Abstract
We report evidence for the electrochemical activity of transition-metal carbodiimides versus lithium and sodium. In particular, iron carbodiimide, FeNCN, can be efficiently used as negative electrode material for alkali-metal-ion batteries, similar to its oxide analogue FeO. Based on 57Fe Mössbauer and infrared spectroscopy (IR) data, the electrochemical reaction mechanism can be explained by the reversible transformation of the Fe-NCN into Li/Na-NCN bonds during discharge and charge. These new electrode materials exhibit higher capacity compared to well-established negative electrode references such as graphite or hard carbon. Contrary to its oxide analogue, iron carbodiimide does not require heavy treatments (such as nanoscale tailoring, sophisticated textures, or coating) to obtain long cycle life with current density as high as 9A g-1 for hundreds of charge-discharge cycles. Similar to the iron compound, several other transition-metal carbodiimides Mx(NCN)y with M=Mn, Cr, Zn can cycle successfully versus lithium and sodium. Their electrochemical activity and performance open the way to the design of a novel family of anode materials.
Original language | English |
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Pages (from-to) | 5090-5095 |
Number of pages | 6 |
Journal | Angewandte Chemie - International Edition |
Volume | 55 |
Issue number | 16 |
DOIs | |
State | Published - Apr 11 2016 |
Funding
M.T.S. acknowledge Dr. Bernard Fraisse for his help in the in situ experiments. X.L. and R.D. happily acknowledge the long-time support of the Deutsche Forschungsgemeinschaft (DFG). R.P.H. acknowledges support from the Materials Sciences and Engineering Division, Office of Basic Energy Sciences, US Department of Energy.
Funders | Funder number |
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U.S. Department of Energy | |
Basic Energy Sciences | |
Division of Materials Sciences and Engineering | |
Deutsche Forschungsgemeinschaft |
Keywords
- batteries
- carbodiimide
- lithium ions
- sodium ions