Molecular Hydrogen Chemisorbed on Unsaturated Coordinate Ti: A New Designed Materials for Hydrogen Storage
Year: 2025
Type: article
Abstract: Solid‐state hydrogen storage materials with optimal binding energy are essential for hydrogen storage and transportation applications and pose long‐standing challenges. Current technologies, including molecular physisorption materials (e.g., metal–organic frameworks (MOFs), carbon nanotubes (CNTs), activated carbons (ACs)) and atomic chemisorption materials (e.g., MgH2, LiBH4, NH4BH4), fall short of meeting practical application requirements. Therefore, designing and constructing new solid‐state hydrogen storage materials at the atomic level is critically important. In this study, the use of defect engineering is explored to modulate hydrogen adsorption sites on TiO2 surfaces. The results demonstrate that low‐coordinated titanium (Ti) atoms on TiO2 can serve as effective hydrogen adsorption sites, storing hydrogen through molecular chemisorption with significantly enhanced adsorption energy compared to Ti atoms in high coordination states. Moreover, the adsorbed hydrogen remains in molecular form, facilitating easy desorption at room temperature, unlike titanium hydride, which requires high temperatures for desorption. This approach provides a promising pathway for developing efficient hydrogen storage materials by leveraging the unique properties of low‐coordinated Ti atoms on TiO2 surfaces.
Source: Advanced Materials Interfaces
Institutions: Griffith University, Sun Yat-sen University, Queensland University of Technology, Tamkang University, South China Agricultural University, Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, South China University of Technology, University of Wollongong, ARC Centre of Excellence for Electromaterials Science, Zhejiang University of Technology
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $3,100
Award: G4991119866
OpenAlex ID: W4410240734
