RESUMEN
O3-type layered oxides have been extensively studied as cathode materials for sodium-ion batteries due to their high reversible capacity and high initial sodium content, but they suffer from complex phase transitions and an unstable structure during sodium intercalation/deintercalation. Herein, we synthesize a high-entropy O3-type layered transition metal oxide, NaNi0.3Cu0.05Fe0.1Mn0.3Mg0.05Ti0.2O2 (NCFMMT), by simultaneously doping Cu, Mg, and Ti into its transition metal layers, which greatly increase structural entropy, thereby reducing formation energy and enhancing structural stability. The high-entropy NCFMMT cathode exhibits significantly improved cycling stability (capacity retention of 81.4% at 1C after 250 cycles and 86.8% at 5C after 500 cycles) compared to pristine NaNi0.3Fe0.4Mn0.3O2 (71% after 100 cycles at 1C), as well as remarkable air stability. Finally, the NCFMMT//hard carbon full-cell batteries deliver a high initial capacity of 103 mAh g-1 at 1C, with 83.8 mAh g-1 maintained after 300 cycles (capacity retention of 81.4%).
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The discovery of the heterostructures that is combining two materials with different properties has brought new opportunities for the development of lithium sulfur batteries (LSBs). Here, C3 N4 -CoSe2 composite is elaborately designed and used as a functional coating on the LSBs separator. The abundant chemisorption sites of C3 N4 -CoSe2 form chemical bonding with polysulfides, provides suitable adsorption energy for lithium polysulfides (LiPSs). More importantly, the spontaneously formed internal electric field accelerates the charge flow in the C3 N4 -CoSe2 interface, thus facilitating the transport of LiPSs and electrons and promoting the bidirectional conversion of sulfur. Meanwhile, the lithiophilic C3 N4 -CoSe2 sample with catalytic activity can effectively regulate the uniform distribution of lithium when Li+ penetrates the separator, avoiding the formation of lithium dendrites in the lithium (Li) metal anode. Therefore, LSBs based on C3 N4 -CoSe2 functionalized membranes exhibit a stable long cycle life at 1C (with capacity decay of 0.0819% per cycle) and a large areal capacity of 10.30 mAh cm-2 at 0.1C (sulfur load: 8.26 mg cm-2 , lean electrolyte 5.4 µL mgs -1 ). Even under high-temperature conditions of 60 °C, a capacity retention rate of 81.8% after 100 cycles at 1 C current density is maintained.
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ZnS has acquired increasing attention for high-performance PIBs anode because of its remarkable theoretical capacity, and redox reversibility for conversion reaction. However, the larger volume variation and delayed reaction kinetics for the ZnS in the discharge/charge processes lead to pulverization and severe capacity degradation. Herein, the trumpet-like ZnS@C composite was synthesized by template method by using sodium citrate as carbon source followed by vulcanization process. As potassium ion batteries (PIB) anode, ZnS@C composite exhibits good rate performance and long life (stable reversible capacity of 107.8â mAh/g over 2000â charge-discharge cycles at 5â A/g and high reversible capacity of 310â mAh/g at 0.1â A/g). The outstanding electrochemical performance of the ZnS@C composite is ascribed to its unique structure, which can mitigate the volume expansion of ZnS in the charge discharge process, expand the contact area between the electrode and electrolyte, and improve the conductivity of electrode materials by the introduction of carbon layer. This method of synthesizing trumpet-like ZnS@C composite provides an important strategy for obtaining potassium ion batteries anode with long cycle.
Asunto(s)
Carbono , Potasio , Conductividad Eléctrica , ElectrodosRESUMEN
Lithium-sulfur (Li-S) batteries have been considered as one of the most promising electrochemical energy storage systems because of their high energy density. However, a series of issues severely limit the practical performances of Li-S batteries such as low conductivity, significant volume change, and shuttle effect. The hollow carbon spheres with huge voids and high electrical conductivity are promising as sulfur hosts. Unfortunately, the nonpolar nature of carbon materials cannot prevent the shuttle effect effectively. In this case, the atomic cobalt is introduced to a nitrogen-doped hollow carbon sphere (ACo@HCS) through polymerization and controlled pyrolysis. The atomic cobalt dopants not only act as active sites to restrict the shuttle effect, but also can promote the kinetics of the sulfur redox reactions. ACo@HCS acting as sulfur host exhibits a high discharge capacity (1003 mAh g-1 ) at a 1.0 C rate after 500 cycles, and the corresponding decay rate is as low as 0.002% per cycle. This exciting work paves a new way to design high-performance Li-S batteries.
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Nb2 O5 possesses superior fast Li+ storage capability for LIB anodes, benefiting from its fast pseudocapacitive behavior and low volumetric change within the cycling processes. However, the poor electric conductivity for Nb2 O5 restricts its reaction kinetics and rate property. Herein, Nb2 O5 /carbon (C) submicrostructures are fabricated by solvothermal method followed by calcination process. The Nb2 O5 /C submicrostructures exhibit outstanding rate behavior and cyclic performance (332â (194)â mAh g-1 after 1000â cycles at 1â (5)â A g-1 ). The superior electrochemical property is attributed to the distinctive structure for Nb2 O5 /C submicrostructures, in which Nb2 O5 nanoparticles uniformly distributed within Nb2 O5 /C composite can protect Nb2 O5 nanoparticles from agglomeration, and the porous carbon matrix can enhance electron/ion conductivity. This work furnishes a novel strategy for fabricating Nb2 O5 /C submicrostructures with superior Li+ storage performance, which can be potentially used to design other metal oxide/C submicrostructures for second battery anode.
RESUMEN
For the past few years, a new generation of energy storage systems with large theoretical specific capacity has been urgently needed because of the rapid development of society. Lithium-sulfur (Li-S) batteries are regarded as one of the most promising candidates for novel battery systems, since their resurgence at the end of the 20th century Li-S batteries have attracted ever more attention, attributed to their notably high theoretical energy density of 2600â W h kg-1 , which is almost five times larger than that of commercial lithium-ion batteries (LIBs). One of the determining factors in Li-S batteries is how to design/prepare the sulfur cathode. For the sulfur host, the major technical challenge is avoiding the shuttling effect that is caused by soluble polysulfides during the reaction. In past decades, though the sulfur cathode has developed greatly, there are still some enormous challenges to be conquered, such as low utilization of S, rapid decay of capacity, and poor cycle life. This article spotlights the recent progress and foremost findings in improving the performance of Li-S batteries by employing multifunctional metal phosphides as host materials. The current state of development of the sulfur electrode of Li-S batteries is summarized by emphasizing the relationship between the essential properties of metal phosphide-based hybrid nanomaterials, the chemical reaction with lithium polysulfides and the latter's influence on electrochemical performance. Finally, trends in the development and practical application of Li-S batteries are also pointed out.
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ZnSe has got extensive attention for high-performance LIBs anode due to its remarkable theoretical capacity and environmental friendliness. Nevertheless, the large volume variation for the ZnSe in the discharge/charge processes brings about rapid capacity fading and poor rate performance. Herein, ZnSe/C hollow polyhedrons are successfully synthesized by selenization of zeolitic imidazolate framework-8 (ZIF-8) with resorcinol-formaldehyde (RF) coating. The protection of C layer derived from RF coating layer and Ostwald ripening during the process of selenization play important roles in promoting formation of ZnSe/C hollow polyhedrons. The ZnSe/C hollow polyhedrons exhibit good rate performance and long-term cycle stability (345â mAh g-1 up to 1000 cycles at 1â A g-1 ) for lithium ion batteries (LIBs) anode. The improved electrochemical performance is benefit from the unique ZnSe/C hollow structure, in which the hollow structure can effectively avoid terrible volume expansion, and the thin ZnSe/C shell can not only provide adequate diffusion paths of lithium ions and but also enhance the electronic conductivity.
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Porous C nanosheet/Cu2S composites were prepared using a simple self-template method and vulcanization process. The Cu2S nanoparticles with an average diameter of 140 nm are uniformly distributed on porous carbon nanosheets. When used as the anode of a potassium-ion battery, porous C nanosheet/Cu2S composites exhibit good rate performance and cycle performance (363 mAh g-1 at 0.1 A g-1 after 100 cycles; 120 mAh g-1 at 5 A g-1 after 1000 cycles). The excellent electrochemical performance of porous C nanosheet/Cu2S composites can be ascribed to their unique structure, which can restrain the volume change of Cu2S during the charge/discharge processes, increase the contact area between the electrode and the electrolyte, and improve the electron/ionic conductivity of the electrode material.
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CeO2, an n-type semiconductor material, has been widely used in microwave absorption (MA) due to its unique structural features such as oxygen vacancies and interstitial atoms. In this paper, Co/CeO2/C composites were prepared by a hydrothermal method followed by a pyrolysis process. The effect of different pyrolysis temperatures (650-950 °C) on the MA property of the composites was investigated. When the pyrolysis temperature was 850 °C, the Co/CeO2/C-850 composite exhibited outstanding MA behavior in the frequency range of 2-18 GHz, displaying a minimum reflection loss (RLmin) of -45.22 dB and an effective absorption bandwidth (EAB) of 4.61 GHz at a thin thickness of 1.75 mm. The MA performance of the Co/CeO2/C composites is mainly attributed to the dielectric loss due to interfacial polarization originating from different interfaces and dipole polarization caused by the oxygen vacancies in CeO2. In addition, the introduction of Co nanoparticles not only provides the magnetic loss but also modulates impendence matching for the current magnetoelectric coupling system.
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The Fe7Se8@Carbon (C) nanotubes are successfully synthesized using Fe3O4@C nanotubes as sacrificial templates. Fe7Se8@C nanotubes exhibit excellent rate behaviour and maintainable capacity (319 mAh g-1 at 2 A g-1 upon 720 cycles), when utilized as SIBs anode. Moreover, for PIBs anode, Fe7Se8@C nanotubes also exhibit outstanding rate behaviour and maintainable capacity 222 mAh g-1 at 2 A g-1 upon 500 cycles). The superior electrochemical performance of Fe7Se8@C nanotubes is ascribed to the unique structure, where the hierarchical hollow tubular characteristic of Fe7Se8@C composites can mitigate the volume expansion of Fe7Se8 and supply effective transmission paths for both Na+(K+) and electrons within repeated cycle processes, and additionally, N-doped carbon layer can further protect the integrality of Fe7Se8@C nanotubes from destruction within the cycle processes, and enhance electronic conductivity.
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The distinctive pomegranate-like Nb2O5/Carbon@N-doped carbon (Nb2O5/C@NC) composites are fabricated using hydrothermal method integrated with nitrogen doped carbon coating procedure. For the SIBs anode, the Nb2O5/C@NC composites present superior rate character and sustainable capacity (117 mAh g-1 upon 1000 cycles at 5 A g-1). The in-situ X-ray diffraction (XRD) is utilized to research its sodium storage mechanism. Furthermore, for PIBs, the Nb2O5/C@NC composites present sustainable capacity (81 mAh g-1 upon 1000 cycles at 1 A g-1). The outstanding performance of Nb2O5/C@NC composites is ascribed to its unique architecture, in which Nb2O5 nanocrystals embedded in porous carbon can restrain agglomeration of Nb2O5 nanocrystals, enhance electron/ion diffusion kinetics, and ensure electrolyte accessibility, and moreover, NC shell layer can provide effective active sites and further increase ions/electrons transfer.
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Potassium-ion batteries (KIBs) have attracted researchers' widespread attention because of the luxuriant reserves of potassium salts and their low cost. Nevertheless, the absence of suitable electrode materials with a stable electrochemical property is a crucial issue, which seriously hampers the practical applications of KIBs. Herein, a scalable anode material consisting of ultrafine ZnS nanoparticles encapsulated in three-dimensional (3D) carbon nanosheets is explored for KIBs. This hierarchical anode is obtained via a simple and universal sol-gel method combined with a typical solid-phase sulfidation route. The special structure of this anode facilitates good contact with electrolytes and has enough voids to buffer the large volumetric stress changing during K+ insertion/extraction. Thus, the 3D ZnS@C electrode exhibitsour stable cycling performance (230 mAh g-1 over 2300 cycles at 1.0 A g-1) and superior rate capability. The kinetic analysis indicates that a ZnS@C anode with considerable pesoudecapactive contribution benefits a fast potassium/depotassium process. Detailed ex-situ and in-situ measurements reveal that this ZnS@C anode combines reversible conversion and alloying-type reactions. This rationally designed ZnS@C material is highly applicable for KIBs, and the current route opens an avenue for the development of highly stable K+ storage materials.
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Vertically aligned CrO(2) nanorods with an areal density as high as 1.2 x 10(10) cm(-2) were obtained via atmospheric pressure CVD assisted by AAO templates for the first time.