have reportedb ismuth oxyhalides (BiOX, X = Cl, I, Br) [12] and their heterojunctions in photocatalytic water splitting, owing to their unique physicochemical properties. [13] Moreover,B iOCl/ BiVO 4 p-n heterojunctions have been reported to enhance the photocatalytic activity and pollutant degradationu nder visiblelight irradiation. [11,14] In ah eterojunction structure, the photocatalytic materials strictly require narrow band gaps, which facilitatev isible-light absorption and proper energy level matching, which in turn facilitates good charget ransfer along with improved oxidation and reductiona bility. [15] Accordingly,t ernary heterojunctions can shown otable improvements through the synergistic effect of the multicomponent,w hich gives rise to the efficient separation of photogenerated electron-hole pairs. Buildingaheterostructure between semiconductors is an encouraging technology to improve photocatalytic activity. [16] Heretofore, numerous designed ternary heterojunction systems have been reported and demonstrated clearly enhanced photocatalytic activity compared with binary systems. [16, 17] Therefore, designing ag -C 3 N 4 -based heterojunction is ag ood approach to enhancing the photocatalytic activity of other materials. [18] The metalfree chemical nature, chemical stability,t unable electronic structure, more abundanta nd inexpensive components,a s well as the more appropriate positionofthe top of the valence band and bottom of the conduction band for photocatalytic water splitting have led to g-C 3 N 4 being considered for the development of heterojunctionp hotocatalysts. [19] Since then, g-C 3 N 4 -based composites, such as g- [18b] have been reported.T he photocatalytic activity of heterojunction materials can be explained in water splitting throughe xamination of suitable properties such as visible-light activity,e lectron-hole pair recombination, overpotential of the heterojunction materials, and the stability in the electrolyte solution.Another issue with hierarchical structured materials is that the synthesis is generally difficult,e xpensive, and requirestoxic templates or surfactants as well as careful control of conditions. The increasingl evel of chemical hazards is as erious problem and various environmental regulations need to be complied with. [24] Therefore, there is an ecessity forr eplacing traditional and hazardous organic solvents in chemical routes of materials synthesis to enable as tep towards more sustainable green chemistry. [25] Deep eutectic solvents (DESs) represent an ewer,n ontoxic,i nexpensive class of alternative mixed solvents ystems, formed upon the mixing of varioush ydrogenbondings alts and charge-neutral species, tof orm al ow-melting liquid that is significantly lower melting than that of the two single components andi si deal around room temperature. [26] DESs are coined as green solvents owing to their properties of high viscosity,c onductivity,s urface tension,a nd biodegradability.A saresult, DESs open new and unrivalled chances to improve the sustainab...