Iron, rhodium-codoped Ni2P nanosheets arrays supported on nickel foam as an efficient bifunctional electrocatalyst for overall water splitting

[Display omitted] •The Fe,Rh-Ni2P/NF were synthesized via hydrothermal treatment and sequential low-temperature phosphorization.•The unique nanosheets arrays effectively enriched the active sites with easy accessibility.•Fe,Rh-codoping had great effects on the electrocatalytic performances.•The elec...

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Published inJournal of colloid and interface science Vol. 605; pp. 888 - 896
Main Authors Chen, Meng-Ting, Duan, Jiao-Jiao, Feng, Jiu-Ju, Mei, Li-Ping, Jiao, Yang, Zhang, Lu, Wang, Ai-Jun
Format Journal Article
LanguageEnglish
Published Elsevier Inc 01.01.2022
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Summary:[Display omitted] •The Fe,Rh-Ni2P/NF were synthesized via hydrothermal treatment and sequential low-temperature phosphorization.•The unique nanosheets arrays effectively enriched the active sites with easy accessibility.•Fe,Rh-codoping had great effects on the electrocatalytic performances.•The electrocatalyst exhibited excellent OER, HER, and overall water splitting activity in the alkaline solutions. To enhance the overall water splitting efficiency, it is widely attractive yet challenging to develop low price, abundance and efficient bifunctional electrocatalysts towards oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Herein, Fe,Rh-codoped Ni2P nanosheets arrays were in situ anchored on three-dimension (3D) Ni foam under hydrothermal condition and successive phosphorization, denoted as Fe,Rh-Ni2P/NF for simplicity. The unique nanosheets arrays effectively enriched the active sites with easy accessibility. By virtue of the unique sheet-like arrays and 3D porous conductive substrate, the prepared Fe,Rh-Ni2P/NF showed the low overpotentials of 226 mV at 30 mA cm−2 towards the OER and 73 mV at 10 mA cm−2 for the HER. Moreover, the electrocatalyst effectively worked as anode and cathode for overall water splitting system, showing a small voltage of 1.62 V to drive a current density of 10 mA cm−2. The present work provides alternative option for fabricating advanced catalysts in electrocatalysis and energy devices.
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ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2021.07.101