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Record-large pore molecular crystals: A leap toward clean energy storage

Record-Large Pore Molecular Crystals: A Leap Toward Clean Energy Storage
(a) Coplanar π-building blocks tend to stack with adjacent molecules, with both sides of the aromatic rings participating, leading to infinite π–π stacks in framework materials. (b) Noncoplanar π-building blocks form discrete π-dimers, as shown in the dashed frame, where only one side of the aromatic rings engages in π–π stacking with neighboring molecules, leaving the opposite side exposed to the channel surface. Credit: Dr. Ruihua Zhang

In our study in the Journal of the American Chemical Society, our team from The University of Hong Kong and Northwestern University, led by the late Nobel Laureate Professor Fraser Stoddart, developed RP-H200, a hydrogen-bonded organic framework (HOF) with the largest pores in its class.

This innovation unlocks new possibilities for sustainable energy storage, gas separation, and catalysis.

The challenge of designing stable, large-pore molecular crystals

Molecular crystals, such as hydrogen-bonded organic frameworks (HOFs), are ordered structures formed by organic molecules linked through noncovalent interactions, such as or π-π stacking. Rock candy, where sucrose molecules form crystals via hydrogen bonds, is a simple example. Endowing molecular crystals with porosity unlocks vast potential for gas separation, sensing, and catalysis.

Yet, a persistent challenge remains: creating molecular crystals with large, stable pores. Large-pore, highly porous crystals often lack stability, while densely packed structures, though robust, have small or no pores. This trade-off has long hindered practical applications.

Our solution

To address this challenge, we designed a mesoporous hydrogen-bonded (HOF) that combines large pores with exceptional stability. The result is RP-H200, a novel molecular crystal featuring 3.6-nanometer pores—the largest ever reported in its class.

Record-Large Pore Molecular Crystals: A Leap Toward Clean Energy Storage
Assembly of noncoplanar molecules into double-walled mesoporous hydrogen-bonded organic frameworks (HOFs), featuring the largest pore size reported in molecular crystals to date. Credit: Dr. Ruihua Zhang

This breakthrough was achieved through a unique noncoplanar assembly strategy using imidazole-annulated triptycene hexaacids. These molecules self-assemble into a double-walled, honeycomb-like structure, creating pores lined with aromatic surfaces.

The material exhibits an impressive surface area of 2313 m²/g—equivalent to one-third of a football field per gram. Remarkably, RP-H200 maintains its at temperatures up to 350°C and in solvents such as ethanol, as confirmed by X-ray diffraction.

High performance in gas storage

RP-H200's large pores, vast surface area, and exceptional stability make it ideal for storing clean-energy gases. At 270 K and 100 bar—typical conditions for methane storage—it captures 0.31 grams of methane per gram, surpassing many existing materials. Its aromatic surfaces form C-H-π interactions with methane, with an adsorption heat of 12 kJ/mol, enabling efficient storage and release without extreme conditions. RP-H200 also stores 6.7% of its weight in hydrogen at 77 K, advancing hydrogen-powered vehicles.

Through repeated adsorption cycles, we confirmed RP-H200's durability, with no significant methane capacity loss after three cycles. It remains stable in humid air and , positioning RP-H200 as a practical solution for real-world energy storage.

Future implications

Our noncoplanar assembly strategy delivers ultra-large pores, robust stability, and solution-processability, enabling cost-effective production. By using , RP-H200 embraces sustainable chemistry, and its recyclability minimizes waste.

This material opens exciting possibilities for HOFs in clean energy, gas separation, and catalysis. Imagine lightweight tanks for methane-fueled vehicles, reducing reliance on , or drug delivery systems that use these pores to transport medications. Our approach can be extended to other HOFs, accelerating the development of functional molecular crystals for diverse applications.

This story is part of , where researchers can report findings from their published research articles. for information about Science X Dialog and how to participate.

More information: Ruihua Zhang et al, Double-Walled Mesoporous Hydrogen-Bonded Organic Frameworks with High Methane Storage Capacity, Journal of the American Chemical Society (2025).

Dr. Ruihua Zhang earned her B.Sc. (2016) and Ph.D. in Chemistry from Xiamen University, mentored by Professors Yang Cao and Chaoyong James Yang. Her doctoral research focused on microfluidics-based single-cell protein analysis, 2D materials electrocatalysis, and single-crystal electronics of nanoclusters and MOFs. In January 2022, she joined the Stoddart Group at Northwestern University as a Postdoctoral Fellow, focusing on hydrogen storage. In 2023, she relocated to HKU with Professor Stoddart and was promoted to Research Assistant Professor in July 2024. Her current research centers on porous crystalline materials for hydrogen and methane storage, separation, and environmental remediation.

Citation: Record-large pore molecular crystals: A leap toward clean energy storage (2025, May 13) retrieved 13 May 2025 from /news/2025-05-large-pore-molecular-crystals-energy.html
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