Several crystal forms of FeOOH are recently reported to be highly promising for lithium storage due to their high capacity, low cost, and environmental friendliness. In particular, β‐FeOOH has shown a capacity of ≈1000 mAh g −1 , which is comparable to other promising iron‐based anodes, such as Fe 2 O 3 and Fe 3 O 4. However, its storage mechanisms are unclear and the potential for further improvement remains unexplored. Here, it is shown that this material can have a very high reversible capacity of ≈1400 mAh g −1 , which is 20%–40% higher than Fe 2 O 3 and Fe 3 O 4 . Such a high capacity is delivered from a series of reactions including intercalation and conversion reactions, formation/deformation of solid‐state electrolyte interface layers and interfacial storage. The mechanisms are studied by a combination of electrochemical and X‐ray absorption near edge spectroscopic approaches. Moreover, very long cycling performance, that is, after even more than 3000 cycles the material still has a significant capacity of more than 800 mAh g −1 , is obtained by a simple electrode design involving introducing a rigid support into porous electrodes. Such long cycling performance is for the first time achieved for high‐capacity materials based on conversion reactions.
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Yu et al. (2014) studied this question.
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