Chambers Andre, Prawer Steven, Ahnood Arman, Zhan Hualin
School of Physics, University of Melbourne, Parkville, VIC, Australia.
School of Engineering, RMIT University, Melbourne, VIC, Australia.
Front Chem. 2022 May 20;10:924127. doi: 10.3389/fchem.2022.924127. eCollection 2022.
Durable and safe energy storage is required for the next generation of miniature bioelectronic devices, in which aqueous electrolytes are preferred due to the advantages in safety, low cost, and high conductivity. While rechargeable aqueous batteries are among the primary choices with relatively low power requirements, their lifetime is generally limited to a few thousand charging/discharging cycles as the electrode material can degrade due to electrochemical reactions. Electrical double layer capacitors (EDLCs) possess increased cycling stability and power density, although with as-yet lower energy density, due to quick electrical adsorption and desorption of ions without involving chemical reactions. However, in aqueous solution, chemical reactions which cause electrode degradation and produce hazardous species can occur when the voltage is increased beyond its operation window to improve the energy density. Diamond is a durable and biocompatible electrode material for supercapacitors, while at the same time provides a larger voltage window in biological environments. For applications requiring higher energy density, diamond-based pseudocapacitors (PCs) have also been developed, which combine EDLCs with fast electrochemical reactions. Here we inspect the properties of diamond-related materials and discuss their advantages and disadvantages when used as EDLC and PC materials. We argue that further optimization of the diamond surface chemistry and morphology, guided by computational modelling of the interface, can lead to supercapacitors with enhanced performance. We envisage that such diamond-based supercapacitors could be used in a wide range of applications and in particular those requiring high performance in biomedical applications.
下一代微型生物电子设备需要耐用且安全的能量存储,由于其在安全性、低成本和高导电性方面的优势,水性电解质是首选。虽然可充电水性电池是功率要求相对较低的主要选择之一,但由于电极材料会因电化学反应而降解,其寿命通常限制在几千次充放电循环。双电层电容器(EDLC)具有更高的循环稳定性和功率密度,尽管由于离子的快速电吸附和解吸而不涉及化学反应,其能量密度目前较低。然而,在水溶液中,当电压超过其工作窗口以提高能量密度时,会发生导致电极降解并产生有害物质的化学反应。金刚石是一种用于超级电容器的耐用且生物相容的电极材料,同时在生物环境中提供更大的电压窗口。对于需要更高能量密度的应用,还开发了基于金刚石的赝电容器(PC),它将EDLC与快速电化学反应相结合。在这里,我们研究了与金刚石相关材料的特性,并讨论了它们用作EDLC和PC材料时的优缺点。我们认为,在界面的计算模型指导下,进一步优化金刚石表面化学和形态,可以制造出性能增强的超级电容器。我们设想,这种基于金刚石的超级电容器可用于广泛的应用,特别是那些在生物医学应用中需要高性能的应用。