.png){kind=icon}
.png){kind=icon}
Return
Structure Sensitivity in CH4 Oxidation: Switching C1 to C2 Selectivity on Mn Single Atoms Versus Nanoparticles
.png){kind=icon}
PRE
AI
W
L
G
X
L
X
林
X
张
DOI：10.1021/jacs.6c06550.png)
.png){kind=icon}
Original request for help.png){kind=icon}
Share.png){kind=icon}
Save
Abstract
En 中文
The direct selective oxidation of methane (DSOM) to high value-added liquid oxygenates using only CH4 and O2 under mild conditions remains a formidable challenge in catalysis. Herein, we report the use of highly dispersed MnOx/ZSM-5 catalysts, in the form of single atoms and nanoparticles, to steer the DSOM reaction toward C1 and C2 oxygenates, respectively. While the Mn single-atom catalysts (SACs) primarily produce C1 products (HCOOH and CH3OH) with a combined selectivity of ∼ 78.8%, the Mn nanoparticle (NP) catalysts exclusively produce liquid oxygenates with excellent stability, achieving a remarkable acetic acid selectivity of 81.8%. Various characterizations and density functional theory calculations reveal that the reaction path is governed by distinct methane activation mechanisms at different Mn sites. On SACs, CH4 is selectively activated to *CH3 at Mn–O sites, leading to C1 oxygenates. In contrast, the multiple MnOx sites on NPs promote further dehydrogenation to *CH2 species, which subsequently couple into a key ethylene intermediate. This intermediate is then oxidized to acetic acid via a nonclassical pathway that circumvents CO carbonylation, thereby effectively suppressing overoxidation. This work provides fundamental insights into structure-sensitive methane activation and offers a practical route for the direct valorization of CH4 into value-added oxygenates using a noble-metal-free catalytic system.
Journal
IF:
15.6
Papers:
20.0W
Citations:
60.2W
Organization
Cited Papers