Cu-based high-entropy two-dimensional oxide as stable and active photothermal catalyst

Cu-based nanocatalysts are the cornerstone of various industrial catalytic processes. Synergistically strengthening the catalytic stability and activity of Cu-based nanocatalysts is an ongoing challenge. Herein, the high-entropy principle is applied to modify the structure of Cu-based nanocatalysts, and a PVP templated method is invented for generally synthesizing six-eleven dissimilar elements as high-entropy two-dimensional (2D) materials. Taking 2D Cu 2 Zn 1 Al 0.5 Ce 5 Zr 0.5 O x as an example, the high-entropy structure not only enhances the sintering resistance from 400 °C to 800 °C but also improves its CO 2 hydrogenation activity to a pure CO production rate of 417.2 mmol g −1 h −1 at 500 °C, 4 times higher than that of reported advanced catalysts. When 2D Cu 2 Zn 1 Al 0.5 Ce 5 Zr 0.5 O x are applied to the photothermal CO 2 hydrogenation, it exhibits a record photochemical energy conversion efficiency of 36.2%, with a CO generation rate of 248.5 mmol g −1 h −1 and 571 L of CO yield under ambient sunlight irradiation. The high-entropy 2D materials provide a new route to simultaneously achieve catalytic stability and activity, greatly expanding the application boundaries of photothermal catalysis. Synergistically enhancing catalytic stability and activity of Cu-based nanocatalysts is an ongoing challenge. Here the authors report Cu-based high-entropy two-dimensional oxide as stable and active catalyst for photothermal CO2 hydrogenation under ambient sunlight irradiation.