Related Experiment Video
Updated: Jul 8, 2026

Electrophoretic Crystallization of Ultrathin High-performance Metal-organic Framework Membranes
Published on: August 16, 2018
Morphology Engineering of Co3O4 via Cetyltrimethylammonium Bromide-Mediated ZIF-67 Synthesis for Efficient
Yurui Zhi1, Lingling Yang1, Meng Li1
1College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu, Sichuan 610059, China.
Abstract:
Co3O4 is a promising nonprecious metal photoelectrocatalyst due to its mixed valence states (Co2+/Co3+) and spinel structure, but the morphology-performance relationship remains unclear. Herein, morphology-engineered Co3O4 was synthesized via a cetyltrimethylammonium bromide (CTAB)-directed ZIF-67 precursor route, yielding four distinct shapes (RD, TRD, NC, TC), whose formation was rationalized by molecular dynamics simulations. The inherited Co3O4 morphologies were systematically correlated with photoelectrocatalytic methanol oxidation performance through multiple descriptors (surface area, pore structure, Co3+/Co2+ ratio, oxygen vacancies, band gap, and •OH adsorption energy). Combined experimental and theoretical results reveal that the TRD morphology exhibits superior activity, benefiting from synergistic effects of dominant {111} facet exposure, high surface area, enriched Co3+, abundant oxygen vacancies, narrow band gap, and efficient charge separation. Moreover, the oxidation pathway of methanol, the contribution of reactive oxygen species, and the catalyst stability are further discussed in conjunction with theoretical calculations. This work elucidates the structure-activity relationship in Co3O4 photoanodes, thereby guiding the design of efficient, low-cost catalysts for photo-assisted direct methanol fuel cells (PDMFCs).
More Related Videos
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Thermal and Photochemical Electrocyclic Reactions: Overview
Hydroboration-Oxidation of Alkenes
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

