Urea is often present in waste water but can be used in powering fuel cells and as an alternative oxidation substrate to water in an electrolyser. However, an insufficient mechanistic understanding and the lack of efficient catalysts for the urea oxidation reaction have hampered the development of such applications. Here we demonstrate that a nickel ferrocyanide (Ni2Fe(CN)(6)) catalyst supported on Ni foam can drive the urea oxidation reaction with a higher activity and better stability than those of conventional Ni-based catalysts. Our experimental and computational data suggest a urea oxidation reaction pathway different from most other Ni-based catalysts that comprise NiOOH derivatives as the catalytically active compound. Ni2Fe(CN)(6) appears to be able to directly facilitate a two-stage reaction pathway that involves an intermediate ammonia production (on the Ni site) and its decomposition to N-2 (on the Fe site). Owing to the different rate-determining steps with more favourable thermal/kinetic energetics, Ni2Fe(CN)(6) achieves a 100 mA cm(-2) anodic current density at a potential of 1.35 V (equal to an overpotential of 0.98 V). Urea oxidation could be a lower-energy alternative to water oxidation in hydrogen-producing electrolysers, but improved catalysts are required to facilitate the reaction. Geng et al. report nickel ferrocyanide as a promising catalyst and suggest that it operates via a different pathway to that of previous materials.
[1]Anhui Univ, Sch Chem & Chem Engn, Hefei, Peoples R China.
[2]Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA, Australia.
[3]Chizhou Univ, Sch Mat & Environm Engn, Chizhou, Peoples R China.
[4]Univ Sci & Technol, Natl Synchrotron Radiat Lab, Hefei, Peoples R China.
[5]Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA.
(8.0+极速模式)