What question did this study set out to answer?

This research aims to evaluate the hydrogen storage capacities of Ben clusters using density functional theory (DFT).

February 8, 2026Open Access

A DFT Study on Ben(n = 10–12) Clusters with Hydrogen Storage Capacity

Key Points

This research aims to evaluate the hydrogen storage capacities of Ben clusters using density functional theory (DFT).
Utilized density functional theory (DFT) for systematic analysis of Ben clusters.
Examined hydrogen adsorption in hollow spherical clusters Be10, Be11, and Be12.
Analyzed adsorption energy, molecular polarization, and forces influencing hydrogen storage.
Conducted desorption temperature calculations to gauge reversible storage potential.
Be10, Be11, and Be12 clusters can store 26, 28, and 30 H2 molecules, respectively.
Achieved hydrogen storage densities well above the target of 5.5 wt%, with values of 31.96 wt%, 31.87 wt%, and 35.87 wt%.
Average adsorption energy measured between 0.16 and 0.19 eV/H2, indicating both physisorption and chemisorption characteristics.
IGMH analysis confirmed physisorption traits of hydrogen molecules.

Abstract

Hydrogen energy has garnered widespread attention as a clean energy source. This study employs density functional theory (DFT) to systematically investigate the hydrogen storage performance of Ben(n = 10–12) clusters. The results reveal that hollow spherical Ben clusters exhibit excellent hydrogen storage capacity while maintaining good thermal stability even after H2 adsorption at room temperature. Specifically, Be10, Be11 and Be12 clusters can adsorb 26, 28, and 30 H2 molecules, achieving hydrogen storage densities of 31.96 wt%, 31.87 wt%, and 35.87 wt%, respectively—far exceeding the U.S. Department of Energy’s target of 5.5 wt%. Calculations indicate an average adsorption energy between 0.16 and 0.19 eV/H2, which lies between physisorption and chemisorption. IGMH isosurface analysis confirms the physisorption characteristics of H2 molecules. PDOS analysis reveals that the hydrogen storage mechanism primarily originates from H2 molecular polarization and van der Waals forces arising from orbital hybridization between hydrogen atoms and the substrate. Desorption temperature calculations show that, above 216 K, this material demonstrates potential for reversible hydrogen storage. This study demonstrates that these three hollow spherical beryllium cluster systems are ideal candidates for achieving ultra-high-capacity reversible hydrogen storage.

Bookmark

View Full Paper