Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Nanostructured anode materials have attracted significant attention for lithium-ion batteries (LIBs) due to their high specific capacity. However, their practical application is hindered by the rather low areal capacity in the ultrathin electrode (∼1 mg cm). Herein, we propose a new strategy of an all-conductive electrode to fabricate a flexible and free-standing vanadium nitride@N-doped carbon/graphene (VN@C/G) thick electrode. Due to the free-standing structure and absence of any nonconductive components in the electrode, the obtained thick electrode displays excellent cycling performances. With the high mass loading of 5 mg cm, VN based electrodes achieve a reversible capacity of 2.6 mAh cm after 200 cycles. Moreover, the all-conductive electrode allows an ultrahigh areal capacity of 7 mAh cm with a high mass loading of 18.3 mg cm, which is comparable to state-of-the-art graphite anodes (4 mAh cm). Theoretical calculations prove the metallic conductivity of VN, which allows fast charge transport in the thick electrode. This strategy of fabricating all-conductive electrodes shows great potentials to achieve high areal capacity in practical lithium-ion batteries.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.0c13859 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!