Hydrogen as an energy carrier: Production pathways, thermochemical constraints, and electrolysis-based green hydrogen prospects

制氢 电解水 电力转天然气 蒸汽重整 氢 高温电解 氢经济 能量载体 析氧 分解水 碱性水电解 吉布斯自由能 氢燃料 可再生能源 高压电解 化学 电解 聚合物电解质膜电解 热力学 热化学循环 化学工程 氢技术 催化作用 材料科学 工艺工程 氧化物 合成气 豆马勃属 甲烷转化炉
作者
Nitesh Subedi,Md Monjur Hossain Bhuiyan,Md. Ariful Islam,Becerril Corral Alfredo,Zahed Siddique
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:220: 154100-154100
标识
DOI:10.1016/j.ijhydene.2026.154100
摘要

Hydrogen is widely recognized as a key energy carrier for enabling deep decarbonization across power generation, transportation, and energy-intensive industrial sectors. However, large-scale deployment from renewable energy remains constrained by the efficiency and cost of current production routes. This review provides a comprehensive assessment of hydrogen production technologies, encompassing both thermochemical processes and electrolysis-based green hydrogen systems. Conventional pathways, including steam methane reforming (SMR) and coal and biomass gasification, are evaluated from thermodynamic and kinetic perspectives, with emphasis on reaction energetics, process efficiency, and carbon emissions. The thermodynamics and kinetics of water electrolysis are examined in detail, highlighting the roles of Gibbs free energy, overpotentials, temperature, and kinetically sluggish oxygen evolution reactions. Recent advances in alkaline, proton exchange membrane (PEM), and solid oxide electrolyzer cells (SOECs) are critically assessed with respect to efficiency, durability, scalability, and compatibility with variable renewable electricity. Emerging electrocatalysts, particularly layered double hydroxide (LDH)-based materials, are discussed as effective routes for accelerating oxygen evolution kinetics and reducing system-level electrolysis losses. By explicitly linking thermodynamic and kinetic constraints with system-level loss analysis and catalyst development, this review presents a unified framework for evaluating hydrogen production technologies beyond conventional efficiency comparisons. The analysis demonstrates that efficiency improvements in hydrogen production are fundamentally constrained by irreversible anodic kinetics rather than thermodynamic minimum work, positioning LDH-based oxygen evolution catalysts as the most impactful lever for near-term cost and performance gains in water electrolysis. • Fossil-based hydrogen supplies >95% via SMR and gasification, emitting ∼830 Mt CO 2 yr −1 . • Reaction enthalpies quantify reforming and gasification thermodynamic limits. • Electrolysis efficiency is limited by OER activation losses. • LDH catalysts reduce anodic overpotential and improve electrolyzer efficiency. • A unified thermodynamic–kinetic framework evaluates hydrogen pathway scalability.
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