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: 1057
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3175
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 development of size- and shape-controlled nanomaterials is essential to tailor their properties and performance for wide-ranging applications from catalysis to sensing. Solid-state synthesis of nanostructures is attractive from a sustainability perspective, but they typically lack the desired size and shape control at small-scale dimensions. This work shows that colloidal precursors can be used in a solid-state route to form hybrid core-shell nanostructures with simultaneous size and morphology control. Encapsulation of PtNPs with a well-defined CuO shell produces CuPt@CuO core-shell nanocubes grown directly from the underlying substrate. The controlled formation of the nanostructures is facilitated by the diamine passivation layer on the Cu substrate. On-substrate growth of the nanocubes gives ease of postsynthesis processing for them to be used directly in electrochemical applications. We show that the synthesized nanostructured substrates have high sensitivity as an electrocatalyst for glucose sensing. We further demonstrate their potential for direct methanol fuel cells by assessing the methanol oxidation reaction (MOR). The mass activity is determined to be 1.656 A mg for MOR, and initial studies indicate the substrates show high CO tolerance.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1021/acsami.4c20674 | DOI Listing |
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