TY - JOUR
T1 - Effects of Oxygen Vacancies and Cation Valence States on the Triboelectric Property of Substoichiometric Oxide Films
AU - Zhu, Yongqiao
AU - Lin, Shiquan
AU - Gao, Wenchao
AU - Zhang, Miao
AU - Yang, Chaogui
AU - Feng, Peizhong
AU - Xu, Cheng
AU - Wang, Zhong Lin
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/8/4
Y1 - 2021/8/4
N2 - Temperature effects on the contact electrification (CE) is of great interest. Here, different kinds of substoichiometric oxide films, such as TiO2-x, Al2O3-x, Ta2O5-x, and Cr2O3-x, are deposited and annealed at different temperatures, and the CE between the films and a Pt-coated tip is performed by using Kelvin probe force microscopy (KPFM). An intriguing finding is that the polarity on the TiO2-x surface changes from negative to positive with the increase of the sample annealing temperature in air atmosphere. Such a result is attributed to the fact that annealing under an oxidative atmosphere repairs oxygen vacancies and helps upgrade the low valency of Ti3+ to a stable high valency of Ti4+. On the contrary, after annealing occurs in an Ar/H2 atmosphere, the polarity on the TiO2-x surface reverses from positive to negative. This is mainly due to the increase of oxygen vacancies after annealing in reducing atmosphere. Through the KPFM results of Al2O3-x, Ta2O5-x, and Cr2O3-x films, the effect of oxygen vacancies is further confirmed, that is, the decrease of oxygen vacancies eases the films at capturing positive charges. Based on this, TiO2-x-based identical material triboelectric nanogenerators (IM-TENGs) are designed and prepared for the first time to control the current direction. Moreover, a surface state model for explaining the CE mechanism between the metal and annealed dielectric is proposed. This study is conducive to the development of the IM-TENGs which regulate the current direction or voltage output accurately in the future and also provides a further understanding of the dominant mechanism of electron transfer in the CE.
AB - Temperature effects on the contact electrification (CE) is of great interest. Here, different kinds of substoichiometric oxide films, such as TiO2-x, Al2O3-x, Ta2O5-x, and Cr2O3-x, are deposited and annealed at different temperatures, and the CE between the films and a Pt-coated tip is performed by using Kelvin probe force microscopy (KPFM). An intriguing finding is that the polarity on the TiO2-x surface changes from negative to positive with the increase of the sample annealing temperature in air atmosphere. Such a result is attributed to the fact that annealing under an oxidative atmosphere repairs oxygen vacancies and helps upgrade the low valency of Ti3+ to a stable high valency of Ti4+. On the contrary, after annealing occurs in an Ar/H2 atmosphere, the polarity on the TiO2-x surface reverses from positive to negative. This is mainly due to the increase of oxygen vacancies after annealing in reducing atmosphere. Through the KPFM results of Al2O3-x, Ta2O5-x, and Cr2O3-x films, the effect of oxygen vacancies is further confirmed, that is, the decrease of oxygen vacancies eases the films at capturing positive charges. Based on this, TiO2-x-based identical material triboelectric nanogenerators (IM-TENGs) are designed and prepared for the first time to control the current direction. Moreover, a surface state model for explaining the CE mechanism between the metal and annealed dielectric is proposed. This study is conducive to the development of the IM-TENGs which regulate the current direction or voltage output accurately in the future and also provides a further understanding of the dominant mechanism of electron transfer in the CE.
KW - annealing
KW - contact electrification
KW - nanogenerator
KW - surface states
KW - triboelectrification
UR - https://www.scopus.com/pages/publications/85112251916
U2 - 10.1021/acsami.1c09248
DO - 10.1021/acsami.1c09248
M3 - Article
C2 - 34297527
AN - SCOPUS:85112251916
SN - 1944-8244
VL - 13
SP - 35795
EP - 35803
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 30
ER -