A simple and feasible strategy was reported to construct NiP nanostructures entwined by graphite layers (NiP/GC). In this process, a commercial amino phosphonic acid chelating resin was adopted as both the phosphorus and carbon resources. Then, Ni was introduced into the resin framework via ionic exchange and chelation to form a resin-Ni precursor. After carbonization, the highly dispersed NiP particles, coupled with thin graphite layers, were simultaneously synthesized in situ. A ternary 7.5% Pt-NiP/GC catalyst was further obtained by loading 7.5 wt % Pt on NiP/GC. For the oxygen reduction reaction in acidic media, the 7.5% Pt-NiP/GC catalyst exhibited even more positive onset (1.03 V) and half-wave (0.93 V) potentials, as well as a rather higher mass activity of 565.3 mA mg and a better long-term stability than those of the commercial 20% Pt/C (JM) electrocatalyst. The improved reaction kinetics is mainly attributed to the synergistic effect between Pt and NiP/GC. This work not only provides a method for the synthesis of phosphides but also gives insight into the synergy between Pt and NiP, which is helpful for the development of more low-Pt catalysts in acidic media.