Enhancing charge storage capacity of cellulose-sweat-based electrolyte flexible supercapacitors with electrochemically exfoliated free-standing carbon yarn electrodes

IF 5.9 3区 材料科学 Q2 CHEMISTRY, PHYSICAL FlatChem Pub Date : 2024-08-05 DOI:10.1016/j.flatc.2024.100724
Amjid Rafique , Isabel Ferreira , Nenad Bundaleski , O.M.N.D. Teodoro , Ana C. Baptista
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Abstract

The Internet of Things (IoT) provides an interface between different electronic devices such as flexible electronics, and e-textiles to capture and receive real-time data and help humans to devise systems that will adequately respond to these environmental stimuli. The main limitations of these devices to work 24/7 are the lack of continuous power supply and easy integration into textiles to perform their functions. The other issues are poor adhesion of active materials with substrates and peeling-off of active material from the electrode substrates and consequently, degradation of electrochemical performance. A potential and evolving strategy is fabricating a current collector-less and integrable carbon yarn-based energy storage device. Herein, we are presenting a facile and novel technique to exfoliate carbon yarn fibers to enhance their electrochemical performance by 3 orders of magnitude. Activated carbon yarn wires acting as current collector-less electrodes along with cellulose acetate-based composite separators offer a large surface area to simulated sweat electrolyte ions and show a gravimetric capacitance of 11.28 Fg−1 at the scan rate of 5 mVs−1. Activated carbon yarn-based symmetric supercapacitor device in a simulated sweat solution electrolyte offers excellent cyclic and bending stability with over 95 % capacitance retention in both tests.

Theoretical insight

Supercapacitors (SCs) comprise many active and passive elements. The most passive and vital elements are current collectors, separators, binders, electrolytes, and packaging. Two key elements, current collector and binders can be eliminated by developing current collector-free or free-standing electrodes. Carbonaceous materials such as graphene [1], [2], carbon nanotubes (CNT) [3], porous carbon [2], and carbon onions[4], [5] are common alternatives of active materials for SCs electrodes owing to their low cost, chemical stability, large surface area, and high electrical conductivity. These active materials show exceptional attributes such as long cyclic life, and high-rate capability owing to their intrinsic operation mechanism e.g., surface charge storage due to large surface area. However, they also suffer from low specific capacitance ascribed to low surface area exposed to electrolyte ions and low charge storage due to poor wettability. The most efficient technique to address this problem is to incorporate doped heteroatoms or surface functional groups such as surface oxygen groups present on the surface of carbon yarn. The inclusion of these doped heteroatoms and functional groups boosts the intrinsic properties, such as electrical conductivity, and wettability. The increased electro-active surface area offers more active sites for electrolyte ions, resulting in more charge storage and higher pseudocapacitance [6], [7], [8].

Carbon yarn comprised of long-chain carbon filaments of 2.5–5 µm in radius, excellent conductivity, high chemical and mechanical stability, and light weightiness make it a potential candidate as an active material or a free-standing electrode for SCs. However, due to its low specific capacitance, limited surface area, and low porosity, carbon yarn failed to be directly exploited as a free-standing or current collector-less electrode for flexible supercapacitor applications.

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利用电化学剥离独立碳纱电极提高纤维素-汗液基电解质柔性超级电容器的电荷存储容量
物联网(IoT)为不同的电子设备(如柔性电子设备和电子纺织品)提供了一个接口,用于捕捉和接收实时数据,帮助人类设计出能够对这些环境刺激做出适当反应的系统。这些设备全天候工作的主要限制因素是缺乏持续的电力供应,以及无法轻松集成到纺织品中以实现其功能。其他问题还包括活性材料与基底的粘附性差,活性材料从电极基底上剥离,从而导致电化学性能下降。一种潜在的、不断发展的策略是制造一种无集流器、可集成的碳纱储能装置。在此,我们将介绍一种简单而新颖的碳纱纤维剥离技术,以将其电化学性能提高 3 个数量级。作为无集流体电极的活性碳纱线以及醋酸纤维素基复合隔板为模拟汗电解质离子提供了较大的表面积,并在 5 mVs 的扫描速率下显示出 11.28 Fg 的重力电容。基于活性碳纱的对称超级电容器装置在模拟汗液电解质中具有出色的循环和弯曲稳定性,在两项测试中电容保持率均超过 95%。超级电容器(SC)由许多主动和被动元件组成。最被动和最重要的元件是集流器、隔膜、粘合剂、电解质和封装。通过开发无电流收集器或独立电极,可以消除电流收集器和粘合剂这两个关键要素。石墨烯、碳纳米管 (CNT)、多孔碳和碳葱等碳质材料具有成本低、化学性质稳定、表面积大和导电率高等特点,是气相沉积物电极活性材料的常见替代品。这些活性材料因其固有的运行机制(如大表面积带来的表面电荷存储)而显示出卓越的特性,如长循环寿命和高速率能力。然而,由于暴露于电解质离子的表面积较小,以及润湿性较差导致电荷存储量较低,它们也存在比电容较低的问题。解决这一问题的最有效技术是在碳纱表面加入掺杂杂原子或表面官能团,如表面氧基团。加入这些掺杂杂原子和官能团可提高导电性和润湿性等固有特性。电活性表面积的增加为电解质离子提供了更多的活性位点,从而产生更多的电荷存储和更高的假电容。
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来源期刊
FlatChem
FlatChem Multiple-
CiteScore
8.40
自引率
6.50%
发文量
104
审稿时长
26 days
期刊介绍: FlatChem - Chemistry of Flat Materials, a new voice in the community, publishes original and significant, cutting-edge research related to the chemistry of graphene and related 2D & layered materials. The overall aim of the journal is to combine the chemistry and applications of these materials, where the submission of communications, full papers, and concepts should contain chemistry in a materials context, which can be both experimental and/or theoretical. In addition to original research articles, FlatChem also offers reviews, minireviews, highlights and perspectives on the future of this research area with the scientific leaders in fields related to Flat Materials. Topics of interest include, but are not limited to, the following: -Design, synthesis, applications and investigation of graphene, graphene related materials and other 2D & layered materials (for example Silicene, Germanene, Phosphorene, MXenes, Boron nitride, Transition metal dichalcogenides) -Characterization of these materials using all forms of spectroscopy and microscopy techniques -Chemical modification or functionalization and dispersion of these materials, as well as interactions with other materials -Exploring the surface chemistry of these materials for applications in: Sensors or detectors in electrochemical/Lab on a Chip devices, Composite materials, Membranes, Environment technology, Catalysis for energy storage and conversion (for example fuel cells, supercapacitors, batteries, hydrogen storage), Biomedical technology (drug delivery, biosensing, bioimaging)
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