Co3ZnC@NC Material Derived from ZIF-8 for Lithium-Ion Capacitors
Ontology highlight
ABSTRACT:
SUBMITTER: Tang Y
PROVIDER: S-EPMC8567260 | biostudies-literature |
REPOSITORIES: biostudies-literature
Similar Datasets
Project description:As a typical metal selenide, CoSe is a kind of foreground anode material for lithium-ion batteries (LIBs) because of its two-dimensional layer structure, good electrical conductivity, and high theoretical capacity. In this work, the original CoSe/N-doped carbon (CoSe/NC) composites were synthesized using ZIF-67 as a precursor, in which the CoSe nanoparticles are encapsulated in NC nanolayers and they are connected through C-Se bonds. The coating structure and strong chemical coupling make the NC nanolayers could better effectively enhance the lithium storage properties of CoSe/NC composites. As a consequence, the CoSe/NC composites deliver a reversible capacity of 310.11 mAh g-1 after 500 cycles at 1.0 A g-1. Besides, the CoSe/NC composites show a distinct incremental behavior of capacity.
| S-EPMC6889125 | biostudies-literature
Project description:Energy consumption is a growing phenomenon in our society causing many negative effects such as global warming. There is a need for the development of new sustainable materials for energy storage. Carbons are materials derivable from biowaste that can rather easily store energy due to their high conductivity and surface area. However, their large-scale processing is challenging as derived materials can be rather heterogeneous and homogenization requires ball milling, a process that can damage carbons in the process of oxidation. Herein, we have prepared caffeine-derived noble nitrogen-doped carbon that withstands the ball milling process without significant oxidation. Additionally, it performs extraordinarily as a cathode material for lithium-ion capacitors, making it an attractive biowaste-derived alternative to commercial heavy metal cathodes.
| S-EPMC8251692 | biostudies-literature
Project description:Transition-metal oxides are attracting considerable attention as anodes for lithium-ion batteries because of their high reversible capacities. However, the drastic volume change and inferior electrical conductivity greatly retard their widespread applications in lithium-ion batteries. Herein, three-dimensional nanoporous composites of CoO x (CoO and Co3O4) quantum dots and zeolitic imidazolate framework-67-derived carbon are fabricated by a precipitation method. The carbon prepared by carbonization of zeolitic imidazolate framework-67 can greatly enhance the electrical conductivity of the composite anodes. CoO x quantum dots anchored firmly on zeolitic imidazolate framework-67-derived carbon can effectively inhibit the aggregation and volume change of CoO x quantum dots during lithiation/delithiation processes. The nanoporous structure can shorten the ion diffusion paths and maintain the structural integrity upon cycling. Meanwhile, kinetics analysis reveals that a capacitance mechanism dominates the lithium storage capacity, which can greatly enhance the electrochemical performance. The composite anodes show a high discharge capacity of 1873 mAh g-1 after 200 cycles at 200 mA g-1, ultralong cycle life (1246 mAh g-1 after 900 cycles at 1000 mA g-1), and improved rate performance. This work may provide guidelines for preparing cobalt oxide-based anodes for LIBs.
| S-EPMC7469398 | biostudies-literature
Project description:Ni-rich cathode LiNixCoyMn1-x-yO2 (NCM, x ≥ 0.5) materials are promising cathodes for lithium-ion batteries due to their high energy density and low cost. However, several issues, such as their complex preparation and electrochemical instability have hindered their commercial application. Herein, a simple solvothermal method combined with calcination was employed to synthesize LiNi0.6Co0.2Mn0.2O2 with micron-sized monodisperse particles, and the influence of the sintering temperature on the structures, morphologies, and electrochemical properties was investigated. The material sintered at 800 °C formed micron-sized particles with monodisperse characteristics, and a well-order layered structure. When charged-discharged in the voltage range of 2.8-4.3 V, it delivered an initial discharge capacity of 175.5 mAh g-1 with a Coulombic efficiency of 80.3% at 0.1 C, and a superior discharge capacity of 135.4 mAh g-1 with a capacity retention of 84.4% after 100 cycles at 1 C. The reliable electrochemical performance is probably attributable to the micron-sized monodisperse particles, which ensured stable crystal structure and fewer side reactions. This work is expected to provide a facile approach to preparing monodisperse particles of different scales, and improve the performance of Ni-rich NCM or other cathode materials for lithium-ion batteries.
| S-EPMC8155954 | biostudies-literature
Project description:Lithium-ion capacitors (LICs) have been proposed as an emerging technological innovation that integrates the advantages of lithium-ion batteries and supercapacitors. However, the high-power output of LICs still suffers from intractable challenges due to the sluggish reaction kinetics of battery-type anodes. Herein, polypyrrole-coated nitrogen and phosphorus co-doped hollow carbon nanospheres (NPHCS@PPy) were synthesized by a facile method and employed as anode materials for LICs. The unique hybrid architecture composed of porous hollow carbon nanospheres and PPy coating layer can expedite the mass/charge transport and enhance the structural stability during repetitive lithiation/delithiation process. The N and P dual doping plays a significant role on expanding the carbon layer spacing, enhancing electrode wettability, and increasing active sites for pseudocapacitive reactions. Benefiting from these merits, the NPHCS@PPy composite exhibits excellent lithium-storage performances including high rate capability and good cycling stability. Furthermore, a novel LIC device based on the NPHCS@PPy anode and the nitrogen-doped porous carbon cathode delivers a high energy density of 149 Wh kg-1 and a high power density of 22,500 W kg-1 as well as decent cycling stability with a capacity retention rate of 92% after 7,500 cycles. This work offers an applicable and alternative way for the development of high-performance LICs.
| S-EPMC8497749 | biostudies-literature
Project description:The non-aqueous asymmetric lithium ion hybrid capacitor (LIHC) is a tactical energy storage device composed of a faradic and non-faradic electrode pair, which aims to achieve both high energy and great power densities. On the other hand, the different types of electrode combinations cause severe imbalances in energy and power capabilities, leading to poor electrochemical performance. Herein, waste pinecone-derived hierarchically porous pyropolymers (WP-HPPs) were fabricated as a surface-driven pseudocapacitive electrode, which has the advantages of both faradic and non-faradic electrodes. The unique materials properties of WP-HPPs possessing high effective surface areas and hierarchically open nanopores led to high specific capacities of ~412 mA h g-1 and considerable rate/cycling performance as a cathode for LIHCs. In particular, nanometer-scale pores, approximately 3 nm in size, plays a key role in the pseudocapacitive charge storage behaviors because open nanopores can transport solvated Li-ions easily into the inside of complex carbon structures and a large specific surface area can be provided by the effective active surface for charge storage. In addition, WP-HPP-based asymmetric LIHCs assembled with a pseudocapacitive counterpart demonstrated feasible electrochemical performance, such as maximum specific energy and specific power of ~340 Wh kg-1 and ~11,000 W kg-1, respectively, with significant cycling stability.
| S-EPMC7118167 | biostudies-literature
Project description:In this manuscript, a dramatic increase in the energy density of ~ 69?Wh kg?¹ and an extraordinary cycleability ~ 2000 cycles of the Li-ion hybrid electrochemical capacitors (Li-HEC) is achieved by employing tailored activated carbon (AC) of ~ 60% mesoporosity derived from coconut shells (CS). The AC is obtained by both physical and chemical hydrothermal carbonization activation process, and compared to the commercial AC powders (CAC) in terms of the supercapacitance performance in single electrode configuration vs. Li. The Li-HEC is fabricated with commercially available Li?Ti?O?? anode and the coconut shell derived AC as cathode in non-aqueous medium. The present research provides a new routine for the development of high energy density Li-HEC that employs a mesoporous carbonaceous electrode derived from bio-mass precursors.
| S-EPMC3801125 | biostudies-literature
Project description:Transition-metal oxides (TMOs) are potential candidates for anode materials of lithium-ion batteries (LIBs) due to their high theoretical capacity (?1000 mA h/g) and enhanced safety from suppressing the formation of lithium dendrites. However, the poor electron conductivity and the large volume expansion during lithiation/delithiation processes are still the main hurdles for the practical usage of TMOs as anode materials. In this work, the CoSnO3@NC@MnO@NC hierarchical nanobox (CNMN) is then proposed and fabricated to solve those issues. The as-prepared nanobox contains hollow cubic CoSnO3 as a core and dual N-doped carbon-"sandwiched" MnO particles as a shell. As anode materials of LIBs, the hollow and carbon interlayer structures effectively accommodate the volume expansion while dual active TMOs of CoSnO3 and MnO efficiently increase the specific capacity. Notably, the dual-layer structure of N-doped carbons plays a critical functional role in the incorporated composites, where the inner layer serves as a reaction substrate and a spatial barrier and the outer layer offers electron conductivity, enabling more effective involvement of active anode materials in lithium storage, as well as maintaining their high activity during lithium cycling. Subsequently, the as-prepared CNMN exhibits a high specific capacity of 1195 mA h/g after the 200th cycle at 0.1C and an excellent stable reversible capacity of about 876 mA h/g after the 300th cycle at 0.5C with only 0.07 mA h/g fade per cycle after 300 cycles. Even after a 250 times fast charging/discharging cycle both at 5C, it still retains a reversible capacity of 422.6 mA h/g. We ascribe the enhanced lithium storage performances to the novel hierarchical architectures achieved from the rational design.
| S-EPMC7304665 | biostudies-literature
Project description:The requirement of energy-storage equipment needs to develop the lithium ion battery (LIB) with high electrochemical performance. The surface modification of commercial LiFePO4 (LFP) by utilizing zeolitic imidazolate frameworks-8 (ZIF-8) offers new possibilities for commercial LFP with high electrochemical performances. In this work, the carbonized ZIF-8 (CZIF-8) was coated on the surface of LFP particles by the in situ growth and carbonization of ZIF-8. Transmission electron microscopy indicates that there is an approximate 10 nm coating layer with metal zinc and graphite-like carbon on the surface of LFP/CZIF-8 sample. The N2 adsorption and desorption isotherm suggests that the coating layer has uniform and simple connecting mesopores. As cathode material, LFP/CZIF-8 cathode-active material delivers a discharge specific capacity of 159.3 mAh g-1 at 0.1C and a discharge specific energy of 141.7 mWh g-1 after 200 cycles at 5.0C (the retention rate is approximate 99%). These results are attributed to the synergy improvement of the conductivity, the lithium ion diffusion coefficient, and the degree of freedom for volume change of LFP/CZIF-8 cathode. This work will contribute to the improvement of the cathode materials of commercial LIB.
| S-EPMC6199046 | biostudies-literature
Project description:Lithium-ion hybrid capacitors (LICs) are regarded as one of the most promising next generation energy storage devices. Commercial activated carbon materials with low cost and excellent cycling stability are widely used as cathode materials for LICs, however, their low energy density remains a significant challenge for the practical applications of LICs. Herein, Na0.76V6O15 nanobelts (NaVO) were prepared and combined with commercial activated carbon YP50D to form hybrid cathode materials. Credit to the synergism of its capacitive effect and diffusion-controlled faradaic effect, NaVO/C hybrid cathode displays both superior cyclability and enhanced capacity. LICs were assembled with the as-prepared NaVO/C hybrid cathode and artificial graphite anode which was pre-lithiated. Furthermore, 10-NaVO/C//AG LIC delivers a high energy density of 118.9 Wh kg-1 at a power density of 220.6 W kg-1 and retains 43.7 Wh kg-1 even at a high power density of 21,793.0 W kg-1. The LIC can also maintain long-term cycling stability with capacitance retention of approximately 70% after 5000 cycles at 1 A g-1. Accordingly, hybrid cathodes composed of commercial activated carbon and a small amount of high energy battery-type materials are expected to be a candidate for low-cost advanced LICs with both high energy density and power density.
| S-EPMC7794966 | biostudies-literature