Interfacial properties of polymeric materials are significantly influenced by their architectural structures and spatial features, while such a study of topologically interesting macromolecules is rarely reported. In this work, we reported, for the first time, the interfacial behavior of catenated poly(L-lactide) (C-PLA) at the air−water interface and compared it with its linear analogue (L-PLA). The isotherms of surface pressure−area per repeating unit showed significant interfacial behavioral differences between the two polymers with different topologies. Isobaric creep experiments and compression−expansion cycles also showed that C-PLA demonstrated higher stability at the air−water interface. Interestingly, when the films at different surface pressures were transferred via the Langmuir−Blodgett method, successive atomic force microscopy imaging displayed distinct nanomorphologies, in which the surface of C-PLA exhibited nanofibrous structures, while that of the L-PLA revealed a smoother topology with less fiber-like structures.