Selective Electrified Propylene-to-Propylene Glycol Oxidation on Activated Rh-Doped Pd
Jianan Erick Huang, Yiqing Chen, Pengfei Ou, Xueda Ding, Yu Yan, Roham Dorakhan, Yanwei Lum, Xiaoyan Li, Yang Bai, Chengqian Wu, Mengyang Fan, Mi Gyoung Lee, Rui Kai Miao, Yanjiang Liu, Colin P. O’Brien, Jinqiang Zhang, Cong Tian, Yongxiang Liang, Yi Xu, Mingchuan Luo, David Sinton, Edward H. Sargent
Abstract
Renewable-energy-powered electrosynthesis has the potential to contribute to decarbonizing the production of propylene glycol, a chemical that is used currently in the manufacture of polyesters and antifreeze and has a high carbon intensity. Unfortunately, to date, the electrooxidation of propylene under ambient conditions has suffered from a wide product distribution, leading to a low faradic efficiency toward the desired propylene glycol. We undertook mechanistic investigations and found that the reconstruction of Pd to PdO occurs, followed by hydroxide formation under anodic bias. The formation of this metastable hydroxide layer arrests the progressive dissolution of Pd in a locally acidic environment, increases the activity, and steers the reaction pathway toward propylene glycol. Rh-doped Pd further improves propylene glycol selectivity. Density functional theory (DFT) suggests that the Rh dopant lowers the energy associated with the production of the final intermediate in propylene glycol formation and renders the desorption step spontaneous, a concept consistent with experimental studies. We report a 75% faradic efficiency toward propylene glycol maintained over 100 h of operation.