Highly Active Electrochemical Hydrogen Production from Water Using CaTiO3 Loaded with Cu2-xO

被引:0
作者
Soltani, Tayyebeh [1 ]
Bergens, Steven H. [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen evolution reaction; Cu2-xO; Non-noble electrocatalysis; PHOSPHIDE NANOPARTICLES; EVOLUTION REACTION; EFFICIENT; CARBON; CO2; ELECTROCATALYST; PHOTOCATALYSTS; REDUCTION; PROGRESS; PAPER;
D O I
10.1007/s11244-024-02018-3
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This study presents the synthesis of calcium titanate (CaTiO3, CTO) perovskite particles via a straightforward flux method, followed by modification with a Cu2-xO cocatalyst to form thin films on both fluorine-doped tin oxide (FTO) and carbon paper substrates. The electrochemical performance of these Cu2-xO/CTO films were rigorously evaluated in the hydrogen evolution reaction (HER). Notably, the CTO modified with 4.0 wt% Cu2-xO on carbon paper exhibited a remarkable increase in HER activity, achieving a current density of 37 mA cm(-2)-significantly higher than that of pristine CTO. The superior performance of the carbon paper-supported films can be attributed to the substrate's unique fibrous porous structure and exceptional conductivity, which collectively enhance electrocatalytic efficiency. This exceptional performance is linked to the high dispersion of Cu2-xO on the CTO surface and the synergistic interactions within the perovskite framework. These findings underscore the potential of Cu2-xO cocatalysts as effective non-noble materials for electrocatalytic water splitting, paving the way for future innovations in sustainable energy technologies.
引用
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页数:9
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