4.8 Article

Highly Efficient Acidic Oxygen Evolution Electrocatalysis Enabled by Porous Ir-Cu Nanocrystals with Three-Dimensional Electrocatalytic Surfaces

Journal

CHEMISTRY OF MATERIALS
Volume 30, Issue 23, Pages 8571-8578

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.8b03620

Keywords

-

Funding

  1. Ministry of Science and Technology [2016YFA0204100, 2017YFA0208200]
  2. National Natural Science Foundation of China [21571135]
  3. Young Thousand Talented Program
  4. Soochow University
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

Ask authors/readers for more resources

The design of efficient Ir-based catalyst for oxygen evolution reaction (OER) in acidic conditions is the key for realizing the commercialization of polymer electrolyte membrane technology. This study reports a class of highly porous Ir-Cu nanocrystals (P-IrCux NCs) through a facile chemical dealloying strategy. Featuring the increased active surface area and plenty of defects, the newly generated P-IrCux NCs are highly active and stable toward OER in acidic conditions. The optimized P-IrCu1.4 NCs exhibit the current density of 12.8 mA cm(-2) at the potential of 1.55 V (vs RHE), presenting 3.5-fold improvement in mass activity and 1.8-fold improvement in specific activity over the pristine solid IrCu1.4 NCs (S-IrCu1.4 NCs). Moreover, the obtained P-IrCu1.4 NCs also show excellent OER stability with negligible potential shift after continuous electrolysis in 0.05 M H2SO4 for 10 h. Further analysis reveals that the coordinatively unsaturated atoms at defects result in the higher oxidation state of iridium, which promotes the optimized intrinsic activity of P-IrCux NCs. This work highlights a promising strategy to create three-dimensional porous Ir-based catalysts for enhancing OER electrocatalysis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available