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
The search for an efficient and stable catalyst for the electrochemical reduction of CO to value-added chemicals is especially critical for lowering the atmospheric CO concentration. In this study, self-supported cobalt/copper nanostructured catalysts were designed, where the influences of the elemental composition and acid-etching on their efficiency towards the CO reduction reaction were studied. The developed Co/Cu catalysts showed superb catalytic activity with a low onset potential at -0.2 V RHE. Gas and liquid product analysis revealed that formate and CO were the main products. It was observed that lower reductive potentials were favourable for formate production, while higher reductive potentials were more favourable for CO formation. electrochemical FTIR studies were further conducted to gain insight into the CO reduction mechanism. The novel synthetic procedure reported in this study leads to promising electrocatalysts with high efficiencies for the conversion of CO into valuable products.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1039/d4nr00909f | DOI Listing |
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