Singlet fission promoted in chiral molecular self-assemblies: researchers provide a valuable guide for molecular design in singlet fission research. Credit: Kyushu University/ Kimizuka lab.

Singlet fission can be promoted by chiral molecular self-assemblies that absorb light, according to new research from Kyushu University.

In organic molecules an exciton is a particle bound pair of an electron (negative charge) and its hole (positive charge). They are held together by Coulombic attraction and can move within molecular assemblies.

Singlet fission (SF) is a process where an exciton is amplified, and two triplet excitons are generated from a singlet exciton. This is caused by the absorption of a single particle of light, or photon, in molecules called chromophores (molecules that absorb specific wavelengths of light).

Controlling the molecular orientation and arrangement of chromophores is crucial for achieving high SF efficiency in materials with strong potential for optical device applications.

So far, studies on SF have been conducted in solid samples, but there is yet to be comprehensive design guidelines for the molecular organisation required for efficient SF.

Professor Nobuo Kimizuka and his colleagues from Kyushu University have now successfully demonstrated that SF can be promoted by introducing chirality (molecules that cannot be superimposed on their mirror images) into chromophores and achieving chiral molecular orientation in self-assembled molecular structures.

The team showed that SF-based triplet excitons in self-assembled aqueous nanoparticles containing chiral π-electron chromophores, a phenomenon not observed in similar racemic nanoparticles (a mixture of equal amounts of molecules that are mirror images of each other).

Kimizuka said: “We have discovered a novel method to enhance SF by achieving chiral molecular orientation of chromophores in self-assembled structures.”

Critical role

The researchers investigated the SF characteristics of aqueous nanoparticles, which self-assembled from ion pairs of tetracene dicarboxylic acid and various chiral or non-chiral amines.

They identified the critical role of the counterion (an ion with a charge opposite to that of another ion in the solution), specifically the ammonium molecule.

The counterion influenced the molecular orientation of the ion pairs, the structural regularity, the spectroscopic properties, and the strength of the intermolecular coupling between tetracene chromophores.

Thus, the counterion played a key role in controlling the alignment of the chromophores and the associated SF process.

Through extensive experimentation with chiral amines, the team achieved a triplet quantum yield of 133% and a rate constant of 6.99 × 10⁹ s⁻¹. In contrast, they observed that nanoparticles with achiral counterions did not exhibit SF.

The racemic ion pair also produced an intermediate correlated triplet pair state by SF.

However, triplet-triplet annihilation was dominant in the triplet pairs; therefore, no dissociation into free triplets was observed.

Kimizuka said: “Our research offers a novel framework for molecular design in SF research and will pave the way for applications in energy science, quantum materials, photocatalysis, and life science involving electron spins.

“Furthermore, it inspires us to continue exploring SF in chiral molecular assemblies in organic media and thin film systems, which are critical for applications in solar cells and photocatalysts.”

The research is published in Advanced Science.