Tuning the Work Function of Ti3C2Tx MXene by Molecular Doping without Changing its Surface Functional Groups

被引:30
作者
El-Demellawi, Jehad K. [1 ]
Mansour, Ahmed E. [1 ]
El-Zohry, Ahmed M. [1 ,2 ]
Hedhili, Mohamed N. [3 ]
Yin, Jun [1 ,4 ]
Emwas, Abdul-Hamid M. [3 ]
Maity, Partha [1 ]
Xu, Xiangming [1 ]
Bakr, Osman M. [1 ]
Mohammed, Omar F. [1 ]
Alshareef, Husam N. [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Phys Sci & Engn PSE Div, Thuwal 239556900, Saudi Arabia
[2] King Fahd Univ Petr Minerals KFUPM, Coll Petr & Geosci CPG, Ctr Integrat Petr Res CIPR, Dhahran 31261, Saudi Arabia
[3] King Abdullah Univ Sci & Technol KAUST, Core Labs, Thuwal 239556900, Saudi Arabia
[4] Hong Kong Polytech Univ, Dept Appl Phys, Kowloon, Hong Kong 999077, Peoples R China
来源
ACS MATERIALS LETTERS | 2022年 / 4卷 / 12期
关键词
ELECTRONIC-PROPERTIES;
D O I
10.1021/acsmaterialslett.2c00796
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Owing to their impressive electronic/optoelectronic properties, MXenes have attracted significant attention among the 2D materials research community. Their work function (WF) tunability, in particular, has permitted efficient interfacial band alignment engineering in several device applications. However, like most of their properties, the WF of MXenes highly depends on their surface terminations, making it hard to individually modify the WF without compromising other fundamental properties, which hinders the exploitation of MXenes to their full potential. Herein, we introduce a surface-terminationindependent method to tune the WF of Ti3C2Tx MXene through molecular doping. The achieved stepwise 500-meV increase in WF, in similar to 120-meV increments, is induced by subsurface electron depletion from Ti(3)C(2)Tx, with no effect on its other key properties. Utilizing electron paramagnetic resonance and ultrafast laser spectroscopy, we reveal that tuning the WF of Ti(3)C(2)Tx is entirely surfacetermination-independent. Such discrete control over the WF renders MXene-based devices with unprecedented operational degrees of freedom.
引用
收藏
页码:2480 / 2490
页数:11
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