In this work, a simplistic composite fabrication of defect pyrochlore Bi1.8Fe0.2WO6 (BFWO) and g-C3N4 (g-CN) was carried out to augment the photocatalytic degradation kinetics and Hydrogen (H2) evolution rate. The structural confirmation through XRD and FTIR confirmed the successful formation of pristine g-C3N4, BFWO NPs, and their composites. FESEM micrographs revealed multilayered sheet-like formation for C3N4 whereas irregular cuboid-shaped structure for BFWO NPs. In the composite formation, the sheets tended to appear wrapped around the BFWO NPs. The UV-DRS absorbance spectra exhibited a highlighted increase in the absorbance region towards the visible light region following a decrease in the band gap. The photoluminescence lifetime studies revealed an enhanced lifetime of excitons to 6.21 ns for 50:50 (g-C3N4: BFWO) composite formation, whereas pristine g-CN displayed an average lifetime of about 4.79 ns. The degradation efficacy in the removal of RhB and MB from water revealed up to 100% and 95.5% removal rates in under 90 mins and 180 mins respectively using the 50:50 composite formation. Similarly, the H2 evolution rate was significantly improved and exhibited up to 370 μmol/h/g. The photo-electrochemical studies revealed a sharp charge separation of excitons for 50:50 (g-C3N4: BFWO) with a maximum photocurrent density of -0.54 μA/cm2 @ 0 V which is 3.6 times and 13.5 times higher than bare g-CN and BFWO. 1.33 V vs. RHE for OER kinetics and -0.09 V vs RHE for HER kinetics were the minimal onset potential exhibited for equal ratios of BFWO and g-CN. Coupled with the heightened charge separation, reduced recombination rate, and optimal band edge positions, the photocatalytic efficiency in the degradation of RhB and MB and water-splitting reactions were improved.