材料科学
锰
污染物
制作
多孔性
纳米线
纳米技术
自组装
化学工程
复合材料
冶金
有机化学
医学
化学
替代医学
病理
工程类
作者
Ran Wang,Jingling Lu,Zeyi Cheng,Tao Yu,S. Chen,Wenxuan Xu,Shaopeng Rong
标识
DOI:10.1002/adfm.202505911
摘要
Abstract The development of 3D macroscopic architectures assembled from inorganic nanoparticles with tailored porous frameworks has garnered substantial attention across academic and industrial domains. These hierarchical structures combine the advantageous features of nanoscale building blocks with macroscopic functionality, offering enhanced surface accessibility and interconnected pathways while preventing nanoparticle reaggregation. This study presents an innovative cross‐linker‐free assembly strategy that enables the rational organization of 1D nanowires into 3D macroscopic architectures, effectively preserving the intrinsic structural advantages of both nanoscale and macroscale components. This methodology employs metal‐cation‐mediated assembly of hydroxylated α‐MnO 2 nanowires, where controlled introduction of cations disrupts electrostatic repulsion between nanowires while facilitating interwire connections through cation‐hydroxyl coordination. The strong coordination interaction between metal cations and surface hydroxyl groups on α‐MnO 2 nanowires drives the formation of 3D interconnected network architecture, resulting in stable hydrogel formation. Subsequent freeze‐drying of these hydrogels yields aerogel materials demonstrating exceptional adsorption capacities for common indoor air pollutants, achieving 34.1 mg g −1 for ammonia and 21.5 mg g −1 for formaldehyde. This cation‐coordination‐driven assembly approach not only establishes a generalizable framework for designing functional macroscopic assemblies from nanowire building blocks but also expands the potential application landscape for such hierarchical architectures, particularly in environmental remediation technologies.
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