promising anode candidates for highenergy rechargeable batteries. [1] Nevertheless, the uncontrolled dendrite formation and poor reversible Li plating/stripping efficiency long hinder its practical application. Fundamentally, the reactive nature of Li metal can spontaneously trigger side reactions with the electrolyte and form a passivation layer (called solid electrolyte interphase, SEI). [2] The chemical heterogeneity and mechanical instability of SEI are generally considered as the reasons for dendrites formation. [3] Therefore, manipulating the electrolyte chemistry is considered as the most effective method, for it can directly impact the properties of SEI and alter Li + deposition behavior. [4] In the electrolyte, Li + is solvated by solvents and anions to form the Li + solvation sheath. [5] The Li + solvation sheath can diffuse freely in bulk electrolyte, which has a higher probability of touching Li surface. Once touching Li metal surface, the solvent molecules and anions from the solvation sheath will be reduced by electrons and compose the main components of SEI, thereby modulating Li + transport and deposition behaviors. [6] Due to the diverse reactivity and proportion in the Li + solvation sheath, the contributions from solvents and anions to the interface chemistry are distinctly different. [7] For the dilute electrolytes (esters and ethers), more solvent molecules dominated the Li + solvation sheath due to high ratio of solvent/anions (e.g., 11.6:1 in 1 m lithium hexafluorophosphate (LiPF 6 )-ethylene carbonate (EC)/diethyl carbonate (DEC)). The reduction species in the SEI depend on the reactivity and proportion of the components (solvents and anions) in the Li + solvation sheath. [8] With a high proportion of solvent molecules in the solvation sheath, the as-obtained SEI was principally composed of solvent-derived organic species (ROLi, RCOOLi, and ROCO 2 Li), accompanied with few inorganic species (LiF, Li 2 S, and Li 2 O) mainly originating from anions. [4a,9] Such solvent-derived SEI with highly resistive nature can bring about sluggish transport and uneven charge distribution of Li + , resulting in notorious dendrite growth with low Coulombic efficiency (CE, 80%). [10] Inducing F atoms to the molecular structure of solvent can tune the reactivity of the Li + solvation sheath. [11] For instance, fluoroethylene carbonate (FEC) has a relatively smaller lowest unoccupied molecular orbital (LUMO) than EC, which can be preferentially reduced to form a SEI The spatial distribution and transport characteristics of lithium ions (Li + ) in the electrochemical interface region of a lithium anode in a lithium ion battery directly determine Li + deposition behavior. The regulation of the Li + solvation sheath on the solid electrolyte interphase (SEI) by electrolyte chemistry is key but challenging. Here, 1 m lithium trifluoroacetate (LiTFA) is induced to the electrolyte to regulate the Li + solvation sheath, which significantly suppresses Li dendrite formation and enables a high Coulombic efficiency of...