Hollow FeP/FeO Hybrid Nanoparticles on Carbon Nanotubes as Efficient Electrocatalysts for the Oxygen Evolution Reaction.

ACS Appl Mater Interfaces

Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology, Institute of Solid State Physics, Chinese Academy of Sciences, Hefei 230031, P. R. China.

Published: March 2020

We develop a method to prepare hollow FeP/FeO hybrid nanoparticles supported on carbon nanotubes (CNTs), which could be used as highly active and efficient electrocatalysts. The Fe@FeO/CNT hybrids were first synthesized by annealing the CNTs adsorbed with Fe(NO), followed by controlled phosphorization treatment. They exhibit an outstanding catalytic activity for oxygen evolution reaction (OER) with a low overpotential of 229 mV at a current density of 10 mA cm, a high turnover frequency value of 0.35 s at an overpotential of 300 mV, and an ultralow Tafel slope of 27.6 mV dec, which is much better than that of FeP/FeO, FeP/CNTs, FeO/CNTs, and the commercial RuO electrocatalyst. More importantly, the Tafel slope is much lower than most non-noble metal-based OER electrocatalysts reported in the previous literature studies as far as we know. The excellent OER performance benefits from the electron transfer from FeO to FeP confirmed by X-ray photoelectron spectroscopy, together with good conductivity of CNTs. This hybrid structure supported on conductive CNTs may offer an efficient method to design earth-abundant and low-cost electrocatalysts for OER in practical applications.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.9b21927DOI Listing

Publication Analysis

Top Keywords

hollow fep/feo
8
fep/feo hybrid
8
hybrid nanoparticles
8
carbon nanotubes
8
efficient electrocatalysts
8
oxygen evolution
8
evolution reaction
8
tafel slope
8
nanoparticles carbon
4
nanotubes efficient
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!