木质素
材料科学
发色团
光催化
极限抗拉强度
光子学
光降解
化学工程
复合材料
纳米技术
有机化学
催化作用
光电子学
化学
工程类
作者
Qinqin Xia,Chaoji Chen,Yonggang Yao,Shuaiming He,Xizheng Wang,Jianguo Li,Jinlong Gao,Wentao Gan,Bo Jiang,Mingjin Cui,Liangbing Hu
标识
DOI:10.1002/adma.202001588
摘要
Abstract Lignin serves as a binder that forms strong matrices of the cell walls of wood. However, it has many photolabile chromophore groups that create a monotonic brownish color and make wood susceptible to photodegradation. Herein, a new strategy is reported for modifying lignin using an in situ, rapid, and scalable process that involves the photocatalytic oxidation of native lignin in wood by H 2 O 2 and UV light. The reaction selectively eliminates lignin's chromophores while leaving the aromatic skeleton intact, thus modulating the optical properties of wood. The resulting “photonic wood” retains ≈80% of its original lignin content, which continues to serve as a strong binder and water‐proofing agent. As a result, photonic wood features a much higher mechanical strength in a wet environment (20‐times higher tensile strength and 12‐times greater compression resistance), significant scalability (≈2 m long sample), and largely reduced processing times (1–6.5 h vs 4–14 h) compared with delignification methods. Additionally, this in situ lignin‐modified wood structure is easily patterned through a photocatalytic oxidation process. This photocatalytic production of photonic wood paves the way for the large‐scale manufacturing of sustainable biosourced functional materials for a range of applications, including energy‐efficient buildings, optical management, and fluidic, ionic, electronic, and optical devices.
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