PAN基凝胶聚合物电解质双电层电容器

为了得到安全、无泄漏、微型、超薄型的双电层电容器,采用内聚合方法制得聚丙烯腈基凝胶聚合物电解质双电层电容器,电解质的增塑剂为碳酸丙烯酯和碳酸乙烯酯,支持电解质为高氯酸锂,电极材料分别为比表面积1000m2/g和2600m2/g的活性炭。采用交流阻抗、循环伏安、恒流充放电、循环寿命等测试方法对内聚合式凝胶聚合物电解质及其组成的双电层电容器的性能进行了测试。结果表明,此种方法制得的双电层电容器的内阻小,比容量较大,其中以比表面积2600m2/g活性炭为电极材料的电容器的双电极比容量达到47.41F/g。     

碳基双电层电容器电极材料的研究进展

双电层电容器是一种介于电池与传统电容器之间的新型储能元件,具有较高的能量密度和功率密度,且充电速度快、循环寿命长、对环境无污染,广泛应用于国防、军工以及电动汽车、数字通讯、计算机等众多民用领域.简述了双电层电容器的基本工作原理,综述了碳基双电层电容器电极材料的研究进展.     

超级电容器准固态聚合物电解质膜的研究

制备了一种介于水凝胶和全固态聚合物电解质之间的聚合物电解质膜,用于活性炭电子双电层电容器。测试表明使用该聚合物电解质膜的双电层电容器的容量为2 15mA·h,其容量、功率特性与KOH水溶液电容器相当。电容器的循环伏安曲线,稳定的充放电循环曲线及交流阻抗谱说明该种聚合物电解质膜在碳基超级电容器的使用电压范围(0～1V)内是稳定的,而且聚合物电解质膜电容器表现出良好的可逆性和循环特性。     

聚酰亚胺超级电容器电极材料研究进展

简述了超级电容器的应用优势及其电极材料的发展与特性,回顾了近几年聚酰亚胺及其衍生碳材料在超级电容器领域的最新研究进展,介绍了聚酰亚胺基多孔碳、碳纳米片、碳气凝胶以及碳纳米纤维等材料作为电极活性材料的研究现状,并分析了各自应用的优缺点及改进的方法。最后讨论了未来推进聚酰亚胺及其衍生碳材料在超级电容器领域的进一步发展应注重的研究方向,指出包括聚酰亚胺碳气凝胶、多孔碳纤维及自支撑膜电极以下几方面仍需研究。     

高表面活性炭电极的制备及其在双电层电容器中的应用

综述了高表面活性炭电极的原料制备、电极成型及修饰技术的研究进展,论述了双电层电容器电化学性能的影响因素,提出了提高双电层电容器电化学性能的方法,主要包括修饰和改善高表面活性炭的微观结构、改进电极成型工艺技术和电极的预处理方式等.并建议根据实际应用过程中双电层电容器的等效电路和Gouy-Chapman-Stern(GCS)模型理论,计算出高表面活性炭电极表面上的电解质的分布形态,以此作为研究双电层电容器的微观结构和吸附储电机理的突破点,为高表面活性炭电极用于双电层电容器的进一步发展提供理论指导.     

双电层电容器电极材料最新研究进展

对双电层电容器炭基电极材料中已经产业化的和颇具产业化前景的活性炭、碳纳米管、炭凝胶等几种材料进行了综述，分析了它们的性质、特点和研究进展。     

导电聚合物复合材料作为超级电容器电极材料

本文综述了基于导电聚合物的复合材料(导电聚合物/碳材料、导电聚合物/金属氧化物材料、导电聚合物/碳材料l金属氧化物材料)作为电极材料在超级电容器中的应用进展,指出将导电聚合物与碳材料或金属氧化物复合,双电层电容与法拉第准电容结合,有机材料与无机材料结合,是超级电容器电极材料研究的重要发展方向.     

碳气凝胶电极用于NaCl溶液电容性除盐的研究

碳气凝胶是一种新型多孔碳材料,具有比表面积大、电导率高的特点。本文通过常压干燥制备了碳气凝胶,研究测试了其结构特性,用N aCl溶液模拟海水,利用CD I原理,以碳气凝胶作电极进行了N aC l溶液的除盐实验。实验表明,决定碳气凝胶的除盐效果的主要因素为比表面积和电导率。在不同配比结构中,以R/C为1500、M值为30%的碳气凝胶电极的除盐效果最佳。利用双电层电容模型解释探讨了碳气凝胶电极的除盐机理。     

碳气凝胶电极用于NaCI溶液电容性除盐的研究

碳气凝胶是一种新型多孔碳材料，具有比表面积大、电导率高的特点。本文通过常压干燥制备了碳气凝胶，研究测试了其结构特性，用NaCl溶液模拟海水，利用CDI原理，以碳气凝胶作电极进行了NaCl溶液的除盐实验。实验表明，决定碳气凝胶的除盐效果的主要因素为比表面积和电导率。在不同配比结构中，以R/C为1500、M值为30％的碳气凝胶电极的除盐效果最佳。利用双电层电容模型解释探讨了碳气凝胶电极的除盐机理。     

碳气凝胶复合材料在超级电容器中应用的研究进展

从碳气凝胶的发展、制备和干燥工艺,以及掺杂碳气凝胶的改性方面叙述了碳气凝胶在超级电容器材料中的研究进展,并展望了碳气凝胶未来的发展方向。     

氧化硅气凝胶绝热材料及其建筑减碳应用

无机氧化硅气凝胶因具有超低导热系数、A级不燃、吸湿率低、轻质等特点,在航天航空、工业及建筑领域的节能减碳方面具有广泛的应用潜力。然而氧化硅气凝胶力学性能差、制备成本高等缺点限制了其发展应用。介绍了氧化硅气凝胶绝热材料制备工艺的研究进展,对氧化硅气凝胶在建筑领域的应用形式（如超轻气凝胶泡沫混凝土、超高性能气凝胶保温隔热板、超低传热系数气凝胶节能玻璃等）进行了综述,并对氧化硅气凝胶在建筑节能领域的发展方向进行了展望。响应碳中和发展目标,随着气凝胶制备技术的发展与成本降低,氧化硅气凝胶绝热材料将在建筑墙体保温隔热方面广泛应用,同时对其性能提出了更多功能性要求,对氧化硅气凝胶材料还需开展更系统的基础研究以及工程应用技术研发,推动建筑领域的节能减碳与可持续发展。     

Preparation of carbon aerogel by ambient pressure drying and its application in lithium/sulfur battery

Formaldehyde, resorcinol, and sodium acetate were used to synthesize the carbon aerogels by ambient pressure drying. The effect of the ratio of resorcinol and sodium acetate for carbon aerogels was researched by scanning electron microscope and Brunauer-Emmett-Teller characterizations. Then the carbon aerogels were applied in synthesizing sulfur/carbon aerogel composites through a melting method, the specific capacity and cycle performance of lithium/sulfur batteries that adopted the prepared composites as cathodes were measured by galvanostatic discharge?Ccharge. X-ray diffraction, conductivity measurement, cyclic voltammetry, and electrochemical impedance spectra tests were also carried out to help explain the electrochemical performance. Finally, the carbon aerogel with the best properties was chosen for the comparative study of replacement of water by acetone as solvent in the preparation of carbon aerogels. According to our study, the carbon aerogel prepared by ambient pressure drying with high electrical conductivity, controllable pore structure, and high specific surface area was proposed to be used for lithium/sulfur batteries, and the key factors to the performance of carbon aerogel/sulfur composites were discussed.     

炭气凝胶的常压干燥制备研究

实验以间苯二酚(Resorcinol,简称R)与甲醛(Formaldehyde,简称F)以一定的摩尔比混合,加入二次去离子水作为溶剂并用碱性试剂作为催化剂,在恒温水浴中生成RF湿凝胶。在常温下用丙酮浸泡湿凝胶以置换水,制备出RF凝胶。最后将RF气凝胶置于管式炉中,在氮气保护气氛下,高温炭化得到炭气凝胶,并用TG-DTA,XRD、高倍显微镜等方法对其表面形貌及结构进行分析。     

石墨烯基气凝胶对有机物的饱和吸附能力

以Pickering乳液法进行了石墨烯基气凝胶(GA)的制备,并以纯有机物和水中乳化油分为吸附对象,对其饱和吸附能力进行了评价,综合对比了不同研究者利用碳纳米材料所制备碳基气凝胶对纯有机化合物的吸附能力,发现包含本文所制备的GA在内的各种碳基气凝胶对不同的有机物的吸附能力与有机物的密度成正比,表明单位质量碳基气凝胶吸附有机物的体积(cm³?g^?1)为定值,与具体的被吸附有机物的种类无关。推断有机物在气凝胶材料中的吸附是一种体积填充行为,气凝胶孔隙体积的大小对于其吸附有机物的能力具有重要影响,但孔隙的占有率也是决定实际吸附有机物能力的关键因素。所制备的GA对水中油分的吸附能力低于其对纯油分的吸附能力,应与水的竞争吸附、有机物的扩散阻力等有关。     

酚醛基炭气凝胶的研究进展

炭气凝胶是一种多孔纳米炭材料,具有低密度、高孔隙率、高比表面积、优异的导电性和良好的成型性能等优点,是炭材料研究的热点和重要方向。本文旨在通过阐明酚醛基炭气凝胶的制备原料和制备工艺的发展过程,从而突出未来酚醛基炭气凝胶的发展方向。基于此,本文首先重点介绍了酚醛基炭气凝胶的制备方法,主要包括溶胶-凝胶化、干燥以及炭化过程三个最主要的步骤;进而详述了以三种不同的前体,即间苯二酚、苯酚、生物质单宁/木质素分别制备酚醛基炭气凝胶的方法及其优缺点;接下来对酚醛基炭气凝胶作为吸附材料（气体吸附/液体吸附）的吸附量以及在电化学储能以及其他领域的应用进行了综述;最后对酚醛基炭气凝胶未来的研究方向和发展前景进行了总结和展望。文章指出,传统的以间苯二酚为原料辅以超临界干燥的方法制备的酚醛基炭气凝胶,原料成本较高,反应条件苛刻,实际生产应用受限;以苯酚取代间苯二酚,亦或是采用冷冻干燥等方法改进其制备工艺,可以大幅度降低原料和生产成本;但未来的发展方向和重点将是绿色、可再生的生物质原料（单宁、木质素、腰果酚等）及复合气凝胶材料的研发。因此,酚醛基炭气凝胶在未来的发展还需要进一步改进其制备工艺和方法,拓宽其原料来源,从而提高性能,扩大应用领域。     

Enhanced thermal shrinkage behavior of phenolic-derived carbon aerogel-reinforced by HNTs with superior compressive strength performance

A novel carbon/m-HNTs composite aerogel was synthesized by introducing the modified halloysite nanotubes (m-HNTs) into phenolic (PR) aerogels through chemical grafting, followed with carbonization treatment. In order to explore the best proportion of HNTs to phenolic, the micromorphology of PR/m-HNTs were investigated by SEM before carbonization, confirming 10 wt% of m-HNTs is most beneficial to the porous network of aerogels. The interaction between PR and HNTs was studied by FTIR spectra, and microstructure evolution of the target product-carbon/m-HNTs composite aerogel were illustrated by SEM and TEM techniques. SEM patterns indicated that the carbon/m-HNTs aerogels maintain a stable porous structure at 1000 °C (carbonization temperature), while a ~20 nm carbon layer was formed around m-HNTs generating an integral unit through TEM analysis. Specific surface area and pore size distribution of composite aerogels were analyzed based on mercury intrusion porosimetry and N₂ adsorption–desorption method, the obtained results stayed around 500 m²g^?1 and 1.00 cm³g^?1 (pore volume) without significant discrepancy, compared with pure aerogel, showing the uniformity of pore size. The weight loss rate (26.76%) decreased greatly compared with pure aerogel, at the same time, the best volumetric shrinkage rate was only 30.83%, contributed by the existence of HNTs supporting the neighbor structure to avoid over-shrinking. The highest compressive strength reached to 4.43 MPa, while the data of pure aerogel was only 1.52 MPa, demonstrating the excellent mechanical property of carbon/m-HNTs aerogels.     

Organic and carbon aerogels from the NaOH‐catalyzed polycondensation of resorcinol–furfural and supercritical drying in ethanol

Organic aerogels and related carbon aerogels were prepared from the NaOH‐catalyzed polycondensation of resorcinol–furfural (RF) and supercritical drying in ethanol. The effect of the preparation conditions, including the RF concentration, molar ratio of resorcinol (R) to NaOH, and molar ratio of R to furfural, on the gelation time and bulk density was studied. The chemical structure of the organic aerogel was revealed by IR spectroscopy. The pyrolysis process of the organic aerogel was investigated by thermogravimetric analysis. According to characterizations of transmission electron microscopy and nitrogen adsorption, the organic and carbon aerogels we obtained had a three‐dimensional network that consisted of around 30‐nm particles, which defined numerous mesopores of less than 30 nm. As a result, the aerogels had high Brunauer–Emmett–Teller surface areas (698–753 m²/g) and large mesopore volumes (1.09–1.64 cm³/g). X‐ray diffraction characterization indicated that the carbon aerogel was more crystalline than activated carbon but less activated than graphite. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1429–1435, 2005     

Superelastic,fatigue resistant and heat insulated carbon nanofiber aerogels for piezoresistive stress sensors

Ultralight flexible carbon aerogels have been applied in many fields but are always hampered due to their weak mechanical stability, large energy dissipation, and complex preparation methods. Here, a novel polyimide-derived carbon nanofiber aerogel with high fatigue resistance and excellent flexibility is prepared by using the designed “fiber gluing” to construct the elastic continuous fibrous network. The as-prepared carbon nanofiber aerogels exhibit ultralow density of 6.6 mg cm⁻³, excellent fire-resistant performance when exposing to alcohol flames (650 °C), and robust elastic resilience even under 55% compressive strain. In particular, the carbon nanofiber aerogels show ultralow plastic deformation (only 1.3%) and low energy dissipation (<0.22) after 1000 cyclic loading-unloading tests at 55% compressive strain. Benefiting from their excellent flexibility and robust mechanical stability, the as-prepared carbon nanofiber aerogel are a promising candidate in the application of wearable devices and piezoresistive stress sensors.     

Carbon Aerogels for Electrochemical Double Layer Capacitors

Carbon aerogels are prepared here via pyrolysis of resorcinol-formaldehyde aerogels. Their open porous and electrically conductive structure renders carbon aerogels suitable for the application in supercapacitors. Different types of electrodes can be derived from the sol-gel-precursors of carbon aerogels: Monolithic fibre-reinforced electrodes and polymer-carbon compounds. Both carbon fibre reinforced and polymeric bound aerogel electrodes based on polytetrafluoroethylene (PTFE) have been investigated in this work with respect to their electrical conductivity, surface area and capacitive performance. The capacitance of both electrode types is above 65 F/cm³ in aqueous electrolytes and this meets the demands of supercapacitor electrodes.     

Nanoporous phloroglucinol-formaldehyde carbon aerogels for electrochemical use

Phloroglucinol-Formaldehyde (PF) organic aerogels were prepared from alcoholic sol-gel polycondensation of phloroglucinol with formaldehyde using KOH as base catalyst and followed by supercritical drying with carbon dioxide. Subsequent pyrolysis of PF organic aerogel under He flow produced carbon aerogels. Textural properties of PF organic and carbon aerogels were obtained by nitrogen adsorption-desorption, and their specific capacitances were measured by cyclic voltammetry. The resultant PF carbon aerogels were mostly mesoporous material with high surface area. The nanoporous structure and electrochemical behavior of PF carbon aerogels could be controlled by the molar ratio of phloroglucinol to catalyst (P/C) and carbonization conditions. PF carbon aerogels exhibited the highest surface area in excess of 1,200 m²/g and specific capacitance up to 250 F/g in comparison to other carbons.