Chemical Society reviews · 2026
Surface-initiated living crystallization-driven self-assembly: from precision nanofabrication to functional interfaces.
СтатьяОбзорНазвание и аннотация: Перевод в очереди
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Tao Jiawei, Lu Yao, Gao Chenchen, Wang Peiwen, Ji Zhenyan, Lv Sen, Cai Xiaomin, Zhang Jingwen, Qiu Huibin
Аннотация
The precise fabrication of nanostructured materials on surfaces is paramount for advancing next-generation technologies in catalysis, electronics, biomedicine, etc. Recently, surface-initiated living crystallization-driven self-assembly (SIL-CDSA) has enabled unprecedented control over the architecture, orientation, and functionality of solid-state nanostructures on desired substrates. This review outlines key principles of SIL-CDSA, including seed immobilization, confined epitaxial growth and micellar brush formation, together with practical methods for dimension control and spatial ordering. Intrinsic core/corona chemistry and the incorporation of exogenous species allowing targeted functionalization are also discussed, covering catalytic, electronic and bioactive features. Case studies are introduced to demonstrate SIL-CDSA as a versatile platform for hierarchically ordered nanostructures, delivering exceptional control over size, periodicity, and composition. By directly translating precision self-assembly to surfaces, SIL-CDSA opens powerful routes to multifunctional, high-performance materials for catalysis, energy systems, sensing, and device fabrication, positioning it as a transformative tool for advanced nanomanufacturing.