Highly efficient and stable bifunctional electrocatalysts with decoupled active sites for hydrogen evolution and oxygen reduction reactions

[Display omitted] •HER and ORR electrocatalyst derived from Ni MOF was synthesized.•N-doped carbon layer was implemented to protect the HER catalyst.•ORR catalytic carbon layer coating increases HER stability.•The proposed method can enhance the stability of various Ni-based catalysts. Alkaline elec...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2021-12, Vol.298, p.120530, Article 120530
Hauptverfasser: Choi, Seunggun, Kwon, Jiseok, Jo, Seonghan, Kim, Sojung, Park, Keemin, Kim, Sungmin, Han, Hyuksu, Paik, Ungyu, Song, Taeseup
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Sprache:eng
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Zusammenfassung:[Display omitted] •HER and ORR electrocatalyst derived from Ni MOF was synthesized.•N-doped carbon layer was implemented to protect the HER catalyst.•ORR catalytic carbon layer coating increases HER stability.•The proposed method can enhance the stability of various Ni-based catalysts. Alkaline electrolysis is one of the most powerful technologies to produce hydrogen energy, where the electrocatalysts play an important role. The cathode electrocatalysts often suffer from undesirable oxidation due to the oxygen gas crossover through the porous separator during electrolysis. This leads to oxygen reduction reaction (ORR) on the cathode electrocatalysts, resulting in the loss of activity for hydrogen evolution reaction (HER). Here, we report a highly efficient and durable HER and ORR bifunctional electrocatalyst derived from Ni metal-organic frameworks to address the above problem. Decoupled active sites for ORR and HER are induced in a hybrid material, NiFeP@Ni_NC, where an ORR catalytic N-doped nanocarbon layer can protect a HER catalytic Niδ+ from the undesired ORR. Therefore, excellent bifunctional stability is secured for NiFeP@Ni_NC. The strategy to enhance HER stability presented herein can be widely extended to design bifunctional electrocatalysts with improved stability in alkaline electrolysis.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2021.120530