阳极
材料科学
兴奋剂
阴极
结晶度
碳纤维
化学工程
纳米技术
电极
光电子学
化学
复合数
复合材料
物理化学
工程类
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI