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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Conventional carbonate electrolytes cannot meet the requirements for lithium-ion batteries (LIBs) with wide temperature range and high safety. Diethyl ethylphosphonate (DEEP) has excellent flame retardancy and a wide temperature range (-83 to 198 °C), which holds promise for developing a non-flammable electrolyte for wide-temperature application in LIBs. However, its limited compatibility with graphite electrodes and slow ionic transport capability must be addressed. Herein, we introduce diethylene glycol dimethyl ether (DEGDME) to reconfigure the solvation structure of DEEP-based electrolyte and enhance its ion transport capacity. The film-forming additives enable the electrolyte to preserve 98% capacity retention after 150 cycles for Li||Graphite cells. The non-flammable DEEP-based electrolytes modified with DEGDME enable improved low-temperature performance with achieving 71% 50th-cycle retention of Graphite||LiFePO cells at -20 °C. This work introduces a new strategy for designing non-flammable phosphate electrolytes, enabling the reliable and safe application of LIBs across a wide temperature range.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12145435 | PMC |
http://dx.doi.org/10.1038/s42004-025-01562-7 | DOI Listing |