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: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
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
Prussian blue analogues (PBAs) have been employed as host materials of aqueous zinc-ion batteries (ZIBs), however, they suffer from low capacity and poor cycling stability due to limited electron transfer and the presence of interstitial water in PBAs. Herein, a vacancy and water-free silver hexacyanoferrate KAgFe(CN) (AgHCF-3) was synthesized by adjusting the ratio of K and Ag in the framework. It offers nearly four electrons involving two sequential redox reactions, namely, Fe/Fe and Ag/Ag, to deliver a large capacity of 179.6 mAh g at 20 mA g with Coulomb efficiency of ~100 %. The Zn//AgHCF-3 cell delivers an estimated energy density of 200 Wh kg, surpassing reported PBAs-based ZIBs. The formation of Ag in the cycling process merits favorable rate performance of AgHCF-3 (156.4 mAh g at 200 mA g with 80.3 % capacity retention after 100 cycles). This investigation paves new pathways for high-capacity PBA cathodes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202416392 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!