Turning sunlight into storable fuels efficiently requires stable Earth-abundant catalysts that efficiently convert a maximum amount of the solar energy into fuel. Previous studies have described a range of catalysts, but a lack of standardized analytic conditions and methods has made objectively comparing catalysts challenging. Researchers standardized measurement techniques to allow a quantitative, objective evaluation of the activity and stability of water-splitting catalysts.
This study fulfills a longstanding need for unbiased comparison of heterogeneous catalysts' performance in electrochemical water-splitting research and helps inform the development of new artificial photosynthesis device components.
Researchers at the Joint Center for Artificial Photosynthesis (JCAP) have developed uniform benchmarking protocols and have used them to make "apples-to-apples" comparisons of the performance of more than forty catalysts for the evolution of hydrogen fuel and oxygen from water. Researchers evaluated the efficiency of each heterogeneous catalyst, measured as the amount of excess energy that would be required to create fuel in an artificial photosynthetic device operating about ten to a hundred times more efficiently than natural photosynthesis that occurs in crop plants. Researchers also determined the catalyst's stability under laboratory testing conditions. While the study confirmed the efficiency of many known catalysts, few of the Earth-abundant catalysts for making hydrogen and oxygen from water proved sufficiently active and stable in the conditions that are required for a practical solar fuels generating system, highlighting a priority for future research.
Explore further: Researchers discover new catalysts to generate renewable fuels
More information: "Benchmarking heterogeneous electrocatalysts for the oxygen evolution reaction." Journal of the American Chemical Society 135, 16977 (2013). DOI: 10.1021/ja407115p
"Benchmarking HER and OER electrocatalysts for solar water splitting devices." Journal of the American Chemical Society 137, 4347 (2015). DOI: 10.1021/ja510442p