Recently, research team led by Prof. ZENG Jie from Hefei National Laboratory for Physical Sciences at the Microscale and Prof. BAO Jun from National Synchrotron Radiation Laboratory of University of Science and Technology of China (USTC) of CAS has made great breakthrough in the controlled synthesis of Pd-Pt tesseracts for oxygen reduction reaction (ORR) and the mechanism investigation of their etching process.
This work was published on Journal of the American Chemical Society.
A proton exchange membrane fuel cell is a chemical cell that converts energy released when a substance reacts into electrical energy with zero emission. It is an excellent substitute for fossil fuel. However, low activity and stability of the Pt-based catalysts in the ORR of the battery cathode restricted the output power and the number of charge and discharge cycles, thus increasing the cost of the whole fuel cells. The preparation of cathode catalysts with high activity and stability has become the hotspot and difficulty in this field.
An animation of a cube to tesseract
Inspired by the evolution from a three-dimensional cube to a four-dimensional tesseracts, the research team carried out oxidation etching on the Pd-Pt uniform alloy nanocubes, and obtained a new tesseracts framework structure of Pd-Pt catalyst by precisely adjusting the removal of Pd atoms and the rearrangement of remaining Pd and Pt atoms.
The structure has high surface ratio and high percentage of active sites, which greatly improve the atomic utilization. The mass activities of tesseracts frames is 1.86 A mg-1Pt, being 11.6 times as high as that of commercial Pt/C catalyst.
In addition, the catalyst obtained by oxidation etching maintains extremely high structural stability in the electrochemical testing environment. After 10,000 times of cyclic charging-discharge tests, its performance did not decrease significantly.
This work not only advance the understanding of the etching mechanism, but also provide efficient strategies for the design of novel hollow frame structures for catalysis.
Paper link:https://pubs.acs.org/doi/10.1021/jacs.0c12282
(Edited by LU Hongyu, USTC News Center)