The valance state of vanadium-key factor in the flexibility of potassium vanadates structure as cathode materials in Li-ion batteries

Potassium hexavanadate (K(2)V(6)O(16)·nH(2)O) nanobelts have been synthesized by the LPE-IonEx method, which is dedicated to synthesis of transition metal oxide bronzes with controlled morphology and structure. The electrochemical performance of K(2)V(6)O(16)·nH(2)O as a cathode material for lithium-ion batteries has been evaluated. The KVO nanobelts demonstrated a high discharge capacity of 260 mAh g(−1), and long-term cyclic stability up to 100 cycles at 1 A g(−1). The effect of the vanadium valence state and unusual construction of the nanobelts, composed of crystalline and amorphous domains arranged alternately were also discussed in this work. The ex-situ measurements of discharged electrode materials by XRD, MP-AES, XAS and XPS show that during the subsequent charge/discharge cycle the potassium in the K(2)V(6)O(16)·nH(2)O structure are replacing by lithium. The structural stability of the potassium hexavandate during cycling depends on the initial vanadium valence state on the sample surface and the presence of the “fringe free” domains in the K(2)V(6)O(16)·nH(2)O nanobelts.