Abstract:Although the successful deployment of lithium-ion batteries (LIBs) in various fields such as consumer electronics, electric vehicles and electric grid, the efforts are still ongoing to pursue the next-generation battery systems with higher energy densities. Interest has been increasing in the batteries relying on the multivalent-ions such as Mg 2+ , Zn 2+ , and Al 3+ , because of the higher volumetric energy densities than those of monovalent-ion batteries including LIBs and Na-ion batteries. Among them, magne… Show more
“…Diverse lithium‐based rechargeable batteries such as lithium ion, 6,7 lithium air, 8,9 and lithium sulfur 10‐12 have been extensively studied to meet this need. However, due to the concerns associated with cost and depletion of global lithium sources as a result of its high demand, other battery alternatives such as sodium ion, 13,14 potassium ion, 15,16 magnesium ion, 17‐19 and aluminum ion 20,21 have been intensively studied amongst others. All these alternatives are geared toward overcoming some of the challenges associated with lithium‐based batteries.…”
Summary
We studied Na0.8Ni0.33Co0.33Mn0.33O2 nanoparticles synthesized using water‐based extract procured from the dried silk of maize (Zea mays lea) plant. The synthesized Na0.8Ni0.33Co0.33Mn0.33O2 was used as the positive electrode in an aqueous sodium ion battery (SIB). X‐ray diffraction (XRD) studies of the biosynthesized material reveal that it can be indexed to the trigonal structure of Na0.8Ni 0.33Co0.33Mn0.33O2 with an R 3m space group (160), (ICSD 184736) although impurities of Mn2O3 and NiO were detected. Surface morphological studies from a scanning electron microscope (SEM) disclose that the nanoparticles consist of an interspersion of sheath‐like particles with quasi‐spherical nanoparticles of uneven dimensions. The sheath‐like particles seem to agglomerate to form layers that coalesce into flower‐like structures that are spread within the quasi‐spherical nanoparticles. The material yielded a rechargeable discharge capacity of about 86 mA h g−1 in a three‐electrode system consisting of platinum, the Na0.8Ni0.33Co0.33Mn0.33O2 and Ag/AgCl as the counter, working and reference electrodes respectively at a current density of 10 mA g−1. However, a full cell using P25 Degussa TiO2 and the biosynthesized Na0.8Ni0.33Co0.33Mn0.33O2 as the negative and the positive electrode, respectively, and having a mass ratio of 1:1 yielded a discharge capacity of 49 mA h g−1 at a current density of 5 mA g−1. Impedance studies for a symmetrical cell developed showed that the magnitude of the impedance is highest at 0% and 100 state of charge (SOC).
“…Diverse lithium‐based rechargeable batteries such as lithium ion, 6,7 lithium air, 8,9 and lithium sulfur 10‐12 have been extensively studied to meet this need. However, due to the concerns associated with cost and depletion of global lithium sources as a result of its high demand, other battery alternatives such as sodium ion, 13,14 potassium ion, 15,16 magnesium ion, 17‐19 and aluminum ion 20,21 have been intensively studied amongst others. All these alternatives are geared toward overcoming some of the challenges associated with lithium‐based batteries.…”
Summary
We studied Na0.8Ni0.33Co0.33Mn0.33O2 nanoparticles synthesized using water‐based extract procured from the dried silk of maize (Zea mays lea) plant. The synthesized Na0.8Ni0.33Co0.33Mn0.33O2 was used as the positive electrode in an aqueous sodium ion battery (SIB). X‐ray diffraction (XRD) studies of the biosynthesized material reveal that it can be indexed to the trigonal structure of Na0.8Ni 0.33Co0.33Mn0.33O2 with an R 3m space group (160), (ICSD 184736) although impurities of Mn2O3 and NiO were detected. Surface morphological studies from a scanning electron microscope (SEM) disclose that the nanoparticles consist of an interspersion of sheath‐like particles with quasi‐spherical nanoparticles of uneven dimensions. The sheath‐like particles seem to agglomerate to form layers that coalesce into flower‐like structures that are spread within the quasi‐spherical nanoparticles. The material yielded a rechargeable discharge capacity of about 86 mA h g−1 in a three‐electrode system consisting of platinum, the Na0.8Ni0.33Co0.33Mn0.33O2 and Ag/AgCl as the counter, working and reference electrodes respectively at a current density of 10 mA g−1. However, a full cell using P25 Degussa TiO2 and the biosynthesized Na0.8Ni0.33Co0.33Mn0.33O2 as the negative and the positive electrode, respectively, and having a mass ratio of 1:1 yielded a discharge capacity of 49 mA h g−1 at a current density of 5 mA g−1. Impedance studies for a symmetrical cell developed showed that the magnitude of the impedance is highest at 0% and 100 state of charge (SOC).
“…Multivalent-ion batteries such as Mg 2+ , Ca 2+ and Al 3+ are reported to deliver higher volumetric energy densities compared with monovalent-ion batteries, including Li-ion and Na-ion batteries. Among these promising multivalent ion batteries, Mg-ion batteries represent a significant advance in battery technology due to their highest theoretical volumetric energy density (3866 mAh cm −3 ), which is higher than that achievable by a Li anode (2066 mAh cm −3 ) [ 2 , 3 , 4 ]. However, several challenges have limited the progress of Mg-ion battery technology maturation [ 3 , 4 , 5 , 6 ], including Mg-ion insulating passivation layer on the anode surface [ 7 ], the solid electrolyte interface (SEI) [ 8 ], safety and stability, and their narrow electrochemical operation window (<2 V vs. Mg/Mg 2+ ) [ 4 , 9 ].…”
Section: Introductionmentioning
confidence: 99%
“…Mg(NO 3 ) 2 , as dopant salt with a high lattice energy of 2429.51 kJ·mol −1 [ 26 ], was chosen to minimise the occurrence of ion association between cations and anions in the complexes. The results revealed in the current work indicate that divalent salts with moderate conductivity can stimulate the development of polymer electrolytes for multivalent batteries [ 4 ].…”
Polymer electrolytes based on agarose dissolved in DMSO solvent complexed with different weight percentages of Mg(NO3)2 ranging from 0 to 35 wt% were prepared using a solution casting method. Electrochemical impedance spectroscopy (EIS) was applied to study the electrical properties of this polymer electrolyte, such as ionic conductivity at room and different temperatures, dielectric and modulus properties. The highest conducting film has been obtained at 1.48 × 10−5 S·cm−1 by doping 30 wt% of Mg(NO3)2 into the polymer matrix at room temperature. This high ionic conductivity value is achieved due to the increase in the amorphous nature of the polymer electrolyte, as proven by X-ray diffractometry (XRD), where broadening of the amorphous peak can be observed. The intermolecular interactions between agarose and Mg(NO3)2 are studied by Fourier transform infrared (FTIR) spectroscopy by observing the presence of –OH, –CH, N–H, CH3, C–O–C, C–OH, C–C and 3,6-anhydrogalactose bridges in the FTIR spectra. The electrochemical properties for the highest conducting agarose–Mg(NO3)2 polymer electrolyte are stable up to 3.57 V, which is determined by using linear sweep voltammetry (LSV) and supported by cyclic voltammetry (CV) that proves the presence of Mg2+ conduction.
“…Energy storage systems based on monovalent cations (Li + , Na + , and K + ) have been widely investigated and significant progress has been achieved (Shen and Yu, 2017;Shen et al, 2018Shen et al, , 2019. Multivalent cations (Mg 2+ , Zn 2+ , Ni 2+ , Ca 2+ , and Al 3+ ) are becoming more attractive, since one mole reacted multivalent ions can provide double or triple the number of electrons as compared to monovalent cations (Bitenc and Dominko, 2018;Cui et al, 2018;Dong et al, 2018;Liu et al, 2019a,b;Zhan et al, 2020). Moreover, multivalent cation-based devices are also more air-resistant and thus more applicable in practice (Sun et al, 2020).…”
Zinc-ion hybrid supercapacitors are a promising energy storage device as they simultaneously combine the high capacity of batteries and the high power of supercapacitors. However, the practical application of Zinc-ion hybrid supercapacitors is hindered by insufficient energy density and poor rate performance. In this study, a symmetrical zinc-ion hybrid supercapacitor device was constructed with hollow mesoporous-carbon nanospheres as electrode materials, and aqueous ZnSO 4 adopted as an electrolyte. Benefiting from the mesoporous structure and high specific area (800 m 2 /g) of the hollow carbon nanospheres, fast capacitor-type ion adsorption/de-adsorption on both the cathode and the anode can be achieved, as well as additional battery-type Zn/Zn 2+ electroplating/stripping on the anode. This device thus demonstrates outstanding electrochemical performance, with high capacity (212.1 F/g at 0.2 A/g), a high energy density (75.4 Wh/kg at 0.16 kW/kg), a good rate performance (34.2 Wh/kg energy density maintained at a high power density of 16.0 kW/kg) and excellent cycling stability with 99.4% capacitance retention after 2,500 cycles at 2 A/g. The engineering of this new configuration provides an extremely safe, high-rate, and durable energy-storage device.
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