wildfire in situ tem heating holder (DENSsolutions)
Structured Review
Wildfire In Situ Tem Heating Holder, supplied by DENSsolutions, used in various techniques. Bioz Stars score: 97/100, based on 594 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/wildfire+in+situ+tem+heating+holder/Wildfire/10__1021_slash_acscatal__5c08070-72-2-1
Average 97 stars, based on 594 article reviews
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In Situ:Article Title: Ligation of Single-Site Ruthenium within Perovskite Oxides for Efficient Conversion of Thermodynamically Stable Molecules Article Snippet: Ru cation ligation in SrTiO3 perovskite and their migration to the surface through exsolution are investigated for the dry reforming of methane (DRM), a chemistry that requires activation of two thermodynamically stable molecules, CH4 and CO2.. Compared to a supported 1 wt % Ru/SrTiO3 benchmark, doped and exsolved Ru-SrTiO3 demonstrate ≥3× higher CH4 turnover rates (873 K), with isolated, ligated Ru exhibiting higher reactivity.. Reactor studies assert that CH4 and CO2 activation are both kinetically relevant for CH4 turnover rates on exsolved RuSrTiO3, unlike for supported Ru systems, where H-abstraction from CH4 is the sole kinetically relevant step. Transmission Electron Microscopy:Article Title: Ligation of Single-Site Ruthenium within Perovskite Oxides for Efficient Conversion of Thermodynamically Stable Molecules Article Snippet: Ru cation ligation in SrTiO3 perovskite and their migration to the surface through exsolution are investigated for the dry reforming of methane (DRM), a chemistry that requires activation of two thermodynamically stable molecules, CH4 and CO2.. Compared to a supported 1 wt % Ru/SrTiO3 benchmark, doped and exsolved Ru-SrTiO3 demonstrate ≥3× higher CH4 turnover rates (873 K), with isolated, ligated Ru exhibiting higher reactivity.. Reactor studies assert that CH4 and CO2 activation are both kinetically relevant for CH4 turnover rates on exsolved RuSrTiO3, unlike for supported Ru systems, where H-abstraction from CH4 is the sole kinetically relevant step. |
