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LiFePO4 (LFP), the attractive commercial cathode materials, exhibits the phase separation between lithium-poor and lithium-rich phase within individual particles due to the wide miscibility gap. The boundaries between such phases develop large stress, lead to cracks within individual particles, and decay the cycle life. There have been lots of interest in investigating the origin of lithium heterogeneity and manipulating the phase boundaries within the particles during cycling. Previously, we revealed that insertion kinetics is dependent on the local lithium composition from which the hysteresis of lithium spatiodynamics originate. [ref.1] In addition, uniformity of ion insertion kinetics at electrolyte-electrode interface governs lithium heterogeneity and spatiodynamics in ether-based organic electrolyte. [ref.1] However, it remains still unclear how the chemical interaction of lithium ions, electrolyte molecules, and solid electrode controls nanoscale ion insertion kinetics. By developing operando scanning transmission x-ray microscopy (STXM) platform which maps lithium composition within individual LFP particles at 50 nm resolution during cycling, we investigated the interfacial lithium transport in various electrolytes: water, carbonates, and ethers. We synthesized LFP particles with platelet morphology and [010] crystallographic axis, which is fast ion diffusion direction, lied parallel to the monochromatic X-ray allowing to visualize lithium transport in the particles. Herein, we discover that aqueous electrolyte greatly accelerates lithium insertion kinetics, completely redirecting lithium heterogenesity and spatiodynamics compared with organic-based electrolyte. Aqueous environment kinetics show higher exchange current density (~700 mAm-2) than organic EC/DMC (~200 mAm-2) and also higher surface diffusion rate which account for the higher degree of intraparticle phase separation within the particles. By extracting kinetics parameters from our result, we experimentally demonstrate that heterogeneity and spatiodynamics in the single particle kinetics is determined by the strong interaction between the electrolyte molecules and the surface of electrode particles. Ref. 1 J. Lim et al. Science (2016) 353 p566 Figure 1