光催化
氮氧化物
相对湿度
吸附
化学
氮气
辐照
环境化学
分析化学(期刊)
材料科学
催化作用
物理化学
有机化学
气象学
物理
核物理学
燃烧
作者
Biwu Chu,Yuan Liu,Hao Li,Yongcheng Jia,Jun Liu,Qing Cao,Tianzeng Chen,Peng Zhang,Qingxin Ma,Xiao Cheng Zeng,Joseph S. Francisco,Hong He
标识
DOI:10.1002/anie.202304017
摘要
N2 O5 is an important intermediate in the atmospheric nitrogen cycle. Using a flow tube reactor, N2 O5 was found to be released from the TiO2 surface during the photocatalytic oxidation of NO2 , revealing a previously unreported source of N2 O5 . The rate of N2 O5 release from TiO2 was dependent on the initial NO2 concentration, relative humidity, O2 /N2 ratio, and irradiation intensity. Experimental evidence and quantum chemical calculations showed that NO2 can react with the surface hydroxyl groups and the generated electron holes on the TiO2 , followed by combining with another NO2 molecule to form N2 O5 . The latter was physisorbed on TiO2 and had a low adsorption energy of -0.13 eV. Box model simulations indicated that the new source of N2 O5 released from TiO2 can increase the daytime N2 O5 concentration by up to 20 % in urban areas if abundant TiO2 -containing materials and high NOx concentrations were present. This joint experimental/theoretical study not only demonstrates a new chemical mechanism for N2 O5 formation but also has important implications for air quality in urban areas.
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