GaN/Surface-modified graphitic carbon nitride heterojunction: Promising photocatalytic hydrogen evolution materials

The coupling of two-dimensional (2D) layered materials is an effective way to realize photocatalytic hydrogen production. Herein, using first-principles calculations, the photocatalytic properties of GaN/CNs heterojunctions formed by two different graphite-like carbon nitride materials and GaN monolayer are discussed in detail. The results show that the GaN/C₂N heterojunction can promote the effective separation of photogenerated electron and hole pairs, which is attributed to its type-II band orientation and high carrier mobility. However, the low overpotential of GaN/C₂N for photocatalytic hydrogen production limits the photocatalytic performance. On this basis, we adjust the CBM position of the GaN/C₂N heterojunction by applying an electric field to enhance its hydrogen evolution capability. In addition, the GaN/g-C₃N₄ is a type-I heterojunction, which is suitable for the field of optoelectronic devices. This work broadens the field of vision for the preparation of highly efficient photocatalysts.     

Green sonochemistry fabrication of pure Gd2Sn2O7 nanoparticles with advanced photocatalytic efficiency for elimination of dye pollutions

The insufficiency of clean water sources has become a perilous tension for the future of the world that one of the eco-friendly and cost-effective solutions is the photocatalytic process for removal of artificial dyes and poisonous organic impurities. In the current research, an eco-friendly sonochemistry process was accomplished to gain Gd₂Sn₂O₇ (GSO) nanoparticles with progressive photo-catalytic proficiency. Lysine amino acid as a green capping agent and ethylenediamine (en) as an alkaline agent were utilized with effective surface categories aiming to manage the growth of formed nuclei with the design of spatial barriers around the metal cations and lastly, stop nano-sample accumulation. The figure and dimension of products was studied by various characterization procedures of spectroscopic and microscopic. The photo-degradation performances of the pure Gd₂Sn₂O₇, Gd₂Sn₂O₇/SnO₂ and Gd₂Sn₂O₇/SnO₂/Gd₂O₃ nanocomposites were tested to the removal of diverse synthetic dyes. The outcome of the type of dye, nano-catalyst composition, pH and scavenger kind was labeled on modifying ability of Gd-Sn-O nano-catalyst task. Optimized Gd₂Sn₂O₇/SnO₂/Gd₂O₃ nanocomposites have an efficiency of 98% for degradation of erythrosine dye that ^?OH radicals support photo-degradation of contamination.     

An infinite chain, {[Ni(tn)2]3[Fe(CN)4(μ-CN)2]2}n,a new catalyst for electrochemical-driven water splitting and photochemical-driven hydrogen evolution from water under blue light

A new catalyst for both water reduction and oxidation, based on an infinite chain, {[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n, is formed by the reaction of NiCl₂, 1,3-propanediamine (tn) and K₃ [Fe(CN)₆]. {[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n can electro-catalyze hydrogen evolution from a neutral aqueous buffer (pH 7.0) with a turnover frequency (TOF) of 1561 mol of hydrogen per mole of catalyst per hour (H₂/mol catalyst/h) at an overpotential (OP) of 837 mV {[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n also can electro-catalyze O₂ production from water with a TOF of ～45 mol O₂ (mol cat)^?1s^?1 at an OP of 591 mV. Under blue light (λ = 469 nm), together with CdS nanorods (CdS NRs) as a photosensitizer, and ascorbic acid (H₂A) as a sacrificial electron donor, {[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n can photo-catalyze hydrogen generation from an aqueous buffer (pH 4.0) with a turnover number (TON) of 11,450 mol H₂ per mole of catalyst (mol of H₂ (mol of cat)^?1) during 10 h irradiation. The average of apparent quantum yield (AQY) is as high as 40.96% during 10 h irradiation. Studies indicate that {[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n exists in two forms: a cyano-bridged chain ({[Ni(tn)₂]₃ [Fe(CN)₄ (μ-CN)₂]₂}_n) in solid, and a salt ([Ni(tn)₂]₃ [Fe(CN)₆]₂) in aqueous media; Catalytic reaction occurs on the nickel center of [Ni(tn)₂]²⁺, and the introduction of [Fe(CN)₆]^3- can improve the catalytic efficiency of [Ni(tn)₂]²⁺ for H₂ or O₂ generation. We hope these findings can afford a new method for the design of catalysts for both water reduction and oxidation.     

Plasmonic semiconductor: A tunable non-metal photocatalyst

Doped semiconductor, a newly discovered plasmonic nanomaterial, has attracted tremendous interest due to its tunable properties. In the field of photocatalysis, the perfect combination of metal-like and semiconductor properties makes it the replacement and supplement of metal plasmonic nanomaterials. This new plasmonic photocatalysis offers high conversion efficiencies and wide optical absorption range with low fabrication costs. This article reviews the recent developments and achievements by which the localized surface plasmon resonance (LSPR) in non-metal plasmonic nanomaterial for photocatalytic applications, including pure non-metal plasmonic photocatalysts and various enhancement strategies such as doping, co-catalyst, heterojunction, LSPR coupling and upconversion luminescence enhancement. It broadens the horizons for plasmonics in the study of photocatalysis and even in energy-related applications.     

Carbon-based TiO2-x heterostructure nanocomposites for enhanced photocatalytic degradation of dye molecules

Application of brown titanium dioxide (TiO_2-x) and its modified composite forms in the photocatalytic decomposition of organic pollutants in the environment is a promising way to provide solutions for environmental redemption. Herein, we report the synthesis of effective and stable TiO_2-x nanoparticles with g-C₃N₄, RGO, and multiwalled carbon nanotubes (CNTs) using a simple hydrothermal method. Among all the as-synthesized samples, excellent photocatalytic degradation activity was observed for RGO-TiO_2-x nanocomposite with high rate constants of 0.075 min^?1_, 0.083 min^?1 and 0.093 min^?1 for methylene blue, rhodamine-B, and rosebengal dyes under UV–Visible light irradiation, respectively. The altered bandgap (1.8 eV) and the large surface area of RGO-TiO_2-x nanocomposite impacts on both absorption of visible light and efficiency of photogenerated charge electron (e^?)/hole (h⁺) pair separation. This resulted in enhanced photocatalytic property of carbon-based TiO_2-x nanocomposites. A systematic study on the influence of different carbon nanostructures on the photocatalytic activity of brown TiO_2-x is carried out.     

Controlled fabrication of Pr(OH)3 nanowires for enhanced photocatalytic activities

In this report, praseodymium hydroxide Pr(OH)₃ nanowires with different aspect ratios (length to diameter ratios) were synthesized by a facile hydrothermal approach. The variations in alkali concentration during synthesis are found to form different aspect ratios of nanowires. The X-ray diffraction and Raman spectroscopy analysis demonstrate the absence of any impurity phases in as-prepared materials. Subsequently, photocatalytic activities of as-prepared nanowires were evaluated by the degradation of methyl orange (MO). Our findings reveal that the nanowires with larger aspect ratios have higher photocatalytic efficiency than the smaller aspect ratio samples. X-ray photospectroscopy investigations reveal that the samples with higher aspect ratio are found to exhibit more oxygen vacancies as compared to lower aspect ratio samples. The enhanced photocatalytic activities can be attributed to the presence of higher percentage of active crystal facet (100), higher concentration of defects densities and narrower band gap. Thus, Pr(OH)₃ nanowires can be considered as a potential candidate for the application of wastewater treatment and related technologies.     

Photocatalytic hydrogen generation by WO3 in synergism with hematite-anatase heterojunction

The present study reports about exploration of a multi-component photocatalytic system comprising of WO₃, TiO₂ and Fe₂O₃ with tandem n-n heterojunctions. The ternary WO₃/TiO₂/Fe₂O₃ nanocomposite with WO₃ nanoparticles over the interfaces of Fe₂O₃ and TiO₂ is synthesized by wet precipitation followed by thermal decomposition. The WO₃/TiO₂/Fe₂O₃ nanocomposite has an enhanced photocatalytic performance towards hydrogen generation by water splitting reaction under visible light irradiation, when compared to the Fe₂O₃/TiO₂ system. A band gap of 2.10 eV, favouring visible light absorption was achieved with the distribution of WO₃ nanopartcles over the interfaces of Fe₂O₃ and TiO_2. The as prepared WTF heterojunction exhibited a maximum hydrogen production rate of 10.2 mL h⁻¹ for a catalyst loading of 0.025 g mL⁻¹. The enhanced photocatalytic performance is tested in presence of various sacrificial agents and proton source. In both cases, the higher photocatalytic efficiency is attributed to the more visible light harnessing ability and pronounced charge separation owing to the tandem n-n heterojunctions generated between TiO₂ with WO₃ and TiO₂ with Fe₂O₃ semiconductors and enhancing the lifetime of the photogenerated electron-hole pairs.     

MoS2-mesoporous LaFeO3 hybrid photocatalyst: Highly efficient visible-light driven photocatalyst

Perovskite type materials have high potential photocatalytic application towards both hydrogen energy generation and organic dye degradation due to their high stability and good reusability. Here, it is the first analysis of photocatalytic degradation of RhB and hydrogen energy evolution under visible light over MoS₂/LaFeO₃ nanocomposite. The physicochemical properties of the materials were characterized using a range of techniques such as XRD, TEM, XPS, FTIR, PL, photocurrent, etc. The optical properties of the nanocomposite show good absorption in UV-Vis spectra as compared to the bare LaFeO₃. In this study, MoS₂/LaFeO₃ nanocomposite was synthesized through single step in situ hydrothermal processes with a narrow bandgap, enhanced photocatalytic application under visible light. This novel MoS₂/LaFeO₃ nanocomposite is an efficient and promising photocatalyst for both hydrogen energy evolution and organic dye degradation.     

A one-pot sealed ammonia self-etching strategy to synthesis of N-defective g-C3N4 for enhanced visible-light photocatalytic hydrogen

Photocatalytic hydrogen (H₂) evolution from water is considered as a prospective approach, which can convert inexhaustible solar energy into chemical energy to alleviate energy crisis and environmental problems. Herein, the N-defective g-C₃N₄ with porous structure was firstly synthesized in a sealed crucible by one-step thermal polymerization method. The experimental data showed that the yield of the catalyst was obviously increased under sealing condition. Moreover, the N-defective g-C₃N₄ prepared from urea precursor under sealed condition reached an optimum photocatalytic H₂ production rate of 597.4 μmol/h and an apparent quantum efficiency of 15.6% at wavelength of 420 nm. This enhanced photocatalytic H₂ production performance is mainly ascribed to the introduction of N-defects, which not only extended of the visible light absorption, but also acted as the electron trap centers to suppress the recombination of the photogenerated electron and hole pairs. This work offers one-step facile strategy for the introduction of N-defects to prepare N-defective g-C₃N₄ with superior photocatalytic activity, which is also a great substitute for the high-energy consuming and complicated synthetic routes.     

Fe、Cr共掺杂TiO_2纳米球的制备

以钛酸丁酯、九水硝酸铁、九水硝酸铬、为原料,采用改进新工艺溶胶-凝胶法制备Fe、Cr共掺杂的TiO_2纳米球光催化材料,且用超声波热处理调控其微结构,通过溶胶-凝胶法加超声波辅助热处理合成了铁铬共掺杂纳米球平均粒径大小约为17.836μm,比普通煅烧处理具有较高的结晶度且平均粒径小。采用X射线衍射仪、激光粒度仪、热重天平、扫描电子显微镜等对样品的形貌和晶型进行了表征。结果表明Fe-Cr-TiO_2纳米球均为高度结晶的锐钛矿晶型,Fe、Cr共掺杂对TiO_2显著的提高其自身的结晶程度,热重分析结果显示制备得到的TiO_2锐钛矿晶体转变为金红石相晶体的相转变温度明显降低。此次研究为改进TiO_2光催化光水解性能提供新的方法,促进太阳能光催化光水解材料的发展。