Journal
JOURNAL OF PHYSICS D-APPLIED PHYSICS
Volume 48, Issue 28, Pages -Publisher
IOP PUBLISHING LTD
DOI: 10.1088/0022-3727/48/28/285303
Keywords
gas sensor; transition metal dichalcogenides; first-principles calculations
Categories
Funding
- National Natural Science Foundation of China [11404271]
- '863' program of China [2014AA032608]
- Natural Science Foundation of Fujian Province of China [2011J05006, 2009J05149, 2014J01026]
- Department of Education of Fujian Province [JA09146]
- Huang Hui Zhen Foundation of Jimei University [ZC2010014]
- Scientific Research Foundation of Jimei University [ZQ2011008, ZQ2009004]
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With the aim of understanding recent experimental data concerning molecular doping in WS2-based FET gas sensors, we have investigated the interaction of NH3 and H2O molecules with monolayer WS2, by means of first-principles calculations. The structural relaxations and total energy calculations are performed to determine the preferential binding configurations and it is found that both NH3 and H2O molecules are physisorbed on monolayer WS2. The Bader analysis combined with the plane-averaged differential charge density results indicate that NH3 acts as the electron donor, while H2O acts as the electron acceptor, leading to n- and p-type doping of WS2, respectively. The charge transfer mechanism is discussed in light of the mixing of the molecular highest occupied molecular orbital and lowest unoccupied molecular orbital with the underlying WS2 orbitals. In addition, the modification of the work function is found to be almost linearly dependent on the total charge transfer. The modification of the work function and the carrier concentration can be obtained by tuning the molecule coverages, without destroying the band structure of monolayer WS2. The electrical sensitivities to the gas adsorption make WS2 a gas sensor that promises wide-ranging applications.
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