التفاصيل البيبلوغرافية
| العنوان: |
Silica-Supported PdGa Nanoparticles: Metal Synergy for Highly Active and Selective CO 2 ‑to-CH 3 OH Hydrogenation |
| المؤلفون: |
Scott R. Docherty (10319921), Nat Phongprueksathat (10319924), Erwin Lam (1412809), Gina Noh (5908415), Olga V. Safonova (1484872), Atsushi Urakawa (1268004), Christophe Copéret (1299531) |
| سنة النشر: |
2021 |
| المجموعة: |
Smithsonian Institution: Digital Repository |
| مصطلحات موضوعية: |
Pharmacology, Evolutionary Biology, Ecology, Cancer, Inorganic Chemistry, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, CH 3 OH, mol, Silica-Supported PdGa Nanoparticles, selectivity, anthropogenic CO 2 emissions, CO 2, silica-supported Pd nanoparticles show, silica-supported Ga III, catalyst, NMR, X-ray absorption spectroscopy, conversion, alloyed PdGa nanoparticles, XAS, IR, surface organometallic chemistry, High CH 3 OH selectivities |
| الوصف: |
The direct conversion of CO 2 to CH 3 OH represents an appealing strategy for the mitigation of anthropogenic CO 2 emissions. Here, we report that small, narrowly distributed alloyed PdGa nanoparticles, prepared via surface organometallic chemistry from silica-supported Ga III isolated sites, selectively catalyze the hydrogenation of CO 2 to CH 3 OH. At 230 °C and 25 bar, high activity (22.3 mol MeOH mol Pd –1 h –1 ) and selectivity for CH 3 OH/DME (81%) are observed, while the corresponding silica-supported Pd nanoparticles show low activity and selectivity. X-ray absorption spectroscopy (XAS), IR, NMR, and scanning transmission electron microscopy–energy-dispersive X-ray provide evidence for alloying in the as-synthesized material. In situ XAS reveals that there is a dynamic dealloying/realloying process, through Ga redox, while operando diffuse reflectance infrared Fourier transform spectroscopy demonstrates that, while both methoxy and formate species are observed in reaction conditions, the relative concentrations are inversely proportional, as the chemical potential of the gas phase is modulated. High CH 3 OH selectivities, across a broad range of conversions, are observed, showing that CO formation is suppressed for this catalyst, in contrast to reported Pd catalysts. |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
unknown |
| Relation: |
https://figshare.com/articles/journal_contribution/Silica-Supported_PdGa_Nanoparticles_Metal_Synergy_for_Highly_Active_and_Selective_CO_sub_2_sub_to-CH_sub_3_sub_OH_Hydrogenation/14233592 |
| DOI: |
10.1021/jacsau.1c00021.s001 |
| الاتاحة: |
https://doi.org/10.1021/jacsau.1c00021.s001 |
| Rights: |
CC BY-NC 4.0 |
| رقم الانضمام: |
edsbas.7985CAEE |
| قاعدة البيانات: |
BASE |