分解水
电解水
微波食品加热
制氢
材料科学
氢
能量载体
除氧
可再生能源
电力转天然气
工艺工程
化学工程
电解
纳米技术
电解质
化学
计算机科学
电极
电气工程
电信
工程类
催化作用
物理化学
有机化学
光催化
作者
José M. Serra,J. F. Borrás-Morell,Beatriz García‐Baños,María Balaguer,Pedro J. Plaza-González,Joaquín Santos,David Catalán‐Martínez,Laura Navarrete,José M. Catalá‐Civera
出处
期刊:Nature Energy
[Springer Nature]
日期:2020-11-02
卷期号:5 (11): 910-919
被引量:104
标识
DOI:10.1038/s41560-020-00720-6
摘要
Supplying global energy demand with CO2-free technologies is becoming feasible thanks to the rising affordability of renewable resources. Hydrogen is a promising vector in the decarbonization of energy systems, but more efficient and scalable synthesis is required to enable its widespread deployment. Here we report contactless H2 production via water electrolysis mediated by the microwave-triggered redox activation of solid-state ionic materials at low temperatures (<250 °C). Water was reduced via reaction with non-equilibrium gadolinium-doped CeO2 that was previously in situ electrochemically deoxygenated by the sole application of microwaves. The microwave-driven reduction was identified by an instantaneous electrical conductivity rise and O2 release. This process was cyclable, whereas H2 yield and energy efficiency were material- and power-dependent. Deoxygenation of low-energy molecules (H2O or CO2) led to the formation of energy carriers and enabled CH4 production when integrated with a Sabatier reactor. This method could be extended to other reactions such as intensified hydrocarbons synthesis or oxidation. Hydrogen is a promising vector in the decarbonization of energy systems, but more efficient and scalable synthesis is required to enable its widespread deployment. Towards that aim, Serra et al. present a microwave-based approach that allows contactless water electrolysis that can be integrated with hydrocarbon production.
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