2023
DOI: 10.1016/j.apcatb.2023.123054
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Enhanced dry reforming of CO2 and CH4 on photothermal catalyst Ru/SrTiO3

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Cited by 28 publications
(15 citation statements)
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“…These indicate that the photoexcited energetic electrons generated from the conduction band of SrTiO 3 can transfer to the adjacent HEA NPs (see also Figure S22). , Therefore, it can be reasonably inferred that HEA NPs act as electron capture centers with high electron density, promoting the activation of CO 2 and thus enhancing the catalytic properties. Taken together, the light-driven DRM process over HEA/SrTiO 3 involves a synergy of photocatalysis and photothermal catalysis .…”
Section: Resultsmentioning
confidence: 99%
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“…These indicate that the photoexcited energetic electrons generated from the conduction band of SrTiO 3 can transfer to the adjacent HEA NPs (see also Figure S22). , Therefore, it can be reasonably inferred that HEA NPs act as electron capture centers with high electron density, promoting the activation of CO 2 and thus enhancing the catalytic properties. Taken together, the light-driven DRM process over HEA/SrTiO 3 involves a synergy of photocatalysis and photothermal catalysis .…”
Section: Resultsmentioning
confidence: 99%
“…Herein, we design HEAs on SrTiO 3 as a highly efficient and coke-resistant catalyst for light-driven DRM without a secondary source of heating, involving a new carbon exchange process (Figure b). In our design, Ni, Rh, Pd, and Ru are explored as the main active metals for CH 4 activation given their previously demonstrated potential for C–H cleavage. ,, SrTiO 3 with moderate alkaline sites is screened as the support to facilitate CO 2 adsorption and activation. ,, HEAs also absorb light in a wide spectrum and act as a “nanoheater” to rapidly elevate the local temperature of the catalyst. Under 4 W cm –2 light irradiation, ultrahigh activity (15.6/16.0 mol g metal –1 h –1 for H 2 /CO production), long-term stability (∼150 h), and remarkable selectivity (∼0.96) are achieved over CoNiRuRhPd loaded on SrTiO 3 (denoted as HEA/SrTiO 3 ).…”
Section: Introductionmentioning
confidence: 99%
“…This suggests that the atomic Ru interface may be a good active site (Figure14a). 119 Thus, the authors optimized the structure of the adsorbed substance to achieve the smallest energy position by placing the adsorbed substance near the interface. The activation energy required for methane to dissociate into methyl* and H* is higher under normal conditions (Figure 14b).…”
Section: Photocatalytic Co 2 Reduction To Comentioning
confidence: 99%
“…The activation energy required for methane to dissociate into methyl* and H* is higher under normal conditions (Figure 14b). 119 Figure 14c shows the H 2 generation pathway in the normal and electronrich states. The electron-rich state of Ru on the catalyst also promotes the formation of H 2 .…”
Section: Photocatalytic Co 2 Reduction To Comentioning
confidence: 99%
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