LAUSR

Abstract Rb-doped K3-xRbxV2(PO4)3/C (x = 0, 0.03, 0.05 and 0.07) composites for high-voltage cathode have been synthesized via a facile sol-gel process. The as-prepared materials have been characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and electrochemical tests. SEM and TEM show that the Rb-doped K3V2(PO4)3/C composites exhibit similar morphology and particle sizes to the undoped one. The electrochemical tests demonstrate that the Rb-doped composites with varied Rb contents deliver better electrochemical performance than the pristine K3V2(PO4)3/C, where K2.95Rb0.05V2(PO4)3/C performs the best. In the voltage range of 2.5–4.6 V (vs. K+/K) at 20 mA g−1, K3V2(PO4)3/C and K2.95Rb0.05V2(PO4)3/C display initial discharge capacities of 41.1 and 55.7 mAh g−1, respectively. The corresponding discharge capacities decrease to 32.1 and 52.6 mAh g−1 after 50 cycles, respectively. At a current density as high as 200 mA g−1, K2.95Rb0.05V2(PO4)3/C still presents higher initial discharge capacity of 34.5 mAh g−1 with a capacity retention of 95.4% after 100 cycles, while K3V2(PO4)3/C only shows the initial discharge of 21.1 mAh g−1 with the capacity retention of 85.7%. The improvement in electrochemical performance of Rb-doped K3V2(PO4)3/C is attributed to the doping of Rb into K sites of K3V2(PO4)3 and this doping can increase the K+ diffusion coefficients in electroactive particles. The results imply that replacement of K+ by larger cations is also helpful to improve the electrochemical performance of other K-containing electrode materials for potassium-ion batteries.