RESUMEN
Metal oxides are well-known materials that have been considered as the prominent photocatalysts. Photocatalysis is a promising way to address the environmental issues which are caused by fossil fuel the combustion and industrial pollutants. Lot of efforts such as doping of metal oxides with metals, non-metals have been made to enhance their photocatalytic activity. More specifically, in this review we have discussed detailed synthesis procedures of rare earth doped metal oxides performed in the past decades. The advantage of doping metal oxides with rare earth metals is that they readily combine with functional groups due to the 4f vacant orbitals. Moreover, doping rare earth metals causes absorbance shift to the visible region of the electromagnetic spectrum which results to show prominent photocatalysis in this region. The effect of rare earth doping on different parameters of metal oxides such as band gap and charge carrier recombination rate has been made in great details. In perspective section, we have given a brief description about how researchers can improve the photocatalytic efficiencies of different metal oxides in coming future. The strategies and outcomes outlined in this review are expected to stimulate the search for a whole new set of rare earth doped metal oxides for efficient photocatalytic applications.
RESUMEN
One of the most efficient ways for the photogenerated charge carriers is by the development of heterojunction between p-type and n-type semiconductors, which creates an interfacial charge transfer between two semiconductors. By enhancing the bifunctional characteristics for hydrogen generation via photocatalytic and electrocatalytic water splitting reaction, we report the type-II Cu2O/g-C3N4 heterostructure in this article. Due to significantly increased catalytically active sites for the hydrogen evolution reaction (HER) reaction during electrocatalysis and decreased charge transfer resistance, the as-prepared heterostructure exhibits a lower overpotential of 47 and 72 mVdec-1 for the HER and oxygen evolution reactions (OER), respectively, when compared to alone g-C3N4. In addition, Cu2O/g-C3N4 heterostructures have a higher photocatalytic hydrogen evolution of 3492 µmol gcat-1 in the presence of Triethanolamine as a sacrificial agent, which is nearly 2-fold times greater than g-C3N4 (1818 µmol gcat-1) after 5 h of continuous light-irradiation. Moreover, produced heterostructure exhibits 81% of Faradaic efficiency and 18% of apparent quantum yield. This work successfully explains how the rise in water splitting is induced by the transfer of photogenerated electrons in a cascade way from p-type Cu2O to the n-type g-C3N4 using density functional theory (DFT) calculations.
RESUMEN
Solar water splitting has emerged as an urgent imperative as hydrogen emerges as an increasingly important form of energy storage. g-C3N4 is an ideal candidate for photocatalytic water splitting as a result of the excellent alignment of its band edges with water redox potentials. To mitigate electron-hole recombination that has limited the performance of g-C3N4, we have developed a semiconductor heterostructure of g-C3N4 with CuFe2O4 nanoparticles (NPs) as a highly efficient photocatalyst. Visible-light-driven photocatalytic properties of CuFe2O4/g-C3N4 heterostructures with different CuFe2O4 loadings have been examined with two sacrificial agents. An up to 2.5-fold enhancement in catalytic efficiency is observed for CuFe2O4/g-C3N4 heterostructures over g-C3N4 nanosheets alone with the apparent quantum yield of H2 production approaching 25%. The improved photocatalytic activity of the heterostructures suggests that introducing CuFe2O4 NPs provides more active sites and reduces electron-hole recombination. The g-C3N4/CuFe2O4 heterostructures furthermore show enhanced electrocatalytic HER activity as compared to the individual components as a result of which by making heterostructures g-C3N4 with CuFe2O4 increased the active catalytic surface for the electrocatalytic water splitting reaction. The enhanced faradaic efficiency of the prepared heterostructures makes it a potential candidate for efficient hydrogen generation. Nevertheless, the designed heterostructure materials exhibited significant photo- and electrocatalytic activity toward the HER, which demonstrates a method for methodically enhancing catalytic performance by creating heterostructures with the best energetic offsets.
RESUMEN
Cr-doped SnO2 nanostructures with a dopant concentration ranging from 1 to 5% have been successfully prepared using low-temperature modified solvothermal synthesis. The as-prepared nanoparticles showed a rutile tetragonal structure with a rough undefined morphology having no other elemental impurities. The particle shape and size, band gap, and specific surface area of the samples were investigated by scanning electron microscopy, transmission electron microscopy (TEM), high-resolution TEM, UV-visible diffused reflectance spectroscopy, and Brunauer-Emmett-Teller surface area studies. The optical band gap was found in the range of 3.23-3.67 eV and the specific surface area was in the range of 108-225 m2/g, which contributes to the significantly enhanced photocatalytic and electrochemical performance. Photocatalytic H2 generation of as-prepared Cr-doped SnO2 nanostructures showed improved effect of the increasing dopant concentration with narrowing of the band gap. Electrochemical water-splitting studies also stressed upon the superiority of Cr-doped SnO2 nanostructures over pristine SnO2 toward hydrogen evolution reaction and oxygen evolution reaction responses.