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Probing CO at a specific site on a metal oxide surface is essential for characterizing various applications such as CO oxidation, hydrogenation, and water–gas shift reaction. Herein, we use atomic force microscopy and Kelvin probe force microscopy to probe the CO on a rutile TiO2(110) surface. Our results indicate that CO can be manipulated along the Ti row by the repulsive lateral force of “pushing” mode. Furthermore, the joint combination of precise manipulation and the distance dependence of local contact potential difference allow us to resolve the interatomic dipole moment and charge state of CO at atomic resolution. Therefore, we found that the negatively charged CO with the dipole moment of negative pole down on the rutile TiO2(110) surface. Our results suppose that both the charge state as well as the on-surface dipole interaction are very effective for CO reaction on rutile TiO2(110) surface.

Publication history
Copyright
Acknowledgements

Publication history

Received: 02 July 2021
Revised: 05 August 2021
Accepted: 09 August 2021
Published: 25 September 2021
Issue date: March 2022

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2021

Acknowledgements

Acknowledgements

This work was supported by a Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science (JSPS) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan (JP16H06327, JP16H06504, and JP17H01061). This work was also supported by the International Joint Research Promotion Program of Osaka University (J171013014, J171013007, and Ja19990011). This project was supported by the National Natural Science Foundation of China (NSFC) JSPS-NSFC (No. J191053055).

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