Jiang Yuewei, Shen Ziyi, Liu Ziyi, Gong Hui, Chen Bo, Su Yingying, Zhou Jinghui, Fei Xu, Li Yao
Liaoning Province Key Laboratory of Pulp and Papermaking Engineering, Liaoning Key Lab of Lignocellulose Chemistry and BioMaterials, Liaoning Collaborative Innovation Center for Lignocellulosic Biorefinery, Dalian Polytechnic University, Dalian, Liaoning Province, 116034, China.
Shandong Tonye Photoresist Material Technology CO., LTD, Weifang, 261206, China; Instrumental Analysis Center, Dalian Polytechnic University, Dalian 116034, China.
J Colloid Interface Sci. 2025 Apr;683(Pt 1):786-798. doi: 10.1016/j.jcis.2024.12.051. Epub 2024 Dec 15.
The poor mechanical properties of biomass-based carbon aerogels after carbonization severely limit their application in pressure sensing and energy storage for wearable devices and electronic skin. In this work, a supramolecular assembly structure was designed inspired by the unique microstructure of natural wood for the preparation of biomass-based carbon aerogels with supercompressibility, elasticity, stable strain electrical signal response, and wide sensitive detection. Bacterial cellulose and lignin were selected as the main components of the biomass-based composite aerogel 'cell wall'. The graphene oxide with an aromatic structure was introduced to induce the assembly of firmly attached lignin and bacterial cellulose. The prepared biomass-based carbon aerogels exhibit supercompressibility (at least 100 cycles at 90 % strain), high elasticity (88.88 % height retention after 1000 cycles at a strain of 50 %), surprising temperature-constant superelasticity and fatigue resistance (shape retention rate greater than 85 %) at -196 ℃. In particular, it exhibits temperature-invariant high linear sensitivity over an extremely wide operating pressure range (0-43 kPa), allowing accurate detection of human signals. In addition, the prepared carbon aerogels exhibit excellent performance in supercapacitors. It has a specific capacitance of 158F/g at a current density of 1 A/g and an energy density of 18.75 Wh/kg at a high power density of 2500 W/g. This strategy also demonstrates its promise as a wearable device in hostile environments.
生物质基碳气凝胶碳化后的力学性能较差,严重限制了它们在可穿戴设备和电子皮肤的压力传感与能量存储中的应用。在这项工作中,受天然木材独特微观结构的启发,设计了一种超分子组装结构,用于制备具有超压缩性、弹性、稳定应变电信号响应和宽敏感检测范围的生物质基碳气凝胶。选择细菌纤维素和木质素作为生物质基复合气凝胶“细胞壁”的主要成分。引入具有芳香结构的氧化石墨烯以诱导紧密附着的木质素和细菌纤维素的组装。所制备的生物质基碳气凝胶表现出超压缩性(在90%应变下至少100次循环)、高弹性(在50%应变下1000次循环后高度保留率为88.88%)、在-196℃时具有惊人的温度恒定超弹性和抗疲劳性(形状保留率大于85%)。特别地,它在极宽的工作压力范围(0-43 kPa)内表现出温度不变的高线性灵敏度,能够准确检测人体信号。此外,所制备的碳气凝胶在超级电容器中表现出优异的性能。在1 A/g的电流密度下比电容为158F/g,在2500 W/g的高功率密度下能量密度为18.75 Wh/kg。该策略还证明了其作为恶劣环境中可穿戴设备的潜力。