Abstract

Herein, the synthesis, characterization, and photoelectrochemical and photocatalytic characteristics of hydrothermally prepared La2O3–g-C3N4, CoO–g-C3N4, and La2O3–CoO–g-C3N4 are discussed. The XRD analysis and crystalline phases unveiled the impregnation of La2O3 and CoO into g-C3N4. The microscopic analysis supports the formation of g-C3N4 nanoflakes and La2O3 and CoO nanoparticles embedded homogeneously in the La2O3–CoO–g-C3N4 nanocomposite, whereas the EDX comprehended their respective elemental composition and ratios. A bandgap energy of 2.38 eV for La2O3–CoO–g-C3N4 was calculated using the Tauc plot method, complementing high visible-light activity. The solar-driven water-splitting reaction exhibited significant photocurrent efficiency (~3.75 mA/cm2), augmenting the hydrogen generation by La2O3–CoO–g-C3N4 compared to that by pure g-C3N4, La2O3–g-C3N4, and CoO–g-C3N4 in 0.5 M Na2SO4 electrolyte. The synergistic effect of La2O3 and CoO impregnation with g-C3N4 led to effective division of the photogenerated charge transporters, enhancing the photocatalytic hydrogen generation by the photocatalysts. Furthermore, photocatalytic pollutant removal, namely greater than 90% decomposition of methylene blue (MB) from water, was investigated with a pseudo-first-order reaction kinetics under 1 sun visible-light irradiation. Thus, La2O3–CoO–g-C3N4 nanocomposite was found to be a prospective material for harnessing solar energy.

Highlights

  • In recent years, the fossil-fuel-based economies have been revolving around a major quest for renewable energy sources

  • It is based on the fabrication of molecular or nanostructured photocatalyst materials to advance our understanding of solar-energy-driven charge distribution and successive photocatalytic water reduction and oxidation processes

  • It is worth mentioning that the intensity of CoO peaks in CoO–g-C3 N4 was somewhat on the lower side as compared to CoO X-ray diffraction (XRD) peak intensity observed in La2 O3 –CoO-g-C3 N4 nanocomposite

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Summary

Introduction

The fossil-fuel-based economies have been revolving around a major quest for renewable energy sources. Robust, and low-cost photocatalysts for renewable energy purposes are highly desired for the future of sustainable energy In this scenario, ample nanomaterials have been explored, but research o fabricate excellent photocatalysts is still ongoing. The photocatalytic activity of pure g-C3 N4 still suffers from sluggish conversion efficiencies, rapid electron–hole reassimilation and concurrent charge recombination, diminutive electrical conduction, low optical absorption, and small surface area [30] These issues have been addressed lately [31], e.g., fabrication of mesoporous materials [32]. We successfully impregnated lanthanum and cobalt oxides with g-C3 N4 hydrothermally to fabricate La2 O3 –g-C3 N4 , CoO–g-C3 N4 , and La2 O3 –CoO–gC3 N4 nanocomposite as effective photocatalysts for photoelectrochemical water-splitting (PECWS) and photodegradation studies. Photoelectrochemical measurements showed improved photocurrent generation in a standard three-electrode electrochemical cell using a neutral electrolyte and enhanced photocatalytic activities compared to the competing photocatalysts

Materials and Chemicals
Synthesis of g-C3 N4
Characterization
Photoelectrochemical Measurements and Setup
Photocatlytic Dye Degradation Studies
Results and Discussion
N4 metal
N4 were coupling effects
Surface Morphology and EDX Analysis
UV–Visible
FTIR Spectroscopy
N4 nanoflakes were hydrothermally pregnated with
N4 nanocomposite were credited the impregnation of3 and
N4 nanocomposite
N4 nanocomposites in a standard three-electrode g-C
Methylene
N4La comparing
N4 to synthesize La
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