Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 144
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 144
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 212
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3106
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
In quantum dot sensitized solar cells (QDSSCs), the photoanode provides a stable support for the quantum dots, and promotes the production of photogenerated electrons and the transfer to external circuit. Therefore, it is very important to search for excellent photoanodes for the commercial application of QDSSCs. In this paper, a core-shell ZnO@TiO hexagonal prism heterogeneous structure was prepared by a two-step hydrothermal method. The ZnO@TiO heterogeneous structure not only has a unique 1D hexagonal prism morphology, but also can effectively inhibit the electron-hole recombination and has a greater light response and higher collection efficiency while speeding up the electron transmission rate. By adjusting the concentration of the TiO source, the best photoanode material Zn@Ti-2 was explored, and it showed excellent cell performance: = 25.4 mA cm, = 0.71 V, PCE = 8.5%, and FF = 0.49. Compared with a single ZnO photoanode, the PCE value is increased by 25%. EIS, Tafel polarization and transient photocurrent responses confirm that the Zn@Ti-2 photoanode has higher catalytic activity and stability. Therefore, Zn@Ti-2 may be a promising photoanode material for QDSSCs.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1039/d3dt03144f | DOI Listing |
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