Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Ionic liquids (ILs) as electrolytes in lithium-sulfur (Li-S) batteries effectively mitigate the shuttle effect. Solvated cationic ether-based ILs, comprising [Li(G1)], [Li(G2)], [LiG3], [LiG4], or [LiG6] paired with bis(trifluoromethyllsulfonyl)imide ([TFSA]) anions, are evaluated for their ability to suppress short-chain lithium polysulfide (LiPS: LiS, LiS, LiS) adsorption on lithium metal. The chelating capacity of solvated cations governs interactions with LiPSs and anions. Solvation via Li chelation prevents free Li fusion with LiPSs, reducing shuttle effects. Remarkably, the cyclic [LiG6] cation exhibits superior Li chelation, stability, and minimized LiPS adsorption compared to linear cations. Ab initio molecular dynamics simulations confirm ether-based ILs stabilize anions and lower LiPS-lithium surface reactivity. These findings highlight solvated cation ILs as tailored electrolytes to control interfacial LiPS behavior, advancing high-performance LiS battery design.
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http://dx.doi.org/10.1002/cphc.202400848 | DOI Listing |