4.6 Article

Electrochemical integration of amorphous NiFe (oxy)hydroxides on surface-activated carbon fibers for high-efficiency oxygen evolution in alkaline anion exchange membrane water electrolysis

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 24, Pages 14043-14051

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta02883a

Keywords

-

Funding

  1. NRF (National Honor Scientist Program) [2010-0020414]
  2. National Research Foundation Korea - Ministry of Science, ICT, and Future Planning [NRF-2018R1A2A1A05077532]

Ask authors/readers for more resources

Developing a high-efficiency and low-cost three-dimensional OER electrode with enriched active sites and improved electrical conductivity is crucial for enhancing the kinetics and mass transport properties of oxygen evolution reaction. The synthesized a-NiFeOOH/N-CFP electrode exhibits excellent OER activity and stability, outperforming state-of-the-art catalysts. These findings signify significant advancements in the utilization of NiFeOOH catalysts for commercial applications.
Developing practical water-splitting devices that convert earth-abundant solar energy and water into renewable fuel holds promise for a sustainable energy future; however, its successful commercialization for practical applications is limited by the sluggish kinetics of the oxygen evolution reaction (OER). Herein, we developed a high-efficiency and low-cost three-dimensional (3D) OER electrode via electrochemical integration of amorphous NiFeOOH on surface activated carbon fiber paper (CFP). The as-synthesized 3D-a-NiFeOOH/N-CFP electrode exhibits an ultra-low overpotential eta(O-2) of 170 mV to afford 10 mA cm(-2) current density, together with a Tafel slope of 39 mV per decade, and excellent stability under OER conditions. Apart from the synergistic effect, the excellent OER activity of a-NiFeOOH/N-CFP is attributed to the unique 3D structure with enriched active sites and the improved electrical conductivity that facilitates the fast OER kinetics and mass transport properties. As a result, the catalyst achieves a high turnover frequency (TOF) of 0.99 s(-1) and mass activity (j(m)) of 2527 A g(-1) at eta(O-2) 270 mV, which outperforms so far reported state-of-the-art OER catalysts and commercial IrO2. Besides, an alkaline anion exchange membrane water electrolyzer fabricated with the a-NiFeOOH/N-CFP anode delivers 1 A current at 1.88 V with a long-term durability of 240 h. These findings highlight the design of high-efficiency OER catalysts and significant advancements towards the utilization of NiFeOOH catalysts for commercial applications.

Authors

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

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available