CAREER: Colloids with programmable surfaces: A polymer approach to self-assembly
CAREER: Colloids with programmable surfaces: A polymer approach to self-assembly
批准号:
1653465
负责人:
Stefano Sacanna
金额:
$76.5万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-06-01 至 2024-05-31
中文摘要
非技术描述有一种令人着迷的方法,可以赋予一种材料新的性质,而不需要改变其化学成分,而是改变材料本身内部物质的结构安排。创造一种潜在的微观结构可以使块状材料以独特和非传统的方式与能量相互作用。其结果是涌现出自然界中通常不存在的新特性。然而,这种材料的实际实现并不简单,因为它需要创造在三维物体上规则间隔的微观特征。虽然这不能通过经典的自上而下的方法来实现,但胶体自组装提供了一种概念上的简单途径,以自下而上的方式赋予这种微观秩序。主要研究人员试图发现新的方法来操纵和合理地将微观构建块组装成复杂的微结构,并最终组装成功能新材料。廉价的聚合物和简单的静电电荷被用来调节构建块之间的结合作用,从而有效地传递组装信息。结果是胶体积木的复杂“汤”,新材料有望从这些“汤”中自我组装和出现。该项目固有的跨学科特性,天然地架起了化学、物理和材料科学之间的桥梁,提供了从高中到研究生的广泛教学机会。教育和更广泛的推广目标包括开发一个公开可用的“胶体图书馆”--一个网络门户,将学生与来自科学和工业各个领域的研究专家联系起来。技术说明尽管整个胶体自组装领域正在迅速汇聚到使用DNA来调节粒子相互作用和传递精确组装指令的方向,但这项研究提出了一种新的、有趣的无DNA编程自组装方法。该研究小组研究聚合物介导的胶体相互作用,并提出将其作为操纵和组装胶体物质的新的通用工具。基于首席研究员在合成胶体化学和软物质物理方面的专业知识,该项目的目标是:(I)开发一个用于聚合物涂层胶体快速原型的模块化合成平台,(Ii)使用所得到的胶体模型系统来研究广泛的聚合物介导的胶体相互作用(包括焓和熵驱动),以及(Iii)利用这些知识来开发廉价且可扩展的方法来编程复杂胶体流体的自组装行为。该项目为下一代可编程自组装胶体材料奠定基础。
英文摘要
Non-Technical DescriptionThere is a fascinating way of imparting new properties to a material that does not require altering its chemical composition, but rather changing the structural arrangement of matter within the material itself. Creating an underlying microstructure can enable bulk materials to interact with energy in unique and unconventional ways. The result are emerging new properties that do not normally exist in nature. The practical realization of such materials, however, is not straightforward, as it requires creating microscopic features that are regularly spaced throughout a three-dimensional object. While this is not achievable via a classic top-down approach, colloidal self-assembly offers a conceptually simple route to impart such microscopic order in a bottom-up fashion.The principal investigator seeks to discover novel methodologies to manipulate and rationally assemble microscopic building blocks into complex micro-architectures and ultimately into functional new materials. Inexpensive polymers and simple electrostatic charges are used to mediate the binding interactions between the building blocks, thus effectively imparting assembly information. The results are complex "soups" of colloidal building blocks from which new materials are expected to self-assemble and emerge.The inherent interdisciplinary character of the project, which naturally bridges between chemistry, physics, and material science, offers a broad range of teaching opportunities from high school to graduate students. Educational and broader outreach goals include the development of a publicly available "colloidal library" - a Web Portal that connects students with research experts from various fields of science and industry.Technical DescriptionWhile the whole field of colloidal self-assembly is rapidly converging towards the use of DNA to mediate particle interactions and impart precise assembly instructions, this research addresses a new and intriguing DNA-free approach to programmable self-assembly. The research team investigates polymer-mediated colloidal interactions and proposes them as new general tools for manipulating and assembling colloidal matter. Building on the principal investigator's expertise in synthetic colloidal chemistry and soft-matter physics, the project aims to: (i) develop a modular synthetic platform for the rapid prototyping of polymer-coated colloids, (ii) use the resulting colloidal model systems to study a broad range of polymer-mediated colloidal interactions (both enthalpy and entropy driven), and (iii) use this knowledge to develop inexpensive and scalable methodologies to program the self-assembly behavior of complex colloidal fluids.This project lays the foundation for the next generation of programmable self-assembling colloidal materials.
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DOI:
10.1038/nature23901
发表时间:
2017-10-12
期刊:
NATURE
影响因子:
64.8
作者:
[Gong, Zhe, Hueckel, Theodore, Sacanna, Stefano]
通讯作者:
Sacanna, Stefano
DOI:
10.1038/s41567-018-0227-4
发表时间:
2018-11-01
期刊:
NATURE PHYSICS
影响因子:
19.6
作者:
[Aubret, Antoine, Youssef, Mena, Palacci, Jeremie]
通讯作者:
Palacci, Jeremie
DOI:
10.1038/s41567-019-0603-8
发表时间:
2019-11-01
期刊:
NATURE PHYSICS
影响因子:
19.6
作者:
[Soni, Vishal, Bililign, Ephraim S., Irvine, William T. M.]
通讯作者:
Irvine, William T. M.
Self-organization in dipolar cube fluids constrained by competing anisotropies
受竞争各向异性约束的偶极立方流体中的自组织
DOI:
10.1039/c7sm02174g
发表时间:
2018
期刊:
Soft Matter
影响因子:
3.4
作者:
[Rossi, Laura, Donaldson, Joe G., Meijer, Janne-Mieke, Petukhov, Andrei V., Kleckner, Dustin, Kantorovich, Sofia S., Irvine, William T., Philipse, Albert P., Sacanna, Stefano]
通讯作者:
Sacanna, Stefano
DOI:
10.1021/acsnano.8b00521
发表时间:
2018-04-01
期刊:
ACS NANO
影响因子:
17.1
作者:
[Hueckel, Theodore, Sacanna, Stefano]
通讯作者:
Sacanna, Stefano
共 8 条
海外基金