DFT study of CO 2 adsorption and hydrogenation on the in 2O 3 surface

Jingyun Ye, Changjun Liu, Qingfeng Ge

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157 Scopus citations

Abstract

Catalytic conversion of CO 2 to liquid fuels or valuable chemicals is an attractive alternative to geological sequestration. In the present study, we applied density functional theory slab calculations in the investigation of the adsorption and hydrogenation of CO 2 on the (110) surface of In 2O 3. Our results indicate that the adsorbed CO 2 is activated, forming a surface carbonate species by combining with surface oxygen, and has an adsorption energy of -1.25 eV. Heterolytic dissociative adsorption of H 2 results in a surface hydroxyl from H binding the surface O site and a hydride from H binding the In site. The migration of H from the In site to the neighboring O site is energetically favorable but has a significant activation barrier of 1.32 eV. Water may adsorb on the surface either molecularly or dissociatively, with adsorption energy of -0.83 eV and -1.19 eV, respectively. Starting from CO 2 coadsorbed with the H adatoms on the In 2O 3 surface, we examined two possible conversion pathways for CO 2: (a) CO 2 is hydrogenated by the H adatom on the In site to form a surface formate species (HCOO); (b) CO 2 is protonated by the H adatom on the O site to form a surface bicarbonate species (COOH). Reaction a is endothermic by +0.33 eV, whereas b is exothermic by -0.78 eV. Although the formation of the bicarbonate species is energetically favorable, the subsequent step to form CO and OH is highly endothermic, with a reaction energy of +1.07 eV. Furthermore, the bicarbonate species can react with a surface hydroxyl easily, resulting in coadsorbed H 2O and CO 2. These results indicate that hydrogenation of CO 2 to the formate species is favorable over protonation to the bicarbonate species on the In 2O 3 surface. These results are consistent with the experimental observations that the indium oxide based catalyst has a high CO 2 selectivity and H 2O resistance.

Original languageEnglish (US)
Pages (from-to)7817-7825
Number of pages9
JournalJournal of Physical Chemistry C
Volume116
Issue number14
DOIs
StatePublished - Apr 12 2012

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