MOFs-like polyoxometalate (POMs) electrodes have already emerged as promising candidates for lithium-ion batteries (LIBs), yet the origins of the underlying redox mechanism in such materials remain a matter of uncertainty. Of critical challenges are the anomalously high storage capacities beyond their theoretical values and the fast ion diffusivity that cannot be satisfactorily comprehended in the theory of crystal lattice. Herein, for the first time we decode t2g electron occupation-regulated dual-redox Li-storage mechanism as the true origin of extra capacity in POMs electrodes. Enhanced V-t2g orbital occupation by Li coordination significantly triggers the Hubbard gap closure and reversible Li deposition/dissolution at surface region. Conjugated V-O-Li configuration at interlayers endow Li+ ion pathways along pore walls as the dominant contribution to the low migration barrier and fast diffusivity. As a result, remarkable cycle stability (~100 % capacity retention after 2000 cycles at 1 A g-1), extremely high specific capacity (1200 mAh g-1 at 100 mA g-1) and excellent rate performance (404 mAh g-1 at 8 A g-1) were achieved, providing new understandings on the underlying mechanism of POMs electrodes and pivotal guidance for dual-storage materials.
Keywords: polyoxometalates * extra capacity * Li-storage mechanism * ion diffusivity * electrochemistry.
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