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
Iridium single atom catalysts are promising oxygen evolution reaction (OER) electrocatalysts for proton exchange membrane water electrolysis (PEMWE), as they can reduce the reliance on costly Ir in the OER catalysts. However, their practical application is hindered by their limited stability during PEMWE operation. Herein, we report on the activation of Ir-doped CoMnO in acidic electrolyte that leads to enhanced activity and stability in acidic OER for long-term PEMWE operation. In-depth material characterization combined with electrochemical analysis and theoretical calculations reveal that activating Ir-doped CoMnO induces controlled restructuring of Ir single atoms to IrO nanoclusters, resulting in an optimized Ir configuration with outstanding mass activity of 3562 A g at 1.53 V (vs RHE) and enhanced OER stability. The PEMWE using activated Ir-doped CoMnO exhibited a stable operation for >1000 h at 250 mA cm with a low degradation rate of 0.013 mV h, demonstrating its practical applicability. Furthermore, it remained stable for more than 400 h at a high current density of 1000 mA cm, demonstrating long-term durability under practical operation conditions.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/jacs.4c11442 | DOI Listing |
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