阳极
材料科学
阴极
兴奋剂
碳纤维
氧气
氮气
化学工程
多孔性
金属
电容器
无机化学
电极
复合数
复合材料
化学
冶金
电压
光电子学
电气工程
有机化学
物理化学
工程类
作者
Yong Min Jung,Jong Hui Choi,Dong Won Kim,Jeung Ku Kang
标识
DOI:10.1002/advs.202301160
摘要
Abstract Sodium‐ion hybrid capacitors (SIHCs) in principle can utilize the advantages of batteries and supercapacitors and satisfy the cost demand of large‐scale energy storage systems, but the sluggish kinetics and low capacities of its anode and cathode are yet to be overcome. Here, a strategy is reported to realize high‐performance dual‐carbon SIHCs using 3D porous graphitic carbon cathode and anode materials derived from metal–azolate framework‐6s (MAF‐6s). First, MAF‐6s, with or without urea loading, are pyrolyzed to synthesize MAF‐derived carbons (MDCs). Then, cathode materials are synthesized via the controlled KOH‐assisted pyrolysis of MDCs (K‐MDCs). K‐MDCs, 3D graphitic carbons, resulting in a record‐high surface area (5214 m 2 g −1 ) being ≈four‐fold higher than pristine MAF‐6, oxygen‐doped sites for high capacity, rich mesopores affording fast ion transport, and high capacity retention over 5000 charge/discharge cycles. Moreover, 3D porous MDC anode materials are synthesized from N‐containing MAF‐6 and exhibited to allow cycle stability over 5000 cycles. Furthermore, dual‐carbon MDC//K‐MDC SIHCs with different loadings (3 to 6 mg cm −2 ) are demonstrated to achieve high energy densities exceeding those of sodium‐ion batteries and supercapacitors. Additionally, it allows an ultrafast‐chargeable high power density of 20000 W kg −1 and robust cycle stability overcoming those of a typical battery.
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