Small Dopants Make Big Differences: Enhanced Electrocatalytic Performance of MoS2 Monolayer for Oxygen Reduction Reaction (ORR) by N– and P–Doping
[Display omitted] The design and development of low-cost and highly efficient electrocatalysts for oxygen reduction reaction (ORR) is crucial to the large-scale commerical application of fuel cells. Herein, by means of comprehensive densty functional theory (DFT) computations, we explored the potent...
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| Published in | Electrochimica acta Vol. 225; pp. 543 - 550 |
|---|---|
| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Elsevier Ltd
20.01.2017
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| Subjects | |
| Online Access | Get full text |
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| Abstract | [Display omitted]
The design and development of low-cost and highly efficient electrocatalysts for oxygen reduction reaction (ORR) is crucial to the large-scale commerical application of fuel cells. Herein, by means of comprehensive densty functional theory (DFT) computations, we explored the potential of the heteroatom doping (N and P) to activate the basal plane of molybdenum disulfide (MoS2) monolayer for ORR in acidic medium. Our computations revealed that substituting S in MoS2 monolayer with N or P atom can introduce high spin density into MoS2 basal plane, leading to its improved chemical reactivity for the O2 activation, and the subsequent ORR steps prefer to proceed though a more efficient 4e pathway. Especially, N-doped MoS2 monolayer exhibits outstanding ORR catalytic performance in terms of its small overpotential (0.67V) and low energy barrier (0.25eV), which is comparable (even lower) to those of Pt–based electrocatalysts. In contrast, the catalytic activity of P–doped MoS2 monolayer is considerably poor due to its very strong interaction with O* and OOH* species in the subsequent reactions. Therefore, we expect that N-doped MoS2 monolayer is a quite promising single-atom-catalyst with high efficiency for ORR in fuel cells. |
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| AbstractList | [Display omitted]
The design and development of low-cost and highly efficient electrocatalysts for oxygen reduction reaction (ORR) is crucial to the large-scale commerical application of fuel cells. Herein, by means of comprehensive densty functional theory (DFT) computations, we explored the potential of the heteroatom doping (N and P) to activate the basal plane of molybdenum disulfide (MoS2) monolayer for ORR in acidic medium. Our computations revealed that substituting S in MoS2 monolayer with N or P atom can introduce high spin density into MoS2 basal plane, leading to its improved chemical reactivity for the O2 activation, and the subsequent ORR steps prefer to proceed though a more efficient 4e pathway. Especially, N-doped MoS2 monolayer exhibits outstanding ORR catalytic performance in terms of its small overpotential (0.67V) and low energy barrier (0.25eV), which is comparable (even lower) to those of Pt–based electrocatalysts. In contrast, the catalytic activity of P–doped MoS2 monolayer is considerably poor due to its very strong interaction with O* and OOH* species in the subsequent reactions. Therefore, we expect that N-doped MoS2 monolayer is a quite promising single-atom-catalyst with high efficiency for ORR in fuel cells. |
| Author | Zhang, Huiying Cai, Qinghai Tian, Yu Chen, Zhongfang Zhao, Jingxiang |
| Author_xml | – sequence: 1 givenname: Huiying surname: Zhang fullname: Zhang, Huiying organization: Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, and College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, China – sequence: 2 givenname: Yu surname: Tian fullname: Tian, Yu organization: Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, and College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, China – sequence: 3 givenname: Jingxiang surname: Zhao fullname: Zhao, Jingxiang email: xjz_hmily@163.com organization: Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, and College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, China – sequence: 4 givenname: Qinghai surname: Cai fullname: Cai, Qinghai organization: Key Laboratory of Photonic and Electronic Bandgap Materials, Ministry of Education, and College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, 150025, China – sequence: 5 givenname: Zhongfang surname: Chen fullname: Chen, Zhongfang organization: Department of Chemistry, Institute of Functional Nanomaterials, University of Puerto Rico, Rio Piedras Campus, San Juan, PR 00931, USA |
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