Loading…
High entropy stabilizing lattice oxygen participation of Ru- based oxides in acidic water oxidation
The development of high-performance oxygen evolution reaction (OER) electrocatalysts for water splitting, particularly in acidic media, remains a difficult challenge. In this work, a Ru-based high entropy oxide (HEO) catalyst, RuNiMoCrFeO x nanoparticles (∼6 nm), loaded onto carbon nanotubes (CNTs)...
Saved in:
Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-10, Vol.1 (4), p.2126-21265 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The development of high-performance oxygen evolution reaction (OER) electrocatalysts for water splitting, particularly in acidic media, remains a difficult challenge. In this work, a Ru-based high entropy oxide (HEO) catalyst, RuNiMoCrFeO
x
nanoparticles (∼6 nm), loaded onto carbon nanotubes (CNTs) was synthesized by a solvent-free microwave method. By optimising its composition, we find that the RuNiMoCrFeO
x
/CNT catalyst shows high performance in 0.5 M H
2
SO
4
, with the overpotential of the HEO being only 219 mV (better than the 280 mV of commercial RuO
2
) at 10 mA cm
−2
and the Tafel slope reaching 47 mV dec
−1
. It is worth noting that this high entropy oxide (HEO) can operate at a high current density of 100 mA cm
−2
for up to 100 hours. The isotopic gas detection and electron spin resonance (ESR) experiments show that the OER tends to proceed through the LOM, and the high conformational entropy stabilizes the involvement of lattice oxygen in acidic solutions.
A novel Ru-based high entropy oxide electrocatalyst RuNiMoCrFeO
x
/CNT was successfully synthesized, where the OER tends to proceed through the LOM on the high entropy surface, high entropy stabilizes the lattice oxygen to participate in the reaction. |
---|---|
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d2ta06128g |