Sulfur-Doped Carbon Nanotemplates for Sodium Metal Anodes
- Authors
- Yoon, Hyeon Ji; Hong, Seungki; Lee, Min Eui; Hwang, Junyeon; Jin, Hyoung-Joon; Yun, Young Soo
- Issue Date
- 2018-05
- Publisher
- AMER CHEMICAL SOC
- Citation
- ACS Applied Energy Materials, v.1, no.5, pp.1846 - 1852
- Abstract
- Sodium metal is a good candidate as an anode for a large-scale energy storage device because of the abundance of sodium resources and its high theoretical capacity (similar to 1166 mA h g(-1)) in a low redox potential (-2.71 V versus the standard hydrogen electrode). In this study, we report effects of sulfur doping on highly efficient macroporous catalytic carbon nanotemplates (MC-CNTs) for a metal anode. MC-CNTs resulted in reversible and stable sodium metal deposition/stripping cycling over similar to 200 cycles, with average Coulombic efficiency (CE) of similar to 99.7%. After heat treatment with elemental sulfur, the sulfur-doped MC-CNTs (S-MC-CNTs) showed significantly improved cycling performances over 2400 cycles, with average CEs of similar to 99.8%. In addition, very small nucleation overpotentials from similar to 6 to similar to 14 mV were achieved at current densities from 0.5 to 8 mA cm(-2), indicating highly efficient catalytic effects for sodium metal nucleation and high rate performances of S-MC-CNTs. These results provide insight regarding a simple but feasible strategy based on bioabundant precursors and an easy process to design a high-performance metal anode.
- Keywords
- ION BATTERIES; LITHIUM; ELECTROLYTE; NUCLEATION; NANOSHEETS; STABILITY; COMPOSITE; LAYER; DOTS; carbon nanotemplate; macroporous carbon; sulfur doping; metal anode; sodium ion battery
- ISSN
- 2574-0962
- URI
- https://pubs.kist.re.kr/handle/201004/121391
- DOI
- 10.1021/acsaem.8b00258
- Appears in Collections:
- KIST Article > 2018
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.