Sustainable electromagnetic shielding graphene/nanocellulose thin films with excellent joule heating and mechanical properties via in-situ mechanical exfoliation and crosslinking with cations

被引:72
作者
Yang, Yi [1 ]
Luo, Cheng-Long [1 ]
Chen, Xu-Dong [2 ]
Wang, Ming [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Chongqing Key Lab Soft Matter Mat Chem & Funct Mfg, Chongqing 400715, Peoples R China
[2] Rongjiang Lab, Chem & Chem Engn Guangdong Lab, Jieyang Branch, Jieyang 515200, Peoples R China
基金
中国国家自然科学基金;
关键词
Electromagnetic shielding; Graphene; Nanocellulose; Cation-? interaction; Joule heating performance; HIGH ELECTRICAL-CONDUCTIVITY; FEW-LAYERED GRAPHENE; MICROWAVE-ABSORPTION; SCALABLE PRODUCTION; NANOCOMPOSITES; COMPOSITES; PERSPECTIVES; FABRICATION; GRAPHITE; SHEETS;
D O I
10.1016/j.compscitech.2023.109913
中图分类号
TB33 [复合材料];
学科分类号
摘要
Herein, a sustainable graphene/nanocellulose electromagnetic shielding composite film was fabricated via nanocellulose inducing graphite in-situ mechanical exfoliation. Cations were added to enhance properties of the films via cation crosslinking. The few-layer graphene produced by this strategy was -3.4 nm in average thickness and good dispersion in the films. The electrical conductivity, electromagnetic shielding effectiveness and mechanical property of the film were enhanced by cation crosslinking, while cation-pi interactions between metal and graphene-enhanced the electrical conductivity and electromagnetic shielding effectiveness. For example, the films cross-linked Cu2+ cations exhibit a tensile strength of 64.3 MPa, elongation at broken of 17.1%, and electromagnetic shielding effectiveness of 30.7 dB and a conductivity of 3172 S/m at a thickness of 40 mu m. In addition, the different Joule heating performance and electromagnetic shielding effectiveness were found in the films by cross-linking with different cations. We provide a new route to prepare low-cost, sustainable, and tunable electromagnetic shielding films with good Joule heating and mechanical property.
引用
收藏
页数:11
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