Hydrogen peroxide (H2O2) has demonstrated applicability in a wide range of applications, spanning from a bleaching agent in the pulp industry, environmental remediation, and fuel cell technology. Industrial scale synthesis, either by the anthraquinone method or catalytic oxidation of hydrogen gas, has serious drawbacks which are related with energy demanding and multi-step processes. An alternative green strategy involves the photocatalytic synthesis of H2O2. All that is needed is the renewable energy of the sun, a semiconducting species absorbing in the visible region, water, and oxygen. In this minireview, we describe the evolution of research milestones that have been achieved within the recent decades regarding the development of functional photocatalytic systems. In the early studies, back in the 1980’s, TiO2-based systems were mostly investigated. However, due to the large band gap of titania (3.2 eV), alternative semiconductors were studied which strongly absorb in the visible region. Thus, a variety of semiconductor families have been investigated, such as doped titania systems, other metal oxides, metal sulfides, organic semiconductors, metal-organic frameworks, carbon nitride systems, etc. In parallel, the development of functional dopants onto the surface of the main semiconductor has lead to both the inhibition of electron-hole recombination and H2O2 degradation. The current minireview collectively provides the studies of the higher H2O2 production rates and offer some suggestions for the near future.
Among the various organic pollutants and industrial chemicals, 4-nitrophenol has been one of the most monitored substances in aqueous environments, due to its enhanced solubility in such systems. This research reports for the first time the microwave-assisted synthesis of CdS/carbon/MoS x hybrids and the subsequent utilization of such systems as photocatalysts for 4-nitrophenol degradation. The hybrids demonstrated a variable photocatalytic activity, by using a variety of organic substances as precursors for the solvothermal carbonization step. By using ascorbic acid as precursor, the corresponding ternary composite exhibited excellent photocatalytic activity, with the 4-nitrophenol concentration been almost quantitatively decayed within 45 min of irradiation. This could be ascribed due to the generation of a high population of heterojunctions as well as the chemical speciation of Mo-based nanostructures. Such ternary hybrids may be utilized as potential photocatalytic systems in processes, where removal of toxic water-soluble substances is the key issue.
The creation of effective Pd‐based architectures with numerous electrocatalytic active sites and efficient charge transfer is of key importance for improving the electrocatalytic performance in water electrolyzer and fuel cell applications. On the other hand, MoS2, possessing multiple electrocatalytic active sites, can act both as support and booster to Pd‐based electrocatalytic structures. Herein, MoSx@Pd hybrids were successfully synthesized by using a one‐pot liquid phase solvothermal strategy with stoichiometric excess of Pd. The optimized MoSx@Pd proves to be an excellent bifunctional electrocatalyst for both hydrogen evolution reaction and oxygen reduction reaction (ORR). Optimized MoSx@Pd operates the process for hydrogen evolution at the same potential as Pt/C and achieves a low overpotential of 76 mV at −10 mA cm−2 due to improved reaction kinetics and charge transfer processes between Pd and MoS2. On top of that, MoSx@Pd exhibits excellent performance and stability as cathode electrocatalyst in a polymer electrolyte membrane water electrolyzer. Simultaneously, the bifunctional electrocatalyst shows enhanced electrocatalytic ORR activity and stability by maintaining 93% of its initial activity outperforming commercial Pt/C. Finally, rotating ring disk electrode analysis reveals that ORR proceeds through the energy efficient 4e− pathway, with water being the main product, rendering MoSx@Pd a promising component for fuel cells.
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