The development of highly efficient, stable, and selective non-precious-metal catalysts for the oxygen reduction reaction (ORR) in alkaline fuel cell applications is essential. A novel nanocomposite of zinc- and cerium-modified cobalt-manganese oxide on reduced graphene oxide mixed with Vulcan carbon (ZnCe-CMO/rGO-VC) was prepared. Physicochemical characterization reveals uniform distribution of nanoparticles strongly anchored on the carbon support resulting in a high specific surface area with abundant active sites. Electrochemical analyses demonstrate a high selectivity in the presence of ethanol compared to commercial Pt/C and excellent ORR activity and stability with a limiting current density of -3.07 mA cm^-2, onset and half-wave potentials of 0.91 and 0.83 V vs reversible hydrogen reference electrode (RHE), respectively, a high electron transfer number, and an outstanding stability of 91%. Such a catalyst could be an efficient and cost-effective alternative to modern noble-metal ORR catalysts in alkaline media.

In this study, Ag-Mn_xO_y/C composite catalysts deposited on reduced graphene oxide (rGO) and, for the first time on N-doped graphene oxide (NGO), were prepared via a facile synthesis method. The influence of the carbon support material on the activity and stability of the oxygen reduction reaction (ORR) and on the tolerance to ethanol in alkaline medium was focused and investigated. The physicochemical properties of the Ag-Mn_xO_y/C catalysts were analyzed by X-ray diffraction (XRD), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS), Brunauer–Emmett–Teller (BET) method, atomic absorption spectroscopy (AAS), inductively coupled plasma-mass spectrometry (ICP-MS), and thermogravimetric gas analysis (TGA). Electrochemical characterization was performed by rotating disk electrode (RDE) experiments. The results show that the active manganese species MnO₂ was assembled as nanorods and nanospheres on rGO and NGO, respectively. Ag was assumed to be present as very small or amorphous particles. Similar redox processes for Ag-Mn_xO_y/rGO and Ag-Mn_xO_y/NGO were examined via cyclic voltammetry. The Ag-Mn_xO_y/rGO resulted in a more negative diffusion limiting current density of −3.01 mA cm⁻² compared to Ag-Mn_xO_y/NGO. The onset potential of approximately 0.9 V vs. RHE and the favored 4-electron transfer pathway were independent of the support material. Ag-Mn_xO_y/NGO exhibited a higher ORR stability, whereas Ag-Mn_xO_y/rGO showed a better ethanol tolerance.

The controlled cation substitution is an effective strategy for optimizing the density of states and enhancing the electrocatalytic activity of transition metal oxide catalysts for water splitting. However, achieving tailored mesoporosity while maintaining elemental homogeneity and phase purity remains a significant challenge, especially when aiming for complex multi-metal oxides. In this study, we utilized a one-step impregnation nanocasting method for synthesizing mesoporous Mn-, Fe-, and Ni-substituted cobalt spinel oxide (Mn_0.1Fe_0.1Ni_0.3Co_2.5O₄, MFNCO) and demonstrate the benefits of low-temperature calcination within a semi-sealed container at 150-200 °C. The comprehensive discussion of calcination temperature effects on porosity, particle size, surface chemistry and catalytic performance for the alkaline oxygen evolution reaction (OER) highlights the importance of humidity, which was modulated by a pre-drying step. The catalyst calcined at 170 °C exhibited the lowest overpotential (335 mV at 10 mA cm^-2), highest current density (433 mA cm^-2 at 1.7 V vs. RHE, reversible hydrogen electrode) and further displayed excellent stability over 22 h (at 10 mA cm^-2). Furthermore, we successfully adapted this method to utilize cheap, commercially available silica gel as a hard template, yielding comparable OER performance. Our results represent a significant progress in the cost-efficient large-scale preparation of complex multi-metal oxides for catalytic applications.

Electrocatalyst development for alkaline direct ethanol fuel cells is of great importance. In this context we have designed and synthesized cerium-modified cobalt manganese oxide (Ce-CMO) spinels on Vulcan XC72R (VC) and on its mixture with reduced graphene oxide (rGO). The influence of Ce modification on the activity and stability of the oxygen reduction reaction (ORR) in absence and presence of ethanol was investigated. The physicochemical characterization of Ce-CMO/VC and Ce-CMO/rGO–VC reveals CeO₂ deposition and Ce doping of the CMO for both samples and a dissimilar morphology with respect to the nature of the carbon material. The electrochemical results display an enhanced ORR performance caused by Ce modification of CMO resulting in highly stable active sites. The Ce-CMO composites outperformed the CMO/VC catalyst with an onset potential of 0.89 V vs. RHE, a limiting current density of approx. −3 mA cm⁻² and a remaining current density of 91% after 3600 s at 0.4 V vs. RHE. In addition, remarkable ethanol tolerance and stability in ethanol containing electrolyte compared to the commercial Pt/C catalyst was evaluated. These outstanding properties highlight Ce-CMO/VC and Ce-CMO/rGO–VC as promising, selective and ethanol tolerant ORR catalysts in alkaline media.

The intermetallic phases Ni ₃ Te ₂ , NiTe, NiTe _{2− x} & NiTe ₂ were synthesized as carbon-black supported nanoparticles using the vapour–solid synthesis approach and were characterized for their performance in electrocatalytic hydrogen evolution.