法拉第效率
材料科学
钾离子电池
阳极
硫黄
碳纤维
电化学
扩散
电极
化学工程
滴定法
电池(电)
无机化学
钾
化学
复合材料
物理化学
复合数
物理
工程类
热力学
磷酸钒锂电池
功率(物理)
冶金
量子力学
作者
Jia Ding,Hanlei Zhang,Hui Zhou,Jun Feng,Xuerong Zheng,Cheng Zhong,Eunsu Paek,Wenbin Hu,David Mitlin
标识
DOI:10.1002/adma.201900429
摘要
Sulfur-rich carbons are minimally explored for potassium-ion batteries (KIBs). Here, a large amount of S (38 wt%) is chemically incorporated into a carbon host, creating sulfur-grafted hollow carbon spheres (SHCS) for KIB anodes. The SHCS architecture provides a combination of nanoscale (≈40 nm) diffusion distances and CS chemical bonding to minimize cycling capacity decay and Coulombic efficiency (CE) loss. The SHCS exhibit a reversible capacity of 581 mAh g-1 (at 0.025 A g-1 ), which is the highest reversible capacity reported for any carbon-based KIB anode. Electrochemical analysis of S-free carbon spheres baseline demonstrates that both the carbon matrix and the sulfur species are highly electrochemically active. SHCS also show excellent rate capability, achieving 202, 160, and 110 mAh g-1 at 1.5, 3, and 5 A g-1 , respectively. The electrode maintains 93% of the capacity from the 5th to 1000th cycle at 3 A g-1 , with steady-state CE being near 100%. Raman analysis indicates reversible breakage of CS and SS bonds upon potassiation to 0.01 V versus K/K+ . The galvanostatic intermittent titration technique (GITT) analysis provides voltage-dependent K+ diffusion coefficients that range from 10-10 to 10-12 cm2 s-1 upon potassiation and depotassiation, with approximately five times higher coefficient for the former.
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