期刊
NANOSCALE
卷 12, 期 26, 页码 14004-14010出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0nr01218a
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资金
- National Natural Science Foundation of China [21531006, 21773163]
- State Key Laboratory of Organometallic Chemistry of Shanghai Institute of Organic Chemistry [2018kf-05]
- Project of Scientific and Technologic Infrastructure of Suzhou [SZS201905]
The development of metal-organic frameworks (MOFs) as high-efficiency electrocatalysts for water splitting has attracted special attention due to their unique structural features including high porosity, large surface areas, high concentrations of active sites, uniform pore sizes and shapes,etc. Most of the related reports focus on thein situgeneration of high-efficiency electrocatalysts by annealed MOFs. However, the pyrolysis process usually destroys the porous structure of MOFs and reduces the number of active sites due to the absence of organic ligands and agglomeration of metal centers. In this work, we prepared unique NiCo-MOF hollow nanospheres (NiCo-MOF HNSs) by a solvothermal method and further fabricated Fe-doped NiCo-MOF HNSs (Fe@NiCo-MOF HNSs) by a simple impregnation-drying method. Significant enhancement of electrocatalytic activity of Fe@NiCo-MOF HNSs was witnessed because of the doped Fe. Compared with the parent NiCo-MOF HNSs, the optimized Fe@NiCo-MOF HNSs exhibited a lower overpotential of 244 mV at 10 mA center dot cm(-2)with a smaller Tafel slope of 48.61 mV center dot dec(-1), which was lowered byca.90 mV due to the influence of Fe doping on the electronic structure of the active centers of Ni and Co. The above materials also displayed excellent stability without obvious activity decay for at least 16 hours. These findings present a new entry in the design and fabrication of high-efficiency MOF-based electrocatalysts for energy conversion.
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