A molecule like a nanobattery

Oldenburg chemical scientists publish results of three interconnected research projects.

How do molecular catalysts – molecules which, like enzymes, can trigger or accelerate certain chemical reactions – function, and what effects do they have? A team of chemists at the University of Oldenburg has come closer to the answers using a model molecule that functions like a molecular nanobattery. It consists of several titanium centres linked to each other by a single layer of interconnected carbon and nitrogen atoms. The seven-member research team recently published its findings, which combine the results of three multi-year PhD research projects, in “ChemPhysChem”. The physical chemistry and chemical physics journal featured the basic research from Oldenburg on its cover.

To gain a better understanding of how the molecule works, the researchers, headed by first authors Dr. Aleksandra Markovic and Luca Gerhards and corresponding author Prof. Dr. Gunther Wittstock, performed electrochemical and spectroscopic experiments and used the university’s high-performance computing cluster for their calculations. Wittstock sees the publication of the paper as a “success story” for both the Research Training Groups within which the PhD projects were conducted and for the university’s computing cluster. “Without the high-performance computing infrastructure, we would not have been able to perform the extensive calculations required to decipher the behaviour of the molecule,” says Wittstock. “This underlines the importance of such computing clusters for current research.”

In the paper, the authors present the results of their analysis of a molecular structure, the prototype for which was the result of an unexpected chemical reaction first reported by the University of Oldenburg’s Chemistry Department in 2006. It is a highly complex molecular structure in which three titanium centres (commonly referred to in high school lessons as titanium ions) are connected to each other by a bridging ligand consisting of carbon and nitrogen. Such a compound would be expected to be able to accept and release several electrons through the exchange of electrons between the metal centres among other reasons.

Gaining a proper understanding of these processes is of particular interest not only for basic research, but also for triggering or accelerating important reactions in which more than one electron is transferred. Such reactions remain a major challenge in technical systems, for which there is still no satisfactory solution. “Many efforts are currently focused on this objective,” says Wittstock. One example is fuel cell technology, which requires the simultaneous transfer of four electrons to one oxygen molecule in order to achieve a flow of electrons from hydrogen to oxygen, he explains. “Such multi-electron reactions also have great potential for saving materials or energy in chemical production.”

The model molecular compound consisting of the bridging ligand and the titanium centres was specifically designed to help the scientists gain a detailed understanding of how compounds with several metal centres are able to accept and release electrons. The scientists excited the molecule by light, to which the molecules responded differently depending on the number of accepted and released electrons. Unfortunately, the molecule made in 2006 proved to be poorly soluble in most solvents and therefore difficult to study. Using chemical synthesis, Dr. Pia Sander, a co-author of the paper, added propeller-like molecular motifs to the compound to improve its solubility. This provided the basis for Markovic’s experiments, which revealed that the model compound could accept a total of three electrons or release six electrons – an unusually high capacity for a single molecule. In each of these reactions, not only the visible colour of the molecule changes, but the absorption of light in the spectral ranges which are invisible to the human eye. Initially, however, the precise changes in the molecule with different numbers of electrons could not be determined on the basis of those spectral ranges.

This is where Luca Gerhards and the university’s computing cluster came into play. Although common explanations are based on the premise that in each transition excited by light only the energy of a single electron changes, co-author Gerhards avoided these simplifying assumptions in his quantum chemical equations. This made the calculations even more complex and kept the high-performance computing cluster busy for months. In the end, the result came as a surprise to everyone involved: Several electrons change their energy levels simultaneously when light hits the molecule under study. Moreover, this charge is not stored in the titanium, as would be expected, but mainly in the bridging ligand, the “link” between the titanium centres.

As Wittstock explains, the metal centres thus provide a positively charged “frame” for electron storage, as in a “nanobattery”. The model molecule – and by extension a whole class of similar compounds – has turned out to be a “mini segment of an energy storage material”. Although their full potential cannot be determined at this stage, Wittstock believes that such “frames” with molecular charge storage motifs could become a new design element in complex molecular catalysts for multi-electron reactions.

The PhD research projects were conducted in research groups led by the Oldenburg chemistry professors Wittstock, Prof. Dr. Rüdiger Beckhaus and Prof. Dr. Thorsten Klüner. The research of the first two projects was interlinked within the framework of the concluded “Nano Energy” Research Training Group, which was funded by the Ministry for Science and Culture of the State of Lower Saxony. The third project involving quantum chemical calculations is part of the Research Training Group “Chemical Bond Activation”, which the German Research Foundation (DFG) has been funding since 2017.

Wissenschaftliche Ansprechpartner:

Prof. Dr Gunther Wittstock, wittstock@uol.de

Originalpublikation:

Aleksandra Markovic, Luca Gerhards, Pia Sander, Carsten Dosche, Thorsten Klüner, Rüdiger Beckhaus, Gunther Wittstock: Electronic Transitions in Different Redox States of Trinuclear 5,6,11,12,17,18‐Hexaazatrinaphthylene‐Bridged Titanium Complexes: Spectroelectrochemistry and Quantum Chemistry. ChemPhysChem, 2020, 21, 2506-2514, doi.org/10.1002/cphc.202000547

Weitere Informationen:

http://uol.de/en/grk-2226 Research Training Group “Chemical Bond Activation”