Poly Meta-Aminophenol (PmAP) as a Solid-State Electron Mediator in the Z-Scheme, Ag3PO4/CoFe2O4 Heterojunction: Mineralization of Highly Concentrated Bisphenol-A and Reactive Dyes Water Pollutants.

This study demonstrated the effectiveness of poly meta-aminophenol (PmAP) as a solid electron mediator in the Z-scheme photocatalytic system for organic pollutants (viz. bisphenol-A and reactive dyes) mineralization and also illustrated how PmAP transported the photogenerated electrons from an O2-emitting photocatalyst (Ag3PO4) to a H2-emitting photocatalyst (CoFe2O4) enabling enhanced photocatalytic activity under visible light irradiation. The PmAP/Ag3PO4-CoFe2O4 (PAC-10), was prepared by a two-step process and characterized by various analytical methods to assess the impact of PmAP on optical, photocatalytic, and electrochemical characteristics of the CoFe2O4 (CFO)/Ag3PO4 composite. The morphological investigation revealed that the PmAP sheet was nicely decorated with evenly distributed Ag3PO4 and CoFe2O4 particles. The M-S plot and impedance analyses were used to assess the electrochemical capabilities of the catalyst. Z-scheme charge transfer pathways were well supported by the radical trapping experiment and HRTEM analysis of Pt photodeposited PAC-10 photocatalysts during the photoreaction. Because of its magnetic nature and ease of synthesis, the PAC-10 offers an easily recyclable Z-scheme photocatalytic system that has the potential for purifying wastewater with high concentrations (up to 100 mg/L) of organic pollutants within 30 min of visible light exposition.

Mini-review on remediation of plastic pollution through photoreforming: progress, possibilities, and challenges.

The increasing plastic pollution has raised significant concerns about the environment and the destruction of its precious resources. Making value-added products out of plastic waste is an effective way to reduce plastic pollution and use it as a valuable resource. Plastic reforming driven by sunlight offers a quick and low-energy way to produce hydrogen from waste. Photoreforming of plastic waste is an emerging technology that cannot only break down plastic polymer waste into value-added chemicals but also produce solar fuel cell quality H2. Technologies, such as pyrolysis, combustion, and advanced oxidation, are right now being studied for converting plastic pollution into energy. A thorough summary and comparison of different technologies have not yet been published. Open dumping and combustion are two main steps to deal with waste plastics, but these processes experience inefficiencies and cannot adequately address the challenges. In this mini-review, we aimed to provide a short overview of the recently reported conventional and novel plastic waste treatment methods. The current research on the photoreforming of plastics conducted by various groups and some advantages and disadvantages of this practice has been discussed thoroughly. Also, some notes were made on the prospective future scope present in this particular research area to achieve a carbon-free fuel system. The purpose of this review is to encourage the utilisation of plastic garbage as an alternative source of energy.

Repercussion of Solid state vs. Liquid state synthesized p-n heterojunction RGO-copper phosphate on proton reduction potential in water.

The same copper phosphate catalysts were synthesized by obtaining the methods involving solid state as well as liquid state reactions in this work. And then the optimised p-n hybrid junction photocatalysts have been synthesized following the same solid/liquid reaction pathways. The synthesized copper phosphate photocatalyst has unique rod, flower, caramel-treat-like morphology. The Mott-Schottky behavior is in accordance with the expected behavior of n-type semiconductor and the carrier concentration was calculated using the M-S analysis for the photocatalyst. And for the p-n hybrid junction of 8RGO-Cu3(PO4)2-PA (PA abbreviated for photoassisted synthesis method), 8RGO-Cu3(PO4)2-EG(EG abbreviated for Ethylene Glycol based synthesis method), 8RGO-Cu3(PO4)2-PEG (PEG abbreviated for Poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol based synthesis method)the amount of H2 synthesized was 7500, 6500 and 4500 µmol/h/g, respectively. The excited electrons resulting after the irradiation of visible light on the CB of p-type reduced graphene oxide (RGO) migrate easily to n-type Cu3(PO4)2 via. the p-n junction interfaces and hence great charge carrier separation was achieved.

3 D Co3 (PO4 )2 -Reduced Graphene Oxide Flowers for Photocatalytic Water Splitting: A Type†II Staggered Heterojunction System.

The design, synthesis, and photoelectrochemical characterization of Co3 (PO4 )2 , a hydrogen evolving catalyst modified with reduced graphene oxide (RGO), is reported. The 3 D flowerlike Co3 (PO4 )2 heterojunction system, consisting of 3 D flowerlike Co3 (PO4 )2 and RGO sheets, was synthesized by a one-pot in situ photoassisted method under visible-light irradiation, which was achieved without the addition of surfactant or a structure-directing reagent. For the first time, Co3 (PO4 )2 is demonstrated to act as a hydrogen evolving catalyst rather than being used as an oxygen evolving photoanode. In particular, 3 D flowerlike Co3 (PO4 )2 anchored to RGO nanosheets is shown to possess dramatically improved photocatalytic activity. This enhanced photoactivity is mainly due to the staggered type II heterojunction system, in which photoinduced electrons from 3 D flowerlike Co3 (PO4 )2 transfer to the RGO sheets and result in decreased charge recombination, as evidenced by photoluminescence spectroscopy. The band gap of Co3 (PO4 )2 was calculated to be 2.35 eV by the Kubelka-Munk method. Again, the Co3 (PO4 )2 semiconductor displays n-type behavior, as observed from Mott-Schottky measurements. These RGO-Co3 (PO4 )2 conjugates are active in the visible range of solar light for water splitting and textile dye degradation, and can be used towards the development of greener and cheaper photocatalysts by exploiting solar light.

Reduced Graphene Oxide-Ag3PO4 Heterostructure: A Direct Z-Scheme Photocatalyst for Augmented Photoreactivity and Stability.

A visible light driven, direct Z-scheme reduced graphene oxide-Ag3PO4 (RGO-Ag3 PO4 ) heterostructure was synthesized by means of a simple one-pot photoreduction route by varying the amount of RGO under visible light illumination. The reduction of graphene oxide (GO) and growth of Ag3PO4 took place simultaneously. The effect of the amount of RGO on the textural properties and photocatalytic activity of the heterostructure was investigated under visible light illumination. Furthermore, total organic carbon (TOC) analysis confirmed 97.1 % mineralization of organic dyes over RGO-Ag3PO4 in just five minutes under visible-light illumination. The use of different quenchers in the photomineralization suggested the presence of hydroxyl radicals ((.)OH), superoxide radicals ((.)O2 (-)), and holes (h(+)), which play a significant role in the mineralization of organic dyes. In addition to that, clean hydrogen fuel generation was also observed with excellent reusability. The 4 RGO-Ag3PO4 heterostructure has a high H2 evolution rate of 3690 µmol h(-1) g(-1), which is 6.15 times higher than that of RGO.

One-Pot Fabrication of RGO-Ag3 VO4 Nanocomposites by in situ Photoreduction using Different Sacrificial Agents: High Selectivity Toward Catechol Synthesis and Photodegradation Ability.

Weak photon absorption and fast carrier kinetics in graphene restrict its applications in photosensitive reactions. Such restrictions/limitations can be overcome by covalent coupling of another photosensitive nanostructure to graphene, forming graphene-semiconductor nanocomposites. Herein, we report one-pot synthesis of RGO-Ag3 VO4 nanocomposites using various sacrificial agents like ethanol, methanol, propanol and ethylene glycol (EG) under visible light illumination. The Raman spectral analysis and (13) C MAS NMR suggest ethanol to be the best sacrificial agent among those studied. Thermal analysis studies, further, confirm the stability of the synthesized nanocomposite with ethanol as sacrificial agent. In view of this, the activity toward dye degradation was focused over the composites prepared via ethanol as sacrificial agent. It was observed and proved that cationic dyes could be degraded quantitatively and swiftly compared to anionic dyes (37.79%) in 1.5 h. This suggests that the surface of the nanocomposites is anionic as partial reduction takes place during synthesis process. In case of mixed dye degradation process, it was noticed that the presence of cationic dye doubles the degradation of anionic dye. The activity of these synthesized nanocomposites is more than five-fold toward the phototransformation of phenol and photodegradation of textile dyes under visible light illumination.