Abstract:The ORCID identification number(s) for the author(s) of this article can be found under https://doi.org/10.1002/smtd.202101131.
Potassium-ion batteries (PIBs) have attracted tremendous attention becauseof their high energy density and low-cost. As such, much effort has focused on developing electrode materials and electrolytes for PIBs at the material levels. This review begins with an overview of the high-performance electrode materials and electrolytes, and then evaluates their prospects and challenges for p… Show more
“…Based on these considerations, ionic conductivity measurements between 10 and 50 °C were performed, considering this as a plausible temperature range for KIB applications in large-scale energy storage plants. 73 , 74 As shown in Figure 8 B, the activated GPEs possessed an appreciable ionic conductivity with values ranging between 10 –3 and 10 –2 S cm –1 when passing from lower (10 °C) to higher temperatures (50 °C), respectively. Interestingly, lower ionic conductivities were found for GAn- and PAn-based membranes over the same temperature interval, in line with their less favorable EUR response as compared with SAn-based systems (see Figure S6 in the Supporting Information ).…”
In this study, biobased
gel polymer electrolyte (GPE) membranes
were developed via the esterification reaction of a cardanol-based
epoxy resin with glutaric anhydride, succinic anhydride, and hexahydro-4-methylphthalic
anhydride. Nonisothermal differential scanning calorimetry was used
to assess the optimal curing time and temperature of the formulations,
evidencing a process activation energy of ∼65–70 kJ
mol
–1
. A rubbery plateau modulus of 0.65–0.78
MPa and a crosslinking density of 2 × 10
–4
mol
cm
–3
were found through dynamic mechanical analysis.
Based on these characteristics, such biobased membranes were tested
for applicability as GPEs for potassium-ion batteries (KIBs), showing
an excellent electrochemical stability toward potassium metal in the
−0.2–5 V voltage range and suitable ionic conductivity
(10
–3
S cm
–1
) at room temperature.
This study demonstrates the practical viability of these biobased
materials as efficient GPEs for the fabrication of KIBs, paving the
path to increased sustainability in the field of next-generation battery
technologies.
“…Based on these considerations, ionic conductivity measurements between 10 and 50 °C were performed, considering this as a plausible temperature range for KIB applications in large-scale energy storage plants. 73 , 74 As shown in Figure 8 B, the activated GPEs possessed an appreciable ionic conductivity with values ranging between 10 –3 and 10 –2 S cm –1 when passing from lower (10 °C) to higher temperatures (50 °C), respectively. Interestingly, lower ionic conductivities were found for GAn- and PAn-based membranes over the same temperature interval, in line with their less favorable EUR response as compared with SAn-based systems (see Figure S6 in the Supporting Information ).…”
In this study, biobased
gel polymer electrolyte (GPE) membranes
were developed via the esterification reaction of a cardanol-based
epoxy resin with glutaric anhydride, succinic anhydride, and hexahydro-4-methylphthalic
anhydride. Nonisothermal differential scanning calorimetry was used
to assess the optimal curing time and temperature of the formulations,
evidencing a process activation energy of ∼65–70 kJ
mol
–1
. A rubbery plateau modulus of 0.65–0.78
MPa and a crosslinking density of 2 × 10
–4
mol
cm
–3
were found through dynamic mechanical analysis.
Based on these characteristics, such biobased membranes were tested
for applicability as GPEs for potassium-ion batteries (KIBs), showing
an excellent electrochemical stability toward potassium metal in the
−0.2–5 V voltage range and suitable ionic conductivity
(10
–3
S cm
–1
) at room temperature.
This study demonstrates the practical viability of these biobased
materials as efficient GPEs for the fabrication of KIBs, paving the
path to increased sustainability in the field of next-generation battery
technologies.
“…Reproduced with permission. [172] Copyright 2021, Wiley. delivered a specific discharge capacity of ≈53 mAh g −1 at 3 mA g −1 , but showed poor cycling efficiency owing to electrolyte consumption during the initial cycles.…”
Section: Full Cell Assemblymentioning
confidence: 99%
“…However, the coulombic efficiency, capacity, and rate capability of organic anode materials must be improved to realize a practical KIB full cell. [21,32,33,172] In summary, the performance of a full cell is dependent on the synergistic effect between the anode, cathode, and electrolyte components. Practical batteries require safe electrode materials with high capacity, high operating voltage, long cycle life, high charge/discharge rate, and structural stability.…”
To meet future energy demands, currently, dominant lithium‐ion batteries (LIBs) must be supported by abundant and cost‐effective alternative battery materials. Potassium‐ion batteries (KIBs) are promising alternatives to LIBs because KIB materials are abundant and because KIBs exhibit intercalation chemistry like LIBs and comparable energy densities. In pursuit of superior batteries, designing and developing highly efficient electrode materials are indispensable for meeting the requirements of large‐scale energy storage applications. Despite using graphite anodes in KIBs instead of in sodium‐ion batteries (NIBs), developing suitable KIB cathodes is extremely challenging and has attracted considerable research attention. Among the various cathode materials, layered metal oxides have attracted considerable interest owing to their tunable stoichiometry, high specific capacity, and structural stability. Therefore, the recent progress in layered metal‐oxide cathodes is comprehensively reviewed for application to KIBs and the fundamental material design, classification, phase transitions, preparation techniques, and corresponding electrochemical performance of KIBs are presented. Furthermore, the challenges and opportunities associated with developing layered oxide cathode materials are presented for practical application to KIBs.
“…There is reason to believe that the electrochemical performance of Al-MOF batteries could be further improved through electrode/ electrolyte engineering. [47,48] Importantly, the repeated alternate storage of opposite charges in bipolar electrode materials has a great impact on the cycling stability of batteries, which can be promoted by adjusting the ratio of anions and cations in IL electrolyte.…”
Section: Alternate Storage Mechanism Of Opposite Chargesmentioning
The limited active sites of cathode materials in aluminum‐ion batteries restrict the storage of more large‐sized Al‐complex ions, leading to a low celling of theoretical capacity. To make the utmost of active sites, an alternate storage mechanism of opposite charges (AlCl4− anions and AlCl2+ cations) in multisites is proposed herein to achieve an ultrahigh capacity in Al–metal–organic framework (MOF) battery. The bipolar ligands (oxidized from 18π to 16π electrons and reduced from 18π to 20π electrons in a planar cyclic conjugated system) can alternately uptake and release AlCl4− anions and AlCl2+ cations in charge/discharge processes, which can double the capacity of unipolar ligands. Moreover, the high‐density active Cu sites (Cu nodes) in the 2D Cu‐based MOF can also store AlCl2+ cations for a higher capacity. The rigid and extended MOF structure can address the problems of high solubility and poor stability of small organic molecules. As a result, three‐step redox reactions with two‐electron transfer in each step are demonstrated in charge/discharge processes, achieving high reversible capacity (184 mAh g−1) and energy density (177 Wh kg−1) of the optimized cathode in an Al–MOF battery. The findings provide a new insight for the rational design of stable high‐energy Al–MOF batteries.
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