Saturated Alcohols Electrocatalytic Oxidations on Ni-Co Bimetal Oxide Featuring Balanced B- and L-Acidic Active Sites
Year: 2025
Type: article
Abstract: Investigating structural and hydroxyl group effects in electrooxidation of alcohols to value-added products by solid-acid electrocatalysts is essential for upgrading biomass alcohols. Herein, we report efficient electrocatalytic oxidations of saturated alcohols (C 1 -C 6 ) to selectively form formate using NiCo hydroxide (NiCo–OH) derived NiCo 2 O 4 solid-acid electrocatalysts with balanced Lewis acid (LASs) and Brønsted acid sites (BASs). Thermal treatment transforms BASs-rich (89.6%) NiCo–OH into NiCo 2 O 4 with nearly equal distribution of LASs (53.1%) and BASs (46.9%) which synergistically promote adsorption and activation of OH − and alcohol molecules for enhanced oxidation activity. In contrast, BASs-enriched NiCo–OH facilitates formation of higher valence metal sites, beneficial for water oxidation. The combined experimental studies and theoretical calculation imply the oxidation ability of C 1 -C 6 alcohols increases as increased number of hydroxyl groups and decreased HOMO–LUMO gaps: methanol (C 1 ) < ethylene glycol (C 2 ) < glycerol (C 3 ) < meso-erythritol (C 4 ) < xylitol (C 5 ) < sorbitol (C 6 ), while the formate selectivity shows the opposite trend from 100 to 80%. This study unveils synergistic roles of LASs and BASs, as well as hydroxyl group effect in electro-upgrading of alcohols using solid-acid electrocatalysts.
Source: Nano-Micro Letters
Institutions: Chinese Academy of Sciences, Shanghai Institute of Ceramics, University of Chinese Academy of Sciences, State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Taizhou University, Taizhou University, Dalian University of Technology, Shanghai Advanced Research Institute, Shanghai Synchrotron Radiation Facility, University at Buffalo, State University of New York
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,690
OpenAlex ID: W4413484926
