Harnessing laser technology to create stable metal halide perovskite-rGO conjugates as promising electrodes for Zn-ion capacitors.

We report that the direct conjugation of metal halide perovskite nanocrystals on rGO sheets can provide high performance and stable electrodes for Zn-ion capacitors. It is the first time that metal halide nanocrystals have been used to enhance the energy storage of 2D materials in capacitors by introducing an additional pseudocapacitance mechanism. In particular, we present a simple, rapid and room temperature laser-induced method to anchor CsPbBr3 nanocrystals on rGO sheets without affecting the initial morphology and crystal structure of the two components. The flexible and high surface area of the rGO sheets enables the conjugation of individual metal halide perovskite nanocrystals, giving rise to new synergetic functionalities. As a result, the specific capacitance of the perovskite-rGO conjugated electrodes can be enhanced by 178- and 152-times compared to those of the plain rGO and perovskite electrodes respectively.

Metal-Ion Intercalation Mechanisms in Vanadium Pentoxide and Its New Perspectives.

The investigation into intercalation mechanisms in vanadium pentoxide has garnered significant attention within the realm of research, primarily propelled by its remarkable theoretical capacity for energy storage. This comprehensive review delves into the latest advancements that have enriched our understanding of these intricate mechanisms. Notwithstanding its exceptional storage capacity, the compound grapples with challenges arising from inherent structural instability. Researchers are actively exploring avenues for improving electrodes, with a focus on innovative structures and the meticulous fine-tuning of particle properties. Within the scope of this review, we engage in a detailed discussion on the mechanistic intricacies involved in ion intercalation within the framework of vanadium pentoxide. Additionally, we explore recent breakthroughs in understanding its intercalation properties, aiming to refine the material's structure and morphology. These refinements are anticipated to pave the way for significantly enhanced performance in various energy storage applications.

Advances in solar energy harvesting integrated by van der Waals graphene heterojunctions.

Graphene has garnered increasing attention for solar energy harvesting owing to its unique features. However, limitations hinder its widespread adoption in solar energy harvesting, comprising the band gapless in the molecular orbital of graphene lattice, its vulnerability to oxidation in oxidative environments, and specific toxic properties that require careful consideration during development. Beyond current challenges, researchers have explored doping graphene with ionic liquids to raise the lifespan of solar cells (SCs). Additionally, they have paid attention to optimizing graphene/Si Schottky junction or Schottky barrier SCs by enhancing the conductivity and work function of graphene, improving silicon's reflectivity, and addressing passivation issues at the surface/interface of graphene/Si, resulting in significant advancements in their power conversion efficiency. Increasing the functional area of graphene-based SCs and designing efficient grid electrodes are also crucial for enhancing carrier collection efficiency. Flaws and contaminants present at the interface between graphene and silicon pose significant challenges. Despite the progress of graphene/Si-based photovoltaic cells still needs to catch up to the efficiency achieved by commercially available Si p-n junction SCs. The low Schottky barrier height, design-related challenges associated with transfer techniques, and high lateral resistivity of graphene contribute to this performance gap. To maximize the effectiveness and robustness of graphene/Si-based photovoltaic cells, appropriate interlayers have been utilized to tune the interface and modulate graphene's functionality. This mini-review will address ongoing research and development endeavors using van der Waals graphene heterojunctions, aiming to overcome the existing limitations and unlock graphene's full potential in solar energy harvesting and smart storage systems.

Effect of Electrolyte Concentration on the Electrochemical Performance of Spray Deposited LiFePO4.

LiFePO4 is a common electrode cathode material that still needs some improvements regarding its electronic conductivity and the synthesis process in order to be easily scalable. In this work, a simple, multiple-pass deposition technique was utilized in which the spray-gun was moved across the substrate creating a "wet film", in which-after thermal annealing at very mild temperatures (i.e., 65 °C)-a LiFePO4 cathode was formed on graphite. The growth of the LiFePO4 layer was confirmed via X-ray diffraction, Raman spectroscopy and X-ray photoelectron spectroscopy. The layer was thick, consisting of agglomerated non-uniform flake-like particles with an average diameter of 1.5 to 3 µm. The cathode was tested in different LiOH concentrations of 0.5 M, 1 M, and 2 M, indicating an quasi-rectangular and nearly symmetric shape ascribed to non-faradaic charging processes, with the highest ion transfer for 2 M LiOH (i.e., 6.2 × 10-9 cm2/cm). Nevertheless, the 1 M aqueous LiOH electrolyte presented both satisfactory ion storage and stability. In particular, the diffusion coefficient was estimated to be 5.46 × 10-9 cm2/s, with 12 mAh/g and a 99% capacity retention rate after 100 cycles.

High electrochemical performance of ink solution based on manganese cobalt sulfide/reduced graphene oxide nano-composites for supercapacitor electrode materials.

Large scale supercapacitor electrodes were prepared by 3D-printing directly on a graphite paper substrate from ink solution containing manganese cobalt sulfide/reduced graphene oxide (MCS/rGO) nanocomposites. The MCS/rGO composite solution was synthesized through the dispersion of MCS NPs and rGO in dimethylformamide (DMF) solvent at room temperature. Their morphology and composition were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray diffraction (EDS). The role of rGO on decreasing charge transfer resistance and enhancing ion exchange was discussed. The MCS/rGO electrode exhibits an excellent specific capacitance of 3812.5 F g-1 at 2 A g-1 and it maintains 1780.8 F g-1 at a high current density of 50 A g-1. The cycling stability of the electrodes reveals capacitance retention of over 92% after 22 000 cycles at 50 A g-1.

Perspectives on Iron Oxide-Based Materials with Carbon as Anodes for Li- and K-Ion Batteries.

The necessity for large scale and sustainable energy storage systems is increasing. Lithium-ion batteries have been extensively utilized over the past decades for a range of applications including electronic devices and electric vehicles due to their distinguishing characteristics. Nevertheless, their massive deployment can be questionable due to use of critical materials as well as limited lithium resources and growing costs of extraction. One of the emerging alternative candidates is potassium-ion battery technology due to potassium's extensive reserves along with its physical and chemical properties similar to lithium. The challenge to develop anode materials with good rate capability, stability and high safety yet remains. Iron oxides are potentially promising anodes for both battery systems due to their high theoretical capacity, low cost and abundant reserves, which aligns with the targets of large-scale application and limited environmental footprint. However, they present relevant limitations such as low electronic conductivity, significant volume changes and inadequate energy efficiency. In this review, we discuss some recent design strategies of iron oxide-based materials for both electrochemical systems and highlight the relationships of their structure performance in nanostructured anodes. Finally, we outline challenges and opportunities for these materials for possible development of KIBs as a complementary technology to LIBs.

Progress and Challenges in Industrially Promising Chemical Vapour Deposition Processes for the Synthesis of Large-Area Metal Oxide Electrode Materials Designed for Aqueous Battery Systems.

The goal of the battery research community is to reach sustainable batteries with high performance, meaning energy and power densities close to the theoretical limits, excellent stability, high safety, and scalability to enable the large-scale production of batteries at a competitive cost. In that perspective, chemical vapour deposition processes, which can operate safely under high-volume conditions at relatively low cost, should allow aqueous batteries to become leading candidates for energy storage applications. Research interest and developments in aqueous battery technologies have significantly increased the last five years, including monovalent (Li+, Na+, K+) and multivalent systems (Mg2+, Zn2+, Al3+). However, their large-scale production is still somewhat inhibited, since it is not possible to get electrodes with robust properties that yield optimum performance of the electrodes per surface area. In this review paper, we present the progress and challenges in the growth of electrodes through chemical vapour deposition at atmospheric pressure, which is one procedure that is proven to be industrially competitive. As battery systems attract the attention of many researchers, this review article might help those who work on large-scale electrical energy storage.

Progress on V2O5 Cathodes for Multivalent Aqueous Batteries.

Research efforts have been focused on developing multivalent ion batteries because they hold great promise and could be a major advancement in energy storage, since two or three times more charge per ion can be transferred as compared with lithium. However, their application is limited because of the lack of suitable cathode materials to reversibly intercalate multivalent ions. From that perspective, vanadium pentoxide is a promising cathode material because of its low toxicity, ease of synthesis, and layered structure, which provides huge possibilities for the development of energy storage devices. In this mini review, the general strategies required for the improvement of reversibility, capacity value, and stability of the cathodes is presented. The role of nanostructural morphologies, structure, and composites on the performance of vanadium pentoxide in the last five years is addressed. Finally, perspectives on future directions of the cathodes are proposed.

Electrochemical Investigation of Phenethylammonium Bismuth Iodide as Anode in Aqueous Zn2+ Electrolytes.

Despite the high potential impact of aqueous battery systems, fundamental characteristics such as cost, safety, and stability make them less feasible for large-scale energy storage systems. One of the main barriers encountered in the commercialization of aqueous batteries is the development of large-scale electrodes with high reversibility, high rate capability, and extended cycle stability at low operational and maintenance costs. To overcome some of these issues, the current research work is focused on a new class of material based on phenethylammonium bismuth iodide on fluorine doped SnO2-precoated glass substrate via aerosol-assisted chemical vapor deposition, a technology that is industrially competitive. The anode materials were electrochemically investigated in Zn2+ aqueous electrolytes as a proof of concept, which presented a specific capacity of 220 mAh g-1 at 0.4 A g-1 with excellent stability after 50 scans and capacity retention of almost 100%.

Special Issue: Perovskite Nanostructures: From Material Design to Applications.

In the past decade, perovskite materials have attracted great scientific and technological interest due to their interesting opto-electronic properties. Nanostructuring of the perovskites, due to their reduced dimensions are advantageous in offering large surface area, controlled transport and charge carrier mobility, strong absorption and photoluminescence, and confinement effects. These features, together with the unique tunability in composition, shape, and functionalities in addition to the ability to form efficient, low-cost, and light-active structures make the perovskite nanostructures efficient functional components for multiple applications, ranging from photovoltaics and batteries to lasing and light-emitting diodes. The purpose of this Special Issue is to give an overview of the latest experimental findings concerning the tunability in composition, shape, functionalities, growth conditions, and synthesis procedures of perovskite structures and to identify the critical parameters for producing materials with functional characteristics.

Towards High Performance Chemical Vapour Deposition V2O5 Cathodes for Batteries Employing Aqueous Media.

The need for clean and efficient energy storage has become the center of attention due to the eminent global energy crisis and growing ecological concerns. A key component in this effort is the ultra-high performance battery, which will play a major role in the energy industry. To meet the demands in portable electronic devices, electric vehicles, and large-scale energy storage systems, it is necessary to prepare advanced batteries with high safety, fast charge ratios, and discharge capabilities at a low cost. Cathode materials play a significant role in determining the performance of batteries. Among the possible electrode materials is vanadium pentoxide, which will be discussed in this review, due to its low cost and high theoretical capacity. Additionally, aqueous electrolytes, which are environmentally safe, provide an alternative approach compared to organic media for safe, cost-effective, and scalable energy storage. In this review, we will reveal the industrial potential of competitive methods to grow cathodes with excellent stability and enhanced electrochemical performance in aqueous media and lay the foundation for the large-scale production of electrode materials.

Special Issue: Advances in Chemical Vapor Deposition.

Pursuing a scalable production methodology for materials and advancing it from the laboratory to industry is beneficial to novel daily-life applications. From this perspective, chemical vapor deposition (CVD) offers a compromise between efficiency, controllability, tunability and excellent run-to-run repeatability in the coverage of monolayer on substrates. Hence, CVD meets all the requirements for industrialization in basically everything including polymer coatings, metals, water-filtration systems, solar cells and so on. The Special Issue "Advances in Chemical Vapor Deposition" has been dedicated to giving an overview of the latest experimental findings and identifying the growth parameters and characteristics of perovskites, TiO2, Al2O3, VO2 and V2O5 with desired qualities for potentially useful devices.

Electrochromic Performance of V2O5 Thin Films Grown by Spray Pyrolysis.

A new approach regarding the development of nanostructured V2O5 electrochromic thin films at low temperature (250 °C), using air-carrier spray deposition and ammonium metavanadate in water as precursor is presented. The obtained V2O5 films were characterized by X-ray diffraction, scanning electron microscopy and Raman spectroscopy, while their electrochromic response was studied using UV-vis absorption spectroscopy and cyclic voltammetry. The study showed that this simple, cost effective, suitable for large area deposition method can lead to V2O5 films with large active surface for electrochromic applications.

Electrochemistry Studies of Hydrothermally Grown ZnO on 3D-Printed Graphene.

A three-dimensional (3D) printer was utilised for the three-dimensional production of graphene-based pyramids and an efficient hydrothermal procedure for ZnO growth. In particular, the 3D-printed graphene pyramids were forwarded in Pyrex glass bottles with autoclavable screw caps filled with 50 mL of an aqueous solution of zinc nitrate hexahydrate and hexamethylenetetramine for 1 h at 95 °C; sufficient enough time to deposit well-dispersed nanoparticles. X-ray diffraction patterns were in accordance with a Raman analysis and presented the characteristic peaks of graphite along with those of wurtzite ZnO. Different positions on the sample were tested, confirming the uniform dispersion of ZnO on graphene pyramids. From the electrochemical studies, it was found that the charging and discharging processes are affected by the presence of ZnO, indicating one well-defined plateau for each process compared to the previously reported bare graphene pyramids. In total, the material shows a value of 325 mAh g-1, a capacitance retention factor of 92% after 5000 scans, and a coulombic efficiency of 100% for the first scan that drops to 85% for the 5000th scan. This excellent performance is the result of the effect of ZnO and graphene that combines two Li+ accommodation sites, and the contribution of graphene pyramids, which provides more available sites to favor lithium storage capacity. Hence, this anode may be a promising electrode material for lithium-ion batteries.

Advancements, Challenges and Prospects of Chemical Vapour Pressure at Atmospheric Pressure on Vanadium Dioxide Structures.

Vanadium (IV) oxide (VO2) layers have received extensive interest for applications in smart windows to batteries and gas sensors due to the multi-phases of the oxide. Among the methods utilized for their growth, chemical vapour deposition is a technology that is proven to be industrially competitive because of its simplicity when performed at atmospheric pressure (APCVD). APCVD's success has shown that it is possible to create tough and stable materials in which their stoichiometry may be precisely controlled. Initially, we give a brief overview of the basic processes taking place during this procedure. Then, we present recent progress on experimental procedures for isolating different polymorphs of VO2. We outline emerging techniques and processes that yield in optimum characteristics for potentially useful layers. Finally, we discuss the possibility to grow 2D VO2 by APCVD.

Field emission properties of low-temperature, hydrothermally grown tungsten oxide.

Tungsten oxide layers have been prepared on conductive glass substrates using aqueous chemical growth from a sodium tungstate precursor at low-temperature hydrothermal conditions. The deposits were then tested as cold electron emitters. Traceable layers could be deposited only within a narrow pH range of 1.5-2 at a time length not exceeding 4 h. Transmittance in the visible spectrum was found to decrease with deposition time. The presence of both monoclinic and hexagonal phases was always detected. At the longest deposition times and highest precursor concentrations, morphologies comprise randomly oriented spikes or rods. The overall emission performance is found to improve with growth time and precursor concentration. The role of morphology on the emission properties of the films is discussed.