阳极
碳化
碳纤维
离子
钠
材料科学
钠离子电池
吸附
电池(电)
空位缺陷
化学工程
复合材料
化学
法拉第效率
电极
冶金
扫描电子显微镜
工程类
热力学
结晶学
有机化学
功率(物理)
物理化学
复合数
物理
作者
Nagmani,Sreeraj Puravankara
标识
DOI:10.1021/acsaem.0c01750
摘要
The sodium-ion storage mechanism of the hard carbon microspheres (HCMSs) synthesized using the microwave technique from the sucrose precursor and a 50% DEG/H2O solvent mixture carbonized at 1000 °C (50DEG-HCMS) is studied. The superior sodium-ion battery (SIB) anode, 50DEG-HCMS delivers the highest reversible capacities of 385 (ICE ∼75.5%) and 265 mAh g–1 (ICE ∼72%) at current densities of 30 and 300 mA g–1, respectively. The plateau related capacity (PRC) solely determines the reversible capacity fade on cycling at all C-rates for the HCMS, validating the insertion/pore-filling mechanism for the low voltage (< ∼0.1 V) capacity. In this study, we substantiate that maximizing PRC may not be the best strategy in designing a high rate, a highly cyclable carbon-based anode for SIBs. HCMSs synthesized using a 20% DEG/H2O solvent mixture and at different carbonization temperatures are also studied to assert the defect/vacancy-assisted adsorption/insertion and insertion/micropore filling Na-ion storage mechanism in hard carbons.
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