Institute for Advanced Materials, School of Materials Science and Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
School of Materials Science and Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013 China.
Acc Chem Res. 2023 Apr 4;56(7):740-751. doi: 10.1021/acs.accounts.2c00705. Epub 2023 Mar 15.
ConspectusSelf-assembly bridges nanoscale and microscale colloidal particles into macroscale functional materials. In particular, self-assembly processes occurring at the liquid/liquid or solid/liquid/air interfaces hold great promise in constructing large-scale two- or three-dimensional (2D or 3D) architectures. Interaction of colloidal particles in the assemblies leads to emergent collective properties not found in individual building blocks, offering a much larger parameter space to tune the material properties. Interfacial self-assembly methods are rapid, cost-effective, scalable, and compatible with existing fabrication technologies, thus promoting widespread interest in a broad range of research fields.Surface chemistry of nanoparticles plays a predominant role in driving the self-assembly of nanoparticles at water/oil interfaces. Amphiphilic nanoparticles coated with mixed polymer brushes or mussel-inspired polydopamine were demonstrated to self-assemble into closely packed thin films, enabling diverse applications from electrochemical sensors and catalysis to surface-enhanced optical properties. Interfacial assemblies of amphiphilic gold nanoparticles were integrated with graphene paper to obtain flexible electrodes in a modular approach. The robust, biocompatible electrodes with exceptional electrocatalytic activities showed excellent sensitivity and reproducibility in biosensing. Recyclable catalysts were prepared by transferring monolayer assemblies of polydopamine-coated nanocatalysts to both hydrophilic and hydrophobic substrates. The immobilized catalysts were easily recovered and recycled without loss of catalytic activity. Plasmonic nanoparticles were self-assembled into a plasmonic substrate for surface-enhanced Raman scattering, metal-enhanced fluorescence, and modulated fluorescence resonance energy transfer (FRET). Strong Raman enhancement was accomplished by rationally directing the Raman probes to the electromagnetic hotspots. Optimal enhancement of fluorescence and FRET was realized by precisely controlling the spacing between the metal surface and the fluorophores and tuning the surface plasmon resonance wavelength of the self-assembled substrate to match the optical properties of the fluorescent dye.At liquid/solid interfaces, infiltration-assisted (IFAST) colloidal self-assembly introduces liquid infiltration in the substrate as a new factor to control the degree of order of the colloidal assemblies. The strong infiltration flow leads to the formation of amorphous colloidal arrays that display noniridescent structural colors. This method is compatible with a broad range of colloidal particle inks, and any solid substrate that is permeable to dispersing liquids but particle-excluding is suitable for IFAST colloidal assembly. Therefore, the IFAST technology offers rapid, scalable fabrication of structural color patterns of diverse colloidal particles with full-spectrum coverage and unprecedented flexibility. Metal-organic framework particles with either spherical or polyhedral morphology were used as ink particles in the Mayer rod coating on wettability patterned photopapers, leading to amorphous photonic structures with vapor-responsive colors. Anticounterfeiting labels have also been developed based on the complex optical features encoded in the photonic structures.Interfacial colloidal self-assembly at the water/oil interface and IFAST assembly at the solid/liquid/air interface have proven to be versatile fabrication platforms to produce functional materials with well-defined properties for diverse applications. These platform technologies are promising in the manufacturing of value-added functional materials.
自组装将纳米级和微级胶体颗粒桥接成宏观功能材料。特别是,发生在液/液或固/液/气界面处的自组装过程在构建大规模二维或三维 (2D 或 3D) 结构方面具有很大的潜力。组装体中胶体颗粒的相互作用导致出现单个构建块中不存在的集体性质,从而提供了更大的参数空间来调整材料性能。界面自组装方法快速、经济高效、具有可扩展性并且与现有制造技术兼容,因此在广泛的研究领域中引起了广泛的关注。
纳米颗粒的表面化学在驱动纳米颗粒在水/油界面处的自组装方面起着主要作用。具有混合聚合物刷或贻贝启发的聚多巴胺涂层的两亲性纳米颗粒已被证明可以自组装成紧密堆积的薄膜,从而在电化学传感器和催化到表面增强光学性能等各种应用中发挥作用。两亲性金纳米颗粒的界面组装与石墨烯纸集成在一起,以模块化方式获得了柔性电极。坚固、生物相容的电极具有出色的电催化活性,在生物传感中表现出出色的灵敏度和重现性。通过将单层聚多巴胺涂层纳米催化剂转移到亲水和疏水基底上,制备了可回收的催化剂。固定化催化剂可以很容易地回收和再利用,而不会损失催化活性。通过合理地将拉曼探针引导到电磁热点,将等离子体纳米颗粒自组装成等离子体基底,用于表面增强拉曼散射、金属增强荧光和调制荧光共振能量转移 (FRET)。通过精确控制金属表面和荧光团之间的间距并调整自组装基底的表面等离子体共振波长以匹配荧光染料的光学特性,实现了强拉曼增强。通过精确控制金属表面和荧光团之间的间距并调整自组装基底的表面等离子体共振波长以匹配荧光染料的光学特性,实现了强拉曼增强。通过精确控制金属表面和荧光团之间的间距并调整自组装基底的表面等离子体共振波长以匹配荧光染料的光学特性,实现了强拉曼增强。
在液体/固体界面上,浸润辅助(IFAST)胶体自组装将液体浸润引入到基底中作为控制胶体组装有序度的新因素。强烈的渗透流导致形成无定形胶体阵列,显示出非虹彩结构色。该方法与广泛的胶体粒子油墨兼容,任何可渗透分散液体但排斥粒子的固体基底都适用于 IFAST 胶体组装。因此,IFAST 技术提供了快速、可扩展的制造具有全光谱覆盖和前所未有的灵活性的各种胶体粒子结构颜色图案的方法。具有球形或多面体形貌的金属有机骨架颗粒被用作 Mayer 棒涂覆在润湿性图案化光纸上的油墨颗粒,导致具有蒸汽响应颜色的无定形光子结构。还基于光子结构中编码的复杂光学特征开发了防伪标签。
水/油界面处的界面胶体自组装和固/液/气界面处的 IFAST 组装已被证明是生产具有明确定义性能的功能性材料的多功能制造平台,适用于各种应用。这些平台技术在增值功能性材料的制造中具有广阔的应用前景。