Over the last two decades, several classes of highly ion-conductive SSEs have been developed which reach or surpass current liquid-state electrolyte conductivity. [5,6] Yet, no ASSB paying in on the above promises has been developed to date. This is mainly due to mechanochemical, chemical, and electrochemical stability issues and interfacial processes that have severely compromised any proposed cell's lifetime. [7][8][9][10][11] While many SSE material inherent (mechano-)chemical processing issues seem amenable to modern engineering approaches, [12][13][14][15][16][17][18][19] the situation is less bright regarding the control of interfacial chemical and electrochemical stability (especially when featuring a LMA), as well as ionic and electronic transport quantities across these interfaces. A hitherto missing deep understanding of the structural, chemical, and physical properties of the buried solid-solid interfaces inside ASSBs at the atomic level is required to overcome these performance limiting interfacial issues.The most studied interfacial properties so far are contact stability and dendrite nucleation and growth. [20][21][22] Both issues are accentuated for LMA/SSE interfaces. In a first approximation, interfacial stability can be traced back to the Dendrite formation and growth remains a major obstacle toward highperformance all solid-state batteries using Li metal anodes. The ceramic Li (1+x) Al (x) Ti (2−x) (PO 4 ) 3 (LATP) solid-state electrolyte shows a higher than expected stability against electrochemical decomposition despite a bulk electronic conductivity that exceeds a recently postulated threshold for dendrite-free operation. Here, transmission electron microscopy, atom probe tomography, and first-principles based simulations are combined to establish atomistic structural models of glass-amorphous LATP grain boundaries. These models reveal a nanometer-thin complexion layer that encapsulates the crystalline grains. The distinct composition of this complexion constitutes a sizable electronic impedance. Rather than fulfilling macroscopic bulk measures of ionic and electronic conduction, LATP might thus gain the capability to suppress dendrite nucleation by sufficient local separation of charge carriers at the nanoscale.