Interfacial
charge transfer and structural proximity effects are
the two essential routes to trigger and tune numerous functionalities
of perovskite oxide heterostructures. However, the cooperation and
competition of these two interfacial effects in one epitaxial system
have not been fully understood. Herein, we fabricate a series of La0.67Ca0.33MnO3/CaRuO3 superlattices
and introduce various chemical doping in the nonmagnetic CaRuO3 interlayers. We found that Ti, Sr, and La doping in the CaRuO3 layer can effectively tune the interfacial charge transfer
and octahedral rotation, thus modulating the ferromagnetism of the
superlattices. Specifically, the B-site Ti doping depletes the Ru
4d band and suppresses the interfacial charge transfer, leading to
a decay of ferromagnetic Curie temperature (T
C). In contrast, the A-site Sr doping maintains a sizable charge
transfer and meanwhile suppresses the octahedral rotation, which facilitates
ferromagnetism and significantly enhances the T
C up to 291 K. The La doping turns out to localize the itinerant
electrons in the CaRuO3 layer, which suppresses both the
interfacial charge transfer and ferromagnetism. The observed intriguing
interfacial engineering of magnetism would pave a new way to understand
the collective effects of interfacial charge transfer and structural
proximity on the physical properties of oxide heterostructures.