![]() Therefore, noble metal and carbon-based materials have been used as supporting and/or co-catalyst to solve this problem and improve its photocatalytic performance 8, 9, 10. Despite this, the photocatalytic efficiency of RP is limited due to the rapid recombination rate of photogenerated electrons and holes. Among them, RP has been reported to be a promising candidate for photocatalysis under the solar spectrum owing to its narrow band gap. Recently, elemental semiconductors, such as α-sulphur 6 and red phosphorus (RP), have attracted considerable attention in the field of photocatalysis because of their unique advantages, such as wide visible light absorption ability, low cost, and earth abundance, which make it suitable for a range of practical applications 6, 7. On the other hand, the catalytic efficiency and absorption ability of TiO 2 over the wide spectrum of solar energy is still feeble and unsatisfactory. Several attempts have been made to enhance the photocatalytic activity and extend the absorption edge of TiO 2 to the visible region via metal and non-metal doping, anchoring of noble metals, textural designing and surface defect engineering 2, 3, 4, 5. On the other hand, the catalytic efficiency of TiO 2 in the wider spectrum of solar energy is still low because of its wide band gap and high recombination rate of photoinduced electrons and holes. Among them, TiO 2 is a more popular photocatalyst for the conversion of solar energy, hydrogen generation via water splitting reaction and dye degradation because of its stability, high catalytic activity, low cost, easy availability etc. Metal oxide-mediated photocatalysis under UV light and/or visible light have been reported widely in terms of stability, efficiency and metal free photocatalysts 1, 2, 3, 4. The design of a photocatalyst for the utilization of solar energy is considered one of the most promising and clean approaches towards pollutant removal from aquatic environments. These findings show that the use of earth abundant and inexpensive red phosphorus instead of expensive plasmonic metals for inducing visible light responsive characteristics in TiO 2 is an effective strategy for the efficient energy conversion of visible light. These photoelectrochemical performances of RP-TiO 2 under visible light irradiation revealed more efficient photoexcited electron-hole separation and rapid charge transfer than under the dark condition, and thus improved photocatalytic activity. Furthermore, as a photoelectrode, electrochemical impedance spectroscopy, differential pulse voltammetry, and linear scan voltammetry were also performed in the dark and under visible light irradiation. The results suggest that the RP-TiO 2 has superior photodegradation ability for model contaminant decomposition compared to other well-known photocatalysts, such as TiO 2 and other reference materials. The resulting RP-TiO 2 nanohybrids were characterized systematically by a range of techniques and the photocatalytic ability of the RP-TiO 2 photocatalysts was assessed further by the photodegradation of a model Rhodamine B pollutant under visible light irradiation. This paper reports that the introduction of elemental red phosphorus (RP) into TiO 2 can shift the light absorption ability from the UV to the visible region, and confirmed that the optimal RP loading and milling time can effectively improve the visible light driven-photocatalytic activity of TiO 2. ![]()
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |