A current perspective for photocatalysis towards the hydrogen production from biomass-derived organic substances and water

Recently, an increasing interest has been devoted to produce chemical energy – hydrogen (H₂) by converting sustainable sunlight energy via water splitting and reforming of renewable biomass-derived organic substances. These photocatalytic processes are very promising, sustainable, economic, and environment-friendly. Herein, this article gives a concise overview of photocatalysis to produce H₂ as solar fuel via two approaches: water splitting and reforming of biomass-derived organic substances. For the first approach – photocatalytic water splitting, there are two reaction types have been used, including photoelectrochemical (PEC) and photochemical (PC) cell reactions. For the second approach, biomass-derived oxygenated substrates could undergo selective photocatalytic reforming under renewable solar irradiation. Significant efforts to date have been made for photocatalysts design at the molecular level that can efficiently utilize solar energy and optimize the reaction conditions, including light irradiation, type of sacrificial reagents. Critical challenges, prospects, and the requirement to give more attention to photocatalysis for producing H₂ are also highlighted.     

Recent development in band engineering of binary semiconductor materials for solar driven photocatalytic hydrogen production

Photocatalytic hydrogen production from water splitting is a promising approach to develop sustainable renewable energy resources and limits the global warming simultaneously. Despite the significant efforts have been dedicated for the synthesis of semiconductor materials, key challenge persists is lower quantum efficiency of a photocatalyst due to charge carrier recombination and inability of utilizing full spectrum of solar light irradiation. In this review, recent developments in binary semiconductor materials and their application for photocatalytic water splitting toward hydrogen production are systematically discoursed. In the main stream, fundamentals and thermodynamic for photocatalytic water splitting and selection of photo-catalysts has been presented. Developments in the binary photocatalysts and their efficiency enhancements though surface sensitization, surface plasmon resonance (SPR) effect, Schoktty barrier and electrons mediation toward enhanced hydrogen production has been deliberated. Different modification approaches including band engineering, coupling of semiconductor catalysts, construction of heterojunction, Z-scheme formation and step-type photocatalytic systems are also discussed. The binary semiconductor materials such as TiO₂, g-C₃N₄, ZnO, ZnS, Fe₂O₃, CdS, WO₃, rGO, V₂O₅ and AgX (Cl, Br and I) are systematically disclosed. In addition, role of sacrificial reagents for efficient photocatalysis through reforming and hole-scavenger are elaborated. Finally, future perspectives for photocatalytic water splitting towards renewable hydrogen production have been suggested.     

A review on copper vanadate‐based nanostructures for photocatalysis energy production

The economic, social, and environmental aspects are important that should be notable before the selection of a method for the production of energy. Various renewable energy sources are used like hydropower, biomass, biofuel, geothermal energy, and wind energy for the production of sustainable energy that are excellent approaches to fulfill energy environmental energy demands. Renewable sources of energy give an excellent chance to extenuate the gas emission in greenhouse and reduction of global warming with the help of renewable sources of energy. The importance and utilization of the variety of renewable sources of energy are elaborated in this article. The emerging and exploring technique for the production of energy is the photocatalysis. In photocatalysis, solar spectrum is the extraneous source that is used with water to produce hydrogen energy (green energy) by the water splitting under the shower of the solar spectrum. The solar spectrum contains heat and intensity of light from which light spectrum is the abundantly used for the splitting of water. The photocatalyst is the key factor to initiate the reaction depending upon the energy band gap by absorbing the energy from the spectrum of the sun. Semiconducting materials having lower forbidden energy band gap are the basic requirements to use them as a photocatalyst for photocatalysis. Copper vanadate and their composites are the promising materials that are used as photocatalyst for the production of hydrogen energy. Copper vanadate is the focusing material that can be used as photocatalyst. It is an n‐type semiconducting material with 2 eV indirect energy band gap having monoclinic structural phase which is tuned by the doping of metals like chromium, molybdenum, and silver to reduce the grain size and energy band gap and increase the surface area and optical absorption of solar light only to enhance the photocatalytic performance towards the production of hydrogen energy by water splitting in the presence of solar light.     

A review on graphitic carbon nitride (g-C3N4) – metal organic framework (MOF) heterostructured photocatalyst materials for photo(electro)chemical hydrogen evolution

Graphitic carbon nitride (g-C₃N₄)-based heterostructured photocatalysts have recently attracted significant attention for solar water splitting and photocatalytic hydrogen (H₂) evolution, because of their alterable physicochemical, optical and electrical properties, such as tunable band structure, ultrahigh specific surface area and controllable pore size, defect formation and active sites. On the other hand, metal-organic frameworks (MOFs) possess a favorable surface area, permanent porosity and adjustable structures that allow them to be suitable candidates for diverse applications. In this review, we therefore comprehensively discuss the structural properties of heterogeneous g-C₃N₄/MOF-based photocatalysts with a special emphasis on their photocatalytic performance regarding the mechanism of heterogeneous photocatalysis, including advantages, challenges and design considerations.     

Photocatalytic water splitting with In-doped H2LaNb2O7 composite oxide semiconductors

The In-doped HLaNb₂O₇ oxide semiconductors synthesized by solid-state reaction followed by an ion-exchange reaction were found to be a novel composite photocatalyst system with enhanced activity for water splitting. Pt was incorporated in the interlayer of In-doped HLaNb₂O₇ by the stepwise intercalation reaction. The In-doped HLaNb₂O₇ powder samples were characterized with X-ray diffraction (XRD) and UV-vis diffuse reflectance spectrometry. The photocatalytic activities of Pt-loaded In-doped HLaNb₂O₇ and individual precursor materials were evaluated by H₂ evolution from aqueous CH₃OH solution under UV light irradiation. It was found that the composite In-doped HLaNb₂O₇ showed a higher H₂ evolution rate in comparison with individual materials. The hydrogen production activity of In-doped HLaNb₂O₇ was greatly enhanced by Pt co-incorporation. The In content in the In-doped HLaNb₂O₇ system was discussed in relation to the photophysical and photocatalytic properties. As In content equal 5 mol%, the HLaNb₂O₇:In/Pt showed a photocatalytic activity of 354 cm³ g⁻¹ hydrogen evolution in 10 vol% methanol solution under irradiation from a 100 W mercury lamp at 333 K for 3 h.     

Photocatalytic membrane reactors for hydrogen production from water

Hydrogen is considered today a promising environmental friendly energy carrier for the next future, since it produces no air pollutants or greenhouse gases when it burns in air, and it possesses high energy capacity. In the last decades great attention has been devoted to hydrogen production from water splitting by photocatalysis. This technology appears very attractive thanks to the possibility to work under mild conditions producing no harmful by-products with the possibility to use renewable solar energy. Besides, it can be combined with the technology of membrane separations making the so-called photocatalytic membrane reactors (PMRs) where the chemical reaction, the recovery of the photocatalyst and the separation of products and/or intermediates simultaneously occur. In this work the basic principles of photocatalytic hydrogen generation from water splitting are reported, giving particular attention on the use of modified photocatalysts able to work under visible light irradiation. Several devices to achieve the photocatalytic hydrogen generation are presented focusing on the possibility to obtain pure hydrogen employing membrane systems and visible light irradiation. Although many efforts are still necessary to improve the performance of the process, membrane photoreactors seem to be promising for hydrogen production by overall water splitting in a cost-effective and environmentally sustainable way.     

Photophysical and photocatalytic water splitting performance of stibiotantalite type-structure compounds,SbMO4 (M = Nb,Ta)

Metal oxides with ferroelectric properties are considered to be a new family of efficient photocatalysts. Here, we investigate stibiotantalite type-structure compounds, SbMO₄ (M = Nb, Ta), with layered crystal structures, and ferroelectric properties as photocatalysts for hydrogen generation from the splitting of pure water. Both compounds were prepared by a conventional solid-state reaction method, and their optical properties, electronic band structure, and photocatalytic water splitting performance were characterized and evaluated. Diffuse reflectance analysis showed that both compounds have moderate band gaps of 3.7 eV for SbTaO₄ and 3.1 eV for SbNbO₄ (cf. 3.0 eV for TiO₂). Mott–Schottky analysis reveals that their conduction-band edge potentials are higher than the water reduction (hydrogen evolution) potential (0 V vs. RHE), indicating both compounds can generate hydrogen from water splitting. The photocatalytic water splitting performance was conducted by using pure water and UV-light irradiation, and photocatalytic H₂ production was confirmed for both compounds. After loading RuO₂ cocatalyst, the rates of hydrogen evolution of SbNbO₄ and SbTaO₄ were 24 μmol/g h and 58 μmol/g h, respectively. It was concluded that both compounds can be used as photocatalysts for water splitting under UV irradiation. The photocatalytic activity difference in both compounds was discussed with regard to electronic band structure and dipole moment difference, resulting from their crystal structures.     

A visible-light-driven heterojunction for enhanced photocatalytic water splitting over Ta2O5 modified g-C3N4 photocatalyst

The photocatalytic water splitting for generation of clean hydrogen energy has received increasingly attention in the field of photocatalysis. In this study, the Ta₂O₅/g-C₃N₄ heterojunctions were successfully fabricated via a simple one-step heating strategy. The photocatalytic activity of as-prepared photocatalysts were evaluated by water splitting for hydrogen evolution under visible-light irradiation (λ > 420 nm). Compared to the pristine g-C₃N₄, the obtained heterojunctions exhibited remarkably improved hydrogen production performance. It was found that the 7.5%TO/CN heterojunction presented the best photocatalytic hydrogen evolution efficiency, which was about 4.2 times higher than that of pure g-C₃N₄. Moreover, the 7.5%TO/CN sample also displayed excellent photochemical stability even after 20 h photocatalytic test. By further experimental study, the enhanced photocatalytic activity is mainly attributed to the significantly improve the interfacial charge separation in the heterojunction between g-C₃N₄ and Ta₂O₅. This work provides a facile approach to design g-C₃N₄-based photocatalyst and develops an efficient visible-light-driven heterojunction for application in solar energy conversion.     

SiI2 monolayer as a promising photocatalyst for water splitting hydrogen production under the irradiation of solar light

The feasibility of SiI₂ monolayer as the candidate for photocatalytic water splitting for hydrogen generation under the irradiation of the solar light is explored. The geometrical structure, the electronic and optical properties, the mobility of carrier and strain engineering of the monolayer are investigated based on the first-principles calculations. The results demonstrate SiI₂ monolayer possesses an indirect gap of 2.33 eV (HSE06), and both the band edge and the bandgap match the redox potential conditions of the water splitting for hydrogen generation. There is an obvious optical absorption in the visible light and near-ultraviolet region and can be enhanced by the compressive strain. Moreover, the mobility of the electron is significantly different from that of the hole, implicating that the effective spatial charge separation is expectable and the ratio of the recombination of the photogenerated charge pairs is low. The primary adsorption site of the water molecule is identified. The Gibbs free energy and the adsorption energies are calculated to demonstrate the H₂ generation from the water molecule splitting on the monolayer. All the considered properties support that SiI₂ monolayer can be achieved as a promising candidate for the photocatalytic water splitting for hydrogen production under the irradiation of the solar light.     

A perspective on the fabrication of heterogeneous photocatalysts for enhanced hydrogen production

This perspective provides an insight to the possibility of adopting hydrogen as a key energy-carrier and fuel source, through Photocatalytic water splitting in the near future. The need of green and clean energy is increasing to overcome the growing demand of sustainable energy throughout globe, owing to CO₂ emission using fossil fuels. To generate highly efficient and cost-competitive hydrogen, the semiconductor based heterojunction nanomaterials have gained tremendous consideration as a promising way. Currently, the efficiency for hydrogen generation through UV–Vis active photocatalysts is relatively low. The key issues are found to be poor separation of photogenerated electron/hole, less surface area, and low absorption region of electromagnetic spectrum. Such issues arise due to inappropriate band edge potentials and large bandgap of present catalyst. A lot of schemes has been devoted to design and fabricate efficient photocatalysts for improved photocatalytic performance in recent years. However, it seems still a challenge and imperative to greatly comprehend the fundamental aspects, photocatalysis and transfer mechanisms for complete deployment of electron/hole pairs. Further, to produce hydrogen to a larger extent through photocatalytic water splitting, the photocatalyst has been modified through co-catalysts/dopants using numerous techniques including the Z-scheme, hybridization, crystallinity, morphology, tuning of band edge positions, reduction of the band gap, surface structure etc., such that these heterogeneous photocatalysts may have ability to absorb enough light in the UV-VIS-IR region. This type of heterogeneous photocatalysts has the ability to improve the rate of efficiency for hydrogen evolution through absorption of sufficient light of solar spectrum and enhance the separation of charge-carriers by inhibiting recombination of electron/hole pairs. We surmise that taking into account the aforesaid factors should support in scheming an efficient photocatalysts for hydrogen production through water splitting, eventually prompting technological developments in this field.     

Exploration of 1D-2D LaFeO3/RGO S-scheme heterojunction for photocatalytic water splitting

Sustainable energy innovation is spearheading the way to achieve decarbonisation through commercially viable and highly competitive renewable technologies for green hydrogen. Photocatalytic water splitting has received global attention, as it promotes the direct conversion of solar energy to chemical energy and hydrogen production. Lanthanum orthoferrite (LaFeO₃) has been selected due to its narrow bandgap perovskite-oxides (ABO₃) type nature, low cost and high chemical stability but it is limited with fast charge recombination. To circumvent its constraint of fast charge recombination, an efficient graphene-based nanocomposite has been prepared by employing reduced graphene oxide (RGO) nanosheets as charge separators for visible light driven photocatalytic water splitting. Here, we present a thorough physical and spectroscopic characterization of the Lanthanum orthoferrite/Reduced Graphene oxide (LaFeO₃/RGO) nanocomposites, and investigate its photocatalytic and photoelectrochemical performance. The photocurrent density of the nanocomposites demonstrated ∼21 times higher in comparison to pure LaFeO₃. The as-prepared nanocomposites have been successfully used as photocatalysts for H₂ generation through water reduction under visible light. A significant enhancement in H₂ generation has been recorded for nanocomposites (∼82 mmol g⁻¹ h⁻¹) as compared to that of bare LaFeO₃ (∼9 mmol g⁻¹ h⁻¹) which is among the highest values obtained using noble-metal-free graphene-based photocatalytic nanocomposites. This work offers a facile approach for fabricating highly efficient 1D-2D heterostructure for photocatalysis application.     

Synthesis of carbon-doped SnO2 nanostructures for visible-light-driven photocatalytic hydrogen production from water splitting

Environmental issues: global warming, organic pollution, CO₂ emission, energy shortage, and fossil fuel depletion have become severe threats to the future development of humans. In this context, hydrogen production from water using solar light by photocatalytic/photoelectrochemical technologies, which results in zero CO₂ emission, has received considerable attention due to the abundance of solar radiation and water. Herein, a single-step thermal decomposition procedure to produce carbon-doped SnO₂ nanostructures (C–SnO₂) for photocatalytic applications is proposed. The visible-light-driven photocatalytic performance of the as-prepared materials is evaluated by photocatalytic hydrogen generation experiments. The bandgaps of the photocatalysts are determined by ultraviolet–visible diffused reflectance spectroscopy. The crystallinity, morphological features (size and shape), and chemical composition and elemental oxidation states of the samples are investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The proposed simple thermal decomposition method has significant potential for producing nanostructures for metal-free photocatalysis.     

Membrane electrode assembly-based photoelectrochemical cell for hydrogen generation

A novel photoelectrochemical cell (PEC) for generation of hydrogen via photocatalytic water splitting is proposed and investigated. At the heart of the PEC is a membrane electrode assembly (MEA) integrated with Degussa P25 TiO₂ powder as a model photocatalyst for the photoanode and Pt catalyst powder for the dark cathode, respectively. It serves as a compact photocatalytic reactor for water splitting as well as an effective separator for the generated hydrogen and oxygen. The unique characteristic of the MEA-based PEC is that the use of co-catalyst, sacrificial reagent and supporting electrolyte in the cell is totally not required. The novel PEC can be operated without addition of water in the cathode compartment resulting in improved photo conversion efficiency. In addition, the application of a Degussa P25/BiVO₄ mixed photocatalyst was found to significantly enhance the hydrogen generation. Further improvements for the MEA-based PEC utilizing solar energy are also proposed.     

Recent progress and challenges in photocatalytic water splitting using layered double hydroxides (LDH) based nanocomposites

The worldwide energy demand is steadily increasing and estimated to be doubled by the year 2050 due to a continuous hike in economies and population. A large part of the global energy requirement procures using traditional energy sources such as fossil fuels, which are non-renewable. Also, their excessive consumption imparts negative impacts on the environment by CO₂, and CO emissions, which constantly increase the average global temperature. Therefore, the need for a more reliable, sustainable, inexpensive, renewable and environmentally-friendly form of energy is imperative. From these perspectives, hydrogen energy is emerging as one of the most promising alternatives to overcome rising energy demand with a zero-carbon footprint.Herein, various layered double hydroxides (LDH) nanocomposite owing to their attractive physicochemical properties and synergistic effect with other materials in the field of hydrogen production are reviewed. Why the class of LDHs materials is critical and their ideographic properties which make them promising materials in the field of water splitting via photocatalysis and electrocatalysis are also discussed. The synthetic methods of LDHs based nanocomposites fabrication are summarized. Various challenges and strategies from the viewpoint of a different method of hydrogen production through LDHs are reported. Additionally, multiple techniques like surface plasmon resonance (SPR), heterojunction formation, and doping with co-catalyst to increase the efficiency for photocatalytic hydrogen production are also presented. Hopefully, this review will help the readers explore highly efficient, inexpensive and stable LDH catalysts toward photocatalytic water splitting.     

Multidisciplinary methods (co-precipitation,ultrasonic, microwave,reflux and hydrothermal) for synthesis and characterization of CaMn3O6 nanostructures and its photocatalytic water splitting performance

Production of hydrogen and oxygen from water splitting reaction under visible light is a simple method for conversion of solar-to-hydrogen energy and it is a hopeful clean and renewable method for H₂ fuel generation. However, there is still a lack of potential materials with significant activity under visible light. Because of safety, chemical inertness, low cost, stability and other characteristics, transition metal oxide semiconductors have been widely applied as photocatalysts for hydrogen generation. Albeit, wide usage of semiconductor photocatalysts were prevented by its inability to exploit solar energy of visible region. Here we show synthesis of a nano-sized mixed metal oxide (MMO) Ca₃MnO₆ through wet-chemistry methods such as co-precipitation, ultrasonic, microwave, reflux, and hydrothermal methods. The nano-sized Ca₃MnO₆ has initially selected based on morphology and respective particle diameters. The selected sample shows a well-defined single crystal, free from any impurities, complete structural formation, and a band gap energy (E_g) of around 5.3 eV. The best product synthesized in ultrasonic method which shows the best morphology, purity and the highest efficiency for splitting of water to hydrogen and oxygen. Irrespective of preparation methods and morphologies, all samples split water into hydrogen and oxygen, as confirmed from their respective photocatalytic analysis. When the selected sample combined with (NH₄)₂Ce(NO₃)₆, the single-crystal Ca₃MnO₆ nanoparticles split water into hydrogen and oxygen more efficiently under visible light. Our findings demonstrate the importance of nanostructured Ca₃MnO₆ single-crystal photocatalysts in solar water splitting.     

A critical review in strategies to improve photocatalytic water splitting towards hydrogen production

Water splitting for hydrogen production under light irradiation is an ideal system to provide renewable energy sources and to reduce global warming effects. Even though significant efforts have been devoted to fabricate advanced nanocomposite materials, the main challenge persists, which is lower efficiency and selectivity towards H₂ evolution under solar energy. In this review, recent developments in photo-catalysts, fabrication of novel heterojunction constructions and factors influencing the photocatalytic process for dynamic H₂ production have been discussed. In the mainstream, recent developments in TiO₂ and g-C₃N₄ based photo-catalysts and their potential for H₂ production are extensively studied. The improvements have been classified as strategies to improve different factors of photocatalytic water splitting such as Z-scheme systems and influence of operating parameters such as band gap, morphology, temperature, light intensity, oxygen vacancies, pH, and sacrificial reagents. Moreover, thermodynamics for selective photocatalytic H₂ production are critically discussed. The advances in photo-reactors and their role to provide more light distribution and surface area contact between catalyst and light were systematically described. By applying the optimum operating parameters and new engineering approach on photoreactor, the efficiency of semiconductor photocatalysts for H₂ production can be enhanced. The future research and perspectives for photocatalytic water splitting were also suggested.     

等离激元效应促进的光催化分解水制氢

  目的  利用光催化分解水的方式直接将太阳能转化并存储为氢气的化学能,是发展清洁能源促进低碳经济的有效途径。文章围绕等离激元效应对光催化分解水制氢的促进机理进行综述,以推进其产业化应用。  方法  阐释了等离激元效应在光催化分解水反应过程中的微观机制,分析了等离激元粒子在增强太阳光的吸收能力、拓展吸收光谱的响应范围、促进光生电子空穴的分离、提升光生载流子的热力学能、以及提供光催化反应活性中心等方面发挥的重要作用。  结果  通过总结当前等离激元效应促进光催化分解水制氢的研究进展,浅析了目前存在的问题,并对该领域的未来发展趋势进行了展望。  结论  基于等离激元效应在太阳能生产燃料中的巨大应用潜力,不同学科背景的相关学者协同合作,对影响光催化剂效率和寿命的各项决定性因素积极研发攻关,将促进该技术领域获得重要突破。     

Recent advances in non-metals-doped TiO2 nanostructured photocatalysts for visible-light driven hydrogen production,CO2 reduction and air purification

The generation of hydrogen and oxygen from the photocatalytic water splitting reaction under visible light is a promisingly renewable and clean source for H₂ fuel. The transition metal oxide semiconductors (e.g. TiO₂, WO_3, ZnO, and ZrO₂) are have been widely used as photocatalysts for the hydrogen generation. Because of safety, low cost, chemical inertness, photostability and other characteristics (bandgap, corrosion resistance, thermal and environmental stability), TiO₂ is considered as a most potential catalyst of the semiconductors being investigated and developed. However, the extensive applications of TiO₂ are hampered by its inability to exploit the solar energy of visible region. Other demerits are lesser absorbance under visible light, and recombination of photogenerated electron-hole pairs. In this review, we focus on the all the possible reactions taking place at the catalyst during photo-induced H₂ from water splitting reaction, which is green and promising technology. Various parameter affecting the photocatalytic water splitting reactions are also studied. Predominantly, this review is focussed on bandgap engineering of TiO₂ such as the upward shift of valence band and downward shift of conduction bands by doping process to extend its light absorption property into the visible region. Furthermore, the recent advances in this direction including various new strategies of synthesis, multiple doping, hetero-junction, functionalization, perspective and future opportunities of non-metals-doped TiO₂-based nanostructured photocatalysts for various photocatalytic applications such as efficient hydrogen production, air purification and CO₂ reduction to valuable chemicals have been discussed.     

Borate particulate photocatalysts for photocatalytic applications: A review

Borate is a kind of wide-bandgap semiconducting material with rich structure and variety, which is usually used in optical properties research. Its unique crystal structure has essential research value for expanding the applications of photocatalysis. This review summarizes the recent research progress of borate photocatalysis, including novel borate photocatalyst, borate-based composite, and borate glass photocatalyst. Furthermore, the energy and environmental photocatalysis applications of borate photocatalysts are discussed, such as overall water splitting reaction, water decomposition to generate hydrogen or oxygen, degradation of pollutants, and others. The strategy of the combination of theoretical calculation and experiment to explore new borate photocatalysts was also introduced. Finally, some developing directions and challenges in borate photocatalytic materials are summarized.     

Photocatalytic water splitting ability of Fe/MgO-rGO nanocomposites towards hydrogen evolution

Photocatalytic water splitting has greatly stimulated as an ideal technique for producing hydrogen (H₂) fuel by employing two renewable sources, i.e., water and solar energy. Here, we have adopted a facile hydrothermal approach for the successful synthesis of reduced graphene oxide (rGO) incorporated Fe/MgO nanocomposites followed by thermal treatment at inert atmosphere to investigate their ability for photodegradation and photocatalytic hydrogen evolution via water splitting. Transmission Electron Microscopy images of Fe/MgO-rGO nanocomposite ensured the distribution of Fe/MgO nanoparticles throughout rGO sheets. Notably, all rGO supported nanocomposites, especially the one, thermally treated at 500 °C at Argon (Ar) atmosphere has demonstrated significantly higher photocatalytic efficiency towards the photodegradation of a toxic textile dye, rhodamine B, than pristine MgO and commercially available Degussa P25 titania nanoparticles as well as other composites. Under solar irradiation, Fe/MgO-rGO (500) nanocomposite exhibited 86% degradation of rhodamine B dye and generated almost four times higher H₂ via photocatalytic water splitting compared to commercially available P25 titania nanoparticles. This promising photocatalytic ability of the Fe/MgO-rGO(500) nanocomposite can be attributed to the improved morphological and surface features due to heat treatment at inert atmosphere as well as escalated charge carrier separation with increased light absorption capacity imputed to rGO incorporation.