The cells developed as part of the project go beyond the state of the art in several ways. First, the in-situ heating cell for thin film studies has a passive dilatation-minimizing mechanism, which makes grazing incidence scattering experiments at elevated temperatures easier due to limited calibration. It is also light-weight, and can be attached both on in-house X-ray diffraction instruments and on goniostats available at synchrotron beamlines. The second cell used for in-situ studies of colloidal synthesis offers unrivaled flexibility in terms of the reactions that can be studied. The advanced materials that were used in the construction allow for heating up to 300C, measuring X-ray absorption at energies as low at 5keV, and greatly facilitate sample preparation, which is of key importance with limited beamline access. The cell also includes a mechanism that enables remote modification of the flight-path during the experiments, which enable facile calibration and tailoring the sample environment to the constraints given by the studied sample. The two cells enables us to study the formation of thin films and colloidal synthesis of nanocrystals in precisely and rapidly, which is key for the development of screening approaches in material searches.
We have also proposed a new synthesis approach for thin films with precisely controlled grain sizes at the nanoscale. Using colloidal metal nanocrystals with exactly controlled sizes as seeds, we were able to fine-tune the crystal domain size in the resulting thin films after annealing. The grain size is directly linked to the performance of photocatalysts, and fine-tuning this parameter has been previously very limited.
Moreover, we have identified a significant limitation in the class of copper vanadates and copper-containing oxides for use as photoanodes. Through a combined theoretical and experimental study we revealed that strong excitonic interactions, arising due to the presence of copper in a certain structural arrangement, strongly limit the performance in this class of materials.
We have also contributed to the fundamental understanding of a certain class of colloidal synthesis of nanocrystals. Using the in-sity cell we identified the exact mechanism of nucleation via disproportionation of a metallo-organic complex, commonly used to obtain monodisperse nanocrystals with different shapes.