期刊
APPLIED SURFACE SCIENCE
卷 537, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apsusc.2020.147970
关键词
Density-functional theory; Chemisorption/Physisorption: adsorbates on surfaces; Adsorption kinetics; Graphene films; Band structure and DOS; Magnetic impurity interaction
类别
资金
- Emirati Center for Environmental and Energy Research at the United Arab Emirates University [31R145, 31R216]
The effect of magnetic moment on hydrogen adsorption and gas-sensing properties in Mn-embedded C2N was investigated using Density Functional Theory. The results showed significant changes in electronic structure due to chemisorption, leading to enhanced sensor responses. C2N:Mn was identified as a promising candidate for a high sensitivity and selectivity hydrogen magnetic gas sensor.
Density functional theory (DFT) has been employed to investigate the effect of magnetic moment on the hydrogen adsorption and gas-sensing properties in Mn-embedded in C2N. Special focus was given to the effects of both magnetization and dimerization on the adsorption properties. Two distinct configurations of embedment were considered: (i) Single atom catalyst (SAC): 1Mn@C2N; and (ii) Dimer atom Catalyst (DAC): Mn-2@C2N. The results showed that the H-2 molecule to exhibit chemisorption processes on both SAC and DAC with weak molecular dissociation. The effect of chemisorption on the electronic structure is so enormous to the extent that the DOS got fragmented near Fermi level with opening of small gaps of order 0.11 eV and 0.20 eV in SAC and DAC, respectively. Such changes would be manifested in enhanced sensor responses. Based upon the huge changes in electronic and magnetic properties induced by the chemisorption and the low recovery time (i.e., tau << 1 s, tau = 92 mu s and 1.8 ms, respectively), we concluded that C2N:Mn should be an excellent candidate for (reusable) hydrogen magnetic gas sensor with high sensitivity and selectivity and rapid recovery time. Our theoretical results were corroborated with good agreement with the available data in literature.
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