MoS <sub>2</sub> Catalysts Selectively Achieve High Yield of Liquid Oxygenate from Direct Conversion of Methane via Hydroxyl Radicals

ABSTRACT Directly converting methane (CH 4 ) into liquid oxygenates (e.g., methanol) can circumvent the cost and engineering limits of natural gas transportation and storage. However, oxygenate yields from CH 4 remain low, and sulfur present in natural gas hinders activity in most catalysts. To overcome these barriers, we employ bulk molybdenum disulfide (MoS 2 ), a low‐cost, robust catalyst which selectively produces large quantities of liquid oxygenates (&gt;900 µmol/g cat ∙hr) from methane in the presence of hydroxyl (OH • ) radicals produced from dilute hydrogen peroxide (H 2 O 2 ) at 75°C. Under realistic reaction conditions, MoS 2 partially and reversibly adopts a metastable, more electrically conductive phase (1T’) that can only be observed through in situ structural probes. Herein, we elucidate that redox synergy between H 2 O 2 and MoS 2 produces active OH • radical species that selectively transform CH 4 to surface methoxy species at the gas‐solid liquid interface, leading to the unitary production of liquid oxygenate at a rate competitive with more costly precious metal catalysts, without additional catalyst preparation steps.

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Publication Details

Journal
Advanced Functional Materials
Published
2026-06-26
DOI
https://doi.org/10.1002/adfm.76526
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

MoS 2 Catalysts Selectively Achieve High Yield of Liquid Oxygenate from Direct Conversion of Methane via Hydroxyl Radicals

Ayaskanta Sahu, Long Qi, Akhil Tayal, Juan D. Jiménez et al.
Advanced Functional Materials
Catalysis and Oxidation Reactions
article

MoS 2 Catalysts Selectively Achieve High Yield of Liquid Oxygenate from Direct Conversion of Methane via Hydroxyl Radicals

Ayaskanta Sahu, Long Qi, Akhil Tayal, Juan D. Jiménez, Dominik Wierzbicki, Sanjaya D. Senanayake, Jorge Moncada, Shannon M. Mahurin, Jordi Llorca, Uddhav Kanbur, Albert Bruix, Eli Stavitski, Michelle K. Kidder, Milinda Abeykoon, Steven L. Farrell, Arephin Islam, Yuting Li, Emanuele Telari, Anna X. Chen, Jie Zhang
article en

Abstract

ABSTRACT Directly converting methane (CH 4 ) into liquid oxygenates (e.g., methanol) can circumvent the cost and engineering limits of natural gas transportation and storage. However, oxygenate yields from CH 4 remain low, and sulfur present in natural gas hinders activity in most catalysts. To overcome these barriers, we employ bulk molybdenum disulfide (MoS 2 ), a low‐cost, robust catalyst which selectively produces large quantities of liquid oxygenates (&gt;900 µmol/g cat ∙hr) from methane in the presence of hydroxyl (OH • ) radicals produced from dilute hydrogen peroxide (H 2 O 2 ) at 75°C. Under realistic reaction conditions, MoS 2 partially and reversibly adopts a metastable, more electrically conductive phase (1T’) that can only be observed through in situ structural probes. Herein, we elucidate that redox synergy between H 2 O 2 and MoS 2 produces active OH • radical species that selectively transform CH 4 to surface methoxy species at the gas‐solid liquid interface, leading to the unitary production of liquid oxygenate at a rate competitive with more costly precious metal catalysts, without additional catalyst preparation steps.

Advanced Functional Materials
Oak Ridge National Laboratory (US), Iowa State University (US), Brookhaven National Laboratory (US), New York University (US), Universitat de Barcelona (ES), University of California, Berkeley (US), Universitat Politècnica de Catalunya (ES)
U.S. Department of Energy, Office of Science, American Chemical Society Petroleum Research Fund, Basic Energy Sciences, Ames Laboratory
Openalex Percentile: Top 19%
Catalysis and Oxidation Reactions
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