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
1,10-Phenanthroline-5,6-dione (phendione)-based transition-metal complexes are known for their use in pharmacological and catalysis applications. However, their application in electrochemical energy storage has not been investigated thus far. Herein, the feasibility of employing phendione-transition-metal complexes was investigated for electrochemical charge storage by taking advantage of the reversible redox activity of both carbonyl groups and transition metal center, contributing to augmented charge storage. Interestingly, the chemistry of the counter ion in the studied complexes effectively tuned the solubility and improved the cycling stability. Although further studies are required to limit the solubility and active-species shuttle, this study explores the bottlenecks of phendione-transition-metal complexes as electrode materials for solid-electrode-format batteries.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1002/cssc.201903290 | DOI Listing |
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