Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Liquid hydrogen in protonic chabazite.

Adriano Zecchina1, Silvia Bordiga, Jenny G Vitillo

  • 1Dipartimento di Chimica IFM and NIS Centre of Excellence, Via P. Giuria 7, I-10125 Torino, Italy.

Journal of the American Chemical Society
|April 28, 2005
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Diamine Grafting of Pyrazole-Based MOF-303 for Diluted-Source CO<sub>2</sub> Capture.

Small (Weinheim an der Bergstrasse, Germany)·2026
Same author

Breaking the 1250 nm Barrier: A Computational Approach to Light Upconversion via Triplet-Triplet Annihilation in the Silica Telecom Band.

ACS applied energy materials·2026
Same author

A Leap toward Quasi-Solid-State Chloride-Ion Batteries with Metal-Organic Frameworks.

ACS energy letters·2026
Same author

Peptide Nucleic Acid Probes for MicroRNA Detection: Mg<sup>2+</sup> Ion Effect, Surface Hybridization, and Surface Plasmon Resonance Biosensing.

ACS measurement science au·2025
Same author

Understanding Surface Properties in CeO<sub>2</sub> Catalysts for the Synthesis of Dimethyl Carbonate: A Combined In Situ IR and NEXAFS Study.

The journal of physical chemistry. C, Nanomaterials and interfaces·2025
Same author

Author Correction: Introducing metal-sulfur active sites in metal-organic frameworks via post-synthetic modification for hydrogenation catalysis.

Nature chemistry·2025

Molecular hydrogen (H2) storage via adsorption is reversible but requires extreme conditions. H-SSZ-13 zeolite, with its unique structure and proton sites, enables efficient H2 densification under favorable conditions.

Area of Science:

  • Materials Science
  • Chemical Engineering
  • Physical Chemistry

Background:

  • Molecular hydrogen (H2) storage via adsorption offers reversible charging/discharging, unlike dissociative methods with kinetic limitations.
  • Current H2 adsorption strategies face challenges due to weak interactions, necessitating low temperatures and high pressures.
  • High surface area materials with polarizing sites are crucial for improving H2 storage working conditions.

Purpose of the Study:

  • To investigate hydrogen adsorption in zeolites under cryogenic conditions.
  • To evaluate the potential of H-SSZ-13 zeolite for enhanced hydrogen storage.
  • To understand the role of material properties in facilitating H2 densification.

Main Methods:

  • Volumetric adsorption measurements at 15 K.

Related Experiment Videos

  • Infrared spectroscopy analysis at 15 K.
  • Characterization of hydrogen adsorption in a series of zeolites, focusing on H-SSZ-13.

    • Main Results:

    • H-SSZ-13 zeolite demonstrated significant hydrogen densification within its nanopores.
    • The cooperative effects of high surface area, internal pore topology, and proton binding sites were identified.
    • Favorable temperature and pressure conditions for hydrogen adsorption were achieved in H-SSZ-13.

    Conclusions:

    • H-SSZ-13 zeolite presents a promising material for efficient molecular hydrogen storage.
    • The unique structural and chemical properties of H-SSZ-13 overcome limitations of traditional adsorption methods.
    • This study highlights the potential of tailored zeolites for practical hydrogen energy applications.