材料科学
化学工程
电催化剂
X射线光电子能谱
碳纳米管
硫黄
碳化物
钼
碳纤维
金属
无机化学
纳米技术
电化学
电极
复合材料
复合数
化学
冶金
物理化学
工程类
作者
Hongchang Hao,Yixian Wang,Naman Katyal,Guang Yang,Hui Dong,Pengcheng Liu,Sooyeon Hwang,Mantha Sai Pavan Jagannath,Graeme Henkelman,Yixin Xu,J. Anibal Boscoboinik,Jagjit Nanda,David Mitlin
标识
DOI:10.1002/adma.202106572
摘要
This is the first report of molybdenum carbide-based electrocatalyst for sulfur-based sodium-metal batteries. MoC/Mo2 C is in situ grown on nitrogen-doped carbon nanotubes in parallel with formation of extensive nanoporosity. Sulfur impregnation (50 wt% S) results in unique triphasic architecture termed molybdenum carbide-porous carbon nanotubes host (MoC/Mo2 C@PCNT-S). Quasi-solid-state phase transformation to Na2 S is promoted in carbonate electrolyte, with in situ time-resolved Raman, X-ray photoelectron spectroscopy, and optical analyses demonstrating minimal soluble polysulfides. MoC/Mo2 C@PCNT-S cathodes deliver among the most promising rate performance characteristics in the literature, achieving 987 mAh g-1 at 1 A g-1 , 818 mAh g-1 at 3 A g-1 , and 621 mAh g-1 at 5 A g-1 . The cells deliver superior cycling stability, retaining 650 mAh g-1 after 1000 cycles at 1.5 A g-1 , corresponding to 0.028% capacity decay per cycle. High mass loading cathodes (64 wt% S, 12.7 mg cm-2 ) also show cycling stability. Density functional theory demonstrates that formation energy of Na2 Sx (1 ≤ x ≤ 4) on surface of MoC/Mo2 C is significantly lowered compared to analogous redox in liquid. Strong binding of Na2 Sx (1 ≤ x ≤ 4) on MoC/Mo2 C surfaces results from charge transfer between the sulfur and Mo sites on carbides' surface.
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