Construction of 2D heterostructure FeP-CoP/MoO nanosheets for efficient oxygen evolution reaction
The oxygen evolution reaction (OER) plays a pivotal role in diverse electrochemical conversion applications, such as water splitting and metal-air batteries. Nevertheless, the formation of several active sites in catalysts made of non-noble metals continues to encounter notable obstacles. To tackle...
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Veröffentlicht in: | CrystEngComm 2023-11, Vol.25 (45), p.6246-6251 |
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Zusammenfassung: | The oxygen evolution reaction (OER) plays a pivotal role in diverse electrochemical conversion applications, such as water splitting and metal-air batteries. Nevertheless, the formation of several active sites in catalysts made of non-noble metals continues to encounter notable obstacles. To tackle this challenge, a 2D heterostructure catalyst composed of Fe
2
P-CoP
2
/MoO
x
nanosheets was designed. The cobalt molybdate (CoMoO
4
) nanosheets and their supported FeOOH nanoflakes were
in situ
transformed into 2D heterostructure Fe
2
P-CoP
2
/MoO
x
nanosheets
via
a simple hydrothermal and phosphorization process. Note that the 2D MoO
x
nanosheets significantly enhance the electrochemically active surface area (ECSA), and there is a synergistic effect between cobalt phosphide (CoP
2
) and iron phosphide (Fe
2
P) nanoparticles, improving the OER reaction activity. When the electrocatalyst was employed for the OER, the Fe
2
P-CoP
2
/MoO
x
nanosheets exhibit remarkable OER efficiency, reducing overpotentials to as low as 235 mV at a current density of 50 mA cm
−2
, accompanied by a Tafel slope of 33.32 mV dec
−1
, along with exceptional enduring stability. The synthesis of the 2D heterostructure Fe
2
P-CoP
2
-MoO
x
nanosheets and their remarkable OER performance represent substantial advancements in developing electrocatalysts that are productive and stable in sustainable energy conversion and storage applications.
2D heterostructure Fe
2
P-CoP
2
/MoO
x
nanosheets on NF were synthesized by simple hydrothermal and phosphorization methods and exhibit remarkable OER performance. |
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ISSN: | 1466-8033 |
DOI: | 10.1039/d3ce00884c |