期刊
ACS NANO
卷 11, 期 1, 页码 453-460出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b06392
关键词
electrocatalysis; CO2 reduction reaction; transition-metal dichalcogenides; atomic doping; ionic liquid
类别
资金
- National Science Foundation [NSF-CBET-1512647]
- MRSEC program at the Materials Research Center [NSF DMR-1121262]
- U.S. Department of Energy from the Division of Materials Science and Engineering, Basic Energy Science [DE-AC0206CH11357]
- NSF [DMR-1620901]
- [NSF-DMR-1420709]
- Direct For Mathematical & Physical Scien
- Division Of Materials Research [1620901] Funding Source: National Science Foundation
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [1512647] Funding Source: National Science Foundation
Electrocatalytic conversion of carbon dioxide (CO2) into energy-rich fuels is considered to be the most efficient approach to achieve a carbon neutral cycle. Transition-metal dichalcogenides (TMDCs) have recently shown a very promising catalytic performance for CO2 reduction reaction in an ionic liquid electrolyte. Here, we report that the catalytic performance of molybdenum disulfide (MoS2), a member of TMDCs, can be significantly improved by using an appropriate dopant. Our electrochemical results indicate that 5% niobium (Nb)-doped vertically aligned MoS2 in ionic liquid exhibits 1 order of magnitude higher CO formation turnover frequency (TOF) than pristine MoS2 at an overpotential range of 50-150 mV. The TOF of this catalyst is also 2 orders of magnitude higher than that of Ag nanoparticles over the entire range of studied overpotentials (100-650 mV). Moreover, the in situ differential electrochemical mass spectrometry experiment shows the onset overpotential of 31 mV for this catalyst, which is the lowest onset potential for CO2 reduction reaction reported so far. Our density functional theory calculations reveal that low concentrations of Nb near the Mo edge atoms can enhance the TOF of CO formation by modifying the binding energies of intermediates to MoS2 edge atoms.
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