Abstract

Vanadium-based materials are promising cathode materials for aqueous rechargeable zinc-ion batteries (ZIBs). However, up to now, the detailed Zn ion intercalation mechanisms are still not fully clear. In this work, we first show a new facile synthesis approach for V 3 O 7 ·H 2 O nanoarray cathode with large mass loadings (1.0–12 mg cm −2 ). An empirical model is proposed to assess the utilization ratio of active materials under different mass loadings. Then, through the combination of first-principles calculations and a series of ex-situ characterizations, we identify for the first time a two-step Zn 2+ intercalation mechanism in V 3 O 7 ·H 2 O. The stepwise and reversible intercalation process is manifested by different diffusion energy barriers and segmented electrochemical kinetics in various discharge depths. The nanoarray binder-free electrode is also applied in pouch cells which show high capacities than state-of-the-art ZIB pouch cells. This study may provide an elucidation for the disputed Zn 2+ intercalation chemistry of vanadium-based cathodes in ZIBs as well as a guidance to the design of high-mass-loading battery materials. By combination of first-principles calculation and comprehensive ex-situ characterizations, a two-step Zn 2+ intercalation mechanism in V 3 O 7 ·H 2 O is demonstrated in this work. An empirical model is proposed to assess the utilization ratio of active materials under different mass loadings. • A facile scalable method is developed to synthesize free-standing V 3 O 7 ·H 2 O cathode with large mass loading. • An empirical model is proposed to assess the utilization ratio of active materials under different loadings. • The two-step Zn 2+ intercalation mechanism is verified for V 3 O 7 ·H 2 O cathode.

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