The development of alternate catalysts that utilize non-precious metal based electrode materials such as the first row transition metal complexes is an important goal for economic fuel cell design. In this direction, a new FeS cubane type cluster, [PPh][FeS(DMET)] (1) (DMET = cis-1,2-dicarbomethoxyethylene dithiolate) and its composite with functionalized graphene, (1@graphene) have been synthesized and characterized. The presence of nanocrystalline structures on graphene matrix in TEM and SEM images of 1@graphene indicate that the cluster (1) has been immobilized. The composite, 1@graphene evolves H gas from p-toluene sulfonic acid (TsOH) in a mixture of HO and CHCN under ambient conditions with a significant turnover number of 3200. 1@graphene electro-catalyzes H evolution at E, -1.2 V with remarkable throughput, catalytic efficiency and stability in only HO or in only CHCN. The FeS cluster (1) alone electro-catalyzes hydrogen evolution at E, -0.75 V from TsOH in CHCN. The X-ray crystal structure of the FeS cluster (1) (λ, CHCl, 823 nm; ε, 2200 mol cm) shows that it is dianionic with a cumulative oxidation state of +2.5 for the iron centers and short C-S bond distances (ca., 1.712 Å & 1.727 Å) indicating the presence of sulfur based radicals.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717245 | PMC |
http://dx.doi.org/10.1038/s41598-017-17121-7 | DOI Listing |
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