E-resources
Peer reviewed
-
Lu, Chao; Chen, Yan; Yang, Yuan; Chen, Xi
Nano letters, 07/2020, Volume: 20, Issue: 7Journal Article
Lithium–sulfur batteries with high energy capacity are promising candidates for advanced energy storage. However, their applications are impeded by shuttling of soluble polysulfides and sluggish conversion kinetics with inferior rate performance and short cycling life. Here, single-atom materials are designed to accelerate polysulfide conversion for Li–S batteries. Nitrogen sites in the structure not only anchor polysulfides to alleviate the shuttle effect but also enable high loading of single-atom irons. Density functional theory calculations indicate that single-atom sites reduce the energy barrier of electrochemical reactions and thus improve the rate and cycling performances of batteries. The coin battery shows impressive energy storage properties, including a high reversible capacity of 1379 mAh g–1 at 0.1 C and a high rate capacity of 704 mAh g–1 at 5 C. The ratio of electrolyte dosage/energy density is as low as 5.5 g Ah1–. It exhibits excellent cycling performance with a capacity retention of 90% even after 200 cycles at 0.2 C.
![loading ... loading ...](themes/default/img/ajax-loading.gif)
Shelf entry
Permalink
- URL:
Impact factor
Access to the JCR database is permitted only to users from Slovenia. Your current IP address is not on the list of IP addresses with access permission, and authentication with the relevant AAI accout is required.
Year | Impact factor | Edition | Category | Classification | ||||
---|---|---|---|---|---|---|---|---|
JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
Select the library membership card:
If the library membership card is not in the list,
add a new one.
DRS, in which the journal is indexed
Database name | Field | Year |
---|
Links to authors' personal bibliographies | Links to information on researchers in the SICRIS system |
---|
Source: Personal bibliographies
and: SICRIS
The material is available in full text. If you wish to order the material anyway, click the Continue button.