RESUMEN
The higher amount of Pt usage and its poisoning in methanol oxidation reaction in acidic media is a major setback for methanol fuel cells. Herein, a promising dual application high-performance electrocatalyst has been developed for hydrogen evolution and methanol oxidation. A low Pt-content nanoalloy co-doped with Cu, Mn, and P is synthesized using a modified solvothermal process. Initially, ultrasmall ≈2.9 nm PtCuMnP nanoalloy is prepared on N-doped graphene-oxide support and subsequently, it is characterized using several analytical techniques and examined through electrochemical tests. Electrochemical results show that PtCuMnP/N-rGO has a low overpotential of 6.5 mV at 10 mA cm-2 in 0.3 m H2 SO4 and high mass activity for the hydrogen evolution reaction. For the methanol oxidation reaction, the PtCuMnP/N-rGO electrocatalyst exhibits robust performance. The mass activity of PtCuMnP/N-rGO is 6.790 mA mg-1 Pt , which is 7.43 times higher than that of commercial Pt/C (20% Pt). Moreover, in the chronoamperometry test, PtCuMnP/N-rGO shows exceptionally good stability and retains 72% of the initial current density even after 20,000 cycles. Furthermore, the PtCuMnP/N-rGO electrocatalyst exhibits outstanding performance for hydrogen evolution and methanol oxidation along with excellent anti-poisoning ability. Hence, the developed bifunctional electrocatalyst can be used efficiently for hydrogen evolution and methanol oxidation.
RESUMEN
The selection and design of new electrode materials for energy conversion and storage are critical for improved performance, cost reduction, and mass manufacturing. A bifunctional anode with high catalytic activity and extended cycle stability is crucial for rechargeable lithium-ion batteries and direct borohydride fuel cells. Herein, a high entropy novel three-dimensional structured electrode with Pr-doped hollow NiFeP nanoflowers inlaid on N-rGO was prepared via a simple hydrothermal and self-assembly process. For optimization of Pr content, three (0.1, 0.5, and 0.8) different doping ratios were investigated. A lithium-ion battery assembled with NiPr0.5 FeP/N-rGO electrode achieved an outstanding specific capacity of 1.61â Ah g-1 at 0.2â A g-1 after 100â cycles with 99.3 % Coulombic efficiencies. A prolonged cycling stability of 1.02â Ah g-1 was maintained even after 1000â cycles at 0.5â A g-1 . In addition, a full cell battery with NiPr0.5 FeP/N-rGOâ¥LCO (Lithium cobalt oxide) delivered a promising cycling performance of 0.52â Ah g-1 after 200â cycles at 0.15â A g-1 . Subsequently, the NiPr0.5 FeP/N-rGO electrode in a direct borohydride fuel cell showed the highest peak power density of 93.70â mW cm-2 at 60 °C. Therefore, this work can be extended to develop advanced electrode for next-generation energy storage and conversion systems.