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Cited 2 time in webofscience Cited 4 time in scopus
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Microwave-assisted ultrafast in-situ growth of N-doped carbon quantum dots on multiwalled carbon nanotubes as an efficient electrocatalyst for photovoltaics

Authors
Ali, MumtazRiaz, RabiaAnjum, Aima SameenSun, Kyung ChulLi, HuiAhn, SeJinJeong, Sung HoonKo, Min Jae
Issue Date
Mar-2021
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Metal-free catalyst; Surface modification; Counter electrodes; Dye-sensitized solar cells
Citation
JOURNAL OF COLLOID AND INTERFACE SCIENCE, v.586, pp.349 - 361
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume
586
Start Page
349
End Page
361
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1549
DOI
10.1016/j.jcis.2020.10.098
ISSN
0021-9797
Abstract
Multiwalled carbon nanotubes (MWCNTs) are at the forefront of metal-free electrocatalysts, however, the performance is still limited due to lack of functionality and dispersion. Coupling of MWCNTs with nitrogen doped carbon quantum dots (NCQDs) can impart the required active sites and dispersion. For the purpose, NCQDs are generally attached to MWCNTs by multistep processing, such as NCQDs synthesis, followed by their complex purification, surface activation, and crosslinking with MWCNT. The scalability of such a multistep process is limited, which is addressed by direct microwave-assisted growth of NCQDs on MWCNT. The concentration of reactants of NCQDs synthesis was optimized (with respect to MWCNTs), to achieve controlled direct growth of NCQDs on MWCNTs. The proposed strategy significantly reduced time and energy consumption, along with providing an overlapped interface for the fast charge transfer. Moreover, NCQDs' growth effectively modulated the surface reactivity and internal band structure of the MWCNTs. In response, dye-sensitized solar cells employing NCQDs modified MWCNT as a counter electrode showed 50% higher photovoltaic performance as compared to bare MWCNTs.
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서울 공과대학 > 서울 화학공학과 > 1. Journal Articles
서울 공과대학 > 서울 유기나노공학과 > 1. Journal Articles

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