An international team has succeeded in considerably increasing the efficiency for direct solar water splitting with a tandem solar cell whose surfaces have been selectively modified. The new record value is 14 percent and thus tops the previous record of 12.4 percent, broken now for the first time in 17 years. Researchers from Helmholtz-Zentrum Berlin, TU Ilmenau, Fraunhofer ISE and California Institute of Technology participated in the collaboration. The results are published in Nature Communications.
Solar energy is abundantly available globally, but unfortunately not constantly and not everywhere. One especially interesting solution for storing this energy is artificial photosynthesis. This is what every leaf can do, namely converting sunlight to chemical energy. That can take place with artificial systems based on semiconductors as well. These use the electrical power that sunlight creates in individual semiconductor components to split water into oxygen and hydrogen. Hydrogen possesses very high energy density, can be employed in many ways and could replace fossil fuels. In addition, no carbon dioxide harmful to the climate is released from hydrogen during combustion, instead only water. Until now, manufacturing of solar hydrogen at the industrial level has failed due to the costs, however. This is because the efficiency of artificial photosynthesis, i.e. the energy content of the hydrogen compared to that of sunlight, has simply been too low to produce hydrogen from the sun economically.
Record value now exceeded
Scientific facilities worldwide have therefore been researching for many years how to break the existing record for artificial photosynthesis of 12.4 %, which has been held for 17 years by NREL in the USA.
Core component: Tandem Solar Cell
Now a team from TU Ilmenau, Helmholtz-Zentrum Berlin (HZB), the California Institute of Technology as well as the Fraunhofer ISE has considerably exceeded this record value. Lead author Matthias May, active at TU Ilmenau and the HZB Institute for Solar Fuels, processed and surveyed about one hundred samples in his excellent doctoral dissertation to achieve this. The fundamental components are tandem solar cells of what are known as III-V semiconductors. Using a now patented photo-electrochemical process, May could modify certain surfaces of these semiconductor systems in such a way that they functioned better in water splitting.
"We have electronically and chemically passivated in situ the aluminium-indium-phosphide layers in particular and thereby efficiently coupled to the catalyst layer for hydrogen generation. In this way, we were able to control the composition of the surface at sub-nanometre scales", explains May. There was enormous improvement in long-term stability as well. At the beginning, the samples only survived a few seconds before their power output collapsed. Following about a year of optimising, they remain stable for over 40 hours. Further steps toward a long-term stability goal of 1000 hours are already underway.
Next goals visible
"Forecasts indicate that the generation of hydrogen from sunlight using high-efficiency semiconductors could be economically competitive to fossil energy sources at efficiency levels of 15 % or more. This corresponds to a hydrogen price of about four US dollars per kilogramme", says Prof. Thomas Hannappel, from the photovoltaics group at TU Ilmenau, who was academic advisor for the work. Prof. Hans-Joachim Lewerenz from the Joint Center for Artificial Photosynthesis at the California Institute of Technology, who worked closely with May, said:"We are nearly there. If we are successful now in reducing the charge carrier losses at the interfaces somewhat more, we might be able to chemically store more than even 17 % of the incident solar energy in the form of hydrogen using this semiconductor system".
Explore further: Objective comparison of catalyst performance for development of artificial photosynthesis systems
May, M. M. et al. Efficient direct solar-to-hydrogen conversion by in situ interface transformation of a tandem structure. Nat. Commun. 6:8286. DOI: 10.1038/ncomms9286 (2015)