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Hydrogen fuel is a non-toxic and source-abundant energetic system, but for its applications in the industry, several issues related to its storage must be resolved. Compounds like NaBH 4 appear as promising hydrogen sources, while can release the latter rapidly under controllable conditions with the use of heterogeneous catalyst systems. In this work, we synthesized a Ni–CoP catalyst by electrodeposition in a three-step process on carbon paper as support. The materials were characterized via SEM-EDS, XRD, and XPS techniques, while the hydrogen evolution reaction (HER) from alkaline NaBH 4 solutions was tested as a batch experiment. Ni–CoP catalyst showed a high amount of H 2 generated in a short time (∼550 mL in 1 min) and remained at 78 and 54% of its initial performance after respectively 100 and 300 h of a continuous hydrolysis process. Our catalyst revealed exceptional performance and stability at higher temperatures and a long process time, which have been a rare subject of investigation in other reports for NaBH 4 hydrolysis in the past. This work paves a new perspective in studying catalysts for hydrogen generation from borohydrides. [Display omitted] • Ni–CoP catalyst was electrodeposited on a carbon support. • Material characterization proved the formation of desired active layers. • High efficiency and stability of the catalyst for a long-term NaBH 4 hydrolysis was revealed. [ABSTRACT FROM AUTHOR]

In recent years, the catalyst efficiency of hydrogen evolution reaction (HER) has been extensively studied. However, the stability of catalysts at high current densities is still a challenge. Herein, layered Ni−Co−P was electrodeposited on carbon fiber paper (CFP) via cyclic voltammetry (CV). This low‐cost electrode exhibits high efficiency and excellent durability for HER in 1 M KOH. To achieve current densities of 10, 100, 500, and 1000 mA cm−2, Ni−Co−P/CFP required overpotentials of 49, 95, 170, and 295 mV, respectively. The layered structure allows the catalyst to fall off layer by layer. After the outer layer of catalyst falls off, the inner layer of catalyst will be exposed to continue working. After 300 h of HER at 1000 mA cm−2, Ni−Co−P/CFP still has a regular morphology and high efficiency. Our work shows that layered Ni−Co−P/CFP has excellent prospects for practical applications. [ABSTRACT FROM AUTHOR]

• Co doped MoS 2 was decorated on nitrogen-doped carbon fiber/carbon paper (NCFCP) by a solvothermal process. • The lattice spacing of (1 0 0) plane of Co-MoS 2 was slightly narrow than that of MoS 2. • The as-prepared Co-MoS 2 /NCFCP hybrids showed enhanced electrochemical activity for HER. In this paper, Co-doped MoS 2 (Co-MoS 2) with various Co/Mo mole ratio (6%–12%) decorated on nitrogen-doped carbon fiber/carbon paper (NCFCP) (Co-MoS 2 /NCFCP) is fabricated by a solvothermal method as an efficient electrocatalyst for hydrogen evolution reaction (HER). The NCFCP substrate is prepared by electrochemical deposition of polypyrrole on carbon paper followed by heat treatment. The obtained 9% Co-MoS 2 /NCFCP hybrid catalyst exhibits an excellent electrocatalytic HER activity with a low overpotential of 174 mV at 10 mA cm−2, a small Tafel slope of 52 mV dec−1 and long-term stability. Thus, Co-MoS 2 /NCFCP hybrid holds high potential as an efficient earth-abundant electrocatalyst material for HER. [ABSTRACT FROM AUTHOR]