Discovery of Catalysts That Prevent Boil-Off Losses in Liquid Hydrogen Production

— Promoting Stabilization of Hydrogen Molecules (= Exothermic Reaction) Before Liquefaction and Contributing to the Realization of a Hydrogen Society —

NIMS (National Institute for Materials Science)
Institute of Science Tokyo
Kochi University of Technology

A joint research team from NIMS, the Institute of Science Tokyo, and Kochi University of Technology discovered high-performance catalysts capable of significantly reducing "boil-off losses," which had been a long-standing issue in liquid hydrogen storage and transportation. These composite catalysts, in which metallic nanoparticles, such as iron, are supported on silicon dioxide (silica) or other low-cost oxide, demonstrate significantly superior performance compared to conventional iron oxide-based catalysts. In this research, the team demonstrated a new mechanism where ortho to para hydrogen conversion is promoted, not by magnetism as in conventional mainstream mechanisms, but by an inhomogeneous electric field on the surface of the catalyst. This research result, which is expected to contribute to a hydrogen energy society, was published in The Journal of Physical Chemistry Letters on March 12, 2026.

Background

Hydrogen, a promising source of next-generation clean energy, needs to be liquefied at a cryogenic temperature of −253°C or lower in order to be stored and transported efficiently. Meanwhile, there are two types of hydrogen molecules with different nuclei spin directions: ortho hydrogen and para hydrogen (Figure). The ortho-para ratio in room-temperature hydrogen gas is 3:1, whereas at a liquid hydrogen temperature, hydrogen is stable when almost 100% is in the para form. However, if hydrogen is rapidly liquefied, the conversion from ortho hydrogen to para hydrogen is delayed, and a substantial quantity of unstable ortho hydrogen will remain in the liquid. This residual ortho hydrogen continues to be converted during storage, causes energy release and partial vaporization of liquid hydrogen, and results in substantial loss (the red broken line in Figure). In order to prevent the loss, a high-performance catalyst that converts ortho hydrogen to para hydrogen before liquefaction (the blue broken line in Figure) is needed. However, conventional catalysts using magnetism, such as iron oxide, were insufficient in performance.

Key Findings

The research team proposed an original hypothesis that ortho-para hydrogen conversion is promoted, not by conventional magnetism, but by an inhomogeneous electric field (uneven static electricity) generated by the cation/anion arrangement on the surface of an oxide catalyst. Based on this hypothesis, the team succeeded in developing high-performance catalysts that surpass conventional catalysts, by combining low-cost oxide like silica (SiO2) and alumina (Al2O3) with common metallic nanoparticles, such as iron (Fe) and cobalt (Co).

Figure. Hydrogen gas is a mixture of ortho hydrogen and para hydrogen. Their ratio depends on temperature, and is also greatly affected by the cooling rate. If hydrogen is rapidly cooled without a catalyst, the conversion from ortho hydrogen to para hydrogen is delayed as shown by the red broken line in the figure, and a substantial quantity of energetically unstable ortho hydrogen will remain in the liquid. The residual ortho hydrogen continues to be converted slowly during storage, and releases energy. This gives rise to partial vaporization of liquid hydrogen, and causes boil-off losses during storage. Therefore, it is essential to use a catalyst that completely converts ortho hydrogen to para hydrogen before the liquefaction process (shown by the blue broken line). Such catalyst prevents boil-off losses during storage and increases the hydrogen handling efficiency.

Future Outlook

Liquid hydrogen plays a particularly important role in long-distance maritime transportation between hydrogen producing/exporting countries, such as Australia and the Middle East, and hydrogen importing countries, such as Japan. The catalysis design approach and high-performance catalysts discovered in this research are expected to contribute to the development of a hydrogen economy in Japan.

Other Information

  • This project was conducted by a research team consisting of Hideo Hosono (Team Leader, ElectroActive Materials Team, Research Center for Materials Nanoarchitectonics (MANA), NIMS [also Honorary Professor, Institute of Science Tokyo]) and Hideki Abe (Group Leader, Hydrogen Production Catalyst Materials Group, Research Center for Energy and Environmental Materials (GREEN), NIMS) as well as Takeshi Fujita (Professor, Kochi University of Technology). The work was supported by JST-Mirai program JPMJMI18A3.
  • This research result was published online in The Journal of Physical Chemistry Letters on March 12, 2026.

Published Paper

Title : Exploring Ortho–Para Hydrogen Conversion Catalysts Based on Surface Electric Field Gradient
Authors : Hiroshi Mizoguchi, Yuichi Shirako, Shusaku Shoji, Hideki Abe, Takeshi Fujita, and Hideo Hosono
Journal : The Journal of Physical Chemistry Letters
DOI : 10.1021/acs.jpclett.6c00357
Publication Date : March 12, 2026

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Contact information

Regarding This Research

Hiroshi Mizoguchi
ElectroActive Materials Team
Research Center for Materials Nanoarchitectonics
National Institute for Materials Science
E-Mail: MIZOGUCHI.Hiroshi=nims.go.jp (Please change "=" to "@")
TEL: +81-29-851-3354 (ext.4705)
Hideki Abe
Hydrogen Production Catalyst Materials Group
Research Center for Energy and Environmental Materials
National Institute for Materials Science
E-Mail: ABE.Hideki=nims.go.jp (Please change "=" to "@")
TEL: +81-29-860-4803
Hideo Hosono
ElectroActive Materials Team
Research Center for Materials Nanoarchitectonics
National Institute for Materials Science,
Honorary Professor
Institute of Science Tokyo
E-Mail: HOSONO.Hideo=nims.go.jp (Please change "=" to "@")
TEL: +81-45-924-5009
Takeshi Fujita
Professor
School of Engineering Science
Kochi University of Technology
E-Mail: fujita.takeshi=kochi-tech.ac.jp (Please change "=" to "@")
TEL: +81-887-57-2508

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