Recent advancement in the performance of solar cells by incorporating transition metal dichalcogenides as counter electrode and photoabsorber

Two‐dimensional (2D) transition metal dichalcogenides (TMDCs) architectures have revealed fascinating characteristics such as direct band gap, strong light absorption, and novel electrochemical properties, which make them promising materials for photovoltaic applications. The review focuses on (1) the study of electrochemical and photovoltaic properties of TMDCs thereby using them as counter electrodes (CEs) in dye‐sensitized solar cells (DSSCs) and (2) analyzing the light absorption and charge transport performance of TMDCs heterostructures with different 3D materials. We have further investigated different materials in combination with TMDCs such as reduced graphene oxide nanocomposite, graphene flakes, and molybdenum as CEs in DSSCs. Conventionally, platinum (Pt) is used as a CE material for DSSCs that displays excellent catalytic activity and high electrical conductivity but due to the high cost and scarcity of Pt limits the large‐scale production. Therefore, the excellent electrochemical properties and cost‐effectiveness of TMDCs make them promising contender to replace Pt as CEs in DSSCs. Additionally, the photovoltaic properties of TMDCs and their heterostructures with various materials such as silicon, gallium arsenide, indium phosphate, tungsten disulfide, boron nitride, and organic polymers are reviewed. TMDCs are also investigated as hole transport layer (HTL) and electron transport layer (ETL) with various organic polymers such as P3HT, PCBM, PEDOT:PSS, PTB7, and spiro‐OmeTAD for organic and perovskite‐based solar cells (SCs). The utilization of TMDCs as CEs and photoabsorbers enhances the power conversion efficiency (PCE) to generate cost‐effective and high performance SC devices that can be exploit for future technological applications.     

Recent developments in reduced graphene oxide nanocomposites for photoelectrochemical water-splitting applications

Graphene oxide (GO) sheets have extremely adjustable electronic characteristics due to their distinctive 2D carbon composition, allowing comprehensive surface modifications. Photodriven water splitting uses semiconducting materials that have water-decomposition electronic structures appropriate for electron and hole injection. Photoelectrochemical (PEC) is regarded as an extremely efficient energy conversion system for the manufacturing of clean solar fuel. There have been tremendous attempts to design and create feasible unassisted PEC systems that can effectively divide water to form hydrogen gas and oxygen with only solar energy input (sunlight) necessary. In particular, in the presence of a photocatalyst modified with an appropriate cocatalyst, overall PEC water splitting can be accomplished. For the development of PEC systems, the fundamental concept of PEC water splitting and enhanced energy-conversion efficiency are essential for solar fuel manufacturing. Therefore, this review paper provides a concise summary of unassisted PEC systems with state-of-the-art advancements towards effective PEC water-splitting equipment for the sustainable future use of solar energy.     

A review on the recent developments in zirconium and carbon-based catalysts for photoelectrochemical water-splitting

In the recent years, considerable interest in the development of clean and renewable alternative energy resources has been observed to overcome the problems of dwindling fossil reserves, environmental pollution and increasing energy demand for a sustainable future. In this respect, hydrogen is considered a sustainable, clean, and energy-rich fuel. Photoelectrochemical (PEC) water-splitting is deemed to be a very promising technology hydrogen production. A number of research endeavors have been dedicated to develop efficient catalysts for this process. An optimum photoelectrocatalyst drives down the energy needed for the disassociation of water by lowering the overpotential of the process and make it competent for commercial applications. Recently, a lot of Zirconium (Zr) and Carbon (C) based compounds have been analyzed for PEC water-splitting. This review article intends to offer insight and timely reference for the progress on Zr and C based catalyst for practical PEC water-splitting in a comprehensive and concise manner. With emphasis on the photoelectrochemical performance, relative design strategies and different approaches to improve or optimize the photoelectrocatalyst materials with Zr and C are discussed. Research approach and recommendations for future PEC water-splitting are also proposed.     

Role of graphene and transition metal dichalcogenides as hole transport layer and counter electrode in solar cells

Photovoltaic (PV) technology got much attention in the past few decades in developing advanced and environment friendly solar cells (SCs). However, high cost, unstable nature, and low efficiency are major limitations towards commercialization of SCs. To overcome the issues, two-dimensional materials (2DMs) have been exploited due to low cost, high catalytic activity, fast charge separation, and better electrochemical performance. The review emphasis on (a) the electrochemical performance of graphene and transition metal dichalcogenides (TMDCs) as a hole transport layer (HTL) in SCs and (b) to explore low-cost and effective counter electrode (CE) based on graphene and TMDCs for dye-sensitized solar cell (DSSC). The review presents a comparative analysis of 2DMs as HTL and CE to attain highly efficient and low-cost PV devices. Multiple combinations of the material with graphene, graphene oxide (GO), reduced graphene oxide (rGO), tungsten disulfide (WS₂), molybdenum disulfide (MoS₂) as HTL, and CE material in PV cells are discussed and comparatively analyzed. Numerous strategies are briefly discussed to enhance the efficiency of SCs by utilizing graphene and TMDCs based HTL and CEs. The review focuses on the recent progress in developing low-cost and highly efficient PV devices by using 2DMs. Our study reveals that GO/PEDOT:PSS demonstrate a maximum power conversion efficiency (PCE) of 13.1% when fabricated at different revolutions. Moreover, our statistical analysis unveils that efficiency of the cell can be enhanced by optimizing the layer thickness, which provide a route to develop highly efficient and better performance SCs that can be exploited for future commercial applications.     

A review of heteroatomic doped two-dimensional materials as electrocatalysts for hydrogen evolution reaction

Emerging two-dimensional (2D) materials, such as graphene, transition metal disulfide compounds (TMDCs), MXenes, layer double hydroxides (LDHs), black phosphorus (BP) and hexagonal boron nitride (h-BN), play an important role in speeding up hydrogen evolution reaction (HER) due to its large specific surface area as well as function of loading and efficient support. However, as an electrocatalyst, pure 2D materials cannot meet HER needs caused by their monotonous performance. Therefore, some nanoparticles are used to load and tune the 2D materials to develop efficient and inexpensive catalysts. Herein, we conduct a thorough analysis for materials based on heteroatoms, especially transition metal atoms and non-metal atoms (N, P, S, etc.) doped with graphene, TMDCs, MXenes, LDHs, BP and h-BN. It can be found that doping or coupling between 2D materials will affect the electronic structure, energy band, active area, conductivity and stability of the catalyst, which will induct a huge change in the catalytic performance. This review reveals the relationship between active centers, H₂O adsorption and chemical reaction processes. It also analyzes and summarizes the design principles and performance improvement mechanisms of hybrid catalysts. These discussions can provide references for other researchers to develop derivatives of related catalysts.     

Current progress on 3D graphene-based photocatalysts: From synthesis to photocatalytic hydrogen production

Hydrogen (H₂) is considered an alternative energy carrier for future clean energy systems in many applications. The three-dimensional (3D) graphene is one of the promising candidates for various applications especially in photocatalytic H₂ production due to its high electron conductivity, mechanical stability, fast electron transfer, and large surface area. Exploring the changes in the physical properties from different dimensionalities can be interesting because a 3D structure may improve the photocatalytic efficiency in terms of enhancing the light adsorption, increasing the accessible active surface, and improving the charge transport. Graphene can act as an electron acceptor and cocatalyst, and combining the graphene with metal oxides, transition metal dichalcogenides, or other semiconducting materials can enhance the photocatalytic activity of composites. Therefore, the synthesis, characterization, mechanism, and performance of the 3D graphene-based photocatalyst in the photocatalytic H₂ production are comprehensively discussed. The current progress and future challenges in the H₂ generation is also discussed in this review.     

Thermoelectric transport in graphene and 2D layered materials

ABSTRACT

In early 90s, Hicks and Dresselhaus proposed that low dimensional materials are advantages for thermoelectric applications due to the sharp features in their density-of-states, resulting in a high Seebeck coefficient and, potentially, in a high thermoelectric power factor. Two-dimensional (2D) materials are the latest class of low dimensional materials studied for thermoelectric applications. The experimental exfoliation of graphene, a single-layer of carbon atoms in 2004, triggered an avalanche of studies devoted to 2D materials in view of electronic, thermal, and optical applications. One can mix and match and stack 2D layers to form van der Waals hetero-structures. Such structures have extreme anisotropic transport properties. Both in-plane and cross-plane thermoelectric transport in these structures are of interest. In this short review article, we first review the progress achieved so far in the study of thermoelectric transport properties of graphene, the most widely studied 2D material, as a representative of interesting in-plane thermoelectric properties. Then, we turn our attention to the layered materials, in their cross-plane direction, highlighting their role as potential structures for solid-state thermionic power generators and coolers.     

Heterostructured two dimensional materials of MXene and graphene by hydrothermal method for efficient hydrogen production and HER activities

Recent development on two-dimensional (2D) heterostructured graphene and MXene materials were explored for electrochemical water splitting hydrogen evolution reaction (HER) activity. The hybrid MXene/reduced graphene oxides as two-dimensional (2D) hybrid structures were prepared by facile hydrothermal techniques at 150 °C with MXene and RG hybrid layered composites. As-prepared electrocatalytic active materials have been confirmed through structural and surface morphological studies such as XRD, RAMAN, FT-IR and SEM analysis. The prepared 2D materials were carried out for HER activities due to attractive conductivity and mass transfer process. HER performance were tested from linear sweep voltammetry (LSV) cures. The prepared MX, RG and MX@RG hybrid electrocatalyst exhibited overpotential values as observed as 220 mV, 193 mV, 121 mV respectively at 10 mAcm^?2 cathodic on set. MX@RG hybrid heterostructure exhibited enhanced HER action with lowest overpotential (η = 121 mV) and good H₂ productions as an active future electrocatalyst for energy storage and conversion applications.     

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.     

Series resistance in n-MoSe2 (TMDC)-based PEC solar cells

Transition metal dichalcogenides (TMDCs) have been noticed as potentials for the PEC solar cells because they are inherently stable against the electrolytic environment. Since MoSe₂—a member of group VI TMDCs—possesses an optically matching band gap of around 1.4 eV, it holds relatively more promise as a better material for such devices. In this article, the authors report their investigations on PEC solar cells fabricated using n-MoSe₂ crystals grown by a direct vapour transport technique. The photoconversion characteristics of n-MoSe₂/I₂/I⁻/pt PEC solar cells were investigated under polychromatic illumination from an incandescent lamp at various intensities. Since the series resistance of TMDC-based PEC solar cells is expected to be high, it may be one of the major parameters blocking the available power on photoconversion from such devices. Efforts have been made here to estimate its value. In addition, the effect of thermal treatment of the photoelectrode on the series resistance was also investigated. It has been found that the series resistance decreases from 4.01 K ohms to 1.93 K ohmson controlled thermal treatment of the photoelectrode. This is accompanied by a marked increase in the photoconversion efficiency (from 3% to around 12%). Thus, it can be concluded that the contribution of the series resistance in TMDC-based PEC solar cells is quite significant and can be reduced by giving controlled thermal treatment to the photoelectrodes.     

Enhanced solar-driven water splitting of 1D core-shell Si/TiO2/ZnO nanopillars

In this work, 1D core-shell Si/metal oxide nanopillar (NP) photoanodes were synthesized for enhanced solar-driven water splitting processes. The core-shell structures were fabricated by atomic layer deposition of different metal oxides (TiO₂ and ZnO) onto Si NP, which were synthesized by metal-assisted chemical etching and nanosphere lithography. In order to characterize produced photoanodes various experimental techniques (SEM/TEM, XRD, Transmittance, Reflectance, Raman spectroscopy) were applied. Photoelectrochemical (PEC) water oxidation of produced photoanodes was studied. It was shown that composition of n-Si/TiO₂/ZnO NP exhibited enhanced photocurrents due to barrier effects. The enhanced PEC properties of core-shell Si/TiO₂/ZnO NP are caused by efficient charge separation of photogenerated electron-hole pairs in the TiO₂/ZnO shell and effective holes transfer to the shell-electrolyte interface. The superior photoelectrochemical performance of a photoanode based on core-shell Si/TiO₂/ZnO NP has been confirmed through electrochemical impedance spectroscopy and voltamperometric measurements under electrode irradiation. 1D core-shell Si/TiO₂/ZnO NP offer a new approach for preparing stable and highly efficient photoanodes for PEC water-splitting process.     

Tin disulfide based ternary composites for visible light driven photoelectrochemical water splitting

Photoelectrochemical (PEC) water splitting could potentially solve the global energy crisis and environmental pollution. In the present work, ternary composites consisting of 2D nanomaterials of SnS₂, reduced graphene oxide (RGO), and mesoporous graphitic carbon nitride (mpg-C₃N₄) are synthesized with layered architecture. The photocurrent density of the ternary composite is 1.45 mA/cm ² at 1.23 V vs RHE, which is over 23 times higher than that of pure SnS₂. The superior photocatalytic activity of mpg-C₃N₄/SnS₂/RGO composite is attributed to synchronous effects of all the materials leading to enhanced electron-hole pair separation, as well as increased visible-light absorption.     

Review on the interface engineering in the carbonaceous titania for the improved photocatalytic hydrogen production

Hydrogen is the prime source of energy with enormous attention in the current research development process as it is safe, clean, eco-friendly, and can be produced from renewable resources through simple catalytic reactions. Scalable production of hydrogen through photocatalysis has been achieved using carbon-modified semiconductors since 2009. In this direction, this review delivers comprehensive understandings into the interface and structural interactions between TiO₂ and carbonaceous materials such as carbon, carbon nanotubes, graphene, activated carbon, graphitic carbon nitride, carbon quantum dots, etc., and their influences toward improving the hydrogen generation activity of these systems. Besides, recently developed carbonaceous materials such as 3-D graphene, carbon nanohorns, and carbon nanocones have also been discussed on their character in the photocatalytic water splitting procedure. In general, the observed improvements in this carbon-modified TiO₂ attributed to the synergetic effects, which offer the active migration of charge carriers and reduced recombination rates in the photocatalyst. Finally, highlighting the future perspectives of the carbonaceous materials in photocatalytic applications are concluded.     

A low-temperature electro-thermochemical water-splitting cycle for hydrogen production based on LiFeO2/Fe redox pair

The thermochemical water-splitting cycles have been paid more attention in recent years because they directly convert thermal energy into stored chemical energy as H₂. However, most thermochemical cycles require extremely high temperatures as well as a temperature switch between reduction and oxidation steps, which are the main obstacles for their development. Herein, we introduced an electrochemical reaction into the thermochemical cycle and established a novel two-step water-splitting cycle based on LiFeO₂/Fe redox pair. The two-step water-splitting process involves a cyclic operation of electrochemical reduction and water-splitting steps. The feasibility of the water-splitting cycle for the hydrogen production was thermodynamically and experimentally investigated. A mechanism of hydrogen production based on LiFeO₂/Fe redox pair was developed. Compared with the traditional high-temperature thermochemical cycles, the electrochemical reduction and water-splitting steps of the process can be isothermally operated in the same cell at a relatively low temperature of 500 °C. The main advantages of the cycle are not only easily available heat sources without involvement of the associated engineering and materials issues, but also without any temperature swings. This is a promising method to achieve water splitting for hydrogen production in the future.     

Rational design and fabrication of surface tailored low dimensional Indium Gallium Nitride for photoelectrochemical water cleavage

Currently several type of energy sources exist in the modern world. The energy makes people's life more comfortable, easy, time savings, fast transformation of information and various modes of transmission. Because of large demand of energy, efforts on production of energy increases day by day which subsequently increase serious environmental concerns such as pollution and lack of existing natural resources. In this respect, several attempts have been proposed for new type of renewable and chemical energy systems to overcome the economic burden, global warming and environmental problems caused by the use of conventional fossil fuels. Hydrogen production via water splitting is a promising and ideal route for renewable energy using the most abundant resources of solar light and water. Cost effective photocatalyst for Photoelectrochemical (PEC) water splitting using semiconductor materials as light absorbers have been extensively studied due to their stability and simplicity. Over the past few decades, various metal oxide photocatalysts for water splitting have been developed and their photocatalytic application was studied under UV irradiation. Alternative semiconductor photocatalyst should harness solar energy in the visible light, one such semiconductor material is indium gallium nitride (InGaN), owing to its suitable and tunable energy band-gap, chemical resistance and notable photoelectrocatalytic activity. This review article is initiated with the brief introduction about the origin and methods of production of hydrogen gas from both renewable and nonrenewable energy sources. Multi-functional properties and applications of InGaN are described along with past and recent efforts of InGaN materials for hydrogen evolution by several investigators are provided in detail. In addition, future prospects and ways to improve the PEC performance of InGaN are presented at the end of this review.     

Nanomaterials for photoelectrochemical water splitting – review

Photoelectrochemical (PEC) water splitting using nanomaterials is one of the promising techniques to generate hydrogen in an easier, cheaper and sustainable way. By modifying a photocatalyst with a suitable band width material can improve the overall solar-to-hydrogen (STH) energy conversion efficiency. Nanomaterials can tune their band width by controlling its size and morphology. In many studies, the importance of nanostructured materials, their morphological and crystalline effects in water splitting is highlighted. Charge separation and transportation is the major concern in PEC water splitting. Nanomaterials are having high surface to volume ratio which facilitates charge separation and suppress electron-hole pair recombination. This review focuses on the recent developments in water splitting techniques using PEC based nanomaterials as well as different strategies to improve hydrogen evolution.     

A critical review on core/shell-based nanostructured photocatalysts for improved hydrogen generation

Photocatalytic water splitting into gaseous hydrogen and oxygen in the presence of semiconductor photocatalysts under a visible spectrum of solar irradiation is one of the most promising processes for plummeting energy demands and environmental pollution. Among the successful photocatalytic materials, the core/shell nanostructures show promising results owing to their fascinating morphology that protects the surface features of the core besides the effective separation of photo-excitons resulting in an enhanced rate of hydrogen production up to 162 mmol h⁻¹g⁻¹_cat, which is a notable highest value reported in the literature. In this review, we have focused on the basic characteristics of the core-shell structure-based semiconductor photocatalytic systems and their efficient water-splitting reactions under light irradiation. Comprehensive detail on various synthesis methods of core-shell nanostructures, shell thickness-dependent properties, charge-transfer reaction mechanisms, and photocatalytic stability are highlighted in this review. Core-shell nanostructured materials have been extensively used as a photocatalyst, co-catalyst, and by coupling with supporting materials to improve the apparent quantum efficiency up to 45.6%. Besides, important photocatalytic properties that influence the redox reactions i.e., effective exciton separation, the effect of different light sources/wavelengths, surface charge modeling, photocatalytic active sites, and turnover frequency (TOF) have also been focused on and extensively described. Finally, the present and future prospects of the core-shell nanostructured photocatalysts for solar energy conversion into green hydrogen production have been expounded.     

Enhanced photoelectrochemical water oxidation on BiVO4 by addition of ZnCo-MOFs as effective hole transfer co-catalyst

Solar-driven water splitting is one of greenways for massive conversion of sustainable and nonpolluting energy applied to meet global energy crisis. Photocatalysts are greatly explored to improve photoelectrochemical (PEC) water oxidation efficiency. Bismuth vanadate (BiVO₄) has been extensively used as photocatalyst for water oxidation, but its passive oxygen evolution kinetics and charge carrier recombination lead to inferior PEC performance under light illumination. Tuning interfacial charge separation and transfer is an eminent way to stimulate water oxidation characteristics of BiVO₄. Herein, a BiVO₄/zinc cobalt metal-organic framework (ZnCoMOF) composite is firstly proposed as photocatalyst for water oxidation. ZnCoMOF nanosheets are loaded on BiVO₄ surface as co-catalyst via solvothermal process. Effects of solvothermal duration and mole ratio of zinc and cobalt are investigated. The optimal BiVO₄/ZnCoMOF electrode shows a photocurrent density of 3.08 mA cm^?2 at 1.23 V vs. reversible hydrogen electrode (RHE), which is 4.21 times greater than that of BiVO₄ electrode. The redox properties of high valence metal ions in ZnCoMOF are used to store photoexcited holes and transfer them to the water oxidation process in the BiVO₄/ZnCoMOF system. This work demonstrates that PEC performance of BiVO₄ can be largely improved via controlling water oxidation kinetics and refining charge recombination and transport properties.     

Improvement of TiO2 nanotubes for photoelectrochemical water splitting: Review

Photoelectrochemical (PEC) water splitting is an ideal method to produce clean hydrogen. Developing photoelectrodes that fulfill the PEC water-splitting criteria has become the greatest challenge for commercialization of this technology. Titanium dioxide, the first material used for this application, remain appealing due to its one-dimensional nanotube structure. However, the bandgap of TiO₂ nanotubes, ~3.0 eV, is relatively wide, leading to problems such as limited utilization of light energy and easy recombination of the photogenerated products, i.e., electrons and holes. Several approaches have been developed to overcome this problem, including (i) modification of surface morphology to enhance the active catalytic area, (ii) band structure modification to reduce photogenerated charge recombination, and (iii) surface sensitization to improve light absorption ability. This review reports the improvements achieved by all of these approaches for TiO₂ nanotubes, including the basic principles of the photocatalytic water-splitting process and the preparation and polymorphs of TiO₂ nanotubes. This review also discusses combinations of several methods that enable high photocurrent density with fabulous stability.     

Recent trends in MXene/Metal chalcogenides for electro-/photocatalytic hydrogen evolution reactions

Hydrogen due to high energy density and ecologically benign characteristics can become an excellent energy carrier for a sustainable energy economy and to appease the energy demand of humankind. Moreover, cost-effective and long-lasting photocatalysts can make the hydrogen generating process more economical and suitable. Recently, MXene have become one of the most sought-after composite materials for photocatalytic hydrogen generation. However, the photocstalytic performance can be further enhanced by doping with other semiconductor materials. Transition metal chalcogenides (Transition metals = Cu, Co, Ni, Zn, Cd, Mo, W)/MXene composites and mixed transition metal chalcogenide/MXene nanocomposites have been extensively investigated for the photocatalytic hydrogen generation. These materials possess unique two-dimensional layered structure that ameliorates the photocatalytic water splitting performance by increasing the light adsorption even at low photon flux density. The 2D design assists in reducing the distance necessary to transverse charge carriers to the surface. Because the layered structure tends to trap electrons in the ultrathin layers, 2D materials have unusual optoelectronic properties. In-plane covalent bonding assisted the creation of various heterojunctions and heterostructures in these 2D materials. Water splitting and hydrogen production are aided by the high surface area of these 2D materials. Due to its diverse elemental composition, unique 2D structure, good photoelectronic characteristics, large surface area, and many surface terminations. The design and production of many types of materials used as catalysts for the hydrogen evolution process are discussed in this article.