钒酸盐
氧化还原
催化作用
氮氧化物
硫酸盐
X射线光电子能谱
化学工程
化学
无机化学
电子转移
吉布斯自由能
异质结
材料科学
光化学
物理化学
有机化学
工程类
光电子学
热力学
燃烧
物理
作者
Rahul Purbia,Sung Yeol Choi,Hee Jun Kim,Bora Ye,Bora Jeong,Duck Hyun Lee,Hyesung Park,Hong‐Dae Kim,Jeong Min Baik
标识
DOI:10.1016/j.cej.2022.135427
摘要
The objective of this study was to demonstrate a facile strategy for vanadate-based catalysts having high NOx conversion efficiency (∼96% @ 220 °C) and improved SO2 resistance by impregnating highly-dispersed CuO–CeO2 nano-heterostructures to V2O5–CeO2–WO3/TiO2 catalysts. The key design of catalysts was based on the maximization of interface chemistry towards synergetic effects of catalytic and redox reactions between Cu and Ce species. The impregnation of 0.1 wt% CuO–CeO2 possessed more surface acid sites and enhanced redox ability at low temperatures (180–220 °C). Based on Gibbs energy calculation and XPS results, thermodynamically favorable reaction of Cu2+ + Ce3+ → Cu+ + Ce4+ made it a perfect candidate for an excellent redox system with V4+/V5+ charge imbalance proportion through electron migration at the adjacent interface. The strong redox interaction and facile electron transfer could also restrain the formation of surface sulfate species and showed an excellent SO2 and water tolerance.
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