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Improved Durability and Activity in Pt/Mo 2 C Fuel Cell Cathodes by Magnetron Sputtering of Tantalum
Author(s) -
Hamo Eliran R.,
Rosen Brian A.
Publication year - 2021
Publication title -
chemelectrochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 59
ISSN - 2196-0216
DOI - 10.1002/celc.202100591
Subject(s) - sputtering , materials science , tantalum , cathode , corrosion , sputter deposition , proton exchange membrane fuel cell , electrochemistry , platinum , electrolyte , chemical engineering , metallurgy , catalysis , electrode , thin film , chemistry , nanotechnology , biochemistry , engineering
Cost reduction together with durability represent the primary challenges for cathode catalysts in polymer electrolyte membrane fuel cells (PEMFCs). The catalyst is often supported by carbon, which suffers from parasitic corrosion, particularly during start‐up and shut‐down operations. Transition metal carbides (TMCs) have attracted attention as a potential replacement for carbon supports because some of them have electronic structures likened to noble metals. Mo 2 C has shown promising activity as platinum support for the oxygen reduction reaction (ORR) but can suffer from oxidation and dissolution. Here, Mo 2 C supports are modified by surface tantalum (Ta) treatment using a variety of DC magnetron sputtering operating parameters. All supports modified by Ta showed improved corrosion resistance compared to the untreated support. Pt/Mo 2 C modified with Ta using a 500 V bias, 6 mTorr working pressure, and 2 min sputter time additionally showed improved kinetic current density and mass activity. Ta sputtering under these conditions were applied to the cathode side of a Pt/Mo 2 C membrane electrode assembly and showed significantly improved durability when subjected to an accelerated stress test. Ta‐modified Pt/Mo 2 C cathodes showed resistance to void formation and loss of electrochemical surface area. Ta magnetron sputtering can therefore be considered a viable surface treatment for improving the activity and stability of PEMFCs using Mo 2 C‐based supports.