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Hydrogen production via water splitting is one of the latest low-cost green hydrogen production technologies. The challenge is to develop inexpensive and highly active catalysts. Herein, we present the preparation of electrocatalysts based on cobalt–phosphorus (Co-P) coatings with different P contents for hydrogen and oxygen evolution reactions (HER and OER). The Co-P coatings were deposited on the copper (Cu) surface using the economical and simple method of electroless metal deposition. The morphology, structure, and composition of the Co-P coatings deposited on the Cu surface were studied via scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX), while their activity for HER and OER in 1 M KOH was investigated using linear sweep voltammetry (LSV) and chrono-techniques. It was found that the catalyst activity for both HER and OER depends on the P content of the catalyst and varies based on the highest efficiency for each reaction. The Co-P coating with 11 wt% P exhibited the lowest overpotential value of 98.9 mV for the HER to obtain a current density of 10 mA cm−2 compared to the Co-P coatings with 8, 5, 1.6, and 0.4 wt% P (107.6, 165.9, 218.2, and 253.9 mV, respectively). In contrast, the lowest OER overpotential (378 mV) was observed for the Co-P coating with 8 wt% P to obtain a current density of 10 mA cm−2 as compared to the Co-P coatings with 5, 11, 1.6, and 0.4 wt% P (400, 413, 434, and 434 mV, respectively). These results suggest that the obtained catalysts are suitable for HER and OER in alkaline media. [ABSTRACT FROM AUTHOR]

The electrolysis of water is one of low-cost green hydrogen production technologies. The main challenge regarding this technology is designing and developing low-cost and high-activity catalysts. Herein, we present a strategy to fabricate flexible electrocatalysts based on nickel–iron (NiFe) alloy coatings. NiFe coatings were plated on the flexible copper-coated polyimide surface (Cu/PI) using the low-cost and straightforward electroless metal-plating method, with morpholine borane as a reducing agent. It was found that Ni90Fe10, Ni80Fe20, Ni60Fe40, and Ni30Fe70 coatings were deposited on the Cu/PI surface; then, the concentration of Fe2+ in the plating solution was 0.5, 1, 5, and 10 mM, respectively. The morphology, structure, and composition of NixFey/Cu/PI catalysts have been examined using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and inductively coupled plasma–optical emission spectroscopy (ICP-OES), whereas their activity has been investigated for hydrogen evolution (HER) and oxygen evolution (OER) reactions in 1 M KOH using linear sweep voltammetry (LSVs). It was found that the Ni80Fe20/Cu/PI catalyst exhibited the lowest overpotential value of −202.7 mV for the HER, obtaining a current density of 10 mA cm−2 compared to Ni90Fe10/Cu/PI (−211.9 mV), Ni60Fe40/Cu/PI (−276.3 mV), Ni30Fe70/Cu/PI (−278.4 mV), and Ni (−303.4 mV). On the other hand, the lowest OER overpotential (344.7 mV) was observed for the Ni60Fe40/Cu/PI catalyst, obtaining a current density of 10 mA cm−2 compared to the Ni35Fe65 (369.9 mV), Ni80Fe20 (450.2 mV), and Ni90Fe10 (454.2 mV) coatings, and Ni (532.1 mV). The developed Ni60Fe40/Cu/PI catalyst exhibit a cell potential of 1.85 V at 10 mA cm−2. The obtained catalysts seem to be suitable flexible catalysts for HER and OER in alkaline media. [ABSTRACT FROM AUTHOR]

In this study, 3D-structured NiMo coatings have been constructed via the widely used electrodeposition method on a Ti surface and decorated with very small Au crystallites by galvanic displacement (Au(NiMo)/Ti). The catalysts have been characterized using scanning electron microscopy, energy dispersive X-ray analysis, and inductively coupled plasma optical emission spectroscopy. Different Au(NiMo)/Ti catalysts, which had Au loadings of 1.8, 2.3, and 3.9 µgAu cm−2, were prepared. The electrocatalytic activity of the Au(NiMo)/Ti catalysts was examined with respect to the oxidation of glucose in alkaline media by cyclic voltammetry. It was found that the Au(NiMo)/Ti catalysts with Au loadings in the range of 1.8 up to 3.9 µgAu cm−2 had a higher activity compared to that of NiMo/Ti. A direct glucose-hydrogen peroxide (C6H12O6-H2O2) single fuel cell was constructed with the different Au-loading-containing Au(NiMo)/Ti catalysts as the anode and Pt as the cathode. The fuel cells exhibited an open circuit voltage of ca. 1.0 V and peak power densities up to 8.75 mW cm−2 at 25 °C. The highest specific peak power densities of 2.24 mW µgAu−1 at 25 °C were attained using the Au(NiMo)/Ti catalyst with the Au loading of 3.9 µg cm−2 as the anode. [ABSTRACT FROM AUTHOR]

In this study, one-pot microwave-assisted synthesis was used to fabricate the graphene (GR)-supported PtCoM catalysts where M = Mn, Ru, and Mo. The catalysts with the molar ratios of metals Pt:Co:Mn, Pt:Co:Ru, and Pt:Co:Mo equal to 1:3:1, 1:2:2, and 7:2:1, respectively, were prepared. Catalysts were characterized using Transmission Electron Microscopy (TEM). The electrocatalytic activity of the GR-supported PtCoMn, PtCoRu, and PtCoMo catalysts was evaluated toward methanol oxidation in an alkaline medium employing cyclic voltammetry and chrono-techniques. The most efficient electrochemical characteristics demonstrated the PtCoMn/GR catalyst with a current density value of 144.5 mA cm−2, which was up to 4.8 times higher than that at the PtCoRu(1:2:2)/GR, PtCoMo(7:2:1)/GR, and bare Pt/GR catalysts. [ABSTRACT FROM AUTHOR]

This paper describes the investigation of electrocatalytic activity of the AuCeO2/C catalyst, prepared using the microwave irradiation method, towards the oxidation of sodium borohydride and oxygen reduction reactions in an alkaline medium. It was found that the obtained AuCeO2/C catalyst with Au loading and electrochemically active surface area of Au nanoparticles (AuNPs) equal to 71 µg cm−2 and 0.05 cm2, respectively, showed an enhanced electrocatalytic activity towards investigated reactions, compared with the Au/C catalyst with an Au loading and electrochemically active surface area of AuNPs equal to 78 µg cm−2 and 0.19 cm2, respectively. The AuCeO2/C catalyst demonstrated ca. 4.5 times higher current density values for the oxidation of sodium borohydride compared with those of the bare Au/C catalyst. Moreover, the onset potential of the oxygen reduction reaction (0.96 V) on the AuCeO2/C catalyst was similar to the commercial Pt/C (0.98 V). [ABSTRACT FROM AUTHOR]