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全碳钾离子和钠离子电容器的直接结构-性能比较

Direct Structure-Performance Comparison of All-Carbon Potassium and Sodium Ion Capacitors.

作者信息

Xu Ziqiang, Wu Mengqiang, Chen Zhi, Chen Cheng, Yang Jian, Feng Tingting, Paek Eunsu, Mitlin David

机构信息

Center for Advanced Electric Energy Technologies (CAEET) School of Materials and Energy University of Electronic Science and Technology of China Chengdu 611731 China.

Chemical & Biomolecular Engineering Clarkson University Potsdam NY 13699 USA.

出版信息

Adv Sci (Weinh). 2019 Apr 24;6(12):1802272. doi: 10.1002/advs.201802272. eCollection 2019 Jun 19.

Abstract

A hybrid ion capacitor (HIC) based on potassium ions (K) is a new high-power intermediate energy device that may occupy a unique position on the Ragone chart space. Here, a direct performance comparison of a potassium ion capacitor (KIC) versus the better-known sodium ion capacitor is provided. Tests are performed with an asymmetric architecture based on bulk ion insertion, partially ordered, dense carbon anode (hard carbon, HC) opposing N- and O-rich ion adsorption, high surface area, cathode (activated carbon, AC). A classical symmetric "supercapacitor-like" configuration AC-AC is analyzed in parallel. For asymmetric K-based HC-AC devices, there are significant high-rate limitations associated with ion insertion into the anode, making it much inferior to Na-based HC-AC devices. A much larger charge-discharge hysteresis (overpotential), more than an order of magnitude higher impedance , and much worse cyclability are observed. However, K-based AC-AC devices obtained on-par energy, power, and cyclability with their Na counterpart. Therefore, while KICs are extremely scientifically interesting, more work is needed to tailor the structure of  "Na-inherited" dense carbon anodes and electrolytes for satisfactory K ion insertion. Conversely, it should be possible to utilize many existing high surface area adsorption carbons for fast rate K application.

摘要

基于钾离子(K)的混合离子电容器(HIC)是一种新型的高功率中能器件,可能在拉贡图空间中占据独特地位。本文对钾离子电容器(KIC)与更为人熟知的钠离子电容器进行了直接性能比较。测试采用基于体相离子插入的不对称结构,部分有序的致密碳阳极(硬碳,HC)与富含氮和氧的离子吸附、高比表面积的阴极(活性炭,AC)相对。同时对经典的对称“类超级电容器”结构AC-AC进行了分析。对于基于钾的不对称HC-AC器件,离子插入阳极存在显著的高倍率限制,使其远不如基于钠的HC-AC器件。观察到更大的充放电滞后(过电位)、超过一个数量级的更高阻抗以及更差的循环稳定性。然而,基于钾的AC-AC器件在能量、功率和循环稳定性方面与基于钠的同类器件相当。因此,虽然钾离子电容器在科学上极具吸引力,但需要开展更多工作来调整“继承自钠”的致密碳阳极和电解质的结构,以实现令人满意的钾离子插入。相反,利用许多现有的高比表面积吸附碳来实现快速钾应用应该是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6bd/6662075/cf9f7a402ef8/ADVS-6-1802272-g001.jpg

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