材料科学
纳米压痕
复合材料
倍半硅氧烷
光致发光
极限抗拉强度
透射率
复合数
耐久性
纳米尺度
网络结构
弹性模量
压痕硬度
堆积
纳米结构
模数
可见光谱
耐化学性
作者
Lili Zhao,Dan Xing,Jingfa Zhang,Yubo Tao,Haigang Wang,Fangong Kong,Peng Li,Fanpu Meng,Ahmed Koubaa
标识
DOI:10.1007/s42114-026-01680-3
摘要
Transparent wood has emerged as a sustainable alternative to glass, yet its limited surface hardness and wear resistance have hindered broader adoption. Here we report a wood-based composite (WG) with glass-like durability and plastic-like flexibility, achieved through an organic–inorganic dual-crosslinked network. Delignified poplar wood is infiltrated with cycloaliphatic epoxy-functionalized oligosiloxane, a cage-type polyhedral oligomeric silsesquioxane precursor, followed by UV-induced cationic polymerization. This forms covalent interfacial bonds and a nanoscale interpenetrating siloxane–cellulose network. The resulting WG exhibits high optical transmittance (~ 92%), tunable haze (~ 40% for privacy), intrinsic blue photoluminescence enabling full UVB shielding, and superior thermal stability. Mechanically, it achieves pencil hardness of 9 H, matching chemically strengthened glass, nanoindentation hardness of 1.7 GPa (sixfold higher than prior transparent woods), ductile impact resistance without shattering, and robust flexibility. The composites demonstrate a tensile strength of 51.2 MPa. These synergistic properties position WG as a multifunctional material for energy-efficient architecture, flexible optoelectronics, and anti-glare building facades, advancing sustainable transparent composites beyond conventional glass and plastics.
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