کد مقاله کد نشریه سال انتشار مقاله انگلیسی ترجمه فارسی نسخه تمام متن
53209 46953 2016 6 صفحه PDF سفارش دهید دانلود کنید
عنوان انگلیسی مقاله ISI
A DFT-based study of surface chemistries of rutile TiO2 and SnO2(110) toward formaldehyde and formic acid
ترجمه فارسی عنوان
یک مطالعه بر اساس DFT مواد شیمیایی سطح TiO2 روتیل و SnO2 (110) نسبت به فرمالدئید و اسید فرمیک
کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی کاتالیزور
چکیده انگلیسی


• Adsorption of formaldehyde and formic acid on rutile TiO2(110) and SnO2(110) results in similar adsorption configurations.
• Stoichiometric SnO2(110) shows a stronger binding towards adsorbates the TiO2(110).
• The presence of bridge-bond oxygen vacancy on the surface makes TiO2(110) bind the adsorbates stronger than SnO2(110).
• TiO2(110) and SnO2(110) show different activities for the conversion of formaldehyde and formic acid.

Rutile TiO2 and SnO2 are two structurally similar metal oxides found applications in catalysis and solid-state sensory devices as well as optics and electronics. In present work, we studied the adsorption and conversion of formaldehyde and formic acid on the (110) surfaces of rutile TiO2 and SnO2 based on density functional theory computational results. As oxygen vacancy is one of the most important and common defects on these metal oxides, the effect of the oxygen vacancy on adsorption and transformation were also examined. The results show that the adsorption of formaldehyde and formic acid resulted in similar adsorption configurations on SnO2(110) and TiO2(110). On the stoichiometric surface, SnO2 exhibits a stronger binding toward the adsorbates than TiO2. On the other hand, TiO2(110) with one bridge-bonded oxygen vacancy shows a stronger binding toward the adsorbates than SnO2(110) with the same type of defects. The bridge-bonded oxygen vacancy played important roles in adsorption and conversion and the Vo-bidentate formate species is the key intermediate in the oxidation of formaldehyde to formic acid. TiO2(110) has a higher activity than SnO2(110) for the reactions examined herein.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Catalysis Today - Volume 274, 1 October 2016, Pages 103–108
نویسندگان
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