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Boosting catalytic activity of niobium/tantalum-nitrogen active-sites for triiodide reduction in photovoltaics
[Display omitted] •Nb/Ta modified NOC was synthesized via simple pyrolysis and ion exchange.•Nb/Ta-NOC with powerful dual-active sites has worthy bifunctional catalytic ability.•Nb/Ta-NOC as electrode for IRR in solar cell showed a conversion efficiency of 8.45%.•Performance of Nb/Ta-NOC for HER is...
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Published in: | Journal of colloid and interface science 2021-12, Vol.603, p.651-665 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Nb/Ta modified NOC was synthesized via simple pyrolysis and ion exchange.•Nb/Ta-NOC with powerful dual-active sites has worthy bifunctional catalytic ability.•Nb/Ta-NOC as electrode for IRR in solar cell showed a conversion efficiency of 8.45%.•Performance of Nb/Ta-NOC for HER is close to that of Pt/C.•Nb/Ta-NOC shows superior electrocatalytic stability in IRR and HER.
To fabricate high-quality catalysts with abundant active sites, a series of transition-metal-modified nitrogenous carbon catalysts (Ta-NOC, Nb-NOC, and Nb/Ta-NOC) was successfully fabricated via pyrolysis and ion exchange. Owing to the high conductivity and ion transport capacity of its unique nitrogen-carbon structure, and synergistic effect of dual-metal active sites on modulating electronic structure, Nb/Ta-NOC catalyst exhibited an excellent catalytic performance and a remarkable electrochemical stability in triiodide reduction reaction (IRR) and hydrogen evolution reaction (HER). Nb/Ta-NOC catalyst achieved an ideal conversion efficiency of 8.45% for IRR in solar cells, which was higher than that of Pt electrode (7.63%). Furthermore, Nb/Ta-NOC catalyst exhibited a small overpotential of 145 mV at a current density of 10 mA·cm-2 and a Tafel slope of 77 mV dec-1 for HER. This work provided a new approach for the rational design of the active-sites-rich electrocatalysts for energy conversion applications. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2021.06.128 |