共 13 条
Pt nanoparticles decorated 3D printed hierarchical porous titanium alloy scaffolds for hydrogen evolution reactions at amper-level current densities
被引:0
|作者:
Song, Hui
[1
]
Ran, Guangshun
[1
]
Xu, Jiangwen
[1
,2
]
Lin, Chunxia
[1
]
Yang, Zicong
[1
]
Chang, Yukun
[1
]
Zhou, Wenyuan
[1
]
Li, Hongyi
[1
,2
]
Wang, Xinxin
[1
]
Wang, Jinshu
[1
]
机构:
[1] Beijing Univ Technol, Coll Mat Sci & Engn, Beijing 100124, Peoples R China
[2] Beijing Univ Technol, Coll Carbon Neutral Future Technol, Beijing 100124, Peoples R China
基金:
中国国家自然科学基金;
北京市自然科学基金;
关键词:
3D Printing;
Self-supporting;
Hierarchical porous;
High current density;
Hydrogen evolution reaction;
ENERGY;
ELECTROCATALYSTS;
D O I:
10.1016/j.jallcom.2025.178941
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Most reported 3D electrodes currently lack a macroscopically ordered porous structure, hindering transport efficiency optimization and reducing the utilization of active materials and the surface area of the electrodes. In this study, a micro- and macroscopic hierarchical porous titanium alloy electrode modified with Pt nanoparticles (Pt/TNTs@3D-TC4) was created using electron beam melting (EBM) technology, anodic oxidation, and a water bath method. The micrometer-scale network structure enhanced electrolyte diffusion and bubble removal, whereas the surface nanostructures provided numerous anchoring sites for Pt nanoparticles. This unique micro- nano structure offers a large specific surface area and efficient mass transport, resulting in excellent acidic HER performance and stability at industrial current densities. X-ray photoelectron spectroscopy (XPS) and X-ray adsorption fine structure (XAFS) analyses confirmed an electronic metal-support interaction (EMSI) between Pt and TiO2 nanotubes (TNTs), with Pt nanoparticles anchored via Pt-O-Ti bonds. The electrode achieved the overpotential of 42 mV at-10 mA cm- 2, and 267 and 378 mV at-0.5 A cm- 2 and 1 A cm- 2, respectively. Exceptional stability was demonstrated, without significant deactivation after 120 h at 0.5 A cm- 2. This study offers a novel strategy in the industrial application of high-performance electrodes for electrochemical energy conversion.
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