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International Journal of
Chemistry Studies
ARCHIVES
VOL. 8, ISSUE 2 (2024)
Exploring transition metal catalysts for hydrogen evolution: Advancements in electrochemical efficiency and stability
Authors
Dr. Randhir Kumar
Abstract
Hydrogen (H₂) is considered a promising clean energy carrier due to its high energy density and zero-emission combustion products. However, the sustainable production and efficient storage of hydrogen present significant challenges. This paper investigates the role of inorganic compounds in overcoming these challenges, with a specific focus on transition-metal catalysts, metal hydrides, and chemical hydrides for hydrogen production and storage. The methodology involves experimental analysis using water electrolysis for hydrogen production, where various transition metal-based catalysts (Ni, Co, Fe) were tested for hydrogen evolution efficiency, and metal hydrides (MgH₂, NaAlH₄) and chemical hydrides (NaBH₄, NH₃BH₃) were examined for hydrogen storage capacity, desorption temperature, and reversibility. The experimental results show that Ni-based catalysts exhibited the highest hydrogen production rate (0.55 m³/kg·hr) with the lowest overpotential (0.09 V), making them the most efficient for hydrogen production. For hydrogen storage, MgH₂ exhibited the highest storage capacity (6.4 wt%) but required a high desorption temperature (400°C). At the same time, NaBH₄ and NH₃BH₃ exhibited good storage capacities (5.5 wt% and 6.0 wt%, respectively) with lower desorption temperatures (200°C and 180°C) and higher reversibility (15 and 18 cycles, respectively). The results highlight the strengths and limitations of each material for hydrogen production and storage, underscoring the need for further optimisation of material design to enable scalable, sustainable hydrogen systems.
Pages:97-102
How to cite this article:
Dr. Randhir Kumar "Exploring transition metal catalysts for hydrogen evolution: Advancements in electrochemical efficiency and stability". International Journal of Chemistry Studies, Vol 8, Issue 2, 2024, Pages 97-102
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