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Methane upgrading into more valuable chemicals has received much attention. Herein, we report oxidative methane conversion to ethane using gaseous O 2 at low temperatures (<400 °C) and atmospheric pressure in a continuous reactor. A highly oxidized Pd deposited on ceria could produce ethane with a productivity as high as 0.84 mmol g cat −1 h −1 . The Pd−O−Pd sites, not Pd−O−Ce, were the active sites for the selective ethane production at low temperatures. Density functional theory calculations confirmed that the Pd−O−Pd site is energetically more advantageous for C−C coupling, whereas Pd−O−Ce promotes CH 4 dehydrogenation. The ceria helped Pd maintain a highly oxidic state despite reductive CH 4 flow. This work can provide new insight for methane upgrading into C 2 species.
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Kwon et al. (2020) studied this question.
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