Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/184961
Title: Pressure-dependent band-bending in ZnO: A near-ambientpressure X-ray photoelectron spectroscopy study
Authors: Zhirui Ma
Xu Lian
Kaidi Yuan
Shuo Sun 
Chengding Gu 
Jia Lin Zhang 
Jing Lyu
Jian-Qiang Zhong|Lei Liue
Hexing Li
Wei Chen 
Keywords: Near-ambient-pressure X-ray photoelectron spectroscopy
Zinc oxide
Carbon dioxide and oxygen activation
Band-bending
Issue Date: 2020
Publisher: Elsevier
Citation: Zhirui Ma, Xu Lian, Kaidi Yuan, Shuo Sun, Chengding Gu, Jia Lin Zhang, Jing Lyu, Jian-Qiang Zhong|Lei Liue, Hexing Li, Wei Chen (2020). Pressure-dependent band-bending in ZnO: A near-ambientpressure X-ray photoelectron spectroscopy study. Journal of Energy Chemistry. ScholarBank@NUS Repository.
Abstract: ZnO-based catalysts have been intensively studied because of their extraordinary performance in lower olefin synthesis, methanol synthesis and water-gas shift reactions. However, how ZnO catalyzes these reactions are still not well understood. Herein, we investigate the activations of CO2, O2 and CO on single crystalline ZnO polar surfaces at room temperature, through in-situ near-ambient-pressure X-ray photoelectron spectroscopy (NAP-XPS). It is revealed that O2 and CO2 can undergo chemisorption on ZnO polar surfaces at elevated pressures. On the ZnO (0001) surface, molecular CO2 (O2) can chemically interact with the top layer Zn atoms, leading to the formation of CO% &' (O% &') or partially dissociative atomic oxygen (O') and hence the electron depletion layer in ZnO. Therefore, an apparent upward bandbending in ZnO (0001) is observed under the CO2 and O2 exposure. On the ZnO (0001() surface, the molecular chemisorbed CO2 (O2) mainly bond to the surface oxygen vacancies, which also results in an upward band-bending in ZnO (0001(). In contrast, no band-bending is observed for both ZnO polar surfaces upon CO exposure. The electron-acceptor nature of the surface bounded molecules/atoms is responsible for the reversible binding energy shift of Zn 2p3/2 and O 1s in ZnO. Our findings can shed light on the fundamental understandings of CO2 and O2 activation on ZnO surfaces, especially the role of ZnO in heterogeneous catalytic reactions.
Source Title: Journal of Energy Chemistry
URI: https://scholarbank.nus.edu.sg/handle/10635/184961
ISBN: 20954956
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