La- and Mn-doped cobalt spinel oxygen evolution catalyst for proton exchange membrane electrolysis

Author:

Chong Lina1ORCID,Gao Guoping2ORCID,Wen Jianguo3ORCID,Li Haixia2,Xu Haiping1ORCID,Green Zach4ORCID,Sugar Joshua D.5,Kropf A. Jeremy1ORCID,Xu Wenqian6ORCID,Lin Xiao-Min3ORCID,Xu Hui4ORCID,Wang Lin-Wang2ORCID,Liu Di-Jia17ORCID

Affiliation:

1. Chemical Science and Engineering Division, Argonne National Laboratory, Lemont, IL 60439, USA.

2. Material Science Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

3. Center for Nanoscale Materials, Argonne National Laboratory, Lemont, IL 60439, USA.

4. Giner Inc., Auburndale, MA 02466, USA.

5. Sandia National Laboratory, Livermore, CA 94550, USA.

6. X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Lemont, IL 60439, USA.

7. Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.

Abstract

Discovery of earth-abundant electrocatalysts to replace iridium for the oxygen evolution reaction (OER) in a proton exchange membrane water electrolyzer (PEMWE) represents a critical step in reducing the cost for green hydrogen production. We report a nanofibrous cobalt spinel catalyst codoped with lanthanum (La) and manganese (Mn) prepared from a zeolitic imidazolate framework embedded in electrospun polymer fiber. The catalyst demonstrated a low overpotential of 353 millivolts at 10 milliamperes per square centimeter and a low degradation for OER over 360 hours in acidic electrolyte. A PEMWE containing this catalyst at the anode demonstrated a current density of 2000 milliamperes per square centimeter at 2.47 volts (Nafion 115 membrane) or 4000 milliamperes per square centimeter at 3.00 volts (Nafion 212 membrane) and low degradation in an accelerated stress test.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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