Designing highly optical active photocatalytic heterojunctions with multi-pronged capabilities for environmental applications is still a challenge. In this work the photocatalytic potential of Ag2CrO4/Ag/BiFeO3@RGO was systematically tested via photo-reduction of BrO3-, degradation of Ciprofloxacin (CIF) and photo-reduction of CO2 under broad light spectrum. Among various samples ABR-8 exhibits 99.6% BrO3- photoreduction and 96.3% CIF photo-oxidation in 90 min (nearly 96% in 60 min). ABR-11 (with 11 wt% RGO) selectively generates 180 mu mol g(-1 )of CH4 in 8 h under visible light (260 mu mol g(-1) under alkali activation) which is approximately 60 times than bare BiFeO3. The excellent performance of ABR series is attributed to successful formation of Zscheme which assists in efficient charge transfer, reduced recombination and wide spectrum response. In addition the electron donation-mediation of plasmonic Ag-0 and adsorption-electron mediation of reduced graphene oxide has a triggering effect on reductive and oxidative capabilities. The band structure analysis, scavenging experiments and electron spin resonance studies make it possible to predict a suitable mechanism for bromate reduction, CIF degradation and CH4 generation. Electron assisted Bro(3)(-) reduction, center dot OH and center dot O-2(-) radicals powered CIF degradation by Z-scheme mechanism and multi-electron single step proton-coupled mechanism for highly selective CH4 production were predicted. The best performing photocatalyst retain over 95% of performance over five consecutive runs. Suitable optimisations lead to higher performance from BiFeo(3) which bears many shortcomings via interfacial junction with Ag2CrO4 with triggering effect from metallic Ag and RGO. Intelligently designed junctions can thus show strong photo-oxidative and reductive capabilities with further scope of fine tuning. Hence this developed heterojunction can be sustainably utilized for multi-pollutant removal and energy/fuel production under broad spectrum of light.