Materials For Electrochemical Energy Storage Research Articles

Nanoporous Carbon Materials Derived from Zanthoxylum Bungeanum Peel and Seed for Electrochemical Supercapacitors

In order to prepare biomass-derived carbon materials with high specific capacitance at a low activation temperature (≤700 °C), nanoporous carbon materials were prepared from zanthoxylum bungeanum peels and seeds via the pyrolysis and KOH-activation processes. The results show that the optimal activation temperatures are 700 °C and 600 °C for peels and seeds. Benefiting from the hierarchical pore structure (micropores, mesopores, and macropores), the abundant heteroatoms (N, S, and O) containing functional groups, and plentiful electrochemical active sites, the PAC-700 and SAC-600 derive the large capacities of ~211.0 and ~219.7 F g−1 at 1.0 A g−1 in 6 M KOH within the three-electrode configuration. Furthermore, the symmetrical supercapacitors display a high energy density of 22.9 and 22.4 Wh kg−1 at 7500 W kg−1 assembled with PAC-700 and SAC-600, along with exceptional capacitance retention of 99.1% and 93.4% over 10,000 cycles at 1.0 A g−1. More significantly, the contribution here will stimulate the extensive development of low-temperature activation processes and nanoporous carbon materials for electrochemical energy storage and beyond.

1T/2H Mixed-phase MoS2 with enlarged interlayer spacing induced via bacteria-derived carbon for long-lifespan pseudocapacitors

Pseudocapacitors (PCs) are considered prospective candidates for large-scale aqueous energy storage systems due to their high power density. However, the poor cycling stability resulting from sluggish metal ion transport kinetics and the instability of the electrode structures hinders their further applications. To address this issue, an effective strategy of 1T/2H mixed-phase MoS2 directly grown on the electrochemically activated carbon (EC) induced via bacteria-derived carbon (BC) from bacillus subtilis was proposed to achieve efficient anodes for potassium ion capacitors. The inherent nitrogen elements found in the bacteria-derived carbon, along with a trace amount of amines and their derivatives generated from amino acid decarboxylation, act as support by inserting into the MoS2 interlayer. Amines and their derivatives as intercalators could suppress the MoS2 layer stacking and mitigate structure damage, which is responsible for preventing rapid capacity fading. Thus, the mixed-phase MoS2 with an expanded interlayer spacing of 0.94 nm achieves a remarkable durability with a capacitance retention of 110.2 % after 40,000 cycles at 10 A g−1. Density Functional Theory (DFT) reveals that the mixed-phase MoS2 could improve electron transfer ability and cyclic stability, in which the rich vacancies introduced by bacteria-derived carbon could enhance the K+ adsorption. To highlight, the asymmetric capacitor device (ASC) adopting mixed-phase MoS2 anode shows a long lifespan (88 % capacitance retention over 10,000 cycles). This work will provide a green approach to boost cycling performance of MoS2 anodes and shed light on developing high-performance MoS2-based materials for electrochemical energy storage.

Synthesis of Ni3V2O8-rGO composite nanostructure for high-performance hybrid supercapacitors via hydrothermal method

To address global energy demand, major efforts have been made to develop cutting-edge electrode materials for electrochemical energy storage (EES) devices. The present article discusses the hydrothermal synthesis of bare nickel vanadate and a nickel vanadate/reduced graphene oxide (Ni3V2O8-rGO) composite for supercapacitor applications. The physicochemical properties of pure Ni3V2O8 (NVO) and the Ni3V2O8-rGO (NVO-rGO) composite were investigated using a variety of characterization tools. The electrochemical traits of the NVO-rGO composite outperform bare NVO due to the synergistic effect. At a current density of 1 mAcm−2, the NVO and NVO-rGO nanostructures exhibit excellent specific capacitances of 85 Fg−1 and 108 Fg−1, respectively. These nanostructures also have energy densities of about 3.82 and 5.02 WhKg−1, with power densities of 141.75 and 151.57 WKg−1 for NVO and NVO-rGO composite, respectively. Electrochemical impedance spectroscopy (EIS) studies revealed a charge resistance of 2.05 Ω. The transfer coefficient and standard rate constant indicate that the charge storage mechanism is based on a quasi-reversible redox process. The present investigation demonstrates that the NVO-rGO composite has exceptional electrochemical performance. The outstanding electrochemical performance of both NVO and NVO/rGO underlines their potential as novel and promising materials for supercapacitor applications, implying significant feasibility for large-scale utilization.

Recent progress on construction and applications of metal‐organic frameworks‐based materials for lithium‐ion batteries and supercapacitors

AbstractMetal‐organic frameworks (MOFs), a special sort of three‐dimensional crystalline porous lattices composed of organic multi‐site connectors and metal nodes, are characterized by unique porosity and high specific surface area, which have attracted a wide range of interest as electrode materials for the electrochemical energy storage devices in recent years. In this contribution, we outline the current research progress on the construction of pristine MOFs, MOF composites, and MOF derivatives and their applications as electrode materials in supercapacitors (SCs) and lithium‐ion batteries (LIBs). Specifically, we discuss the shortcomings of MOFs‐based electrode materials for SCs and LIBs. The innovative work on performance improvements by combining MOFs with other conductive materials and derivating MOFs into metal sulfides, metal oxides, metal phosphides, and porous carbon is also presented in detail. Finally, our perspectives on the challenges in the future for a grasp of the potential mechanisms are tentatively provided. This review will inspire more developments and applications of MOFs‐based electrode materials for electrochemical energy storage.

Electrochemical Investigation of Lithium Perchlorate-Doped Polypyrrole Growing on Titanium Substrate

Lithium perchlorate-doped polypyrrole growing on titanium substrate (LiClO4-PPy/Ti) has been fabricated to act as electroactive electrode material for feasible electrochemical energy storage. A theoretical and experimental investigation is adopted to disclose the conductivity, electroactivity properties and interfacial interaction-dependent capacitance of LiClO4-PPy/Ti electrode. The experimental measurement results disclose that LiClO4-PPy/Ti reveals lower ohmic resistance (0.2226 Ω cm−2) and charge transfer resistance (2116 Ω cm−2) to exhibit higher electrochemical conductivity, a more reactive surface, and feasible ion diffusion to present higher double-layer capacitance (0.1930 mF cm−2) rather than LiClO4/Ti (0.3660 Ω cm−2, 65,250 Ω cm−2, 0.0334 mF cm−2). LiClO4-PPy/Ti reveals higher Faradaic capacitance caused by the reversible doping and dedoping process of perchlorate ion on PPy than the electrical double-layer capacitance of LiClO4/Ti caused by the reversible adsorption and desorption process of the LiClO4 electrolyte on Ti. Theoretical simulation calculation results prove that a more intensive electrostatic interaction of pyrrole N···Ti (2.450 Å) in LiClO4-PPy/Ti rather than perchlorate O···Ti (3.537 Å) in LiClO4/Ti. LiClO4-PPy/Ti exhibits higher density of states (57.321 electrons/eV) at Fermi energy and lower HOMO-LUMO molecule orbital energy gap (0.032 eV) than LiClO4/Ti (9.652 electrons/eV, 0.340 eV) to present the enhanced electronic conductivity. LiClO4-PPy/Ti also exhibits a more declined interface energy (−1.461 × 104) than LiClO4/Ti (−5.202 × 103 eV) to present the intensified interfacial interaction. LiClO4-PPy/Ti accordingly exhibits much higher specific capacitances of 0.123~0.0122 mF cm−2 at current densities of 0.01~0.10 mA cm−2 rather than LiClO4/Ti (0.010~0.0095 mF cm−2, presenting superior electroactivity and electrochemical capacitance properties. LiClO4-PPy/Ti could well act as the electroactive supercapacitor electrode for feasible energy storage.

Carbon and Nitrogen‐Co‐Doped Se/NiSe2/CoSe2 Nanocomposite as Superior Performance Electrode Material in Hybrid Supercapacitors

AbstractMetal selenides are essential electrode materials for promising electrochemical energy storage with comparable or improved electrochemical performance than metal oxides. Herein, Se/NiSe2/CoSe2 (S/NS/CS) is fabricated using a solvothermal approach with the assistance of polyethyleneimine, followed by annealing at different temperatures (300, 400, 500, and 600 °C) for one hour under an argon atmosphere. After annealing, all electrodes’ physical and electrochemical properties were examined, which determined that the best electrode is NiCo2O4/NiO (NCO/NO) formed at 500 °C. Additional hydrothermal method uses NCO/NO with SeO2 as a selenium source to prepare S/NS/CS nanocomposite, with a specific surface architecture that enables easy ion movement and robust conductivity, giving it exceptional electrochemical energy storage properties. It exhibited a remarkable capacitance of 468 F g−1 at a current density of 0.5 A g−1. For practical applications, the hybrid S/NS/CS//AC device was designed using S/NS/CS as a positive electrode and commercial activated carbon (AC) as a negative electrode. The asymmetric device demonstrated an excellent capacitance of 142 F g−1 (189 C g−1) and a superb specific energy of 44 Wh kg−1 at a specific power of 840 W kg−1 at a current density of 1 A g−1, providing 80 % capacity retention and 100 % coulombic efficiency after 5000 cycles.

Unlocking Spin Gates of Transition Metal Oxides via Strain Stimuli to Augment Potassium Ion Storage

Transition metal oxides (TMOs) are key in electrochemical energy storage, offering cost‐effectiveness and a broad potential window. However, their full potential is limited by poor understanding of their slow reaction kinetics and stability issues. This study diverges from conventional complex nano‐structuring, concentrating instead on spin‐related charge transfer and orbital interactions to enhance the reaction dynamics and stability of TMOs during energy storage processes. We successfully reconfigured the orbital degeneracy and spin‐dependent electronic occupancy by disrupting the symmetry of magnetic cobalt (Co) sites through straightforward strain stimuli. The key to this approach lies in the unfilled Co 3d shell, which serves as a spin‐dependent regulator for carrier transfer and orbital interactions within the reaction. We observed that the opening of these 'spin gates' occurs during a transition from a symmetric low‐spin state to an asymmetric high‐spin state, resulting in enhanced reaction kinetics and maintained structural stability. Specifically, the spin‐rearranged Al‐Co3O4 exhibited a specific capacitance of 1371 F g‐1, which is 38% higher than that of unaltered Co3O4. These results not only shed light on the spin effects in magnetic TMOs but also establish a new paradigm for designing electrochemical energy storage materials with improved efficiency.

Unlocking Spin Gates of Transition Metal Oxides via Strain Stimuli to Augment Potassium Ion Storage.

Transition metal oxides (TMOs) are key in electrochemical energy storage, offering cost-effectiveness and a broad potential window. However, their full potential is limited by poor understanding of their slow reaction kinetics and stability issues. This study diverges from conventional complex nano-structuring, concentrating instead on spin-related charge transfer and orbital interactions to enhance the reaction dynamics and stability of TMOs during energy storage processes. We successfully reconfigured the orbital degeneracy and spin-dependent electronic occupancy by disrupting the symmetry of magnetic cobalt (Co) sites through straightforward strain stimuli. The key to this approach lies in the unfilled Co 3d shell, which serves as a spin-dependent regulator for carrier transfer and orbital interactions within the reaction. We observed that the opening of these 'spin gates' occurs during a transition from a symmetric low-spin state to an asymmetric high-spin state, resulting in enhanced reaction kinetics and maintained structural stability. Specifically, the spin-rearranged Al-Co3O4 exhibited a specific capacitance of 1371 F g-1, which is 38% higher than that of unaltered Co3O4. These results not only shed light on the spin effects in magnetic TMOs but also establish a new paradigm for designing electrochemical energy storage materials with improved efficiency.

Enhanced Photocatalytic and Electrochemical Performance of MOF-Derived NiO-ZnO Oxide Composites for Wastewater Treatment and Sustainable Energy Storage

Solar energy is a crucial and sustainable resource, necessitating material optimization for efficient use in solar-driven applications, particularly photocatalysis. Mixed-metallic nanocomposites, notably those derived from metal-organic frameworks (MOFs), have emerged as promising functional materials for environmental remediation and electrochemical energy storage. MOFs provide unique platforms for synthesizing diverse nanostructures, incorporating metals, oxides, sulfides, and nitrides within a porous carbon matrix. These resulting nanocomposites exhibit high crystallinity, retained morphologies, and tunable textural features. This study focuses on synthesizing a MOF-derived Ni/Zn nanocomposite (i.e., MD-Ni/Zn) from a bimetallic MOF to exploit its potential in photocatalytic pollutant degradation and electrochemical energy storage. Under UV irradiation, the MD-Ni/Zn nanocomposite efficiently degrades 98% of mixed (RhB+CV) dye within 60 minutes. This remarkable photocatalytic performance is attributed to the occurrence of mixed phases in the MD-Ni/Zn nanocomposite, minimizing the recombination efficiency of photoinduced e-/h+ through the p-n heterojunction mechanism. Electrochemical analysis reveals outstanding capacitance in the MD-Ni/Zn nanocomposite, reaching 1002 F/g at 5 A/g, emphasizing its suitability for enhanced electrochemical energy storage.

Dual-gate design enables intrinsic safety of high-energy batteries

The safety issue hampers the application of high-energy lithium-ion batteries in electric vehicles, grid energy storage, electric ships and aircrafts. The chemical cross-talk, which refers to the migration of energetic intermediates between cathode and anode, initiates battery self-heating and accelerates the intensive heat release during battery thermal failure. However, blocking the chemical cross-talk is extremely hard. Previously, we may expect a thermally stable separator can guard the gate between battery cathode and anode, however, large amount of hot gas breaks the defense mechanically not thermally. Draining the cross-talk gas is of equal importance with blocking it. Herein, a dual-gate design notion is proposed, using separator as “block gate” and vent valve as “removal gate” to regulate the spatial distribution of energetic species to reduce the major heat release during battery thermal runaway. The design is validated by more than 50 battery chemistries. Typically, the maximum temperature of NMC811||Gr pouch cell decreases from >800 °C to <300 °C, the highest temperature rising rate decreases from 761.0 °C/s to 0.013 °C/s. The morphology and crystalline change of cathode verify that the chemical cross-talk is successfully suppressed. Moreover, such design has little side effect on the electrochemical performance of batteries. The dual-gate design breaks the bottleneck for the safety design of high energy batteries, providing insight into the safe utilization of electrochemical energy storage materials.

Supercapacitor Performance of MXene-Coated Carbon Nanofiber Electrodes

MXenes consisting of thin layers of transition metal carbides or nitrides are good candidates for electrode materials due to their excellent electrical conductivity and fast ion transfer. Electrospun carbon nanofibers are highly porous and electrically conductive, making them attractive for electrode materials. In this study, free-standing electrodes were prepared by the dip-coating of carbon nanofibers (CNFs) in the MXene (Ti3C2) colloidal solution, which was synthesized via the wet-etching of MAX (Ti3AlC2) phase, and their chemical structures were investigated by X-ray diffraction and Fourier transform infrared spectroscopy. In addition, scanning and transmission electron microscopy were used to investigate the morphological and crystallographic features of MXene-coated CNFs. Surface area and pore volumes were investigated by nitrogen adsorption/desorption measurements. Supercapacitor performance was studied by assembling a 3-electrode system with 1M aqueous sodium sulfate solution as an electrolyte. MXene-coated CNFs exhibited a maximum specific capacitance of 514 F/g at 0.5 A/g, with energy and power densities of 71.4 Wh/kg at 0.5 A/g and 2.3 kW/kg at 5 A/g, respectively, which are relevantly higher compared to the pristine CNFs due to the pseudocapacitive behavior of MXenes. They also showed comparable cyclic stability during 5000 cycles with the CNFs. This result indicates that MXene-coated carbon nanofibers can be effective electrode materials for electrochemical energy storage.

Cycling Stability of a 2D Pristine MOF Supercapacitors

Two‐dimensional (2D) metal–organic frameworks (MOFs) have been a worldwide research interest due to their potential application in supercapacitors. Herein, a cobalt‐based layered MOF ([Co2(μ‐SO4)(Hppza)2(H2O)3]n, namely, SEU‐1; H2ppza = 3‐(pyridin‐4‐yl)‐1H‐pyrazole‐5‐carboxylic acid) has been synthesized via a one‐step solvothermal method. Single X‐ray diffraction analysis shows that the SEU‐1 exhibits a (3,3,4)‐connected 2D structure with a Schläfli symbol of (62·8)(63)(64·8·10). Variable‐temperature magnetic susceptibility data display that antiferromagnetic interactions between two CoII ions exist in SEU‐1. The supercapacitive performance has been evaluated in the three‐electrode system. Its maximum specific capacitance is 145.5 F g−1 at 1 A g−1, along with the specific capacitance retention of 92.7% at the current density of 5 A g−1 after 6000 cycles in 3 M KOH solution. These results demonstrate that SEU‐1 is a good candidate for electrode material for electrochemical energy storage.

Integrated free-standing WS2 3D-printed carbon supercapacitor with solid state electrolyte

ABSTRACT There is a huge need for energy storage devices due to the depletion of natural gas and the increasing requirement for portable electronic gadgets. Fused deposition modeling (FDM) 3D-printing has drawn tremendous interest for the fabrication of batteries and supercapacitors (SCs) due to its tabletop manufacturing technique, bespoke design, fast prototyping and user-friendly process. However, there are fewer available conductive filaments for FDM printing that are ideal from an energy storage standpoint. 2D transition metal dichalcogenide WS2 has been discovered to be a favourable material for electrochemical energy storage. As a result, in this work, we modified a carbon electrode that was 3D-printed by incorporating WS2 in order to enhance the capacitive performance of the SC electrode. The WS2-coated 3D-printed carbon electrode (WS2/3D-PCE) exhibits 2.8 times higher specific capacitance than the 3D-printed carbon electrode at 50 mV s−1. A solid-state symmetric supercapacitor (SS-SC) was fabricated with WS2/3D-PCE and polyvinyl alcohol (PVA)/Li2SO4 as gel electrolytes. Such modified 3D-PCE opens up the opportunities to design any custom-shaped electrode with tailored properties and pave a route for future research that will lead to more electrochemical devices for portable electronics.

In‐suit synthesis of FeP/C/CNT composites with excellent performance in supercapacitors and lithium‐ion batteries

AbstractIron phosphide (FeP) is a promising electrochemical energy storage material due to easy to obtain and high theoretical capacity. However, the intrinsic poor conductivity and the large volume change during charging and discharging process, result in a sharp decline in capacity and short cycle life for FeP. In this work, the FeP/C/CNT nanocomposite was synthesized efficiently and conveniently by one‐step solid‐phase synthesis method. Amorphous carbon‐coated FeP particles are embedded in a three‐dimensional network structure composed of highly conductive carbon nanotubes, drastically enhancing the conductivity of FeP and reducing the volume expansion during charging and discharging. In the three‐electrode system, the FeP/C/CNT composites showed good electrochemical performance, with a specific capacity as high as 124.4 mAh g−1 at 1 A g−1. Meanwhile, the constructed Ni2P@C/CNT//FeP/C/CNT asymmetric supercapacitor delivered a high energy density (70.73 Wh kg−1), power density (7.9 kW kg−1) and a long cycle life (10000 cycles). In addition, as served as an anode material in the lithium ion battery, the FeP/C/CNT composite also displayed as high as 601.8 mAh g−1of specific capacity at 0.1 A g−1 and a good cycle stability, showing superior electrochemical performance. The above work provides a promising composite material for supercapacitors and lithium ion batteries. Moreover, the solid‐state preparation methods can provide a reference for the synthesis of transition metal phosphides.

Supercapacitor Electrodes: Is Nickel Foam the Right Substrate for Active Materials?

Ni foam is an extensively used current collector and substrate in investigations of electrochemically active materials such as supercapacitors and electrocatalysts for oxygen and hydrogen evolution reactions. This material is relatively cheap, porous, and conductive and has a large specific surface area, all of which make it a good substrate. We investigated Ni-Mg ferrites and NiMn2O4 as active materials for electrochemical energy storage. These materials, when loaded on Ni foam, gave promising capacitance values: 172 F/g (at 2 mV/s) for NiMn2O4 in 6 M KOH and 242 F/g (at 2 mV/s) for MgFe2O4 in 3 M KOH. Nevertheless, during the authors' work, many experimental problems occurred. Inconsistencies in the results directed further investigation towards measuring the capacitance of the active materials using GCE and platinum electrodes as substrates to discover if Ni foam was the culprit of the inconsistencies. When non-nickel substrates were used, both NiMn2O4 and MgFe2O4 showed reduced capacitance. Experimental problems associated with the utilization of Ni foam as a substrate for active materials in supercapacitor electrodes are discussed here, combined with other problems already addressed in the scientific literature.

Hydrothermally decorating MnO2 onto NiCo layered double hydroxide nanosheets for electrochemical energy storage

In research out of the sustainable electrochemical energy storage material, NiCo-LDH/MnO2 composite has been prepared via simple hydrothermal method. The experimental characterizations of XRD, SEM/TEM and XPS have been utilized to explore the structure and morphology of prepared composite. The needle-like MnO2 was found adhered to NiCo-LDH sheet. The composite's electrochemical properties were evaluated through cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy. It has been realized that the MnO2 dosage not only changes the composite's microstructure but also affects its electrochemical properties. The best specific capacitance (2602 F g−1 at a current density of 1 A g−1) was achieved for the composite sample with 38% MnO2 (mass), which is almost two times high from the same composite in previous reports. With the sample, the assembled asymmetric supercapacitor exhibits a remarkable energy density of 19.56 Wh.Kg−1 at 800.29 W Kg−1. It could be attributed to the synergetic effects of two components as well as their good interfacial coupling. The good electrochemical activity makes our synthesized composite feasible to be applied as electrode material and provides valuable insights for the development of smart capacitors utilizing NiCo-LDH.

Protonated C3N4 Nanosheets for Enhanced Energy Storage in Symmetric Supercapacitors through Hydrochloric Acid Treatment.

Next-generation electrochemical energy storage materials are essential in delivering high power for long periods of time. Double-layer carbonaceous materials provide high power density with low energy density due to surface-controlled adsorption. This limitation can be overcome by developing a low-cost, more abundant material that delivers high energy and power density. Herein, we develop layered C3N4 as a sustainable charge storage material for supercapacitor applications. It was thermally polymerized using urea and then protonated with various acids to enhance its charge storage contribution by activating more reaction sites through the exfoliation of the C-N framework. The increased electron-rich nitrogen moieties in the C-N framework material lead to better electrolytic ion impregnation into the electrode, resulting in a 7-fold increase in charge storage compared to the pristine material and other acids. It was found that C3N4 treated with hydrochloric acid showed a very high capacitance of 761 F g-1 at a current density of 20 A g-1 and maintained 100% cyclic retention over 10,000 cycles in a three-electrode configuration, outperforming both the pristine material and other acids. A symmetric device was fabricated using a KOH/LiI gel-based electrolyte, exhibiting a maximum specific capacitance of 175 F g-1 at a current density of 1 A g-1. Additionally, the device showed remarkable power and energy density, reaching 600 W kg-1 and 35 Wh kg-1, with an exceptional cyclic stability of 60% even after 5000 cycles. This study provides an archetype to understand the underlying mechanism of acid protonation and paves the way to a metal-carbon-free environment.

The Synthesis of Three-Dimensional Hexagonal Boron Nitride as the Reinforcing Phase of Polymer-Based Electrolyte for All-Solid-State Li Metal Batteries.

Powdery hexagonal boron nitride (h-BN), as an important material for electrochemical energy storage, has been typically synthesized in bulk and one/two-dimensional (1/2D) nanostructured morphologies. However, until now, no method has been developed to synthesize powdery three-dimensional (3D) h-BN. This work introduces a novel NaCl-glucose-assisted strategy to synthesize micron-sized 3D h-BN with a honeycomb-like structure and its proposed formation mechanism. We propose that NaCl acts as the template of 3D structure and promotes the nitridation reaction by adsorbing NH3 . Glucose facilitates the homogeneous coating of boric acid onto the NaCl surface via functionalizing the NaCl surface. During the nitridation reaction, boron oxides (BO4 and BO3 ) form from a dehydration reaction of boric acid, which is then reduced to O2 -B-N and O-B-N2 intermediates before finally being reduced to BN3 by NH3 . When incorporated into polyethylene oxide-based electrolytes for Li metal batteries, 5 wt % of 3D h-BN significantly enhances ionic conductivity and mechanical strength. Consequently, this composite electrolyte demonstrates superior electrochemical stability. It delivers 300 h of stable cycles in the Li//Li cell at 0.1 mA cm-2 and retains 89 % of discharge capacity (138.9 mAh g-1 ) after 100 cycles at 1 C in the LFP//Li full cell.

Conductive MOFs: Synthesis and Applications in Supercapacitors and Batteries

AbstractConductive metal‐organic frameworks (c‐MOFs) have uniform, adjustable pore sizes and customizable functional groups and excellent electrical conductivity, making them promising electrode materials for electrochemical energy storage. However, the synthesis of high crystallinity c‐MOFs remains a significant challenge. The purpose of this review is to provide guidance for the synthesis of high crystallinity c‐MOFs and emphasize their applications in the field of energy storage. We begin with reviewing the influence of various reaction conditions on the morphology, size, and crystallinity of c‐MOFs, and then summarize the current work on c‐MOFs in the field of electrochemical energy storage from both experiment and modeling. Furthermore, the existing issues are discussed in the development of c‐MOFs and the primary directions for future research.

Biomass-Derived Carbon Materials for Electrochemical Energy Storage.

The environmental impact from the waste disposal has been widely concerned around the world. The conversion of wastes to useful resources is important for the sustainable society. As a typical family of wastes, biomass materials basically composed of collagen, protein and lignin are considered as useful resources for recycle and reuse. In recent years, the development of carbon material derived from biomasses, such as plants, crops, animals and their application in electrochemical energy storage have attracted extensive attention. Through the selection of the appropriate biomass, the optimization of the activation method and the control of the pyrolysis temperatures, carbon materials with desired features, such as high-specific surface area, variable porous framework, and controllable heteroatom-doping have been fabricated. Herein, this review summarized the preparation methods, morphologies, heteroatoms doping in the plant/animal-derived carbonaceous materials, and their application as electrode materials for secondary batteries and supercapacitors, and as electrode support for lithium-sulfur batteries. The challenges and prospects for the controllable synthesis and large-scale application of biomass-derived carbonaceous materials have also been outlooked.