Experimental methodology and static absorption spectra of P3HT. a The experimental setup for time-resolved soft X-ray spectroscopy. A 15 fs visible pump pulse excites the π→π* transition in P3HT, and a temporally delayed attosecond soft X-ray pulse probes the carbon and sulfur absorption edges. b The visible absorption spectrum of the P3HT samples used in this work, and the pump pulse spectrum which is centered at the maximum of the π→π* resonance in P3HT. c A typical soft X-ray spectrum extending to ~330 eV (black line). The red line is the X-ray absorption spectrum of the P3HT sample, absorption features at the sulfur L1,2,3 and carbon K-edges are resolved simultaneously. Credit: Nature Communications (2022). DOI: 10.1038/s41467-022-31008-w

Researchers have tracked the first fractions of a second after light strikes solar cells, providing insights into how they produce electricity.

Probing the very first moments of the process of converting light into electricity could help researchers improve new solar cells, allowing them to produce energy more efficiently.

The method, developed by Imperial College London researchers, uses ultrafast lasers and X-rays to provoke a reaction and then to measure the changes it causes over just femtoseconds (quadrillionths of a second).

Now, a team of researchers at Imperial and Newcastle University has used the technique to study organic photovoltaic (OPV) materials that harvest the to produce energy or to split water.

OPV materials are under intense study as they can provide cheaper renewable energy. However, many of the materials currently used are unstable or inefficient, due to the complex interaction of electrons that are excited by light.

Closer study of the fast interactions of these electrons, like the paper published today in Nature Communications that combines fast time resolution with measurements localized to atoms, provide valuable insights into methods for improving and catalysts.

More efficient devices

Professor Jon Marangos, from the Department of Physics at Imperial, says that "OPVs are cheap and flexible alternatives to silicon-based photovoltaics, and so are an attractive prospect for use in future solar energy generation infrastructure.

"This work demonstrates the power of our new time-resolved X-ray technique, which can now be applied to a wider range of materials and may provide the understanding needed for making more efficient OPV devices."

The team probed the first step of solar energy conversion—the reactions in the material caused by the striking of light. They first fired a laser pulse lasting 15 femtoseconds at the material to excite the reaction. They followed this with an X-ray pulse lasting just attoseconds (less than millionths of a billionth of a second), which measured the resultant changes in the material.

Rapidly evolving states

The team observed, for the first time, direct X-ray signatures of the of the material when electrons are knocked out of position. This creates an electron and "hole" pair, that can move through the material.

This initial state rapidly evolved into a new, more stable state in just 50 femtoseconds. Calculations by Professor Tom Penfold at Newcastle University agreed well with the observations, showing the initial state depended on the distance between chains of molecules in the material.

Dr. Artem Bakulin, from the Department of Chemistry at Imperial, says that "this sensitivity of the time-resolved X-ray method to the initial electron dynamics occurring directly after excitation by light paves the way for new insights into the photophysics of a wide range of organic optoelectronic and other materials."

The team now plan to explore the ultrafast charge dynamics in other organic semiconductor materials, including recently discovered that use different molecules as electron acceptors, which show enhanced OPV efficiency.

More information: D. Garratt et al, Direct observation of ultrafast exciton localization in an organic semiconductor with soft X-ray transient absorption spectroscopy, Nature Communications (2022). DOI: 10.1038/s41467-022-31008-w

Journal information: Nature Communications