阳极
材料科学
兴奋剂
阴极
结晶度
碳纤维
化学工程
储能
钠离子电池
功率密度
电容器
电化学
电极
光电子学
化学
复合数
复合材料
物理化学
量子力学
物理
工程类
法拉第效率
功率(物理)
电压
作者
Tianhao Yao,Hongkang Wang,Yuanbin Qin,Jian‐Wen Shi,Yonghong Cheng
标识
DOI:10.1016/j.compositesb.2023.110557
摘要
Sodium-ion capacitors (SICs) have been viewed as promising energy storage devices because of their high power/energy density, cycling stability and cost-efficiency, but they are also restricted by the unmatched reaction kinetics between the battery-type anode and capacitor-type cathode. Herein, we present a novel way to enhance the pseudocapacitive storage behavior and reaction kinetics of TiO2-based anode via Mo-doping and carbon hybridization, using the Mo-doped titanium metal-organic framework (Ti-MOF, MIL-125) as the precursor. Appropriate amount of Mo-doping (Mo:Ti = 1:9) induces the shape evolution from the round MIL-125 nanotablets to square Mo-MIL-125 nanocubes, which can be readily converted to Mo-doped TiO2-x@carbon composite with conformal morphology (namely, Mo0.1-TiO2-x@C). Mo-doping increases the concentration of Ti3+/oxygen vacancy and decreases its crystallinity, which greatly enhances the reaction kinetics and sodium storage performance. When examined in half-cells, the Mo0.1-TiO2-x@C anode exhibits higher pseudocapacitive contribution (∼85%), higher reversible capacity (216 mAh g−1 at 0.5 A g−1), and better cycling and rate capability (185 mAh g−1 even after 3000 cycles at 1 A g−1). When paired with commercial activated carbon (AC) as cathode, the Mo0.1-TiO2-x@C//AC SICs deliver a maximum energy density of 269.37 Wh kg−1 at a power density of 80.4 W kg−1 and 61.75 Wh kg−1 even at a high power density of 5421.95 W kg−1.
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