Black phosphorus-based materials for energy storage and electrocatalytic applications

Dual hetero atom containing bio-carbon: Multifunctional electrode material for High Performance Sodium-ion Batteries and Oxygen Reduction Reaction

Recent advances of two-dimensional transition metal nitrides for energy storage and conversion applications

Transition metal oxides (TMOs) have been extensively explored as promising electrode materials for electrochemical energy storage and catalysis. However, TMOs intrinsically have low electronic conductivity and suffer severe volume change during electrochemical cycling. In this study, we develop an effective strategy to enhance conductivity and buffer volume changes of TMOs, in which networked nitrogen-doped carbon nanotubes (N-CNTs) are incorporated into Co3O4 nanosheets system. Based on the whole mass of Co3O4 and N-CNT, the composites can maintain a stable discharge capacity of ~590 mAh g−1 after 80 cycles at a current density of 0.5 A g−1. Moreover, the composites also exhibit greatly enhanced catalysis ability towards oxygen evolution reaction (OER), ie, small Tafel slope of 84 mV dec−1, low overpotential of 310 mV at a current density of 10 mA cm−2, and almost no activity decay throughout 30-hour continuous operation. This study lays a new route for smartly designing advanced electrode materials for energy storage and electrochemical catalysis.

Ion-conducting membranes are crucial in electrochemical storage and energy conversion technologies such as fuel cells, alkaline ion batteries, and redox-flow batteries. The purpose of the membrane is to prevent direct contact between the electrodes while allowing selective ions to pass through. The characteristics of the ion-conducting membranes include excellent mechanical and thermal stability, chemical resistance, high ionic conductivity, and selectivity. Polymers and polymer-based precursors make up the majority of the materials that have been used as ion-conducting membranes. However, most polymer-based membranes have issues related to poor chemical resistance, recyclability, and thermal and mechanical stability. In addition, as more sustainable materials are being sought to create a sustainable society, new environmentally friendly and economically viable materials are in high demand. The clay-based material could be an alternative for ion-conducting applications due to its porous structure, high surface area, tunable interlayer spacing, excellent thermal and mechanical stability, and high ion conductivity. Clay minerals are primarily used in water treatment, pharmaceutics, ceramics, paints, and coating industries. Furthermore, clay minerals have been used as a filler material in energy storage and conversion system to improve the thermal stability and ion conductivity in electrodes, electrolytes, and separators.Herein, we report a novel approach to making non-polymeric hybrid clay membranes using environmentally benign materials such as clay and zwitterion (i.e., sulfobetaine). These membranes with improved ionic conductivity will find immense potential in applications in energy storage and conversion systems. Such membranes have been synthesized by intercalating sulfobetaine molecules into the interlayer spacing of the bentonite clay matrix. Sulfobetaine is a zwitterion composed of quaternary ammonium cations and sulfonate anions. Leveraging the unique structure-property features that exist in zwitterions helps to alter the interlayer spacings in the clay matrix, thereby enabling ion diffusion through the silicate layers. Furthermore, it helps in the formation of a self-supporting membrane. The functionalized membrane's crystal structure and chemical composition were investigated using XRD, XPS, and ATR-FTIR. XRD was used to identify the layered structure of the silicates in clay and the increased interlayer spacing (1.15 nm to 1.8 nm) of the hybrid clay membrane. Data from XPS and ATR-FTIR confirmed the successful functionalization of clay with sulfobetaine. Furthermore, the ionic conductivity of the hybrid clay membrane was characterized using a non-aqueous lithium electrolyte solution, and found a conductivity of . This is one of the first reports showcasing how zwitterions can impart conductivity in clay silicate motifs. It suggests an easy and novel approach to transport lithium-ion through silicate layers, thereby making it suitable for use as membranes in batteries and supercapacitors. The current study demonstrates an easy and versatile approach to developing cost-effective and eco-friendly membranes from sustainable materials such as clay, which, when functionalized, has the potential to be a highly efficient ion-conducting material with applications in energy storage, devices, and technologies.

Transition metal oxalates as energy storage materials. A review

Silica-derived nanostructured catalysts (SDNCs) are a class of materials synthesized using nanocasting and templating techniques, which involve the sacrificial removal of a silica template to generate highly porous nanostructured materials. The surface of these nanostructures is functionalized with a variety of electrocatalytically active metal and non-metal atoms. SDNCs have attracted considerable attention due to their unique physicochemical properties, tunable electronic configuration, and microstructure. These properties make them highly efficient catalysts and promising electrode materials for next generation electrocatalysis, energy conversion, and energy storage technologies. The continued development of SDNCs is likely to lead to new and improved electrocatalysts and electrode materials. This review article provides a comprehensive overview of the recent advances in the development of SDNCs for electrocatalysis and energy storage applications. It analyzes 337,061 research articles published in the Web of Science (WoS) database up to December 2022 using the keywords "silica", "electrocatalysts", "ORR", "OER", "HER", "HOR", "CO2RR", "batteries", and "supercapacitors". The review discusses the application of SDNCs for oxygen reduction reaction (ORR), oxygen evolution reaction (OER), hydrogen evolution reaction (HER), carbon dioxide reduction reaction (CO2RR), supercapacitors, lithium-ion batteries, and thermal energy storage applications. It concludes by discussing the advantages and limitations of SDNCs for energy applications.

The performance of energy storage devices is highly related to the properties of electrode materials, such as components, morphology, configurations and so on. As a typical hierarchical carbon material, three-dimensional ordered porous carbon (3D-OPC) has unique characteristics of low cost, large specific surface area, highly ordered channels, and high electronic and ionic conductivity, which shows great potential in energy storage and conversion applications. In this mini review, we summarize various template-assisted preparation methods for 3D-OPC, including hard-, ice- and self-templated approaches, and their applications in electrocatalysis, batteries and supercapacitors. Additionally, the critical roles of vertical channels in 3D-OPC when used as electrodes are also discussed. Finally, the current challenges and future research outlook of 3D-OPC are proposed.

Mixed transition metal oxides with favorable electrochemical properties are promising electrode materials in energy storage and conversion systems. In this work, uniform porous yolk-shell MnCo2O4 (denoted as YSM-MCO) microrugby balls have been synthesized by simple annealing treatment of metal carbonates with a microrugby ball shape in air. Benefiting from the desired porous structure and composition, the as-synthesized YSM-MCO exhibits enhanced electrochemical performance when investigated as anode materials for lithium-ion batteries and electrocatalysts for the oxygen evolution reaction. The YSM-MCO demonstrates remarkable lithium storage properties with a good cycling stability (94% capacity retention over 200 cycles at 0.5 A g-1) and superior rate capability (414 mA h g-1 at 5 A g-1). In addition, the YSM-MCO also exhibits better OER activity than most of the reported MnCo2O4-based electrocatalysts.

Disposal and recycling of the large scale biomass waste is of great concern. Themochemically converting the waste biomass to functional carbon nanomaterials and bio-oil is an environmentally friendly apporach by reducing greenhouse gas emissions and air pollution caused by open burning. In this work, we reported a scalable, "green" method for the synthesis of the nanofibers/mesoporous carbon composites through pyrolysis of the Fe(III)-preloaded biomass, which is controllable by adjustment of temperature and additive of catalyst. It is found that the coupled catalytic action of both Fe and Cl species is able to effectively catalyze the growth of the carbon nanofibers on the mesoporous carbon and form magnetic nanofibers/mesoporous carbon composites (M-NMCCs). The mechanism for the growth of the nanofibers is proposed as an in situ vapor deposition process, and confirmed by the XRD and SEM results. M-NMCCs can be directly used as electrode materials for electrochemical energy storage without further separation, and exhibit favorable energy storage performance with high EDLC capacitance, good retention capability, and excellent stability and durability (more than 98% capacitance retention after 10,000 cycles). Considering that biomass is a naturally abundant and renewable resource (over billions tons biomass produced every year globally) and pyrolysis is a proven technique, M-NMCCs can be easily produced at large scale and become a sustainable and reliable resource for clean energy storage.

Efficient production of ammonia using environmentally friendly techniques under ambient conditions is crucial to renewable energy storage and industrial applications, and catalysts with new reaction pathways are highly desirable. In this work, black phosphorus (BP) is used as a metal‐free 2D catalyst for the photoelectrochemical (PEC) nitrogen reduction reaction (NRR). The electrode is fabricated by layer‐by‐layer assembly of BP nanosheets on an indium tin oxide substrate. The PEC NRR activity in the N2 saturated aqueous electrolyte without a sacrificial agent is excellent, as exemplified by an ammonia yield rate of 102.4 µg h−1 mgcat.−1 and Faradaic efficiency of 23.3% at −0.4 V, which are the best among nonmetal catalysts for synthesis of ammonia by photocatalysis and electrocatalysis. Furthermore, the BP electrode shows excellent stability after 6 consecutive cycles. The excellent PEC catalytic properties are attributed to the light excitation enhanced electrocatalytic process and that the external bias promoted photocatalytic process improves ammonia production synergistically. The results not only demonstrate the great potential of BP in PEC catalysis, but also identify a promising technique to produce ammonia under ambient conditions using solar energy and electric energy.

Nanomaterials provide many desirable properties for electrochemical energy storage devices due to their nanoscale size effect, which could be significantly different from bulk or micron-sized materials. Particularly, confined dimensions play important roles in determining the properties of nanomaterials, such as the kinetics of ion diffusion, the magnitude of strain/stress, and the utilization of active materials. Nanowires, as one of the representative one-dimensional nanomaterials, have great capability for realizing a variety of applications in the fields of energy storage since they could maintain electron transport along the long axis and have a confinement effect across the diameter. In this review, we give a systematic overview of the state-of-the-art research progress on nanowires for electrochemical energy storage, from rational design and synthesis, in situ structural characterizations, to several important applications in energy storage including lithium-ion batteries, lithium-sulfur batteries, sodium-ion batteries, and supercapacitors. The problems and limitations in electrochemical energy storage and the advantages in utilizing nanowires to address the issues and improve the device performance are pointed out. At the end, we also discuss the challenges and demonstrate the prospective for the future development of advanced nanowire-based energy storage devices.

Sustainability is highly desired for human beings due to a rapidly changing global climate and numerous environmental issues. In past decades, state-of-the-art studies have been extensively conducted to achieve sustainable energy conversion and storage. However, the remaining challenges in the commercialization of energy conversion and storage devices are to develop novel materials and advanced manufacturing processes. Furthermore, the engineering of nanostructures and device-architectures is of great importance for the energy conversion and storage flat forms. This Special Issue “Novel Materials for Sustainable Energy Conversion and Storage” aims the state-of-the-art research reports of novel nanomaterials and the engineering of device architectures for divergent energy conversion and storage applications with high sustainability involving solar energy systems, electrochemical cells, artificial photosynthesis or secondary (rechargeable) batteries, as highlighted in this editorial.

Developing efficient multifunctional materials for the oxygen evolution reaction (OER) and supercapacitors has become essential for storing and converting energy. Taking advantage of the structural flexibility of metal–organic frameworks (MOFs), bifunctional electrochemical nanomaterial LaFeCoOOH with high performance is successfully synthesized by doping rare earth La atoms in transition metals. La doping modifies the coordination environment of active sites and material morphology, modulates the energy structure, improves material conductivity, and optimizes the adsorption and desorption performance of oxygen intermediates. LaFeCoOOH demonstrates exceptional electrocatalytic activity for OER, achieving a remarkably low overpotential of 177 mV at 10 mA cm −2 current density in 1 m KOH alkaline electrolyte. The material exhibits outstanding operational stability, maintaining consistent performance for over 1000 h at an elevated current density of 100 mA cm −2 under identical alkaline conditions. Furthermore, LaFeCoOOH electrode displays superior electrochemical energy storage capabilities, demonstrating an impressive specific capacitance of 3508 mF cm −2 at 1 mA cm −2 current density. When configured as an asymmetric supercapacitor (LaFeCoOOH//Activated Carbon (AC)) using 6 m KOH electrolyte, the device achieves an exceptional energy density of 118.52 µWh cm −2 while delivering a power density of 1700 µW cm −2 , highlighting its dual functionality for both energy conversion and storage applications. Hence, this study provides a new perspective for the exploration of new multifunctional transition metal composites modified with rare earth elements for energy storage and conversion applications.

MXenes: An exotic material for hybrid supercapacitors and rechargeable batteries

Hybrid or composite heterostructured electrode materials have been widely studied for their potential application in electrochemical energy storage. Whereas their physical or chemical properties could be affected significantly by modulating the heterogeneous interface, the underlying mechanisms are not yet fully understood. In this work, we fabricated an electrochemical energy storage device with a MoS2 nanosheet/MnO2 nanowire heterostructure and designed two charge/discharge channels to study the effect of the heterogeneous interface on the energy storage performances. Electrochemical measurements show that a capacity improvement of over 50% is achieved when the metal current collector was in contact with the MnO2 instead of the MoS2 side. We propose that this enhancement is due to the unidirectional conductivity of the MoS2/MnO2 heterogeneous interface, resulting from the unimpeded electrical transport in the MnO2-MoS2 channel along with the blocking effect on the electron transport in the MoS2-MnO2 channel, which leads to reaction kinetics optimization. The present study thus provides important insights that will improve our understanding of heterostructured electrode materials for electrochemical energy storage.