CeO2 has played an important role in improving the oxygen evolution reaction (OER) performance of transition metals-based catalysts whether as a hybrid, substrate, or interface. The high OER activity is ascribed to the optimized transition metals and/or the formed oxygen vacancies. In this work, the interface effect between CoO and CeO2 is reported to be the reason for the excellent OER performance of CoO/CeO2. Compared with sole CoO or CoO/CeO2-L (larger CoO nanosheets), CoO/CeO2 has exhibited higher OER performance due to the faster kinetics and higher OER intrinsic activity because of the large amount of Co/Ce interfaces. Theoretical calculations reveal the generation of the reconstructed active center of the Co–O–Ce configuration due to...
CO elimination through oxidation over highly active and cost-effective catalysts is a way forward fo...
The development of electrocatalysts with high activity and stability for oxygen evolution reaction (...
ABSTRACT: DFT+U calculations of the structure of CeO2(111)-supported Au-based bimetallic nanocluster...
Catalysts are urgently needed to remove the residual CO in hydrogen feeds through selective oxidatio...
The unique interface synergistic catalytic properties for metal oxide-supported catalysts have long ...
The bottom-up design strategy can more rationally optimize the composition and structure of the mate...
The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are considered as the core r...
Understanding the inherent catalytic nature of the interface between metal nanoparticles (NPs) and o...
Catalysts are urgently needed to remove the residual CO in hydrogen feeds through selective oxidatio...
The development of high-performance and inexpensive electrocatalysts for the oxygen evolution reacti...
To reveal the richer chemistry of CO oxidation by CeO2 supported Au Nanoclusters NCs)/Nanoparticles,...
The amorphous Co-Ce binary metal oxides Co1-yCeyOx prepared by the photochemical metal–organic depos...
Oxygen is the most abundant element in the Earth’s crust. The oxygen reduction reaction (ORR) is als...
The bottleneck of large-scale implementation of electrocatalytic water-splitting technology lies in ...
ABSTRACT: DFT+U calculations of CO oxidation by Au13 nanoclusters (NCs) supported on either CeO2 or ...
CO elimination through oxidation over highly active and cost-effective catalysts is a way forward fo...
The development of electrocatalysts with high activity and stability for oxygen evolution reaction (...
ABSTRACT: DFT+U calculations of the structure of CeO2(111)-supported Au-based bimetallic nanocluster...
Catalysts are urgently needed to remove the residual CO in hydrogen feeds through selective oxidatio...
The unique interface synergistic catalytic properties for metal oxide-supported catalysts have long ...
The bottom-up design strategy can more rationally optimize the composition and structure of the mate...
The oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are considered as the core r...
Understanding the inherent catalytic nature of the interface between metal nanoparticles (NPs) and o...
Catalysts are urgently needed to remove the residual CO in hydrogen feeds through selective oxidatio...
The development of high-performance and inexpensive electrocatalysts for the oxygen evolution reacti...
To reveal the richer chemistry of CO oxidation by CeO2 supported Au Nanoclusters NCs)/Nanoparticles,...
The amorphous Co-Ce binary metal oxides Co1-yCeyOx prepared by the photochemical metal–organic depos...
Oxygen is the most abundant element in the Earth’s crust. The oxygen reduction reaction (ORR) is als...
The bottleneck of large-scale implementation of electrocatalytic water-splitting technology lies in ...
ABSTRACT: DFT+U calculations of CO oxidation by Au13 nanoclusters (NCs) supported on either CeO2 or ...
CO elimination through oxidation over highly active and cost-effective catalysts is a way forward fo...
The development of electrocatalysts with high activity and stability for oxygen evolution reaction (...
ABSTRACT: DFT+U calculations of the structure of CeO2(111)-supported Au-based bimetallic nanocluster...