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| URI | http://purl.tuc.gr/dl/dias/0B7D783B-3B40-46EA-8817-5461E6D60C1F | - |
| Αναγνωριστικό | https://doi.org/10.3390/catal10020160 | - |
| Αναγνωριστικό | https://www.mdpi.com/2073-4344/10/2/160/htm | - |
| Γλώσσα | en | - |
| Μέγεθος | 53 pages | el |
| Μέγεθος | 8,76 megabytes | en |
| Τίτλος | Recent advances on the rational design of non-precious metal oxide catalysts exemplified by CuOx/CeO2 binary system: implications of size, shape and electronic effects on intrinsic reactivity and metal-support interactions | en |
| Δημιουργός | Konsolakis Michail | en |
| Δημιουργός | Κονσολακης Μιχαηλ | el |
| Δημιουργός | Lykaki Maria | en |
| Δημιουργός | Λυκακη Μαρια | el |
| Εκδότης | MDPI | en |
| Περιγραφή | This article belongs to the special issue Rational design of non-precious metal oxide catalysts by means of advanced synthetic and promotional routes | en |
| Περίληψη | Catalysis is an indispensable part of our society, massively involved in numerous energy and environmental applications. Although, noble metals (NMs)-based catalysts are routinely employed in catalysis, their limited resources and high cost hinder the widespread practical application. In this regard, the development of NMs-free metal oxides (MOs) with improved catalytic activity, selectivity and durability is currently one of the main research pillars in the area of heterogeneous catalysis. The present review, involving our recent efforts in the field, aims to provide the latest advances—mainly in the last 10 years—on the rational design of MOs, i.e., the general optimization framework followed to fine-tune non-precious metal oxide sites and their surrounding environment by means of appropriate synthetic and promotional/modification routes, exemplified by CuOx/CeO2 binary system. The fine-tuning of size, shape and electronic/chemical state (e.g., through advanced synthetic routes, special pretreatment protocols, alkali promotion, chemical/structural modification by reduced graphene oxide (rGO)) can exert a profound influence not only to the reactivity of metal sites in its own right, but also to metal-support interfacial activity, offering highly active and stable materials for real-life energy and environmental applications. The main implications of size-, shape- and electronic/chemical-adjustment on the catalytic performance of CuOx/CeO2 binary system during some of the most relevant applications in heterogeneous catalysis, such as CO oxidation, N2O decomposition, preferential oxidation of CO (CO-PROX), water gas shift reaction (WGSR), and CO2 hydrogenation to value-added products, are thoroughly discussed. It is clearly revealed that the rational design and tailoring of NMs-free metal oxides can lead to extremely active composites, with comparable or even superior reactivity than that of NMs-based catalysts. The obtained conclusions could provide rationales and design principles towards the development of cost-effective, highly active NMs-free MOs, paving also the way for the decrease of noble metals content in NMs-based catalysts. | en |
| Τύπος | Ανασκόπηση | el |
| Τύπος | Review | en |
| Άδεια Χρήσης | http://creativecommons.org/licenses/by/4.0/ | en |
| Ημερομηνία | 2021-09-16 | - |
| Ημερομηνία Δημοσίευσης | 2020 | - |
| Θεματική Κατηγορία | Copper-ceria | en |
| Θεματική Κατηγορία | Rational design | en |
| Θεματική Κατηγορία | Size | en |
| Θεματική Κατηγορία | Shape | en |
| Θεματική Κατηγορία | Electronic/chemical functionalization | en |
| Θεματική Κατηγορία | CO oxidation | en |
| Θεματική Κατηγορία | N2O decomposition | en |
| Θεματική Κατηγορία | Preferential oxidation of CO (CO-PROX) | en |
| Θεματική Κατηγορία | Water gas shift reaction (WGSR) | en |
| Θεματική Κατηγορία | CO2 hydrogenation | en |
| Βιβλιογραφική Αναφορά | M. Konsolakis and M. Lykaki, “Recent advances on the rational design of non-precious metal oxide catalysts exemplified by CuOx/CeO2 binary system: implications of size, shape and electronic effects on intrinsic reactivity and metal-support interactions,” Catalysts, vol. 10, no. 2, Feb. 2020. doi: 10.3390/catal10020160 | en |
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