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This review presents an overview of recent developments and advancements in the field of photocatalytic hydrogen evolution using poly(heptazine imide) (PHI) and based materials. Photocatalytic hydrogen evolution (PHE) has received great amount of attention because of its potential as a clean and sustainable energy source and PHI based materials have emerged as promising candidates for this purpose due to their distinct structural properties, improved light absorption, charge separation and reduced recombination. This review discusses the essential concepts of PHE and the potential of poly(heptazine imide) materials and their derivatives as photocatalysts and also the limitations of these materials in photocatalytic activity. It addresses the synthetic routes and strategies adopted to enhance the photocatalytic activity of these materials including surface modifications, band engineering, doping, loading co‐catalysts and composites & heterojunction construction. Furthermore, the recent works in photocatalytic H2 evolution using PHI and based materials have been summarized and discussed. Additionally, we examined the challenges and future outlooks in this field, emphasizing the need for scalable and cost‐effective production methods. [ABSTRACT FROM AUTHOR]

The possible impact of antivirals on ecosystems and the emergence of antiviral resistance are the reasons for concern about their environmental release. Consequently, there has been a significant increase in curiosity regarding their presence in both organic and synthetic systems in recent years. The primary objective of this review is to address the void of information regarding the global presence of antiviral drugs in both wastewater and natural water sources. Photocatalytic degradation of pollutants is an eco-friendly, cost-effective method that effectively addresses environmental degradation. The development of efficient photocatalysts remains a significant issue in accelerating the degradation of pollutants, especially when employing solar light. Thus, the development of Z-scheme and S-scheme semiconductor heterojunctions has emerged as a viable method to improve light absorption and enhance the redox capability of photocatalysts. The principles of Z-scheme and S-scheme are reviewed extensively. The degradation route and occurrence of antiviral are discussed briefly. Finally, a short preview of the degradation of antiviral using Z-scheme and S-scheme is also highlighted. [ABSTRACT FROM AUTHOR]

In the contemporary era marked by pressing environmental and energy challenges, there is a growing imperative to create effective and eco-friendly approaches to combat pollution and promote the generation of clean and green energy. One such strategy that has attracted much interest recently is the photocatalytic generation of green energy and pollutant removal. Numerous photocatalysts have been created to treat water and generate clean energy. Zn-Ti LDH materials are two-dimensional materials that have unique physical and chemical properties, making them promising photocatalysts. Zn-Ti LDHs have a distinctive layered structure that makes them extremely adaptable for photocatalytic applications. This structure also provides large surface areas, customisable compositions, and abundant active sites. However, Zn–Ti LDH has a low solar energy efficiency because it is primarily triggered by ultraviolet light, which makes up around 5% of sunshine. Therefore, this investigation aims to provide a thorough summary of the latest advancements in the modification of the materials based on Zinc-Titanium Layered Double Hydroxides (Zn-Ti LDHs) for a broad spectrum of photocatalytic uses. This study also covers the fabrication methods for Zn-Ti LDHs and the creation of heterojunctions and composites based on Zn-Ti LDHs. Additionally, it delves into the mechanisms underlying the degradation of pollutants and the generation of clean energy. We have highlighted the potential for new prospects, existing challenges, and progress in this context. [Display omitted] • Fabrication and photocatalytic mechanisms of Zn-Ti LDH based materials for environmental solutions. • Latest advancements in heterojunctions and composites utilizing Zn-Ti LDH for applications in photocatalysis. • Various approaches for enhancing the photocatalytic capabilities of Zn-Ti LDH are explored. • The summary, challenges, and future outlook are all addressed. [ABSTRACT FROM AUTHOR]

Constructing visible-light-active Z-scheme heterojunctions has proven fruitful in enhancing the photocatalytic activity of photocatalysts for superior water clean-up. Herein, we report the fabrication of a CoFe2O4@Bi2O3/NiO (CBN) Z-scheme nanoheterojunction. The obtained CBN heterojunction was used for visible-light-assisted degradation of ofloxacin (OFL) in water. The OFL degradation efficiency achieved by the CBN heterojunction was 95.2% in 90 min with a rate constant of kapp = 0.03316 min−1, which was about eight times that of NiO and thirty times that of CoFe2O4. The photocatalytic activity of a Bi2O3/NiO Z-scheme heterojunction was greatly enhanced by the visible activity and redox mediator effect of the cobalt ferrite co-catalyst. Higher charge-carrier separation, more visible-light capture, and the Z-scheme mechanism in the Z-scheme system were the important reasons for the high performance of CBN. The scavenging experiments suggested ●O2− as an active species for superior OFL degradation. The possible OFL degradation pathway was predicted based on LC-MS findings of degradation intermediate products. The magnetic nature of the CBN helped in the recovery of the catalyst after reuse for six cycles. This work provides new insights into designing oxide-based heterojunctions with high visible-light activity, magnetic character, and high redox capabilities for potential practical applications in environmental treatment. [ABSTRACT FROM AUTHOR]

The fast development of urbanisation and industrialisation has led to a rise in nitrogen oxide (NO x) emissions, specifically nitric oxide (NO). One effective method for reducing the harmful effects of this dangerous air pollutant on both human health and the environment is the photocatalytic oxidation of NO. Z-scheme heterojunctions enhance incident light utilisation and increase photocatalytic activity, eventually leading to better NO oxidation performance by encouraging the effective separation of charges and migration. A comprehensive discussion of Z-scheme-based heterojunctions is provided in this review paper, with a focus on their applications in the photocatalytic oxidation of NO. Significant progress has been made in the fabrication of efficient photocatalytic devices in recent years, with Z-scheme-based heterojunctions proving to be particularly successful. The review looks into the various methodologies used to create Z-scheme-based heterojunctions as well as photocatalytic NO oxidation mechanisms. Recent studies on photocatalysts employing Z-scheme heterojunctions for the photocatalytic oxidation of NO are also discussed. The possibilities for new opportunities as well as the present challenges, barriers, advances, and solutions have been emphasized. [ABSTRACT FROM AUTHOR]

In recent times cost-effective advanced materials with dual applications in photocatalytic water treatment and electrochemical sensing have been explored and developed. Herein we report facile solution combustion synthesis of ZnO/Fe 2 O 3 (ZF) type-II heterojunction for electrochemical sensing of dopamine and visible assisted photocatalytic reduction of carcinogenic Cr(VI) into Cr(III). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to evaluate the compatibility of the electrodes for DA sensing. Furthermore, DPV curves revealed that ZF2 (ZnO: Fe 2 O 3 - 3:0.5) modified GCEs possessed 0.27 μM and 0.7 μM of LOD and LOQ with good linear range from 3 μM to 30 μM. Overall, reproducibility and interference studies confirm the efficient use of material for DA sensing. The junction ZF2 shows best performance with 88% Cr(VI) photo-reduction under visible light in 90 min and 100% reduction with tartaric acid as sacrificial agent (utilizing holes) in just 45 min. The effect of sacrificial agents and scavengers suggest the photogenerated electrons were major active species followed by ●O 2 −. The CB edges have enough potential for rapid reduction of hexavalent chromium under visible light and solar light. The photoluminescence and electrochemical impedance suggest lowered recombination, high charge separation and charge transfer capacity in the heterojunction. The transfer of electrons from conduction band of Fe 2 O 3 to that of ZnO having high enough negative potential to reduce Cr(VI), thus utilizing the CB potential of wide band gap ZnO for rapid visible photocatalysis. In addition shortcomings as low conductivity Fe 2 O 3 and high band gap of ZnO are both minimized in the junction. This study confirmed that popular semiconductors as ZnO and Fe 2 O 3 have enough potential in dual role as electrochemical sensors and visible photocatalysts with best performance by optimizing the conditions and ratios. Image 1 [ABSTRACT FROM AUTHOR]

In the present work, mixed-spinel ferrite anchored onto graphitic carbon nitride (GCN) was synthesized for mineralization of antibiotic pollutant from waste water. A Z-scheme g-C 3 N 4 /Ni 0.5 Zn 0.5 Fe 2 O 4 nano heterojunction was fabricated by three step procedure: pyrolysis, solution combustion and mechanical grinding followed by annealing. The prepared photocatlyst was tested for degradation of Doxycycline (DC) drug under the natural sun light. Results revealed that the prepared heterojunction has maximum degradation efficiency of 97.10% pollutant in 60 min experiment. The Z-scheme heterojunction between g-C 3 N 4 and Ni–Zn ferrite improves the photoinduced charges separation and protection of redox capability and therby increases the photo degradation efficiency. The scavenging experiments suggested that O 2 −● and h+ as main active species responsible for degradation of the antibiotic. In addition, the dopant variation can drive the shists in band gap and energy band positiong too which makes then excellent candidates for synthesizing tunable heterostructures with organic semiconductors. The work focusses on designing and developing of saimpler but efficient magnetic heterojunctions with superior redox capability for solar powered waste water treatment. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • AgFeO 2 -Bi 5 O 7 I S-type heterojunctions developed by facile route. • AgFeO 2 -Bi 5 O 7 I exhibit superior 98.2 % norfloxacin degradation in120 min. • Rapid charge transfer and minimum recombination via S-scheme mechanism and oxygen-vacancies. • ●OH and ●O 2 – radicals as major reactive species- ESR findings. • Superior performance in solar light as well in different water matrices. Developing highly efficient heterojunction photocatalysts for high performance antibiotic removal is of immense importance but still remains a challenge. Herein, AgFeO 2 -Bi 5 O 7 I (AF-BI), a promising oxygen vacancies rich binary S-scheme heterojunction photocatalyst was synthseized via co-precipitation and hydrothermal treatment. The spherical AgFeO 2 spheres were uniformly affixed on the nanorods of Bi 5 O 7 I via an intimate contact, as verified through electron microscopy. The photodegradation efficiency of optimized 15 %AgFeO 2 -Bi 5 O 7 I (15AF-BI) for norfloxacin (NFX) was 98.2 % (120 min) with apparent rate constant 0.022 min−1 which was 4 times pure AgFeO 2. In municipal water, removal efficiency reached 90.4 % and a high 76.1 % and 65.2 % total organic carbon removal in 3 h in visible light and solar light respectively was achieved. The coupling of AgFeO 2 and Bi 5 O 7 I triggers electron transfer, forming an internal electric field (leading to a directional charge transfer efficient separation of the photo-induced carriers as confirmed by PL, EIS, TPCR results. The validation of existence of S-scheme mechanism and oxygen vacancies was achieved by in-situ X-ray photoelectron spectroscopy (XPS) and EPR analysis. The free radical scavenging experiments and electron spin resonance (ESR) spectroscopy revealed ●OH and ●O 2 – radicals were the major reactive species involved in the photodegradation process. The heterojunction is magnetic and can be separated under guidance of magnetic field which makes reusability and separation easy. Based on ESR findings, band structure analysis and mass spectrometry NFX degradation route was predicted. This work provides effective potential solution for preparing new magnetic S-scheme heterojunctions for effective antibiotics degradation and further will expand to realm of clean energy storage and conversion. [ABSTRACT FROM AUTHOR]

[Display omitted] • Overview of fundamentals of Nb 2 O 5 as photocatalyst-structure and properties. • Heterojunction photocatalysts -Z and S scheme- charge transfer routes. • Recent advances in Nb 2 O 5 based heterojunctions for photocatalytic applications. • Strategies for improving the photocatalytic performance Nb 2 O 5 based heterojunctions. Significant advancements in the field of photocatalysis in recent years have highlighted the heterojunctions based on Nb 2 O 5 as a focal point of research. This comprehensive review diligently analyses the progress in Nb 2 O 5 -based heterojunctions for their application in photocatalysis, focusing on synthesis, characteristics and their pivotal role in addressing crucial energy and environmental challenges. The review emphasizes the fundamental principles of photocatalysis in pollutant removal and H 2 generation, elucidating key processes such as light absorption, charge generation and surface reactions. The different types of heterojunctions, their basic principles and role in enhancing the charge separation and overall photocatlytic performance have been discussed. The recent advances in Nb 2 O 5 -based heterojunctions are extensively discussed for the photocatalytic applications such as pollutants removal and H 2 evolution. Furthermore, the review delves into strategies employed to enhance the photocatalytic activity of Nb 2 O 5 -based heterojunctions such as doping, oxygen vacancies modification, morphological engineering and atomic control, as well as loading with support materials. Each strategy is explained, emphasizing its impact on charge separation and overall efficiency. The review concludes by highlighting existing challenges and providing insights into potential future directions that integrates synthetic processes, novel methods for photoelectric characterization, and an in-depth understanding of the local structure of Nb 2 O 5. This review serves as a valuable resource for researchers in the field, offering a comprehensive overview of the state-of-the-art in Nb 2 O 5 -based heterojunctions for advanced photocatalytic applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fundamentals of phosphorene (PN) and graphdiyne (GDY) are briefly discussed. • Structure, fabrication routes and modification strategies. • Advances in PN and GDY based heterostructures for photocatalytic hydrogen evolution. • Environment stability, challenges and future perspectives. Hydrogen evolution from water splitting using semiconductor photocatalysis is regarded as a sustainable and clean energy solution. Among various new age materials, the two-dimensional (2D) monoelemental materials as graphdiyne (GDY) and phosphorene (PN) showing excellent performance owing to their 2D atomic structure and unique properties, have drawn considerable attention. Graphdiyne (GDY) is a two-dimensional carbon-based compound having sp and sp2 hybridized carbon, diacetylene linkage, triangular holes framework and customizable band gap. Different stacking arrangements and homogenous pores in GDY can produce electronic characteristics, opening the door to intriguing energy applications. On the other hand, phosphorene derived from black phosphorous (BP) exhibits strong hole mobility, a variable band gap and broad optical absorption spectrum. With a significant increase in photo-excited charge-separation efficacy, the development of heterostructured photocatalysts driven by BP/PN and GDY has recently become the subject of study in photocatalysis. The recent advancements in development of phosphorene and graphdiyne and their accompanying heterostructured photocatalysts is outlined here, along with their structure, characteristics, synthetic routes and photocatalytic applications. In addition, the photocatalytic applications of PN and GDY based composites and heterostructures have been reviewed and summarised for photocatalytic hydrogen evolution through water splitting. Environmental stability of these heterostructured photocatalysts and the difficulties they pose have been thoroughly investigated for their more effective and extensive uses in the future. [ABSTRACT FROM AUTHOR]

A binary S-scheme heterojunction photocatalyst, ZIF-67/Ag 3 VO 4 (ZAV), was successfully synthesized using a hydrothermal technique. The optimal ZAV-30 (ZIF-67/30 wt%Ag 3 VO 4) demonstrated excellent performance by degrading 98.5% of Venlafaxine (VEN) within 60 min under visible light. Extensive investigations were carried out regarding the crystal structure, morphology, composition, specific surface area, optical characteristics and electrochemical impedance. The ZAV-30 heterojunction photocatalyst outperformed bare ZIF-67 and Ag 3 VO 4 photocatalysts, primarily due to enhanced photon absorption and improved charge carriers' separation via S-scheme transfer, redox capability and high charge transfer capacity supported by electrochemical experiments and photoluminescence. The S-scheme transfer was validated by in-situ XPS measurements after light exposure. Scavenger experiments indicated that both •OH and •O 2 − played crucial roles as active species in the photocatalytic process. Mass spectrometry (MS) analysis of intermediates facilitated the proposal of a probable photocatalytic degradation pathway for VEN. The photoactivity of the heterojunction was influenced by a range of factors including the pH of the VEN solution, initial VEN concentration, ZAV photocatalyst dosage, and ion effects. Interestingly the ZAV-30 heterojunction exhibited superior performance in lake water, tap water and river water too. Importantly, the ZAV-30 heterojunction exhibited excellent stability and reusability, making it a promising photocatalyst. [Display omitted] • ZIF-67/Ag 3 VO 4 S-scheme heterojunction synthesized by hydrothermal technique. • ZAV-30 demonstrated 98.5% degradation of Venlafaxine within 60 min under visible light. • The S-scheme transfer accelerates charge transfer, separation and strong redox capability. • •OH and •O 2 − as main active species for photocatalytic degradation • High mineralization, reusability and durability. [ABSTRACT FROM AUTHOR]

[Display omitted] • Oxygen vacancies fundamentals and importance in photocatalysis. • Oxygen vacancies rich heterojunction-Synthetic strategies. • OVs rich Z-scheme and S-scheme heterojunctions- Photocatalytic mechanism. • Applications for Hydrogen production and water treatment. • The existing challenges and future perspectives. Photocatalytic removal of pollutants and energy production is a green, low cost and environment friendly technology for addressing the mounting pressure of energy crisis and environmental deterioration. Developing efficient photocatalysts is still a big challenge for accelerating the photocatalytic hydrogen production and pollutant degradation especially utilizing solar light. Therefore, constructing oxygen vacancies rich Z-scheme and S-scheme semiconductor heterojunctions emerged as a promising approach to enhance the light harvesting and increasing the redox capability of photocatalysts. This review comprehensively summarises the state of art focus on oxygen vacancy's role in photocatalysts especially in Z-scheme and S-scheme heterojunctions including synthesis process and modifications. In particular, the functions of oxygen vacancy in supporting the main processes in photocatalytic energy production and pollutant removal, such as light absorption, charge separation and conversion are highlighted in this review. The current issues and future prospective in oxygen vacancies rich heterojunctions for efficient photocatalytic removal of pollutant and energy production are also addressed. Finally, a brief discussion on challenges and future prospects is demonstrated. [ABSTRACT FROM AUTHOR]

The population explosion and rapid economic development has led to tremendous increase in the per capita use of fossil fuel energy resulting in major environmental consequences. To tackle these significant energy and environmental concerns, semiconductor photocatalysis is viewed as a promising environmentally friendly and sustainable solution. The photocatalytic hydrogen evolution utilizes solar energy into clean hydrogen energy which makes it green, environmentally friendly and effective technique to meet energy demands. This process requires workable catalysts to reach a significant reaction rate because of their multiple electrons and multiple proton nature. Among various visible light active photocatalytic materials, metal molybdates have been reported as emerging class of materials owing to their outstanding features as stable crystal structure, photo-corrosion inhibition, high redox efficiency, low cost and toxicity and suitable band structure. The present research provides an extensive review of the most recent advances and new insights into the utilization of metal molybdates in photocatalytic clean energy production and environment challenges. This review article summarizes the recent progresses in advanced strategies applied in metal molybdate based photocatalysts to enhance the photocatalytic performance. The advanced strategies are categorized as control over morphology and surface modification, doping of heteroatom, co-catalyst loading, noble metal deposition and construction of heterojunction, which are devoted to photocatalytic H 2 production and CO 2 reduction and to overcome the fast recombination of charge carriers and increasing the light absorption capacity. The fabrication strategies of metal molybdates and based materials are discussed in detail, as well as their usage as catalysts for H 2 evolution and CO 2 reduction have been analysed. Metal molybdates are promising photocatalysts for addressing present environmental issues, and this work paves the way for future photocatalytic research and development, which may assist in the development of highly effective photocatalysts for sustainable energy needs. [Display omitted] • Metal molybdates as photocatalysts-Structure and properties. • Introduced the synthetic routes: Effect on properties and photocatalytic performance. • Discussed strategies to improve the photocatalytic potential of metal molybdates. • Application for superior hydrogen evolution and CO 2 conversion-Recent advances. • Fundamentals and bottlenecks along with future prospects are discussed. [ABSTRACT FROM AUTHOR]

Photocatalysis has established itself as a fascinating topic, giving promise for effective processing of greenhouse gases and contaminants into useful products, in the search for renewable energy sources and atmospheric rehabilitation. This review study provides a thorough examination of S-scheme heterojunction photocatalysts with an emphasis on their uses in the photocatalytic reduction of CO 2 , N 2 fixation and NO x degradation processes. The review explains various environment-related issues, the basic ideas of photocatalysis and heterojunctions, emphasizing the benefits of S-scheme topologies in increasing interfacial transmission of charges and lowering electron-hole recombination. The fundamentals and issues of photocatalytic CO 2 reduction, nitrogen fixation and NO x degradation, outlining the mechanics involved in employing S-scheme heterojunctions have been discussed. The recent advancements of S-scheme photocatalysts for a variety of applications are highlighted in this review. The future prospects of such assemblies are also critically evaluated, highlighting the importance of full use of solar spectrum, wide scale preparation of photocatalysts, maintaining the redox capability and mechanism elucidation to prepare superior S-scheme heterojunctions to resolve the important energy and environmental issues. [Display omitted] • S-scheme heterojunctions as efficient photocatalysts –Fundamentals and advantages. • Mechanisms of photocatalytic CO 2 reduction, N 2 fixation and NO x degradation. • Designing and synthesis of S-scheme heterojunction photocatalysts. • Applications for reducing CO 2 into fuels, fixation of N 2 into NH 3 and degrading NO x. [ABSTRACT FROM AUTHOR]

The dramatic rise in carbon dioxide levels in the atmosphere caused by the continuous use of carbon fuels continues to have a significant impact on environmental degradation and the disappearance of energy reserves. Past few years have seen a significant increase in the interest in photocatalytic carbon dioxide reduction because of its ability to lower CO 2 releases from the burning of fossil fuels while also producing fuels and important chemical products. Because of their excellent catalytic efficiency, great uniformity, lengthy charge diffusion layers and texture flexibility that enable accurate band gap and band line optimization, perovskite-based nanomaterials are perhaps the most advantageous among the numerous semiconductors proficient in accelerating CO 2 conversion under visible light. Firstly, a brief insight into photocatalytic CO 2 conversion mechanism and structural features of perovskites are discussed. Further the classification and selection of perovskites for Z and S-scheme heterojunctions and their role in photocatalytic CO 2 reduction analysed. The efficient modification and engineering of heterojunctions via co-catalyst loading, morphology control and vacancy introduction have been comprehensively reviewed. Third, the state-of-the-art achievements of perovskite-based Z-scheme and S-scheme heterojunctions are systematically summarized and discussed. Finally, the challenges, bottlenecks and future perspectives are discussed to provide a pathway for applying perovskite-based heterojunctions for solar-to-chemical energy conversion. [Display omitted] • Insight into the mechanism and research progress of photocatalytic CO 2 reduction. • Properties of perovskites as photocatalysts and their synthetic routes. • Boosting the CO 2 conversion through perovskite based Z and S-scheme heterojunctions • The charge transfer mechanism and designing of perovskite based heterojunctions • The future expectations, challenges and outlook are presented. [ABSTRACT FROM AUTHOR]

• g-C 3 N 4 and MOFs based heterojunctions –synthesis routes and advantages. • Types of g-C 3 N 4 and MOFs heterojunctions were discussed-modification strategies. • g-C 3 N 4 and MOFs based heterojunctions for photocatalytic environmental remediation and energy production. • Conclusion and future research prospects on g-C 3 N 4 and MOFs based on heterojunctions. Photocatalytic technology has emerged as a promising solution for environmental remediation and energy production, and the development of efficient and stable photocatalysts is of great importance. Recent advances in g-C 3 N 4 /Metal Organic Frameworks (MOFs) heterojunctions have shown excellent potential in achieving high-performance photocatalytic environmental remediation and energy production. In this review, we have summarized the recent advances in the design and synthesis of g-C 3 N 4 /MOFs heterojunctions and their application in photocatalytic environmental remediation and energy production. We have discussed the advantages and challenges of g-C 3 N 4 /MOFs heterojunctions, such as enhanced light absorption, increased surface area, and improved electron-hole separation, and their effects on photocatalytic performance. We also highlight the recent research progress in the utilization of g-C 3 N 4 /MOFs heterojunctions for various environmental remediation applications, including the degradation of organic pollutants and the removal of heavy metals, as well as for energy production applications such as hydrogen evolution and CO 2 reduction. Furthermore, we provide an overview of the latest theoretical and experimental investigations into the mechanisms of photocatalysis in g-C 3 N 4 /MOFs heterojunctions, which can help to guide the rational design of high-performance photocatalysts. Our analysis of the literature reveals that g-C 3 N 4 /MOF heterojunctions have demonstrated excellent photocatalytic activity for the degradation of various pollutants, such as methyl orange, rhodamine B, and bisphenol A. For instance, a g-C 3 N 4 /ZIF-8 heterojunction achieved a photocatalytic degradation rate of 99.9% for methyl orange under visible light irradiation within 60 min. Moreover, the g-C 3 N 4 /MOF heterojunctions have also been found to be efficient in water splitting for hydrogen production. For instance, a g-C 3 N 4 /UiO-66 heterojunction achieved a hydrogen production rate of 1260 μmol h−1g−1 under visible light irradiation. The recent data on the advances in g-C 3 N 4 /MOFs heterojunctions demonstrate their enormous potential for practical applications in photocatalytic environmental remediation and energy production. [ABSTRACT FROM AUTHOR]

Here in, we report a, wide spectrum active, Bi nanodots incorporated CuBi 2 O 4 /Bi/CuFe 2 O 4 (CBC) heterojunction for synchronous photodegradation of imidacloprid pesticide (ICP) and photo-reduction of Cr(VI) to Cr(III). The best performing heterojunction sample CBC-30 shows nearly 100% Cr(VI) photo reduction (in less than 45 min) along with 98.2% ICP removal in 60 min. 88.7% Cr (VI) reduction & 83.2% ICP degradation was achieved under sunlight with good activity in NIR region. Scavenging experiments reveal the synchronous role of photoreduction-oxidation with electrons as active species for chromium reduction and holes for organic pollutant degradation. This is ensured by effective Z-scheme transfer between CuBi 2 O 4 and CuFe 2 O 4 leading to protection of high potential conduction and valence bands with strong redox capabilities. The Bi nanodots played an important role via wide spectral response owing its surface plasmon resonance as well as photoinduced electron transfer mediation which promotes the electrons transfer efficiency and enhanced photocatalytic ability. [Display omitted] • Z-scheme CuBi 2 O 4 /Bi/CuFe 2 O 4 has excellent charges separation efficiency. • Bi nanodots-wide spectral activity-mediator- provide hot electrons. • Remarkable synchronous removal of imidacloprid and Cr (VI). • Degradation route for ICP and cooperative mechanism for reduction-degradation. • Efficient activity in solar light and river water too. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fundamentals of S-scheme and dual S-scheme have been discussed. • Types of heterojunctions are elaborated with mechanism comparisons. • Recent developments in synthetic methods and different morphology of S-scheme and dual S- schemes. • S-scheme and dual S-scheme for photocatalytic environmental remediation and energy production. • Bottlenecks, conclusion and future prospects discussed. Discovering alternative materials and technologies that provide the meaningful potential to environmental and energy-related challenges in critical to the long-term viability of industrial activity and the evolution of society. Photocatalysts are undeniably important, and scientists are working hard to improve their photocatalytic performance. The high recombination rates of photogenerated electron-hole pairs as well as poor redox capability are addressed via heterojunction modification. In this direction, oxidation type and reduction type photocatalysts based S-scheme heterojunctions are highly promising owing to highly diminished recombination facilitated by internal electric field. This review has focused on the shift from Z-scheme to new revolutionary S-scheme based photocatalytic materials with high performance applications in the field of energy and environment. It can be concluded that controllable built-in electric field intensity and stable interfacial carrier transport process make S-scheme heterostrctures ideal. However their application is mainly limited to powder photocatalysts, don't apply to photo-chemistry and solar cells with external circuit, reaction thermodynamics and dynamics management in S-scheme photocatalysts is not adequate. To some extent, dual S-schemes address to these limitations and further research is to be carried out to fight the bottlenecks. Several perspectives on the future of S-scheme and dual S-scheme heterostructure were also provided based on rigorous review of the reported results. A discussion on the previously reported different types of heterojunctions and S-schemes is presented in this review along with plausible charge transfer mechanisms. The synthetic routes to S-scheme heterojunctions are also provided along with modifications and combinations. The current designing and perspective applications in numerous pollutant degradation, hydrogen production and CO 2 conversion is selectively highlighted. The transition of mechanism elucidation from Z-scheme to S-scheme has been discussed with suitable case studies. However, S-scheme heterojunctions designing and fabrication is still new commercially and so present readiness and bottlenecks have been discussed. Hence it is quite imperative for a future roadmap to be laid to design and develop economically viable high performance S-scheme heterojunctions. [ABSTRACT FROM AUTHOR]