In the race to build a practical hydrogen economy, one stubborn problem has shadowed every optimistic forecast: how to store and release hydrogen safely, cheaply, and on demand. Hydrogen itself is the cleanest fuel imaginable—burning it produces nothing but water—but the gas is notoriously difficult to contain. Compressed tanks are heavy and energy-intensive, liquefied hydrogen must be chilled to a frigid minus 253 degrees Celsius, and metal hydrides tend to be bulky and slow to recharge. Now, a team of researchers working across Malaysia and China has reported a striking advance in an alternative approach: chemically unlocking hydrogen from a solid, stable compound called ammonia borane, using a new catalyst built from inexpensive nickel, copper, and molybdenum oxides. Their work, published in Catalysis Letters, describes a hierarchical nanocatalyst that releases hydrogen from ammonia borane dissolved in methanol with remarkable speed, low energy input, and durability that survived repeated use.
Ammonia borane, a white crystalline solid with the formula NH₃BH₃, has long been considered one of the most attractive chemical hydrogen carriers. It is stable in air at room temperature, non-toxic by the standards of many industrial chemicals, and packs a high gravimetric hydrogen content—nearly 20 percent by mass, meaning that every kilogram of the material holds the equivalent of almost 200 liters of hydrogen gas at standard conditions. The challenge lies in getting that hydrogen out. Ammonia borane can release hydrogen through several pathways: hydrolysis, where water breaks the compound apart; thermolysis, which requires heating to elevated temperatures; and alcoholysis, where an alcohol such as methanol attacks the B–N framework and liberates three equivalents of hydrogen gas per molecule. Methanolysis is particularly appealing because methanol is liquid at ambient conditions, easy to pump and dose, and the reaction can proceed at room temperature or slightly above—provided a good catalyst is present.
The catalyst problem is where most of the field’s difficulties have concentrated. The most active catalysts reported to date for ammonia borane dehydrogenation rely on precious metals such as ruthenium, platinum, or palladium, which deliver superb kinetics but at costs that make large-scale deployment questionable. Researchers have therefore intensively explored cheaper alternatives built from copper, nickel, and cobalt, often in the form of mixed oxides, phosphides, or heterostructured composites. Each of these first-row transition metals brings something useful to the table: copper sites interact with the B–H bonds of ammonia borane and methanol molecules, while nickel and its oxides are known to activate N–H bonds and assist in electron transfer. Combining them effectively, however, has proven tricky—simple physical mixtures rarely match the performance of well-engineered interfaces.
The team behind the new study, led by Wei Gong of Qingdao University of Technology and Meng Guan Tay of Universiti Malaysia Sarawak, with contributions from Hao Li at Huizhou University, took a one-pot hydrothermal synthesis route followed by calcination to produce a composite they denote NiO–Cu₃Mo₂O₉. The hydrothermal step—essentially growing crystals from an aqueous precursor solution inside a sealed, pressurized vessel at elevated temperature—allowed the copper molybdate phase to form hierarchical, flower-like architectures, a morphology previously associated with high surface areas and abundant exposed active sites. The subsequent calcination converted the nickel precursor into nickel oxide nanosheets intimately intergrown with the Cu₃Mo₂O₉ framework. The result is not merely a blend of two oxides but a chemically and electronically coupled system in which the two phases share interfaces at the nanometer scale.
Characterization of the material was thorough and multitechnique. Powder X-ray diffraction confirmed the crystalline phases of both NiO and Cu₃Mo₂O₉, ruling out unwanted impurity phases. Scanning and transmission electron microscopy revealed the hierarchical morphology, showing how the composite’s structure provides short diffusion pathways for reactants and abundant boundary regions where the two oxides meet. X-ray photoelectron spectroscopy provided evidence of electronic interaction between the components—shifts in binding energies consistent with charge redistribution at the NiO–Cu₃Mo₂O₉ interfaces, the kind of electronic coupling that underlies synergistic catalysis. Brunauer–Emmett–Teller nitrogen adsorption measurements quantified the surface area and porosity, parameters that matter enormously for a heterogeneous catalyst because reactions can only occur where the reactants can physically reach the surface.
The catalytic performance numbers are the heart of the story. When ammonia borane was dissolved in methanol in the presence of the NiO–Cu₃Mo₂O₉ catalyst, hydrogen was released at a rate of about 170 milliliters of H₂ per minute under the optimized conditions. Normalized to catalyst mass, the hydrogen generation rate reached 1,200 milliliters of hydrogen per gram of catalyst per minute—a figure that dwarfs the 360 milliliters per gram per minute achieved by Cu₃Mo₂O₉ alone. In other words, adding the NiO component more than tripled the activity, a clear signature of the synergistic effect the synthesis was designed to create. The turnover frequency, a measure of how many hydrogen molecules a single active site produces per minute, was 49.8 per minute—high for a non-precious-metal oxide system and competitive with many literature catalysts that rely on far more expensive ingredients.
Perhaps even more important for real-world viability is the catalyst’s stability and its low energy barrier. Kinetic analysis across a range of temperatures yielded an activation energy of just 18.9 kilojoules per mole, a remarkably low value indicating that the reaction proceeds with only a modest thermal push; the optimum operating temperature was found to be a mild 30 degrees Celsius, essentially ambient. Low activation energy translates directly into lower operational costs and simpler reactor engineering, since no elaborate heating systems are required. And when the researchers recovered the catalyst and reused it, the material retained more than 90 percent of its initial activity after six consecutive cycles—an encouraging sign that the hierarchical structure and interfacial coupling resist the sintering, leaching, and deactivation that commonly plague oxide-based catalysts in liquid-phase reactions.
The kinetic studies also mapped how the reaction responds to its conditions. The rate increased with both ammonia borane dosage and catalyst loading, consistent with a heterogeneous process whose speed is governed by the number of available active sites and the concentration of the substrate in solution. Such systematic kinetic profiling, the authors note, provides the foundation for mechanistic understanding: it suggests that the rate-determining steps likely involve the interaction of methanol molecules with copper sites and the activation of B–H and N–H bonds at the coupled oxide interfaces, with the NiO component tuning the electron density of adjacent copper molybdate regions. Real-time Fourier transform infrared spectroscopy, performed by the Huizhou team, allowed the researchers to track intermediate species during the reaction, offering direct spectroscopic windows into the catalytic sequence.
The broader context makes this work more than a single data point. Research groups worldwide have been building a library of non-noble catalysts for ammonia borane conversion—hollow cobalt oxide shells decorated with copper and nickel oxides, heterostructured NiO–CuO nanosheets that harness visible light, copper molybdate–nickel molybdate microspheres, and phosphide-based systems among them. Each design probes a different facet of the same underlying question: how to engineer interfaces where cheap metals cooperate to break strong chemical bonds. The new NiO–Cu₃Mo₂O₉ composite fits squarely into this trend but stands out for the combination of exceptionally low activation energy, high hydrogen generation rate, and robust recyclability achieved in a single material prepared by a simple, scalable one-pot method. The hydrothermal–calcination route requires no exotic equipment, and the constituent elements—nickel, copper, molybdenum, and oxygen—are abundant and inexpensive compared with the platinum-group metals that dominate the most active catalysts.
What remains to be demonstrated is the path from laboratory flask to practical system. A hydrogen fuel cell vehicle or a stationary power application would need not just fast hydrogen release but a complete cycle: hydrogenation of a spent fuel to regenerate ammonia borane, efficient catalyst recovery, and control of byproducts. Methanolysis of ammonia borane yields ammonium borate derivatives in solution, and regenerating the carrier from those spent products remains an energy-intensive step that the field has not fully solved. Nevertheless, advances on the release side of the cycle are essential, and the numbers reported here—1,200 milliliters of hydrogen per gram per minute, a turnover frequency approaching 50 per minute, an activation energy under 19 kilojoules per mole, and stability across six cycles—move the benchmark for what Earth-abundant oxide catalysts can achieve. As the search for practical hydrogen storage chemistry intensifies, catalysts like this one suggest that the missing piece may not be exotic chemistry at all, but clever engineering of the humble interfaces between common metal oxides.
Subject of Research: Development of a NiO–Cu₃Mo₂O₉ hierarchical nanocatalyst for efficient hydrogen production via ammonia borane methanolysis.
Subject of Research: Chemistry
Article Title: Fabrication of NiO–Cu₃Mo₂O₉ Catalyst for Efficient Hydrogen Gas Production via Ammonia Borane Methanolysis
Article References: Gong, W., Li, X., Quan, X., Liu, X., An, Q., Li, H., & Tay, M. G. (2026). Fabrication of NiO–Cu3Mo2O9 Catalyst for Efficient Hydrogen Gas Production via Ammonia Borane Methanolysis. Catalysis Letters, 156(9), Article 269. https://doi.org/10.1007/s10562-026-05521-2
Image Credits: AI Generated
DOI: 10.1007/s10562-026-05521-2
Keywords: Hydrogen production, Ammonia borane, Methanolysis, NiO–Cu₃Mo₂O₉ catalyst, Heterogeneous catalysis, Activation energy, Turnover frequency, Nickel oxide, Copper molybdate, Hydrogen storage, Chemical hydride, Nanocatalyst
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Bethany Barker. (September 4, 2026). New NiO–Cu3Mo2O9 Catalyst Boosts Hydrogen Production from Ammonia Borane. Scienmag. https://scienmag.com/new-nio-cu3mo2o9-catalyst-boosts-hydrogen-production-from-ammonia-borane/
Bethany Barker. “New NiO–Cu3Mo2O9 Catalyst Boosts Hydrogen Production from Ammonia Borane.” Scienmag, 4 September 2026, https://scienmag.com/new-nio-cu3mo2o9-catalyst-boosts-hydrogen-production-from-ammonia-borane/. Accessed 4 September 2026.
Bethany Barker. “New NiO–Cu3Mo2O9 Catalyst Boosts Hydrogen Production from Ammonia Borane.” Scienmag. September 4, 2026. https://scienmag.com/new-nio-cu3mo2o9-catalyst-boosts-hydrogen-production-from-ammonia-borane/
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