Tuning the electronic and molecular structures of catalytic active sites with titania nanoligands

Elizabeth I Ross-Medgaarden; Israel E Wachs; William V Knowles; Andrew Burrows; Christopher J Kiely; Michael S Wong

doi:10.1021/ja711456c

Tuning the electronic and molecular structures of catalytic active sites with titania nanoligands

J Am Chem Soc. 2009 Jan 21;131(2):680-7. doi: 10.1021/ja711456c.

Authors

Elizabeth I Ross-Medgaarden¹, Israel E Wachs, William V Knowles, Andrew Burrows, Christopher J Kiely, Michael S Wong

Affiliation

¹ Operando Molecular Spectroscopy and Catalysis Laboratory, Department of Chemical Engineering, Lehigh University, Bethlehem, Pennsylvania 18015, USA.

PMID: 19102648
DOI: 10.1021/ja711456c

Abstract

A series of supported 1-60% TiO(2)/SiO(2) catalysts were synthesized and subsequently used to anchor surface VO(x) redox and surface WO(x) acid sites. The supported TiO(x), VO(x), and WO(x) phases were physically characterized with TEM, in situ Raman and UV-vis spectroscopy, and chemically probed with in situ CH(3)OH-IR, CH(3)OH-TPSR and steady-state CH(3)OH dehydration. The CH(3)OH chemical probe studies revealed that the surface VO(x) sites are redox in nature and the surface WO(x) sites contain acidic character. The specific catalytic activity of surface redox (VO(4)) and acidic (WO(5)) sites coordinated to the titania nanoligands are extremely sensitive to the degree of electron delocalization of the titania nanoligands. With decreasing titania domain size, <10 nm, acidic activity increases and redox activity decreases due to their inverse electronic requirements. This is the first systematic study to demonstrate the ability of oxide nanoligands to tune the electronic structure and reactivity of surface metal oxide catalytic active sites.