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Venkataswamy Perala Jampaiah Deshetti Kandjani Ahmad Esmaielzadeh Sabri Ylias M. Reddy Benjaram M. Vithal M. 《Research on Chemical Intermediates》2018,44(4):2523-2543
Research on Chemical Intermediates - In this work, various transition and rare earth metal ions (M3+; M = Mn3+, Fe3+, La3+, and Pr3+) doped CeO2 solid solutions were prepared by a... 相似文献
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Deshetti Jampaiah Anastasios Chalkidis Ylias M. Sabri Suresh K. Bhargava 《Chemical record (New York, N.Y.)》2019,19(7):1407-1419
The necessity to drastically act against mercury pollution has been emphatically addressed by the United Nations. Coal‐fired power plants contribute a great deal to the anthropogenic emissions; therefore, numerous sorbents/catalysts have been developed to remove elemental mercury (Hg0) from flue gases. Among them, ceria (CeO2) has attracted significant interest, due to its reversible Ce3+/Ce4+ redox pair, surface‐bound defects and acid‐base properties. The removal efficiency of Hg0 vapor depends among others, on the flue gas composition and temperature. CeO2 can be incorporated into known materials in such a way that the abatement process can be effective at different operating conditions. Hence, the scope of this account is to discuss the role of CeO2 as a promoter, active phase and support in the design of composite Hg0 sorbents/catalysts. The elucidation of each of these roles would allow the integration of CeO2 advantageous characteristics to such degree, that tailor‐made environmental solution to complex issues can be provided within a broader application scope. Besides, it would offer invaluable input to theoretical calculations that could enable the materials screening and engineering at a low cost and with high accuracy. 相似文献
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Dr. Hamidreza Arandiyan Dr. Sajjad S. Mofarah Dr. Yuan Wang Dr. Claudio Cazorla Dr. Deshetti Jampaiah Dr. Magnus Garbrecht Prof. Karen Wilson Prof. Adam F. Lee Prof. Chuan Zhao Prof. Thomas Maschmeyer 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(58):14418-14426
Perovskite oxides are regarded as promising electrocatalysts for water splitting due to their cost-effectiveness, high efficiency and durability in the oxygen evolution reaction (OER). Despite these advantages, a fundamental understanding of how critical structural parameters of perovskite electrocatalysts influence their activity and stability is lacking. Here, we investigate the impact of structural defects on OER performance for representative LaNiO3 perovskite electrocatalysts. Hydrogen reduction of 700 °C calcined LaNiO3 induces a high density of surface oxygen vacancies, and confers significantly enhanced OER activity and stability compared to unreduced LaNiO3; the former exhibit a low onset overpotential of 380 mV at 10 mA cm−2 and a small Tafel slope of 70.8 mV dec−1. Oxygen vacancy formation is accompanied by mixed Ni2+/Ni3+ valence states, which quantum-chemical DFT calculations reveal modify the perovskite electronic structure. Further, it reveals that the formation of oxygen vacancies is thermodynamically more favourable on the surface than in the bulk; it increases the electronic conductivity of reduced LaNiO3 in accordance with the enhanced OER activity that is observed. 相似文献
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