Splitting water using renewable electricity to produce green hydrogen is seen by many as essential for achieving net-zero carbon emissions. Currently the cost and efficiency of such hydrogen production is a critical barrier to increasing the use of green hydrogen in replacing fossil fuel.
Using by the Advanced Photon Source (APS), a U.S. Department of Energy (DOE) Office of Science user facility at DOE’s Argonne National Laboratory, a group of scientists have recently demonstrated a new type of low-cost catalyst that could slash the cost and boost the efficiency of green hydrogen production through water splitting. Their results were published in the journal Science.
In 2021, to accelerate the development of affordable hydrogen, DOE launched its first Energy Earthshot–the “Hydrogen Shot”–with the goal of cutting the cost of green hydrogen to $1 per kilogram in one decade, the so-called “1-1-1” goal. Proton exchange membrane water electrolysis is seen as a key technology for meeting this goal.
A proton exchange membrane water electrolyzer consists of a cathode and an anode, separated by a solid proton-conducting membrane. During the electrochemical reaction, water is split at the anode into oxygen, protons and electrons. The protons then migrate across the membrane to the cathode where they re-combine with electrons to produce hydrogen.
The challenge with the current water electrolyzer technology is its use of iridium as the catalyst at the anode. Iridium is one of the rarest and most pricy elements on Earth. Its usage adds a significant capital cost and market uncertainty in meeting the 1-1-1 goal. A low-cost alternative is needed.
In a bid to replace iridium, a team of researchers led by scientists at Argonne explored a new anode catalyst made from manganese and lanthanum-doped cobalt oxide. The catalyst was produced using electrospinning of a metal-organic framework (MOF)-based precursor to create a highly porous crystalline structure with a large surface area, leading to a substantially increased electrocatalytic reaction efficiency. Furthermore, by controlling the manganese and lanthanum doping and distribution, they improved the catalyst conductivity and activity, as well as its stability in the acid environment of the electrolyzer.
The team used several X-ray techniques to analyse the structure of the lanthanum and manganese-doped cobalt catalysts before, during and after water electrolysis. These included X-ray absorption spectroscopy carried out at beamlines 12-BM and 20-BM of the APS and high-energy X-ray diffraction at 17-BM.
The anode was also found to be more stable than previous cobalt oxide catalysts. Interestingly, it was not that stable when first placed in the acidic electrolysis cell, but its stability improved once current started running through it.
X-ray absorption spectroscopy showed that there was a major change in the crystalline structure under electrolysis conditions. According to the researchers, this is critical to decipher the enhanced efficiency and improved stability of this lanthanum and manganese-doped cobalt catalyst. Particularly, it helped the researchers to understand why the catalyst can be stable in the acid environment under the electrolyzer operating condition.
This structural change revealed by X-ray studies was unexpected and could help scientists improve their fundamental understanding of electrocatalysis using metal oxides. It also provides valuable insight into the direction for further improvement of these earthly abundant metal oxide materials as replacements for iridium, which would remove the major cost barrier for widespread uptake of green hydrogen production. – Michael Allen
See: L. Chong1, G. Gao2, J. Wen1, H. Li1, H. Xu1, Z. Green3, J. D. Sugar4, A. J. Kropf1, W. Xu1, X.-M. Lin1, H. Xu3, L.-W. Wang2, D.-J. Liu1,5, “La- and Mn-doped cobalt spinel oxygen evolution catalyst for proton exchange membrane electrolysis” Science 380 6645 609-616 (2023)
Author affiliations: 1Argonne National Laboratory; 2Lawrence Berkeley National Laboratory; 3Giner Inc.; 4Sandia National Laboratories; 5University of Chicago
This work is supported by the US Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office (D. Peterson, project manager), and by Laboratory Directed Research and Development (LDRD) funding of Argonne National Laboratory, provided by the Director, Office of Science, of the US DOE under contract no. DEAC02-06CH11357 through a Maria Goeppert Mayer Fellowship to L.C. Work performed at the Center for Nanoscale Materials and Advanced Photon Source, both US DOE Office of Science User Facilities, was supported by the US DOE, Office of Basic Energy Sciences, under contract no. DE-AC02-06CH11357. The work at Lawrence Berkeley National Laboratory was supported by the Assistant Secretary for Energy Efficiency and Renewable Energy of the US DOE under the Hydrogen Generation program. Sandia National Laboratories is a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia, LLC, a wholly owned subsidiary of Honeywell International, Inc., for the US DOE’s National Nuclear Security Administration under contract no. DE-NA0003525.
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