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In the present work, we investigate the potential of modified barium titanate (BaTiO3), an inexpensive perovskite oxide derived from earth-abundant precursors, for developing efficient water oxidation electrocatalysts using first-principles calculations. Based on our calculations, Rh doping is a way of making BaTiO3 absorb more light and have less overpotential needed for water to oxidize. It has been shown that a TiO2-terminated BaTiO3 (001) surface is more promising from the point of view of its use as a catalyst. Rh doping expands the spectrum of absorbed light to the entire visible range. The aqueous environment significantly affects the ability of Rh-doped BaTiO3 to absorb solar radiation. After Ti→Rh replacement, the doping ion can take over part of the electron density from neighboring oxygen ions. As a result, during the water oxidation reaction, rhodium ions can be in an intermediate oxidation state between 3+ and 4+. This affects the adsorption energy of reaction intermediates on the catalyst’s surface, reducing the overpotential value.

Zinc–air batteries (ZABs) have garnered significant interest as a viable substitute for lithium-ion batteries (LIBs), primarily due to their impressive energy density and low cost. However, the efficacy of zinc–air batteries is heavily dependent on electrocatalysts, which play a vital role in enhancing reaction efficiency and stability. This scholarly review article highlights the crucial significance of electrocatalysts in zinc–air batteries and explores the rationale behind employing Fe-Co-Ni-Zn-based metal–organic framework (MOF)-derived hybrid materials as potential electrocatalysts. These MOF-derived electrocatalysts offer advantages such as abundancy, high catalytic activity, tunability, and structural stability. Various synthesis methods and characterization techniques are employed to optimize the properties of MOF-derived electrocatalysts. Such electrocatalysts exhibit excellent catalytic activity, stability, and selectivity, making them suitable for applications in ZABs. Furthermore, they demonstrate notable capabilities in the realm of ZABs, encompassing elevated energy density, efficacy, and prolonged longevity. It is imperative to continue extensively researching and developing this area to propel the advancement of ZAB technology forward and pave the way for its practical implementation across diverse fields.

The ice-templated method (ITM) has drawn significant attention to the improvement of the electrochemical properties of various materials. The ITM approach is relatively straightforward and can produce hierarchically porous structures that exhibit superior performance in mass transfer, and the unique morphology has been shown to significantly enhance electrochemical performance, making it a promising method for energy storage and conversion applications. In this review, we aim to present an overview of the ITM and its applications in the electrochemical energy storage and conversion field. The fundamental principles underlying the ITM will be discussed, as well as the factors that influence the morphology and properties of the resulting structures. We will then proceed to comprehensively explore the applications of ITM in the fabrication of high-performance electrodes for supercapacitors, batteries, and fuel cells. We intend to find the key advances in the use of ITM and evaluate its potential to overcome the existing challenges in the development of efficient energy storage and conversion systems.

The leakage behavior of ferroelectric film has an important effect on energy storage characteristics. Understanding and controlling the leakage mechanism of ferroelectric film at different temperatures can effectively improve its wide-temperature storage performance. Here, the structures of a 1 mol% SiO2-doped BaZr0.35Ti0.65O3 (BZTS) layer sandwiched between two undoped BaZr0.35Ti0.65O3 (BZT35) layers was demonstrated, and the leakage mechanism was analyzed compared with BZT35 and BZTS single-layer film. It was found that interface-limited conduction of Schottky (S) emission and the Fowler-Nordheim (F-N) tunneling existing in BZT35 and BZTS films under high temperature and a high electric field are the main source of the increase of leakage current and the decrease of energy storage efficiency at high temperature. Only an ohmic conductive mechanism exists in the whole temperature range of BZT35/BZTS/BZT35(1:1:1) sandwich structure films, indicating that sandwich multilayer films can effectively simulate the occurrence of interface-limited conductive mechanisms and mention the energy storage characteristics under high temperature.

Layered vanadium-based materials are considered to be great potential electrode materials for aqueous Zn-ion batteries (AZIBs). The improvement of the electrochemical properties of vanadium-based materials is a hot research topic but still a challenge. Herein, a composite of Zn-ion pre-intercalated V2O5·nH2O combined with reduced graphene oxide (ZnVOH/rGO) is synthesized by a facile hydrothermal method and it shows improved Zn-ion storage. ZnVOH/rGO delivers a capacity of 325 mAh·g−1 at 0.1 A·g−1, and this value can still reach 210 mAh·g−1 after 100 cycles. Additionally, it exhibits 196 mAh·g−1 and keeps 161 mAh·g−1 after 1200 cycles at 4 A·g−1. The achieved performances are much higher than that of ZnVOH and VOH. All results reveal that Zn2+ as “pillars” expands the interlayer distance of VOH and facilitates the fast kinetics, and rGO improves the electron flow. They both stabilize the structure and enhance efficient Zn2+ migration. All findings demonstrate ZnVOH/rGO’s potential as a perspective cathode material for AZIBs.

N, S-doped ultramicroporous carbons (NSUC-x) with a high nitrogen/sulfur content and a narrow pore-size distribution of around 0.55 nm were firstly prepared using L-cysteine as a nitrogen and sulfur source. The phase, graphitization degree, morphology, specific surface area, pore structure and surface condition of NSUC-x are investigated to analyze the key role in electrochemical performance. Such an ultramicroporous structure and N, S doping not merely provide a high-specific surface area and a suitable pore size, but also induce a good wettability for the fast transport and adsorption of electrolyte ions. Due to the above strategies, the typical NSUC-0.4 exhibits a high gravimetric capacitance of 339 F g−1 at 0.5 A g−1 as well as a capacity retention of 91.6% after 10,000 cycles in a three-electrode system using a 6 M KOH electrolyte. More attractively, a NSUC-0.4-assembled symmetrical supercapacitor delivers an energy output of 7.4 Wh kg−1 at 100 W kg−1 in 6 M KOH as well as a capacity retention of 92.4% after 10,000 cycles, indicating its practical application prospect. Our findings open up new prospects for the design and electrochemical application of N, S-doped ultramicroporous carbons.

Lithium-ion batteries (LIBs) as a predominant power source are widely used in large-scale energy storage fields. For the next-generation energy storage LIBs, it is primary to seek the high capacity and long lifespan electrode materials. Nickel and purified terephthalic acid-based MOF (Ni-PTA) with a series amounts of zinc dopant (0, 20, 50%) are successfully synthesized in this work and evaluated as anode materials for lithium-ion batteries. Among them, the 20% atom fraction Zn-doped Ni-PTA (Zn0.2-Ni-PTA) exhibits a high specific capacity of 921.4 mA h g−1 and 739.6 mA h g−1 at different current densities of 100 and 500 mA g−1 after 100 cycles. The optimized electrochemical performance of Zn0.2-Ni-PTA can be attributed to its low charge transfer resistance and high lithium-ion diffusion rate resulting from expanded interplanar spacing after moderate Zn doping. Moreover, a full cell is fabricated based on the LiFePO4 cathode and as-prepared MOF. The Zn0.2-Ni-PTA shows a reversible specific capacity of 97.9 mA h g−1 with 86.1% capacity retention (0.5 C) after 100 cycles, demonstrating the superior electrochemical performance of Zn0.2-Ni-PTA anode as a promising candidate for practical lithium-ion batteries.

A general rise in environmental and anthropogenically induced greenhouse gas emissions has resulted from worldwide population growth and a growing appetite for clean energy, industrial outputs, and consumer utilization. Furthermore, well-established, advanced, and emerging countries are seeking fossil fuel and petroleum resources to support their aviation, electric utilities, industrial sectors, and consumer processing essentials. There is an increasing tendency to overcome these challenging concerns and achieve the Paris Agreement’s priorities as emerging technological advances in clean energy technologies progress. Hydrogen is expected to be implemented in various production applications as a fundamental fuel in future energy carrier materials development and manufacturing processes. This paper summarizes recent developments and hydrogen technologies in fuel refining, hydrocarbon processing, materials manufacturing, pharmaceuticals, aircraft construction, electronics, and other hydrogen applications. It also highlights the existing industrialization scenario and describes prospective innovations, including theoretical scientific advancements, green raw materials production, potential exploration, and renewable resource integration. Moreover, this article further discusses some socioeconomic implications of hydrogen as a green resource.

The nanocomposites of reduced graphene oxide (rGO) supported zinc tungstate nanoparticles (ZnWO4-NPs) receive considerable attention in electro-catalytic hydrogen evolution reactions (HER) and reveal significantly higher electro-catalytic performances than pure ZnWO4-NPs in alkaline media (i.e., 0.5 M KOH electrolyte). The polarization studies show that the ZnWO4-NPs@rGO nanocomposites exhibit low energy loss and good electrode stability during electrochemical reactions for HER. Furthermore, the Tafel slope of ZnWO4-NPs@rGO nanocomposites is found to be approximately 149 mV/dec, which closely agrees with the reported Tafel values of the noble metal electrocatalyst. In contrast, the performance of the ZnWO4-NPs@rGO nanocomposite is found to be approximately 1.5 times higher than that of ZnWO4-NPs in hydrogen production efficiency. Our results emphasize the significance of the nanocomposites with enhanced electro-catalytic activities by lowering the energy loss during electro-catalysis in an alkaline medium.

Nanostructured β-FeSi2 and β-Fe0.95Co0.05Si2 specimens with a relative density of up to 95% were synthesized by combining a top-down approach and spark plasma sintering. The thermoelectric properties of a 50 nm crystallite size β-FeSi2 sample were compared to those of an annealed one, and for the former a strong decrease in lattice thermal conductivity and an upshift of the maximum Seebeck’s coefficient were shown, resulting in an improvement of the figure of merit by a factor of 1.7 at 670 K. For β-Fe0.95Co0.05Si2, one observes that the figure of merit is increased by a factor of 1.2 at 723 K between long time annealed and nanostructured samples mainly due to an increase in the phonon scattering and an increase in the point defects. This results in both a decrease in the thermal conductivity to 3.95 W/mK at 330 K and an increase in the power factor to 0.63 mW/mK2 at 723 K.

The incorporation of nonmetal group dopants into a graphitic carbon nitride (g-C3N4) framework is fabricated by adding a small amount of hexamethylenetetramine during the thermal polymerization process. The material shows an excellent visible-light photocatalytic H2 production performance that is eight times higher than bulk g-C3N4. This outstanding performance is ascribed to the introducing of N-doped carbon, which not only enhances the light absorption and favorsa narrower band gap, but also upshifts the conductionband (CB) potential, resulting in a better reduction ability of electrons. This discovery has potential significancefor the designing of high performance, economic, and environmental friendly photocatalyst for solar energy conversion.

NiMn2O4 (NMO) is a good alternative anode material for lithium-ion battery (LIB) application, due to its superior electrochemical activity. Current research shows that synthesis of NMO via citric acid-based combustion method envisaged application in the LIB, due to its good reversibility and rate performance. Phase purity and crystallinity of the material is controlled by calcination at different temperatures, and its structural properties are investigated by X-ray diffraction (XRD). Composition and oxidation state of NMO are further investigated by X-ray photoelectron spectroscopy (XPS). For LIB application, lithiation delithiation potential and phase transformation of NMO are studied by cyclic voltammetry curve. As an anode material, initially, the average discharge capacity delivered by NMO is 983 mA·h/g at 0.1 A/g. In addition, the NMO electrode delivers an average discharge capacity of 223 mA·h/g after cell cycled at various current densities up to 10 A/g. These results show the potential applications of NMO electrodes for LIBs.

Biochar is a byproduct generated from the hydrothermal liquefaction of biomass, such as corn stover, in an anaerobic environment. This work aims to convert biochar into a value-added product of carbon nanofibrous felt. First, the biochar-containing precursor membrane was prepared from simultaneous electrospinning and electrospraying. After thermal stabilization in air and carbonization in argon, the obtained precursor membrane was converted into a mechanically flexible and robust carbon nanofibrous felt. Electrochemical results revealed that the biochar-derived carbon nanofibrous felt might be a good candidate as a supercapacitor electrode with a good rate capability and high kinetic performance.

Zinc-air batteries (ZABs) have garnered significant interest as a viable substitute for lithium-ion batteries (LIBs), primarily due to their impressive energy density and low cost. However, the efficacy of zinc-air batteries is heavily dependent on electrocatalysts, which play a vital role in enhancing reaction efficiency and stability. This scholarly review article highlights the crucial significance of electrocatalysts in zinc-air batteries and explores the rationale behind employing Fe-Co-Ni-Zn-based metal-organic framework (MOF)-derived hybrid materials as potential electrocatalysts. These MOF-derived electrocatalysts offer advantages such as abundancy, high catalytic activity, tunability, and structural stability. Various synthesis methods and characterization techniques are employed to optimize the properties of MOF-derived electrocatalysts. Such electrocatalysts exhibit excellent catalytic activity, stability, and selectivity, making them suitable for applications in ZABs. Furthermore, they demonstrate notable capabilities in the realm of ZABs, encompassing elevated energy density, efficacy, and prolonged longevity. It is imperative to continue extensively researching and developing this area to propel the advancement of ZAB technology forward and pave the way for its practical implementation across diverse fields.

In this work, hierarchical three-dimensional (3D) urchinlike WO3 microspheres with a self-assembled nanorod core, and a connected and quasiconnected nanothorn network shell were synthesized with the hydrothermal method. For the surface or near-surface regions of pseudocapacitive materials that are involved in the Faradaic reaction, the urchinlike WO3 special microstructure provided more effective charge-storage area, exhibiting a high specific capacitance of 488.78 F g−1, low average equivalent-series resistance of 0.966 Ω cm−2, and excellent cycling stability (84.75% of its initial value after the 10,000 cycles). This performance indicates the urchinlike WO3 microspheres are promising electrode materials for high-performance supercapacitors.

Ni-doped VO2(B) samples (NixVO2(B)) were fabricated by a facile one-step hydrothermal method. When evaluated as a cathode material for lithium ion batteries (LIBs), these Ni-doped VO2(B) exhibited improved lithium storage performance as compared to the pure VO2(B). In particular, when the doping amount is 3%, NixVO2(B) showed the highest lithium storage capacity, best cycling stability, smallest electrochemical reaction resistance, and largest lithium diffusion coefficient. For example, after 100 cycles at a current density of 32.4 mA/g, NixVO2(B) delivered a high specific discharge capacity of 163.0 mAh/g, much higher than that of the pure VO2(B) sample (95.5 mAh/g). Therefore, Ni doping is an effective strategy for enhancing the lithium storage performance of VO2(B).

Carbon nanotubes (CNTs) are known as nano-architectured allotropes of carbon, having graphene sheets that are wrapped forming a cylindrical shape. Rolling of graphene sheets in different ways makes CNTs either metals or narrow-band semiconductors. Over the years, researchers have devoted much attention to understanding the intriguing properties CNTs. They exhibit some unusual properties like a high degree of stiffness, a large length-to-diameter ratio, and exceptional resilience, and for this reason, they are used in a variety of applications. These properties can be manipulated by controlling the diameter, chirality, wall nature, and length of CNTs which are in turn, synthesis procedure-dependent. In this review article, various synthesis methods for the production of CNTs are thoroughly elaborated. Several characterization methods are also described in the paper. The applications of CNTs in various technologically important fields are discussed in detail. Finally, future prospects of CNTs are outlined in view of their commercial applications.

Biomorphic Mn3O4 nanocrystal/porous carbon microfiber composites were hydrothermally fabricated and subsequently calcined using cotton as a biotemplate. The as-prepared material exhibited a specific capacitance of 140.8 F·g−1 at 0.25 A·g−1 and an excellent cycle stability with a capacitance retention of 90.34% after 5000 cycles at 1 A·g−1. These characteristics were attributed to the introduction of carbon fiber, the high specific surface area, and the optimized microstructure inherited from the biomaterial.

Manganese dioxides, inorganic materials which have been used in industry for more than a century, now find great renewal of interest for storage and conversion of energy applications. In this review article, we report the properties of MnO2 nanomaterials with different morphologies. Techniques used for the synthesis, structural, physical properties, and electrochemical performances of periodic and aperiodic frameworks are discussed. The effect of the morphology of nanosized MnO2 particles on their fundamental features is evidenced. Applications as electrodes in lithium batteries and supercapacitors are examined.

A photoanode material ZnO nanoflower (ZNFs) for efficient dye-sensitized solar cell (DSSC) was prepared. This unique structure can significantly increase the specific surface area and amount of light absorption, leading to a higher short-circuit current density. Furthermore, ZNFs resulted in closer spacing between the nanorods and more direct conduction paths for electrons, leading to higher open-circuit voltage. The overall promising power conversion efficiency of 5.96% was obtained with photoanodes of 8.5 μm thickness. This work shows that ZNFs is an attractive material and has good potential for application in high efficiency ZnO-based DSSCs.

The Co-B amorphous alloys were prepared via a chemical reduction method by sodium borohydride, using three different cobalt salts (CoCl2·6H2O, CoSO4·7H2O, and Co(NO3)2·6H2O) as sources of cobalt. As anode materials in alkaline rechargeable batteries, the Co-B alloy prepared from CoCl2·6H2O has a maximum specific discharge capacity of 844.6 mAh/g, and 306.4 mAh/g is retained even after 100 cycles at a discharge current of 100 mA/g. When Co(NO3)2·6H2O is used as a raw material, the formation of Co3(BO3)2 worsens the electrochemical properties of the sample, i.e., a maximum capacity of only 367.0 mAh/g.

Cobalt sulfide (Co9S8) particles are compounded as the electrode materials of supercapacitors by a mechanical alloying method. They show excellent properties including good cycling stability and high specific capacitance. A supercapacitor is assembled using Co9S8 as the anode and activated carbon (AC) as the cathode. It gains a maximum specific capacitance of 55 F·g−1 at a current density of 0.5 A·g−1, and also an energy density of 15 Wh·kg−1. Those results show that the novel and facile synthetic route may be able to offer a new way to synthesize alloy compounds with excellent supercapacitive properties.

Nanostructured β-FeSi 2 and β-Fe 0.95 Co 0.05 Si 2 specimens with a relative density of up to 95% were synthesized by combining a top-down approach and spark plasma sintering. The thermoelectric properties of a 50 nm crystallite size β-FeSi 2 sample were compared to those of an annealed one, and for the former a strong decrease in lattice thermal conductivity and an upshift of the maximum Seebeck's coefficient were shown, resulting in an improvement of the figure of merit by a factor of 1.7 at 670 K. For β-Fe 0.95 Co 0.05 Si 2 , one observes that the figure of merit is increased by a factor of 1.2 at 723 K between long time annealed and nanostructured samples mainly due to an increase in the phonon scattering and an increase in the point defects. This results in both a decrease in the thermal conductivity to 3.95 W/mK at 330 K and an increase in the power factor to 0.63 mW/mK 2 at 723 K.

The incorporation of nonmetal group dopants into a graphitic carbon nitride (g-C 3 N 4 ) framework is fabricated by adding a small amount of hexamethylenetetramine during the thermal polymerization process. The material shows an excellent visible-light photocatalytic H 2 production performance that is eight times higher than bulk g-C 3 N 4 . This outstanding performance is ascribed to the introducing of N-doped carbon, which not only enhances the light absorption and favorsa narrower band gap, but also upshifts the conductionband (CB) potential, resulting in a better reduction ability of electrons. This discovery has potential significancefor the designing of high performance, economic, and environmental friendly photocatalyst for solar energy conversion.

Manganese dioxides, inorganic materials which have been used in industry for more than a century, now find great renewal of interest for storage and conversion of energy applications. In this review article, we report the properties of MnO₂ nanomaterials with different morphologies. Techniques used for the synthesis, structural, physical properties, and electrochemical performances of periodic and aperiodic frameworks are discussed. The effect of the morphology of nanosized MnO₂ particles on their fundamental features is evidenced. Applications as electrodes in lithium batteries and supercapacitors are examined.