Selective catalytic reduction (SCR) is probably the most widespread process for limiting NO emissions under lean conditions (O excess) and, in addition to the currently used NH or urea as a reducing agent, many other alternative reductants could be more promising, such as CH/CHO, H and CO. Different catalysts have been used thus far for NO abatement from mobile (automotive) and stationary (fossil fuel combustion plants) sources, however, perovskites demand considerable attention, partly due to their versatility to combine and incorporate various chemical elements in their lattice that favor deNO catalysis. In this work, the CH/CHO, H, and CO-SCR of NO on perovskite-based catalysts is reviewed, with particular emphasis on the role of the reducing agent nature and perovskite composition. An effort has also been made to further discuss the correlation between the physicochemical properties of the perovskite-based catalysts and their deNO activity. Proposed kinetic models are presented as well, that delve deeper into deNO mechanisms over perovskite-based catalysts and potentially pave the way for further improving their deNO efficiency.
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http://dx.doi.org/10.3390/nano12071042 | DOI Listing |
Adv Sci (Weinh)
December 2024
School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.
The significant interest in perovskite oxides stems from their compositional and structural flexibility, particularly in the field of electrochemistry. In this study, the double E strategy (exsolution and electrodeposition strategies) is successfully devised for synthesizing perovskite-based bifunctional electrocatalysts, enabling simultaneous OER and HER applications with exceptional catalytic performance. The synthesized R-LCTFe/Ni catalyst exhibits outstanding electrocatalytic activity, delivering low overpotentials of 349 and 309 mV at 10 mA cm for OER and HER, respectively, indicating substantial improvements in the inherent electrocatalytic activity.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Xi'an Key Laboratory of Functional Supramolecular Structure and Materials, College of Chemistry and Material Science, Northwest University, Xi'an 710127, China.
The oxygen evolution reaction (OER) poses a significant kinetic challenge for various critical energy conversion and storage technologies including electrocatalytic water splitting and metal-air batteries. In this study, a LaCoO/NiFe layered double hydroxide (LDH) catalyst was synthesized through the growth of n-type NiFe LDH on the surface of the p-type LaCoO semiconductor, resulting in a p-n heterostructure for a photogenerated carrier-assisted electrocatalytic OER (PCA-eOER). The alignment of their band structures facilitates the formation of an internal electric field at the heterojunction interface, which promotes the creation of oxygen vacancies and enhances electron transport.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
Henan Key Laboratory of Quantum Materials and Quantum Energy, School of Quantum Information Future Technology, Henan University, Zhengzhou 450046, China.
Co and Ni codoped strontium ferrite particles were prepared by a solid-state strategy and employed as catalysts for the OER. They exhibited a Tafel slope of 55 mV dec and required an overpotential of 334 mV to afford a current density of 10 mA cm, which is lower than that of Co and Ni separately doped samples. The DFT calculations reveal the redistribution of local charge around Fe atoms, decrease of energy barriers, and increase of conductivity by doping.
View Article and Find Full Text PDFACS Sens
December 2024
Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.
Chemistry
January 2025
School of Chemical and Environmental Engineering, China University of Mining & Technology (Beijing), Beijing, 100083, P. R. China.
Bifunctional catalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) are essential components of rechargeable zinc-air batteries. In this study, we synthesized a PrBaMnCoRuO (PBMCRO) perovskite composite with in situ exsolved CoRu nanoparticles and Co-N-C, functioning as an efficient bifunctional electrocatalyst for zinc-air batteries. The in situ exsolution of CoRu nanoparticles from the perovskite oxide was facilitated by the reducing action of 2-methylimidazole (2-MIM).
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