Dicarboxylic
acids and cyclic ketones, such as adipic
acid (AA)
and cyclohexanone (CHN), are essential compounds for the chemical
industry. Although their production by electrosynthesis using electricity
is considered one of the most promising strategies, the application
of such processes has been hampered by a lack of efficient catalysts
as well as a lack of understanding of the mechanism. Herein, a series
of monolithic msig/ea-NiOOH-Ni(OH)2/NF
were prepared by means of self-dissolution of metal matrix components,
interface growth, and electrochemical activation (denoted as msig/ea). The as-synthesized catalysts have three-dimensional
cuboid-like structures formed by interconnecting nanosheets composed
of NiOOH. By theoretically guided regulation of the amounts of Ni3+ and oxygen vacancies (OV), a 96.5% yield of CHN
from cyclohexanol (CHA) dehydrogenation and a 93.6% yield of AA from
CHN oxidation were achieved. A combined experimental and theoretical
study demonstrates that CHA dehydrogenation and CHN oxidation were
promoted by the formation of Ni3+ and the peroxide species
(*OOH) on OV. This work provides a promising approach for
directional electrosynthesis of high-purity chemicals with in-depth
mechanistic insights.