Heterostructure engineering of the Fe-doped Ni phosphides/Ni sulfide p-p junction for high-efficiency oxygen evolution
Regulating charge distribution through heterostructure engineering is an encouraging approach to achieving efficient alkaline water electrolysis. Here, a Fe-doped Ni phosphides/Ni sulfide p-p heterojunction (NiFe-PS) for oxygen evolution reaction (OER) is constructed on nickel foam. It is shown that...
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Veröffentlicht in: | Journal of alloys and compounds 2022-11, Vol.924, p.166613, Article 166613 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Regulating charge distribution through heterostructure engineering is an encouraging approach to achieving efficient alkaline water electrolysis. Here, a Fe-doped Ni phosphides/Ni sulfide p-p heterojunction (NiFe-PS) for oxygen evolution reaction (OER) is constructed on nickel foam. It is shown that the built-in electric field at the interface of Fe-doped Ni phosphides/Ni sulfide facilitates the charge transfer and modifies the electronic properties of the catalyst, thereby enhancing its conductivity and catalytic activity. Profiting from the rational electronic structure modulation, the designed NiFe-PS electrode possesses excellent OER performance among phosphides with low overpotentials of 204 and 256 mV at current densities of 10 and 100 mA cm-2, respectively. Meanwhile, the prepared catalyst displays high stability in the long-term chronopotentiometric test (125 h @ 100 mA cm-2). Structural characterizations confirm that the outer phosphide layer can withstand long-term surface oxidation and operate as a robust shield to prevent oxidation of the inner sulfide, ensuring rapid electron transport within the catalyst throughout the OER process.
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•The built-in field guarantees the rapid charge transfer, and the heterostructure preventsthorough structural degradation.•NiFe-PS shows a small overpotential (256 mV @ 100 mA cm-2) and a low Tafel slope (53.7 mV dec-1).•NiFe-PS can maintain its core intact even after a long-term OER test (125 h @ 100 mA cm-2 without attenuation). |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2022.166613 |