Platinum group metal-free NiMo hydrogen oxidation catalysts: high performance and durability in alkaline exchange membrane fuel cells. Issue 46 (16th November 2017)

• Record Type: Journal Article
• Authors: Kabir, Sadia; Lemire, Kenneth; Artyushkova, Kateryna; Roy, Aaron; Odgaard, Madeleine; Schlueter, Debbie; Oshchepkov, Alexandr; Bonnefont, Antoine; Savinova, Elena; Sabarirajan, Dinesh C.; Mandal, Pratiti; Crumlin, Ethan J.; Zenyuk, Iryna V.; Atanassov, Plamen; Serov, Alexey
• Is Part Of: Journal of materials chemistry. Volume 5:Issue 46(2017)
• Page Start: 24433
• Page End: 24443
• Publication Date: 2017-11-16
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c7ta08718g
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : A highly active NiMo electrocatalyst for HOR in alkaline media with power density at 0.5 V higher than 100 mW cm −2 (peak value of 120 mW cm −2 ), which is similar to palladium was synthesized and comprehensively studied. Abstract : We introduce a new platinum group metal-free (PGM-free) hydrogen oxidation electrocatalyst with superior performance in anodes of alkaline exchange membrane fuel cells (AEMFCs). A carbon-supported bimetallic nickel–molybdenum catalyst was synthesized by thermal reduction of transition metal precursors on the surface of a carbon support (KetjenBlack 600J). The mass-weighted activity of 4.5 A gMe −1 determined in a liquid electrolyte 0.1 M NaOH using a rotating disk electrode (RDE) technique is comparable to the value reported for Pd/C with a comparable particle size under similar conditions. This NiMo/KB catalyst was integrated in a membrane electrode assembly (MEA) using an alkaline exchange membrane and ionomer. Single AEMFC tests performed in a H2 /O2 configuration resulted in a record power density output of 120 mW cm −2 at 0.5 V, the MEA was found to be durable under the conditions of potential hold of 0.7 V for 115 h. For the first time, operando X-ray computed tomography (CT) experiments were performed demonstrating liquid water formation at the PGM-free anode during cell operation, and in situ ambient pressure X-ray photoelectron spectroscopy (APXPS) and X-ray absorption spectroscopy (APXAS) were used to study the role of molybdenum in hydrogen adsorption.