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: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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Combining the new two-dimensional conductive MXene with transition metal oxide to build composite structure is a promising path to improve the conductivity of metal oxide. However, a critical challenge still remains in how to achieve a good combination of MXene and metal oxide. Herein, we develop a facile hydrothermal route to synthesize the MnO/TiCTcomposite electrode for supercapacitors by synergistically coupling MnOnanowires with TiCTMXene nanoflakes. Compared with the pure MnOelectrode, the morphology of the MnO/TiCTcomposite electrode changes from nanowires to nanoflowers. Moreover, the overall conductivity and electrochemical performance of the composite electrode are greatly improved due to an addition of TiCTMXene. The specific capacitance of the MnO/TiCTcomposite electrode achieves 210.8 F·gat a scan rate of 2 mV·s, while that of the pure MnOelectrode is only 55.2 F·g. Furthermore, the specific capacitance of the MnO/TiCTcomposite electrode still can remain at 97.2% even after 10 000 charge-discharge cycles, revealing an excellent cycle stability. The synthesis strategy of this work can pave the way for the research and practical application of the electrode materials for supercapacitors.
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http://dx.doi.org/10.1088/1361-6528/acc744 | DOI Listing |