Tran Van Chinh, Mastantuoni Gabriella, Garemark Jonas, Dreimol Christopher H, Wang Xin, Berggren Magnus, Zhou Qi, Kroon Renee, Engquist Isak
Laboratory of Organic Electronics, Department of Science and Technology, Linköping University, SE-601 74, Norrköping, Sweden.
Wallenberg Wood Science Center, Department of Science and Technology, Linköping University, SE-601 74 Norrköping, Sweden.
ACS Appl Mater Interfaces. 2024 Dec 11;16(49):68416-68425. doi: 10.1021/acsami.4c16298. Epub 2024 Dec 3.
The 3D micro- and nanostructure of wood has extensively been employed as a template for cost-effective and renewable electronic technologies. However, other electroactive components, in particular native lignin, have been overlooked due to the absence of an approach that allows access of the lignin through the cell wall. In this study, we introduce an approach that focuses on establishing conjugated-polymer-based electrical connections at various length scales within the wood structure, aiming to leverage the charge storage capacity of native lignin in wood-based energy storage electrodes. We demonstrate that poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) PEDOT/PSS, integrated within the cell wall lumen, can be interfaced with native lignin through the wood cell wall through in situ polymerization of a water-soluble S-EDOT monomer. This approach increases the capacitance of the conductive wood to 315 mF cm at a scan rate of 5 mV s, which is seven and, respectively, two times higher compared to the capacitance of conductive wood made with the single components PEDOT/PSS or S-PEDOT. Moreover, we show that the capacitance is contributed by both the electroactive polymers and native lignin, with native lignin accounting for over 70% of the total charge storage capacity. We show that accessing native lignin through in situ creation of electrical interconnections within the wood structure offers a pathway toward sustainable, wood-based electrodes with improved charge-storage capacity for applications in electronics and energy storage.
木材的三维微观和纳米结构已被广泛用作具有成本效益和可再生的电子技术的模板。然而,由于缺乏一种能够使木质素穿过细胞壁的方法,其他电活性成分,特别是天然木质素,一直被忽视。在本研究中,我们引入了一种方法,该方法专注于在木材结构内的各种长度尺度上建立基于共轭聚合物的电连接,旨在利用木材基储能电极中天然木质素的电荷存储能力。我们证明,整合在细胞壁腔中的聚(3,4-乙撑二氧噻吩)-聚(苯乙烯磺酸盐)(PEDOT/PSS)可以通过水溶性S-EDOT单体的原位聚合穿过木材细胞壁与天然木质素连接。这种方法在5 mV s的扫描速率下将导电木材的电容提高到315 mF cm,分别比由单一成分PEDOT/PSS或S-PEDOT制成的导电木材的电容高7倍和2倍。此外,我们表明电容由电活性聚合物和天然木质素共同贡献,天然木质素占总电荷存储容量的70%以上。我们表明,通过在木材结构内原位创建电互连来获取天然木质素,为实现可持续的、具有改进电荷存储容量的木材基电极提供了一条途径,可用于电子和储能应用。