Currently,　lanthanide　(Ln(3+))　doped　Pb-free　double　perovskites　(DPs)　suffer　from　competitive　emissions　of　the　self-trapped　exciton　(STE)　and　Ln(3+).　Herein,　a　new　type　of　Nd3+-doped　Cs2AgInCl6　DPs　with　Na+/Bi3+　co-alloying　is　developed.　Benefiting　from　Na+/Bi3+-induced　local　structural　modification,　both　STE　broadband　visible　luminescence　and　Nd3+　near-infrared　(NIR)　emissions　are　boosted　via　free　exciton　sensitization.　Specifically,　a　total　648-fold　enhancement　in　emitting　intensities　compared　to　the　Na+/Bi3+-free　counterpart　is　realized,　with　a　significantly　improved　NIR　photoluminescence　quantum　yield　(PLQY)　from　0.16%　to　30.3%.　First-principles　density　functional　theory　calculations,　Raman　spectra,　and　steady/transient-state　PL　spectra　verify　the　modification　of　local　site　symmetry,　breakdown　of　parity-forbidden　absorption,　and　reduction　of　electron-phonon　coupling　via　Na+/Bi3+　doping.　Finally,　a　compact　vis-NIR　broadband　light-emitting　diode　(LED)　is　designed　by　coupling　the　Na/Bi/Nd:　Cs2AgInCl6　DP　with　a　commercial　ultraviolet　LED　chip,　which　shows　promising　applications　in　spectroscopic　analyses　and　multifunctional　lighting.