Iron Phosphide (Fe2P) particles embedded within in-situ generated tubular carbon structures uniformly doped with nitrogen heteroatoms (Fe2P @ NC) have been investigated as an anode in all-solid-state lithium-ion batteries (ASSLIBs). The designed morphology offered a number of suitable features, such as high conductivity, robust framework, and abundant redox active sites for augmenting overall battery performance. As anode, Fe2P @ NC has provided a high lithiation/delithiation capacity of 1214.8 mA h/g /1367.01 mA h/g at a current density of 66.6 mA/g (100 μA) with a high coulombic efficiency (>100%). Further, Fe2P @ NC also demonstrated an excellent rate performance and moderate structural stability during cycling. The charge storing mechanism for Fe2P @ NC investigated via ex-situ X-ray diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS) studies indicates irreversible conversion of Fe2P → Li3P & Fe in the initial cycle and reversible Li3P ↔ LiP reaction in subsequent cycles. Analysis of reaction kinetics for Fe2P @ NC nanocomposite is carried out using CV measurements at different scan rates. This study explores the possibility of MOF-derived iron-phosphide-based composite material as a high-performance anode for ASSLIBs.