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Novel direct dual Z-scheme ZnO-Er 2 O 3 -Nd 2 O 3 @rGO heterostructured nanocomposite along with simple ZnO-Er 2 O 3 -Nd 2 O 3 nanocomposite was prepared by co-precipitation route. The X-ray diffraction pattern exhibited the diffraction peaks associated with ZnO (hexagonal), Er 2 O 3 (cubic), and Nd 2 O 3 (hexagonal) in both nanocomposites. The FTIR spectra further confirmed the formation of nanocomposites. The energy bandgap of simple and rGO decorated nanocomposites were 3.1 and 2.82 eV. The antibacterial characteristics of grown samples showed that the rGO anchored nanocomposite has higher antibacterial activity as compared to simple nanocomposite. The ZnO-Er 2 O 3 -Nd 2 O 3 @rGO nanocomposite exhibited higher photodegradation (97.0%) against methylene blue (MB) than simple nanocomposite (86.0%). The effectiveness of grown ZnO-Er 2 O 3 -Nd 2 O 3 @rGO nanocomposite as photocatalyst was also tested for degradation of other dyes such as RhB, MO, CR, and SO. The effect of operating parameters was investigated for ZnO-Er 2 O 3 -Nd 2 O 3 @rGO nanocomposite. A possible conventional heterojunction and Z-scheme for the degradation using ZnO-Er 2 O 3 -Nd 2 O 3 @rGO nanocomposite has been designed to elucidate the photocatalytic mechanism. • ZnO-Er 2 O 3 -Nd 2 O 3 and ZnO-Er 2 O 3 -Nd 2 O 3 @rGO nanocomposites successfully prepared. • The photocatalytic application was studied using MB, RhB, MO, CR and SO dyes. • The effect of operating parameters for the degradation of SO dye investigated. • The antibacterial activity against different bacterial strains was investigated. [ABSTRACT FROM AUTHOR]

Developing effective and noble-metal-free electrocatalysts for the grim oxygen evolution reaction (OER) and photocatalysts for pollutant elimination is critical for long-term energy supply and environmental remediation. Herein a simple sol-gel technique is used to synthesize NiO/C60 electrophotocatalyst and is characterized via different state-of-art techniques. All the characteristic analytical studies have discovered that the structural components dramatically increased the OER and photocatalytic activity for grown NiO/C60 nanocomposite. TEM results showed that the C60 uniformly covering NiO has a particle size of 46 nm. NiO/C60 electrocatalyst has outperformed the overpotential of 310 mV at a current density of 10 mA/cm2. At the applied voltage, electrochemical impedance spectroscopy showed that the catalytically active surfaces of NiO/C60 and charge transfer rate are much greater than simple NiO. It was also discovered that the grown nanocomposite remained stable for 30 h without degrading, outlasting numerous recent noble-metal-free electrocatalysts. In addition, the NiO/C60 has also exhibited excellent photocatalytic reduction efficiency for Methylene blue (MB) dye and completely degraded after 40 min under sunlight with the stability of up to six cycles. Our findings show that NiO-based water oxidation electrocatalysts and efficient photocatalysts may now be produced at a low cost with outstanding performance. Recycleable core-shell NiO/C60 photocatalyst and electrocatalyst. [Display omitted] • Development of NiO/C60 core-shell electrocatalyst/photocatalyst. • Lower overpotential 310 mV and Tafel slope 43 mV/dec at 10 mA/cm2 for OER. • Complete MB dye degradation in 40 min under natural sunlight. • Remarkable stability 1500 cycles for OER and 6 cycles for photocatalysis. • Dual-functional, low-cost, noble-metal-free catalyst with outstanding performance. [ABSTRACT FROM AUTHOR]