Light-driven
synthesis of hourglass-shaped metal–organic frameworks. Credit: Dongling Ma,
INRS
Metal-organic frameworks, better
known as MOFs, are among the most intensely studied materials for addressing
major environmental challenges. Their highly ordered, ultra-porous architecture
enables applications ranging from CO2 capture and air or water purification to catalysis and hydrogen
production. It is therefore no surprise that MOFs have drawn global attention
in recent years, notably with their recognition by the 2025 Nobel Prize in
Chemistry, as they play an increasingly central role in the development of
sustainable technologies.
Despite their promise, MOFs remain
challenging to synthesize with high precision. Conventional solvothermal
methods typically require high temperatures (up to 200° C) and long reaction
times, making them energy-intensive and difficult to control. These harsh
conditions can compromise structural precision and limit functional
performance.
This constraint has now been
overcome by Professor Dongling Ma, a nanomaterials expert at the Institut
national de la recherche scientifique (INRS) and Canada Research Chair in
Advanced Functional Nanocomposites. In collaboration with researchers from McGill
University, her team has developed a photochemical synthesis strategy that
enables MOFs to be formed under mild, ambient conditions.
"Our work demonstrates that
photons can be used not only to initiate MOF synthesis, but also to guide it
with exceptional precision. This strategy opens a sustainable pathway for
engineering advanced materials while dramatically reducing energy consumption,"
says Prof. Ma.
In a study published in Nature Communications, the team
at INRS Énergie Matériaux Télécommunications Research Centre reports the
ambient-temperature synthesis (15° C, four hours) of a cobalt–porphyrin-based MOF—named phoPPF-3—using light as the sole driving force.
Rather than relying on thermal
energy, this light-driven approach uses photons to initiate and control the
assembly process at the atomic scale. The strategy enables multidimensional
control over framework formation, resulting in unique two-dimensional hourglass-like
morphologies. Crucially, it also induces selective Co2+–carboxylate coordination, preserving free-base porphyrin cores that cannot
be maintained using conventional solvothermal synthesis. The outcome is a MOF
with enhanced structural precision, improved thermal stability, and a level of
control previously inaccessible under traditional conditions.
Enhanced photocatalytic performance for future energy technologies
Beyond its innovative synthesis,
phoPPF-3 exhibits superior functional performance. Compared with solvothermally
synthesized analogs, it demonstrates higher photocatalytic activity in both
benzyl alcohol oxidation and photocatalytic hydrogen evolution. In some cases,
performance improvements reach up to 50%, highlighting the strong link between
synthesis precision and functional efficiency.
"MOFs already play a strategic
role in the energy transition. By enabling atomically precise synthesis under
ambient conditions, this approach accelerates the development of more efficient
and scalable technologies," notes Yong Wang, a Ph.D. student in the
Materials and Energy program in Dongling Ma's laboratory at the time the study
was conducted.
Importantly, the researchers also
demonstrated that this photochemical methodology is not limited to a single
system. Its successful extension to other MOFs underscores the generality and
versatility of the approach.
By drastically lowering the energy requirements for MOF synthesis while enhancing structural and functional control, this strategy opens new possibilities for large-scale production and applications such as CO₂ capture, environmental remediation, industrial catalysis, and solar energy conversion and storage.
Provided by INRS
Source: Creating green materials with light could transform clean energy

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