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通过交联聚二茂铁基硅烷网络的热解制备纳米结构、磁可调陶瓷,以及通过在硅片内微成型形成宏观形状物体和微米级图案。

Genesis of nanostructured, magnetically tunable ceramics from the pyrolysis of cross-linked polyferrocenylsilane networks and formation of shaped macroscopic objects and micron scale patterns by micromolding inside silicon wafers.

作者信息

Ginzburg Madlen, MacLachlan Mark J, Yang San Ming, Coombs Neil, Coyle Thomas W, Raju Nandyala P, Greedan John E, Herber Rolfe H, Ozin Geoffrey A, Manners Ian

机构信息

Polymer and Materials Chemistry Research Group, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.

出版信息

J Am Chem Soc. 2002 Mar 20;124(11):2625-39. doi: 10.1021/ja0107273.

Abstract

The ability to form molded or patterned metal-containing ceramics with tunable properties is desirable for many applications. In this paper we describe the evolution of a ceramic from a metal-containing polymer in which the variation of pyrolysis conditions facilitates control of ceramic structure and composition, influencing magnetic and mechanical properties. We have found that pyrolysis under nitrogen of a well-characterized cross-linked polyferrocenylsilane network derived from the ring-opening polymerization (ROP) of a spirocyclic [1]ferrocenophane precursor gives shaped macroscopic magnetic ceramics consisting of alpha-Fe nanoparticles embedded in a SiC/C/Si(3)N(4) matrix in greater than 90% yield up to 1000 degrees C. Variation of the pyrolysis temperature and time permitted control over the nucleation and growth of alpha-Fe particles, which ranged in size from around 15 to 700 A, and the crystallization of the surrounding matrix. The ceramics contained smaller alpha-Fe particles when prepared at temperatures lower than 900 degrees C and displayed superparamagnetic behavior, whereas the materials prepared at 1000 degrees C contained larger alpha-Fe particles and were ferromagnetic. This flexibility may be useful for particular materials applications. In addition, the composition of the ceramic was altered by changing the pyrolysis atmosphere to argon, which yielded ceramics that contain Fe(3)Si(5). The ceramics have been characterized by a combination of physical techniques, including powder X-ray diffraction, TEM, reflectance UV-vis/near-IR spectroscopy, elemental analysis, XPS, SQUID magnetometry, Mössbauer spectroscopy, nanoindentation, and SEM. Micromolding of the spirocyclic [1]ferrocenophane precursor within soft lithographically patterned channels housed inside silicon wafers followed by thermal ROP and pyrolysis enabled the formation of predetermined micron scale designs of the magnetic ceramic.

摘要

对于许多应用而言,能够形成具有可调性能的模制或图案化含金属陶瓷是很有必要的。在本文中,我们描述了一种由含金属聚合物衍生而来的陶瓷的演变过程,其中热解条件的变化有助于控制陶瓷的结构和组成,进而影响其磁性和机械性能。我们发现,由螺环[1]二茂铁环戊烷前体通过开环聚合(ROP)得到的具有良好表征的交联聚二茂铁基硅烷网络在氮气气氛下热解,可得到形状规整的宏观磁性陶瓷,其由嵌入SiC/C/Si₃N₄基体中的α-Fe纳米颗粒组成,在高达1000℃的温度下产率大于90%。热解温度和时间的变化使得能够控制α-Fe颗粒的成核和生长,这些颗粒的尺寸范围约为15至700 Å,同时也能控制周围基体的结晶。当在低于900℃的温度下制备时,陶瓷中含有较小的α-Fe颗粒并表现出超顺磁性行为,而在1000℃制备的材料则含有较大的α-Fe颗粒且具有铁磁性。这种灵活性对于特定的材料应用可能是有用的。此外,通过将热解气氛改为氩气,可以改变陶瓷的组成,从而得到含有Fe₃Si₅的陶瓷。这些陶瓷通过多种物理技术进行了表征,包括粉末X射线衍射、透射电子显微镜、反射紫外-可见/近红外光谱、元素分析、X射线光电子能谱、超导量子干涉仪磁力测量、穆斯堡尔光谱、纳米压痕和扫描电子显微镜。在硅片内部软光刻图案化通道内对螺环[1]二茂铁环戊烷前体进行微成型,然后进行热ROP和热解,能够形成磁性陶瓷的预定微米级设计。

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