2020
DOI: 10.1016/j.apcatb.2019.118189
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Integrating photocatalysis and thermocatalysis to enable efficient CO2 reforming of methane on Pt supported CeO2 with Zn doping and atomic layer deposited MgO overcoating

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Cited by 137 publications
(102 citation statements)
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“…Employing CeO 2 in photocatalytic methane reforming is promising because CeO 2 is known to have many oxygen vacancies, which provides various merits in catalytic activity [45]. Pan et al doped zinc ions into CeO 2 and loaded Pt, and finally coated it with atomic layer MgO (Figure 23) [46]. They focused on photocatalytic DRM, but they claimed that both the input of photon energy and thermal energy boosted the conversion.…”
Section: Methodsmentioning
confidence: 99%
“…Employing CeO 2 in photocatalytic methane reforming is promising because CeO 2 is known to have many oxygen vacancies, which provides various merits in catalytic activity [45]. Pan et al doped zinc ions into CeO 2 and loaded Pt, and finally coated it with atomic layer MgO (Figure 23) [46]. They focused on photocatalytic DRM, but they claimed that both the input of photon energy and thermal energy boosted the conversion.…”
Section: Methodsmentioning
confidence: 99%
“…Recently, an approach of photothermocatalysis for CO 2 reduction by water, [ 33–35 ] hydrogen, [ 36–40 ] and methane [ 41–49 ] was developed. The approach is very efficient and promising as it well integrates low energy consumption of photocatalysis with high efficiency of thermocatalysis.…”
Section: Introductionmentioning
confidence: 99%
“…For photothermocatalytic CRM, VIII group metal catalysts were reported to demonstrate catalytic activity. [ 41–49 ] Among the catalysts, nonprecious metal catalysts such as Ni and Co are appealing due to their earth abundance, low cost, and good catalytic activity. [ 43,45–48 ] However, unlike noble metal catalysts with good resistance to carbon deposition, nonprecious metal catalysts are prone to deactivation due to two side‐reactions of carbon deposition such as CO disproportionation (2CO = C + CO 2 , Δ H 298 = −171 kJ mol −1 ) and methane dissociation (CH 4 = C + 2H 2 , Δ H 298 = 75 kJ mol −1 ).…”
Section: Introductionmentioning
confidence: 99%
“…Recently, Li's group developed a new composite catalyst comprising atomic MgO layers over Pt supported by Zn‐doped CeO 2 , which promoted the production of syngas via photothermal catalytic CRM. [ 143 ] This catalyst showed outstanding activity for the reaction, with the formation rate of CO and H 2 reaching 516 and 356 mmol g −1 h −1 under 30 suns at 600 °C (Figure 14c,d). This report provided a new photothermal catalytic process to convert CH 4 and CO 2 into high‐value chemicals…”
Section: Photocatalytic Conversion Of Methanementioning
confidence: 99%