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DMREF: Collaborative Research: Strain Adaptive Materials

DMREF: Collaborative Research: Strain Adaptive Materials
DMREF:合作研究:应变自适应材料
批准号:
1921858
负责人:
Krzysztof Matyjaszewski
金额:
$57.71万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-10-01 至 2023-09-30

项目摘要

项目成果

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中文摘要
翻译
非技术描述:软机器人、可穿戴电子产品和个性化医疗的出现引发了对模拟活组织机械反应的合成材料的需求。活组织是独特的,因为它们在触摸时是柔软的,但抵抗变形。这种应变适应性硬化代表了大自然的防御机制之一,防止意外的组织破裂,并注入了一个坚定的特点感觉。已经探索了各种分子和宏观构建体来再现组织力学;然而,它们未能在分子尺度上整合柔软性和坚固性。该项目旨在开发一个材料设计平台,利用建筑代码对从超软脑组织到超硬皮肤的机械响应的巨大变化进行编程。通过软物质理论家,合成化学家和实验物理学家的闭环合作,这种架构设计方法将激发合成化学和软物质物理学的新方向,以创建具有编码结构-性质相关性的新型分子架构。根据材料基因组计划的使命,这种方法将构成材料设计搜索引擎的基础,该搜索引擎将指导和加速具有目标机械性能的组织复制品的合成。这些新型材料将催化许多技术的根本性转变,包括但不限于软机器人、主动伪装系统和生物医学设备。技术描述:传统凝胶和弹性体无法复制组织的应变适应性硬化。变形时从超软到超硬的机械响应的转变需要不同结构图案的分级组织,其在不同应力水平下触发变形机制的级联。因此,该项目将解决三个基本和日益复杂的挑战。首先,理论建模将建立网络结构和机械性能(如刚度和硬度)之间的普遍相关性,并将形成用于在设计的聚合物系统中编码精确机械“表型”的定量指导方针。其次,将自组装部分引入网络结构代码将使聚合物组件具有应变自适应硬化。第三,动态交联的结合将赋予可编程的粘弹性响应,并将平台扩展到应变率响应的机械表型。该项目目标的实现将产生一个分子代码-共同实现可编程和有效开发下一代组织样合成材料,同时具有应变和应变率适应性机械性能。该奖项反映了NSF的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
Non-technical Description: The advent of soft robotics, wearable electronics, and personalized medicine has sparked a demand for synthetic materials that mimic the mechanical responses of living tissues. Living tissues are unique as they are soft at touch, yet resistant to deformation. This strain-adaptive stiffening represents one of Nature's defense mechanisms that prevents accidental tissue rupture and imbues a characteristic feeling of firmness. Various molecular and macroscopic constructs have been explored to reproduce the tissue mechanics; however, they fail to integrate softness and firmness on a molecular scale. This project aims at the development of a materials design platform that harnesses architectural codes for programming the grand variation of mechanical responses, ranging from that of ultra-soft brain tissue to super-firm skin. Through closed-loop collaboration of soft matter theoreticians, synthetic chemists, and experimental physicists, this design-by-architecture approach will inspire new directions in synthetic chemistry and soft-matter physics towards creation of novel molecular architectures with encoded structure-property correlations. In line with the mission of the Materials Genome Initiative, this approach will constitute the foundation for a materials design search engine that will guide and accelerate the synthesis of tissue replicas with targeted mechanical properties. The novel classes of materials will catalyze fundamental shifts in many technologies, including - but not limited to - soft robotics, active camouflage systems, and biomedical devices. Technical Description: Conventional gels and elastomers cannot replicate tissue's strain-adaptive stiffening. Transition from the super-soft to super-firm mechanical response upon deformation requires a hierarchical organization of different structural motifs that trigger a cascade of deformation mechanisms at different stress levels. As such, the project will address three fundamental and increasingly complex challenges. First, theoretical modeling will establish universal correlations between network architecture and mechanical properties such as stiffness and firmness, and will form quantitative guidelines for encoding precise mechanical "phenotypes" in designed polymeric systems. Second, introduction of self-assembling moieties into network architectural code will empower polymer assemblies with strain-adaptive stiffening. Third, incorporation of dynamic crosslinks will impart programmable viscoelastic response and extend the platform to strain-rate responsive mechanical phenotypes. Fulfillment of the project goals will yield a molecular code - collectively enabling the programmable and efficient development of next-generation of tissue-like synthetic materials with both strain- and strain rate-adaptive mechanical properties.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
期刊论文(12)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1021/acs.macromol.2c01712
发表时间: 2022-11-28
期刊: MACROMOLECULES
影响因子: 5.5
作者: [Martinez, Michael R., Schild, Dirk, Matyjaszewski, Krzysztof]
通讯作者: Matyjaszewski, Krzysztof
DOI: 10.1021/acs.macromol.2c00006
发表时间: 2022-04-12
期刊: MACROMOLECULES
影响因子: 5.5
作者: [Maw, Mitchell, Morgan, Benjamin J., Sheiko, Sergei S.]
通讯作者: Sheiko, Sergei S.
DOI: 10.1002/pola.29481
发表时间: 2019-12
期刊: Journal of Polymer Science Part A: Polymer Chemistry
影响因子: --
作者: [Mateusz Olszewski;Lingchun Li;Guojun Xie;A. Keith;S. Sheiko;K. Matyjaszewski]
通讯作者: Mateusz Olszewski;Lingchun Li;Guojun Xie;A. Keith;S. Sheiko;K. Matyjaszewski
Poor Solvents Improve Yield of Grafting-Through Radical Polymerization of OEO 19 MA
不良溶剂提高了 OEO 19 MA 自由基聚合接枝的产率
DOI: 10.1021/acsmacrolett.0c00245
发表时间: 2020
期刊: ACS Macro Letters
影响因子: 7.015
作者: [Martinez, Michael R., Krys, Pawel, Sheiko, Sergei S., Matyjaszewski, Krzysztof]
通讯作者: Matyjaszewski, Krzysztof
共 6 条
    Collaborative Research: DMREF:Programmable Design, Synthesis, and Forensics of Soft Materials
    • 批准号:
      2324168
    • 项目类别:
      Standard Grant
    • 资助金额:
      $47.5万
    • 财政年份:
      2023
    • 负责人:
      Krzysztof Matyjaszewski
    • 依托单位:
    Controlled Interphases by ATRP: Polymeric Brushes and Functional Networks
    • 批准号:
      2202747
    • 项目类别:
      Continuing Grant
    • 资助金额:
      $100.0万
    • 财政年份:
      2022
    • 负责人:
      Krzysztof Matyjaszewski
    • 依托单位:
    Collaborative Research: Polar-Polyolefin Block Copolymers via MILRad Functionalization: A Platform for Amphiphilic Nanostructured Material Synthesis
    • 批准号:
      2108901
    • 项目类别:
      Standard Grant
    • 资助金额:
      $22.5万
    • 财政年份:
      2021
    • 负责人:
      Krzysztof Matyjaszewski
    • 依托单位:
    Development of More Active and More Selective Catalysts for ATRP
    • 批准号:
      2000391
    • 项目类别:
      Standard Grant
    • 资助金额:
      $60.0万
    • 财政年份:
      2020
    • 负责人:
      Krzysztof Matyjaszewski
    • 依托单位:
    海外基金