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Heteroatom‐doped transition metal oxides have attracted great attention as advanced anode materials for lithium‐ion batteries due to their high theoretical capacity and superior properties. However, the limited resource availability has led to a substantial rise in prices for valuable metals such as Ni and Co, posing a significant challenge for their application. To address this issue, recycling of these metals from waste materials have gained prominence, and particularly the recovery of Co has been mostly focused on its economic benefits. Herein, we introduced a novel recycling strategy for fabrication of heteroatom‐doped CoO x (comprising mainly Co 3 O 4 with a minor CoO phase) anode with a yolk–shell structure for lithium‐ion batteries, by separating Co from cemented tungsten carbide waste. By employing a simple leaching process and subsequent spray pyrolysis, the yolk–shell structured microsphere comprising CoO x was successfully synthesized. Moreover, the presence of other waste metals in the leachate facilitated multi‐heteroatom doping during synthesis. Interestingly, the introduction of various dopants into CoO x induced oxygen vacancy formation, thereby enhancing the electrochemical properties of the CoO x anode. As a result, compared with the phase‐pure (un‐doped) CoO x yolk–shell, the heteroatom‐doped CoO x yolk–shell exhibited robust cycling stability (602 mAh·g −1 for 200 cycles at 1 A·g −1 ) and excellent rate capability (210 mAh·g −1 at 10 A·g −1 ).
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Kim et al. (2024) studied this question.
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