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纳米材料的特殊结构决定了其具有大的比表面积、高的表面活性等特点,因而在力学、热学、光学、电磁学等方面都具有广泛的应用。以表面活性剂形成的胶束和乳液等为模板制备纳米材料是一种常见的方法,该方法可以大大降低溶剂的表面张力并改变体系的界面组成和结构,已经引起了研究者们的高度重视。有序介孔材料具有规则可调的纳米级孔道,可用作吸附剂、催化剂、催化剂载体或模板。以表面活性剂自组装形成的聚集体为模板合成有序介孔材料由于操作简单,且材料的孔道分布更为均一,因而成为了最常见的制备方法。但目前在纳米材料及介孔材料的制备中,普遍使用传统的单链表面活性剂作为模板剂,由于该种表面活性剂结构单一,因而以其为模板所生成的纳米材料及介孔材料暴露出形貌单一且结构不易调控等缺点。双子表面活性剂由于具有特殊的胶束自组装行为、高的表面活性及分子结构中疏水链段与联结基组成可调等特点,可实现纳米材料更加良好的分散及制备具有独特形貌的纳米材料和介孔材料。根据国内外研究进展,本文从双子表面活性剂在溶液中形成的各种有序聚集体——胶束(反胶束)、囊泡及液晶等角度出发,综述了以其为模板或者微反应器制备纳米材料的研究进展,同时对以双子表面活性剂为稳定剂辅助制备纳米材料的研究进展进行了阐述,并总结了双子表面活性剂辅助制备介孔材料过程中其结构参数变化对介孔材料形貌的影响,最后对双子表面活性剂辅助制备纳米材料及介孔材料的前景进行了展望。 相似文献
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Biomorphic mineralization: From biology to materials 总被引:4,自引:0,他引:4
Tong-Xiang Fan 《Progress in Materials Science》2009,54(5):542-659
Since material properties are structure-dependent, new and interesting properties are expected from unusual or complex structures. Biomorphic mineralization is a technique that produces materials with morphologies and structures resembling those of nature living things, through employing bio-structures as templates for mineralization. The products, biomorphic materials, combine natural geometry with synthetic material chemistry. Fundamental information along with recent advances in biomorphic mineralization and biomorphic materials are provided in this review through discussions on the following aspects: biomorphic materials produced through synthesis or assembly using a range of templates including biomolecules, microorganisms, plants and animals; processing methods and mechanisms of biomorphic mineralization; properties and emerging applications of biomorphic materials in multiple areas including electronics, magnetics, photonics, biotech, sensing, and filtration. The potential of various natural structures for biomimicking to produce advanced materials will be also discussed. We conclude by making a prospect on biomorphic mineralization and biomorphic material, which is the product of close conversations between human and nature and the product of close co-operation between scientists from diverse fields. 相似文献
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应用DNA模版自组装CdS纳米线 总被引:1,自引:0,他引:1
近年来,由于具有双螺旋补偿结构,DNA分子作为智能模版被广泛应用于设计棒状或管状类的纳米结构.本文报道了应用DNA双螺旋模版将CdS纳米粒子自组装为CdS纳米线.制备的CdS纳米线由几根纳米线紧密缠绕在一起,也呈螺旋形结构,该结构在无机材料中是很少见的.该结构形成的主要原因归功于CdS纳米粒子和DNA分子间的强烈静电互作用,由于含自由基的CdS纳米粒子带负电荷,而氨基的DNA核酸根带正电荷.研究结果表明应用DNA模版制备纳米线是一种简便、高效的技术和方法.同时,DNA模版法也为从底上制备纳米级的材料和物体提供了广阔的空间. 相似文献
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Nature provides lots of inspiration for material and structural design for various applications. Deriving design principles from the investigation of nature can provide a rich source of inspiration for the development of multifunctional materials. The bioinspired design templates mainly include mussels, nacre, and various plant species. As a sustainable and renewable feedstock, nanocellulose can be used to fabricate advanced materials with multifunctional properties through bioinspired designs. However, challenges and opportunities remain for realizing the full potential in the design of novel materials. This article reviewed recent development in the bioinspired nanocellulose based materials and their application. This article summarizes the functions (e.g., surface wetting) and applications (e.g., composite) of bioinspired nanocellulose-based materials. The bioinspired design templates are discussed along with strategies, advantages, and challenges to the development of synthetic mimics. Additionally, mechanisms and processes (e.g., chemical modification, self-assembly) leading to biomimetic design are discussed. Finally, future research directions and opportunities of bioinspired nanocellulose-based materials are highlighted. 相似文献
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以碳化后的梧桐木块作为碳模板,采用金属锆作为锆源,在KCl和KF的混合熔盐体系中制备了多孔ZrC/C复合陶瓷材料。研究了不同碳化温度对碳模板的显微形貌、显气孔率和体积密度的影响。并采用X射线光电子能谱(XPS)、傅里叶变换红外光谱(FTIR)、X射线衍射仪(XRD)和扫描电子显微镜(SEM)表征了梧桐木的碳化过程以及复合材料的物相组成和显微形貌。结果表明:梧桐木的碳化分为有机物的热分解和石墨化两个过程;碳化后的梧桐木保留了多孔的特征结构,随着碳化温度的升高,碳模板显气孔率变大,体积密度减小;反应时间的延长有利于增强ZrC层与碳模板基体表面的结合力;KF的加入量需要严格控制,过量的KF会破坏复合材料的结构。 相似文献
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Zhengjie Li Sida Wu Wei Lv Jiao‐Jing Shao Feiyu Kang Quan‐Hong Yang 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(20):2674-2688
Graphene and its derivatives are emerging as a class of novel but versatile templates for the controlled preparation and functionalization of materials. In this paper a conceptual review on graphene‐based templates is given, highlighting their versatile roles in materials preparation. Graphene is capable of acting as a low‐dimensional hard template, where its two‐dimensional morphology directs the formation of novel nanostructures. Graphene oxide and other functionalized graphenes are amphiphilic and may be seen as soft templates for formatting the growth or inducing the controlled assembly of nanostructures. In addition, nanospaces in restacked graphene can be used for confining the growth of sheet‐like nanostructures, and assemblies of interlinked graphenes can behave either as skeletons for the formation of composite materials or as sacrificial templates for novel materials with a controlled network structure. In summary, flexible graphene and its derivatives together with an increasing number of assembled structures show great potentials as templates for materials production. Many challenges remain, for example precise structural control of such novel templates and the removal of the non‐functional remaining templates. 相似文献
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Yuanqing Gu 《Materials Research Bulletin》2010,45(5):536-541
Inspired by the complicated structure of natural substances, we designed and fabricated nanotube/hollow sphere hybrid structured functional anatase titania material. Cellulosic substance (commercial filter paper) was chosen as nanotube template while silica and polystyrene colloidal microspheres with different diameters were employed as hollow sphere templates. The ultrathin nature of titania layer enabled faithful replication of the nanoscopic structural details of both the template substances. The microsphere and cellulose templates were removed by calcination for polystyrene microsphere template case, and further alkali treatment was carried out to dissolve away the silica component for silica microsphere template case. The obtained anatase titania nanotubes were decorated with nanoscale titania hollow spheres with wall thickness of about 7.5 nm. The resulted hybrid materials exhibited similar but superior photocatalytic efficiency compared with simple titania nanotube structured materials due to the higher surface area endowed by the complex highly porous structure. 相似文献
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Marcos Fernández-Leyes Valeria Verdinelli Natalia Hassan Juan M. Ruso Olga Pieroni Pablo C. Schulz Paula Messina 《Journal of Materials Science》2012,47(6):2837-2844
Since the trabecular bone exhibit sponge-like bicontinuity there is a growing interest in the synthesis of spongy-like sieves
for the construction of bio-active implantable materials. Here, we propose a one step sol–gel method for the synthesis of
bicontinuous pore silica materials using different bile salts aqueous mixtures as templates. The influences of the type and
amount of bile salt on the synthesis processes are investigated and correlated with the final material morphology. As a final
point, their structural properties are interrelated with their ability to induce a bone-like apatite layer in contact with
simulated body fluid (SBF). We have confirmed that under specific template conditions, the synthesized material has an open
bio-active macropore structure that is blanched in a 3D-disordered sponge-like network similar than those existed in trabecular
bone. 相似文献
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介孔材料SBA-15/环氧树脂复合材料的制备和固化动力学 总被引:1,自引:0,他引:1
通过溶胶-凝胶方法合成并接枝修饰介孔材料SBA-15,再通过热分析方法研究了介孔材料SBA-15和环氧树脂复合材料的固化动力学。主要对环氧树脂体系的固化过程和介孔材料(SBA-15)表面羟基和甲基对该固化过程的影响进行研究。结果表明,SBA-15对环氧树脂固化的催化作用主要表现在两个方面:一方面是表面羟基基团催化作用,另一方面是其空间限制的较微弱催化作用。从固化动力学角度来说,低分子量液体双酚A型环氧树脂(DGEBA)和二乙基甲苯二胺(DETDA 80)体系和SBA15-CH3的体系都能很好地符合Kamal自催化动力学模型,在加入SBA15-OH体系使固化初始阶段醚化反应强烈,不能符合Kamal模型。 相似文献
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Silica-precipitating peptides isolated from a combinatorial phage display peptide library 总被引:2,自引:0,他引:2
Many biological organisms contain specialized structures composed of inorganic materials. Cellular processes in vivo facilitate the organized assembly of mineral building blocks into complex structures. The structural hierarchy and complexity across a range of length scales are providing new ideas and concepts for materials chemistry. Proteins that direct biomineralization can be used to control the production of nanostructured materials and facilitate the fabrication of new structures. Here, we demonstrate that some of the silica-binding peptides isolated from a combinatorial phage peptide display library can be used in precipitating silica from a solution of silicic acid. The results described in this report demonstrate that peptides displayed by phages act as templates in inorganic material synthesis and provide a means of understanding how some of the biological systems may be carrying out materials chemistry in vivo. 相似文献