材料科学
超级电容器
锐钛矿
化学工程
阳极
纳米孔
石墨烯
电解质
纳米技术
碳纤维
电容
电极
复合材料
有机化学
工程类
复合数
物理化学
催化作用
光催化
化学
作者
Wenbin Fu,Enbo Zhao,Ruiying Ma,Zifei Sun,Yang Yang,Marta Sevilla,Antonio B. Fuertes,Alexandre Magasinski,Gleb Yushin
标识
DOI:10.1002/aenm.201902993
摘要
Abstract Li‐ion hybrid supercapacitors (Li‐HSCs) hold great promise in future electrical energy storage due to their relatively high power and energy density. However, a major challenge lies in the slow kinetics of Li‐ion intercalation/extraction within metal‐oxide electrodes. Here, it is shown that ultrafast charge storage is realized by confining anatase TiO 2 nanoparticles in carbon nanopores to enable a high‐rate anode for Li‐HSCs. The porous carbon with interconnected pore walls and open channels not only works as a conductive host to protect TiO 2 from structural degradation but also provides fast pathways for ion/electron transport. As a result, the assembled cells exhibit remarkable rate capabilities with a specific capacity of ≈140 mAh g −1 at a slow charge and ≈60 mAh g −1 at a 3.5 s fast charge. While the charge/discharge process can be completed as fast as that of state‐of‐the‐art electrical double‐layer capacitors (EDLCs), the produced nanocomposites show three to seven times higher volumetric capacitance than activated carbons used in commercial EDLCs with acetonitrile‐based electrolytes. Equally important for some applications in cold climates or the space, the Li‐HSCs can operate at subzero temperatures as low as −40 °C, which is likely only limited by thermal properties of the acetonitrile (melting point of −45 °C).
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