对H2O2具有良好的电催化还原性能,其线性响应范围为1～138μmol·L-1,检测限为0.32μmol·L-1(S/N=3),并具有较低的米氏常数(0.143 mmol·L-1).该电极操作简单,响应迅速,稳定性和重现性好,有望用于蛋白质的固定化及第三代生物传感器的制备.     

有序介孔碳/石墨烯/镍泡沫的制备及其对多巴胺的高灵敏度和高选择性检测（英文）

柔性生物传感器在可穿戴电子设备中有着广泛的应用前景.为了获得柔性电化学多巴胺传感器,作者在本工作中首先在镍泡沫表面通过化学气相沉积生长石墨烯,随后通过高温碳化嵌段共聚物与酚醛树脂在石墨烯表面共组装形成的薄膜制备了有序介孔碳/石墨烯/镍泡沫(OMC/G/Ni)复合材料.其中,镍泡沫可以为复合材料提供具有高导电性和良好柔韧性的金属骨架,而具有垂直排列介孔阵列的有序介孔碳层为复合材料提供了高的电活性表面积,且有利于活性位点的暴露.值得注意的是,夹在有序介孔碳层和镍泡沫之间的石墨烯极大地增强了各组分之间的相容性,有利于进一步提升复合材料的电化学性能.作为电化学传感器中的工作电极,OMC/G/Ni体现出优异的多巴胺检测能力.不但具有宽的线性检测范围(0.05～58.75μmol·L~(-1))和低检测限(0.019μmol·L~(-1)),还具有良好的选择性、重现性和稳定性.此外,OMC/G/Ni在弯曲状态下依旧能够保持对多巴胺的高检测能力,证明了其在柔性生物传感器中的应用潜力.     

有序介孔碳/石墨烯/镍泡沫的制备及其对多巴胺的高灵敏度和高选择性检测

柔性生物传感器在可穿戴电子设备中有着广泛的应用前景. 为了获得柔性电化学多巴胺传感器,作者在本工作中首先在镍泡沫表面通过化学气相沉积生长石墨烯,随后通过高温碳化嵌段共聚物与酚醛树脂在石墨烯表面共组装形成的薄膜制备了有序介孔碳/石墨烯/镍泡沫（OMC/G/Ni）复合材料. 其中,镍泡沫可以为复合材料提供具有高导电性和良好柔韧性的金属骨架,而具有垂直排列介孔阵列的有序介孔碳层为复合材料提供了高的电活性表面积,且有利于活性位点的暴露. 值得注意的是,夹在有序介孔碳层和镍泡沫之间的石墨烯极大地增强了各组分之间的相容性,有利于进一步提升复合材料的电化学性能. 作为电化学传感器中的工作电极,OMC/G/Ni体现出优异的多巴胺检测能力. 不但具有宽的线性检测范围（0.05 ~ 58.75 μmol·L^-1）和低检测限（0.019 μmol·L^-1）,还具有良好的选择性、重现性和稳定性. 此外,OMC/G/Ni在弯曲状态下依旧能够保持对多巴胺的高检测能力,证明了其在柔性生物传感器中的应用潜力.     

柔性导电高分子复合材料在应变传感器中的应用*

柔性和可穿戴传感器最近十几年来的发展,使得它们在个性化医疗、人机交互和智能机器人等方面拥有良好的应用前景。由导电材料和弹性聚合物组成的柔性导电高分子复合材料具有高的可拉伸性、良好的柔韧性、优异的耐久性等优点,可用来制备传感范围宽、灵敏度高的柔性应变传感器。本文综述了基于柔性导电高分子复合材料的可拉伸应变传感器的分类(填充型、三明治型、吸附型应变传感器)和传感机理(隧穿效应,分离机制,裂纹扩展),并详细介绍了传感器所用复合材料的结构设计,包括内部结构(双逾渗网络、隔离、多孔、“砖混”结构)、表面结构(微裂纹、褶皱结构)和宏观结构(纤维状、网状、薄膜结构)。内部结构设计可降低材料的逾渗阈值,表面结构设计可提高传感器性能,每个宏观结构都有自己的特点。最后对应变传感器的材料选择、制备工艺、结构设计、附加性能、集成技术和应用方向等方面进行了展望。     

基于仿生MXene纤维导电网络的柔性透明电极及电容传感器

为了开发具有优良性能的智能伪装隐身器件,使用预模板法制备了柔性透明电极.以叶脉纤维为预模板,在其表面沉积金属碳化物/氮化物（MXene）,从而开发了具有透明有序导电网络结构的透明电极.叶脉表面的羟基基团与导电材料的表面活性基团的相互作用极大地提高了导电材料与基底的表面结合力.此柔性透明电极在透光率为80.6%时,方阻为11.4Ω/sq,有效地避免了光电特性之间的“权衡”效应,且在1000次弯曲循环下电阻几乎保持不变,具备良好的耐久性和稳定性.将此透明电极成功制备透明电容式传感器,其灵敏度可达0.09 kPa^-1,且在1000次循环之后相对电容基本保持不变,具有出色的传感性能和耐久性,可以在人难以察觉的状态下监测人体运动信号.此柔性透明电极和透明电容传感器在可穿戴伪装电子领域具有巨大潜力.     

基于CuO-Co3O4的催化燃烧型一氧化碳传感器

采用共沉淀法制备了CuO-Co3O4复合材料,并以其为催化剂,负温度系数热敏电阻(NTCT)为加热电阻,制备了一种催化燃烧型CO传感器,该传感器对CO的定量限为0.034 9 mg.L-1。利用X射线衍射(XRD)和场发射扫描电子显微镜(FESEM)对复合材料的物相和表面形貌进行表征。当CuO-Co3O4的煅烧温度为400℃时,传感器对CO的灵敏度最高。在桥电压为9 V,CO的浓度为0.034 9~0.582 mg.L-1时,传感器的响应信号与CO浓度之间呈现良好的线性关系,线性相关系数为0.979。90%的响应和恢复时间分别为24 s和68 s。     

Flexible Broad‐Range Pressure Sensors Enabled by Deformation‐Induced Conductive Channels in 3D Graphene Foam@Polydimethylsiloxane Composite for Precise Vibrational Signal Detection

Here we report the design and fabrication of high‐performance pressure sensors based on three‐ dimensional (3D) graphene foam filled polydimethylsiloxane (GF@PDMS) composite with a broad sensing range spaning from 0.05 kPa to 130 kPa. The interpretation of device functioning mechanism can be classified into low and high pressure sensing regions. In the low pressure region (<15 kPa), the pressure loading leads to the temporal connection of micro‐cracks in GF scaffold and forming conductive channels. In the high pressure region (15 kPa to 130 kPa), the pressure induced deformation of GF results in the better connections among micro‐cracks and the shortening of conductive pathway to further decrease the electrical resistance. The GF@PDMS sensors exhibited accuracy, sensibility and reproducibility to detect pressure signals with remarkable stability for over 16000 loading‐unloading cycles, indicating its great potential for practical applications. Moreover, the GF@PDMS sensors also showed high performances in the detection of dynamic pressures, such as subtle mechanical vibration signals, as well as physiology vibrational signals generated by human throats. We expect this technology could be integrated into different sensing systems for the applications in wearable smart electronics and human‐machine communications.     

The influence of bending on the performance of flexible carbon black/polymer composite gas sensors

The performance of electronics on flexible substrates suffers under substrate bending leading to reduced device performance. In this article, we highlighted the influence of bending strain on a conductive polymer composite gas sensor and developed a model to investigate the influence of strain. We evaluated the strain influence on the resistance of a gas sensor with respect to sensitivity, filler content, cyclic loading, and electrode orientation. The sensitivity of gas sensors increased with decreasing tensile bending radii. The influence of strain was dominant for gas sensors with less carbon black concentration. Cyclic bending tests showed a decrease of sensor resistance versus time and a plastic deformation. A sensor geometry orientations effect to reduce the sensitivity to bending strain was achieved by aligning the electrode fingers parallel to the strain. A model was successfully implemented to simulate strain influences inside the polymer incorporating the Poisson ratio. We suggest a concept to achieve a strain insensitive gas sensor by creating an orientation between single particles inside the composite. Implementing this results into existing gas sensors will improve the measurement quality and reliability of sensors on flexible substrates. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

Non‐oxidized graphene/elastomer composite films for wearable strain and pressure sensors with ultra‐high flexibility and sensitivity

It remains challenging to prepare wearable strain and pressure sensors with excellent mechanical properties, ultra‐high flexibility and sensitivity. Electrically conductive graphene platelets (GnPs) with high structural integrity are used in making a composite film fabricated using robust fabrication techniques. The gauge factor for the strain is up to 100 at 0%‐5% strain and 50 at 5%‐30% strain, and the sensitivity to pressure is 2.7×10^‐2 kPa^‐1 between 0 and 10 kPa and 1.5×10^‐4 kPa^‐1 between 300 and 1000 kPa. In addition, the flexible sensor demonstrates good repeatability and durability after 1000 cycles of tensile and compression tests. The flexible sensor has fast response ability and a wide operating temperature range, suggesting the excellent response to temperature. The flexible sensor is applied in monitoring several human motions as a wearable device with high accuracy. The ability to detect strain, pressure and temperature of the flexible sensor extends its applications to multifunctional wearable devices.     

Thin and high conductive multi-walled carbon nanotubes/polydimethylsiloxane composite film prepared via solvent method as strain sensors

Flexible strain sensors based on conductive fillers and flexible polymers possessed significant advantages in human motion detection. Preparing a strain sensing layer with high electrical conductivity and excellent mechanical property under high content of conductive filler contributed to the stability of flexible strain sensors. In this study, MWCNTs/PDMS composite film was prepared by the organic solvent method. The microstructure, electrical conductivity, mechanical property, and piezoresistive characteristics of the composite film at different MWCNTs contents were characterized and discussed. When the mass fraction of MWCNTs in the composite film was 5%, the composite film exhibited a high electrical conductivity of 9.56 S/m while maintaining ideal mechanical properties, and the film thickness was just about 180 μm. The relationship between electrical signals and film strain was performed. The piezoresistive characteristic results demonstrated that the prepared composite film could be used as flexible strain sensor for human motion detection. The prepared thin MWCNTs/PDMS composite film in this paper illustrated high conductive and desired flexibility, and was an alternative material for human motion detection.     

Changes in electrical resistance of carbon‐black‐filled silicone rubber composite during compression

We studied the changes in the electrical resistance of carbon black filled silicone rubber composite, which is the sensitive element of the flexible force sensor, as a function of time during compression. The experimental results show that there is a sudden increase of the electrical resistance along with the sudden increase of the stress immediately after the compression. When the sample strain is kept constant, the electrical resistance and the stress both decay with time. The data of the stress relaxation and the resistance relaxation both can be fitted by the linear combination of two exponential functions. Based on the shell structure theory, the experimental phenomena are explained from the view that the uniaxial pressure induces the changes in the effective conductive paths. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 2700–2706, 2007     

交流阻抗谱在聚乙烯/碳黑导电复合材料导电机理研究中的应用

用交流阻抗谱论证了聚乙烯/碳黑(PE/CB)导电复合材料的网络导电机理,分析了热处理过程对复合材料电性能的影响。通过在不同频率和低电压下测定热处理前后及不同长度的导电复合材料样品的导电能力(A)、导电方式(B)和电阻值(Ra Rc),证明了材料内部存在着直通碳链、小间隙的碳链和大间隙的碳链,呈现三维网络导电结构。     

低压近场静电纺丝ZnO/PVDF复合微米纤维阵列的制备及压力传感性

利用低压近场静电纺丝技术制备了ZnO/PVDF(聚二偏氟乙烯)微米纤维平行阵列, 通过光学显微镜、扫描电子显微镜(SEM)和X射线能量色散光谱(EDS)对ZnO/PVDF微米纤维进行了表征. 该复合纤维的平均直径约为40 μm. EDS分析测试证明ZnO纳米颗粒已经掺杂进入了平行微米纤维中. 压电性能和电学性能测试结果表明, ZnO/PVDF微米纤维阵列的压电性能增强. 研究结果表明, 近场电纺丝ZnO/PVDF复合微米纤维阵列在压电型压力传感器和纳米发电机领域具有潜在的应用价值.     

聚乙烯醇/聚吡咯复合导电水凝胶应变传感器的制备及性能

以聚乙烯醇(PVA)为原料, 植酸(PA)和氨基-聚倍半硅氧烷(NH₂-POSS, NP)为交联剂, 通过冻融循环法制得PVA/PA/NP复合水凝胶, 再以其为模板, 通过吡咯的原位聚合制得PVA/PA/NP-PPy复合导电水凝胶, 克服了聚吡咯材料易脆、 疏水的特性, 进一步改善了水凝胶的导电性和灵敏性. 循环拉伸实验结果表明该水凝胶具有良好的自回复能力, 电导率高达7.53 S/m, 从I-V曲线可知其作为柔性可穿戴应变传感器的最高检测电流可达 9.029 mA, 灵敏度因子可达6.796, I-T曲线表明该传感器可以准确地通过电流信号变化来监测人体的各种微小运动.     

The piezoresistive behaviors of polyethylene/foliated graphite nanocomposites

A conductive nanocomposite with an ordered conductive network and low-percolation threshold were prepared by adding foliated graphite (FG) nanosheets to high-density polyethylene (HDPE). The piezoresistive behavior of the nanocomposites was investigated under different pressure ranges. There existed a critical pressure below which composite resistance decrease with the increase of pressure and above which resistance increased sharply with increasing of pressure. The critical pressure is a function of the concentration of FG and the sensitivity of the change in resistivity against the applied pressure strongly depended on the FG content. The critical pressures of the nanocomposites with FG concentration at 6 vol.%, 11 vol.%, 12 vol.%, are about 7 MPa, 10 MPa, and 12 MPa, respectively. After repeated pressure treatment, there was a gradual decrease in the change of conducting structure although a permanent damage occurred due to the irreversible deformation of polymer matrix. As a result, the piezoresistive behavior of HDPE/FG nanocomposites tended to be constant under cyclic compression. The behavior was accounted for by an extension of tunneling conduction theory to which provides a good approximation to the piezoresistive effect.