Abstract:Sodium-ion batteries are regarded as one of the most promising energy storage systems, but the choice of anode material is still facing great challenges. Biomass carbon materials were explored for their low cost and wide range of sources. Here, a hard carbon material with a "honeycomb" structure using pine pollen (PP) as a precursor was successfully prepared and applied as an anode. The initial discharge capacity can reach 370 mA h g −1 at a current density of 0.1 A g −1 . After cycling 200 times, the reversib… Show more
“…Figure 4b and Additional file 1: Figure S5b display the charge/discharge curves for different cycles of Co 9 S 8 @NSC and NSC with the initial coulombic efficiency (CE) of 54.1% and 28.3%, respectively. The relatively low CE is caused by the irreversible formation of SEI film and electrolyte consumption [7]. The curves of these two samples manifest distinctive voltage platform of Co 9 S 8 and carbon, which are in accord with the results of CV tests (Fig.…”
Section: Resultssupporting
confidence: 86%
“…And the electrochemical potential of Na (− 2.71 V vs the standard hydrogen electrode, SHE) is higher than that of Li (− 3.04 V) with 330 mV, which makes SIBs possible to meet large-scale energy storage demands [4][5][6]. However, the most important challenge in SIBs is the large volume expansion during the process of sodiation originated from the great strain derived from the larger radius of Na + (1.02 Å) than Li + (0.76 Å) [7,8]. This will result in severe pulverization and exfoliation of active materials from copper foil and further lead to poor cycling performance.…”
Co 9 S 8 is a potential anode material for its high sodium storage performance, easy accessibility, and thermostability. However, the volume expansion is a great hindrance to its development. Herein, a composite containing Co 9 S 8 nanofibers and hollow Co 9 S 8 nanospheres with N, S co-doped carbon layer (Co 9 S 8 @NSC) is successfully synthesized through a facile solvothermal process and a high-temperature carbonization. Ascribed to the carbon coating and the large specific surface area, severe volume stress can be effectively alleviated. In particular, with N and S heteroatoms introduced into the carbon layer, which is conducive to the Na + adsorption and diffusion on the carbon surface, Co 9 S 8 @NSC can perform more capacitive sodium storage mechanism. As a result, the electrode can exhibit a favorable reversible capacity of 226 mA h g −1 at 5 A g −1 and a favorable capacity retention of 83.1% at 1 A g −1 after 800 cycles. The unique design provides an innovative thought for enhancing the sodium storage performance.
“…Figure 4b and Additional file 1: Figure S5b display the charge/discharge curves for different cycles of Co 9 S 8 @NSC and NSC with the initial coulombic efficiency (CE) of 54.1% and 28.3%, respectively. The relatively low CE is caused by the irreversible formation of SEI film and electrolyte consumption [7]. The curves of these two samples manifest distinctive voltage platform of Co 9 S 8 and carbon, which are in accord with the results of CV tests (Fig.…”
Section: Resultssupporting
confidence: 86%
“…And the electrochemical potential of Na (− 2.71 V vs the standard hydrogen electrode, SHE) is higher than that of Li (− 3.04 V) with 330 mV, which makes SIBs possible to meet large-scale energy storage demands [4][5][6]. However, the most important challenge in SIBs is the large volume expansion during the process of sodiation originated from the great strain derived from the larger radius of Na + (1.02 Å) than Li + (0.76 Å) [7,8]. This will result in severe pulverization and exfoliation of active materials from copper foil and further lead to poor cycling performance.…”
Co 9 S 8 is a potential anode material for its high sodium storage performance, easy accessibility, and thermostability. However, the volume expansion is a great hindrance to its development. Herein, a composite containing Co 9 S 8 nanofibers and hollow Co 9 S 8 nanospheres with N, S co-doped carbon layer (Co 9 S 8 @NSC) is successfully synthesized through a facile solvothermal process and a high-temperature carbonization. Ascribed to the carbon coating and the large specific surface area, severe volume stress can be effectively alleviated. In particular, with N and S heteroatoms introduced into the carbon layer, which is conducive to the Na + adsorption and diffusion on the carbon surface, Co 9 S 8 @NSC can perform more capacitive sodium storage mechanism. As a result, the electrode can exhibit a favorable reversible capacity of 226 mA h g −1 at 5 A g −1 and a favorable capacity retention of 83.1% at 1 A g −1 after 800 cycles. The unique design provides an innovative thought for enhancing the sodium storage performance.
“…Therefore, numerous biomass-based carbon combining hierarchical pores and heteroatom doping have gained considerable attentions, resulting in pesudocapacitance and electrical double layer capacitance. Carbonization of natural biomass materials, including seaweeds (Kang et al, 2015), peanut shell (Ding et al, 2015), rice bran (Hou et al, 2014), plant leaves (Liu B. et al, 2017; Zhang et al, 2018; Zhao et al, 2018), fruit (Wu et al, 2014), and wheat flour (Wu et al, 2015; Yu et al, 2016), has been investigated. It is demonstrated as a feasible approach, which could result in a low cost and eco-friendly way to prepare hierarchical porous carbon electrodes.…”
Porous carbon materials produced by biomass have been widely studied for high performance supercapacitor due to their abundance, low price, and renewable. In this paper, the series of nitrogen-doped hierarchical porous carbon nanospheres (HPCN)/polyaniline (HPCN/PANI) nanocomposites is reported, which is prepared via
in-situ
polymerization. A novel approach with one-step pyrolysis of wheat flour mixed with urea and ZnCl
2
is proposed to prepare the HPCN with surface area of 930 m
2
/g. Ultrathin HPCN pyrolysised at 900°C (~3 nm in thickness) electrode displays a gravimetric capacitance of 168 F/g and remarkable cyclability with losing 5% of the maximum capacitance after 5,000 cycles. The interconnected porous texture permits depositing of well-ordered polyaniline nanorods and allows a fast absorption/desorption of electrolyte. HPCN/PANI with short diffusion pathway possesses high gravimetric capacitance of 783 F/g. It can qualify HPCN/PANI to be used as cathode in assembling asymmetric supercapacitor with HPCN as anode, and which displays an exceptional specific capacitance of 81.2 F/g. Moreover, HPCN/PANI//HPCN device presents excellent cyclability with 88.4% retention of initial capacity over 10,000 cycles. This work will provide a simple and economical protocol to prepare the sustainable biomass materials based electrodes for energy storage applications.
“…From the viewpoint of sustainability, carbon materials derived from waste biomass are especially interesting . In recent years, carbons made from rice husks, corn or wheat straw, coir pith, soy bean residues (from tofu production), pistachio shells, wood chips or fibers, grass, pine pollen, lignin, tannic acid, or shrimp shells, among others, have been introduced as anode materials in lithium‐ or sodium‐based batteries. Similarly, all kinds of biowaste have been carbonized and used as host materials in the cathodes of lithium–sulfur, lithium–selenium, or lithium–oxygen batteries.…”
Sustainable sources of energy have been identified as a possible way out of today's oil dependency and are being rapidly developed. In contrast, storage of energy to a large extent still relies on heavy metals in batteries. Especially when built from biomass‐derived organics, organic batteries are promising alternatives and pave the way towards truly sustainable energy storage. First described in 2008, research on biomass‐derived electrodes has been taken up by a multitude of researchers worldwide. Nowadays, in principle, electrodes in batteries could be composed of all kinds of carbonized and noncarbonized biomass: On one hand, all kinds of (waste) biomass may be carbonized and used in anodes of lithium‐ or sodium‐ion batteries, cathodes in metal–sulfur or metal–oxygen batteries, or as conductive additives. On the other hand, a plethora of biomolecules, such as quinones, flavins, or carboxylates, contain redox‐active groups that can be used as redox‐active components in electrodes with very little chemical modification. Biomass‐based binders can replace toxic halogenated commercial binders to enable a truly sustainable future of energy storage devices. Besides the electrodes, electrolytes and separators may also be synthesized from biomass. In this Review, recent research progress in this rapidly emerging field is summarized with a focus on potentially fully biowaste‐derived batteries.
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