“…18 In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. 24,59 A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle. 60 Besides, a pair of redox peaks at 0.07/0.20 V are observed, which are probably ascribed to the sodium ion insertion and extraction into/from the carbon cloth substrate.…”
Section: Resultssupporting
confidence: 86%
“…Figure A displays the first three cycles of CV profiles for the NiSe 2 /C-2G-500 electrode within the voltage range of 0.01–3.0 V tested at a scan rate of 0.1 mV s –1 . During the first cathodic scan, the strong reduction peak at around 1.30 V is ascribed to the intercalation of sodium ions into NiSe 2 to form Na x NiSe 2 , while the weak and broad peak at around 0.60 V is attributed to the further conversion reaction of Na x NiSe 2 to metallic Ni and Na 2 Se, and the formation of an irreversible solid electrolyte interface (SEI) film. ,, In the first anodic scan, the predominant oxidation peak at 2.00 V with a shoulder correlates to the desodiation process with the regeneration of NiSe 2 from metallic Ni and NaSe 2 . In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. , A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle .…”
Section: Results
and Discussionmentioning
confidence: 99%
“…During the first cathodic scan, the strong reduction peak at around 1.30 V is ascribed to the intercalation of sodium ions into NiSe 2 to form Na x NiSe 2 , while the weak and broad peak at around 0.60 V is attributed to the further conversion reaction of Na x NiSe 2 to metallic Ni and Na 2 Se, and the formation of an irreversible solid electrolyte interface (SEI) film. ,, In the first anodic scan, the predominant oxidation peak at 2.00 V with a shoulder correlates to the desodiation process with the regeneration of NiSe 2 from metallic Ni and NaSe 2 . In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. , A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle . Besides, a pair of redox peaks at 0.07/0.20 V are observed, which are probably ascribed to the sodium ion insertion and extraction into/from the carbon cloth substrate. , In the third cycle, the two reduction peaks at 1.44 and 1.10 V move to 1.43 and 1.07 V, and the oxidation peak at 1.94 V changes to 1.90 V, which might be caused by the rearranged material structure formed in the electrode after the first and second cycles .…”
As one type of promising anode for
sodium-ion batteries
(SIBs),
nickel diselenide (NiSe2) has stimulated considerable attention.
However, its wide practical application has been greatly limited by
the sluggish kinetics, low electrical conductivity, as well as severe
volume changes and aggregation of particles during repeated cycling.
In this work, we demonstrate a facile strategy to achieve self-supporting
carbon nanosheet arrays densely decorated with NiSe2 nanoparticles
on carbon cloth through the one-pot hydrothermal formation of intermediate
glucose-intercalated Ni(OH)2 as both the nickel precursor
and carbon source, followed by carbonization and selenization processes.
The strongly coupled NiSe2 nanoparticles with a carbon
nanosheet matrix can endow the improved sodium storage performance
owing to the robust structural integrity, abundant active sites, as
well as accelerated charge transfer kinetics. As expected, the optimal
anode of NiSe2/C hybrid arrays exhibits a remarkable reversible
capacity of 465 mAh g–1 at a current density of
0.5 A g–1 after 350 cycles and an outstanding rate
capability of 259 mAh g–1 at 5 A g–1. We propose that the present study shall unravel more insights into
the delicate design and exploration of NiSe2-based anode
materials for SIBs with high performance.
“…18 In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. 24,59 A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle. 60 Besides, a pair of redox peaks at 0.07/0.20 V are observed, which are probably ascribed to the sodium ion insertion and extraction into/from the carbon cloth substrate.…”
Section: Resultssupporting
confidence: 86%
“…Figure A displays the first three cycles of CV profiles for the NiSe 2 /C-2G-500 electrode within the voltage range of 0.01–3.0 V tested at a scan rate of 0.1 mV s –1 . During the first cathodic scan, the strong reduction peak at around 1.30 V is ascribed to the intercalation of sodium ions into NiSe 2 to form Na x NiSe 2 , while the weak and broad peak at around 0.60 V is attributed to the further conversion reaction of Na x NiSe 2 to metallic Ni and Na 2 Se, and the formation of an irreversible solid electrolyte interface (SEI) film. ,, In the first anodic scan, the predominant oxidation peak at 2.00 V with a shoulder correlates to the desodiation process with the regeneration of NiSe 2 from metallic Ni and NaSe 2 . In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. , A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle .…”
Section: Results
and Discussionmentioning
confidence: 99%
“…During the first cathodic scan, the strong reduction peak at around 1.30 V is ascribed to the intercalation of sodium ions into NiSe 2 to form Na x NiSe 2 , while the weak and broad peak at around 0.60 V is attributed to the further conversion reaction of Na x NiSe 2 to metallic Ni and Na 2 Se, and the formation of an irreversible solid electrolyte interface (SEI) film. ,, In the first anodic scan, the predominant oxidation peak at 2.00 V with a shoulder correlates to the desodiation process with the regeneration of NiSe 2 from metallic Ni and NaSe 2 . In the second cycle, the reduction peaks shift to two new peaks situated at 1.44 and 1.10 V, while the oxidation peak is split into two peaks at a low voltage of 1.79 and 1.90 V correlating to the multiple-step sodium ion removal process. , A similar phenomenon is also found in previously reported literature, which is mainly attributed to the structural rearrangement of the electrode materials and the decomposition of electrolytes to form the SEI in the initial cycle . Besides, a pair of redox peaks at 0.07/0.20 V are observed, which are probably ascribed to the sodium ion insertion and extraction into/from the carbon cloth substrate. , In the third cycle, the two reduction peaks at 1.44 and 1.10 V move to 1.43 and 1.07 V, and the oxidation peak at 1.94 V changes to 1.90 V, which might be caused by the rearranged material structure formed in the electrode after the first and second cycles .…”
As one type of promising anode for
sodium-ion batteries
(SIBs),
nickel diselenide (NiSe2) has stimulated considerable attention.
However, its wide practical application has been greatly limited by
the sluggish kinetics, low electrical conductivity, as well as severe
volume changes and aggregation of particles during repeated cycling.
In this work, we demonstrate a facile strategy to achieve self-supporting
carbon nanosheet arrays densely decorated with NiSe2 nanoparticles
on carbon cloth through the one-pot hydrothermal formation of intermediate
glucose-intercalated Ni(OH)2 as both the nickel precursor
and carbon source, followed by carbonization and selenization processes.
The strongly coupled NiSe2 nanoparticles with a carbon
nanosheet matrix can endow the improved sodium storage performance
owing to the robust structural integrity, abundant active sites, as
well as accelerated charge transfer kinetics. As expected, the optimal
anode of NiSe2/C hybrid arrays exhibits a remarkable reversible
capacity of 465 mAh g–1 at a current density of
0.5 A g–1 after 350 cycles and an outstanding rate
capability of 259 mAh g–1 at 5 A g–1. We propose that the present study shall unravel more insights into
the delicate design and exploration of NiSe2-based anode
materials for SIBs with high performance.
“…At a scan rate of 0.5 mV s À1 , 79% of the total charge is assigned to the capacitive contributions, which illustrates the excellent rate capability of the VOH-CNTs cathode (Figure 4C). 42,43 At various scan rates, the percentage of capacitive contributions gradually dominates as a high scanning rate that increased from 70% to 87%, benefiting fast charge transfer dynamics (Figure 4D). 44,45 The typical GITT curves are displayed in Figure 4E.…”
Advanced wearable portable electronic products are needed energy storage devices with foldable properties. Zinc-ion batteries (ZIBs) are one of the most promising alternatives for energy storage devices due to their significant advantages, such as low cost, high reliability, and safety for folding. Herein, V 5 O 12 Á 6H 2 O (VOH) was obtained by facile electrodeposition strategy on carbon nanotube (CNTs) film, forming the freestanding V 5 O 12 Á 6H 2 O-CNTs (VOH-CNTs) composite films. The resultant VOH-CNTs composite films with high mechanical properties can be directly used as the cathode for foldable aqueous zinc-ion batteries (AZIBs). The VOH-CNTs electrode at a current density of 1 A g À1 shows a high specific capacity of 356 mAh g À1 and the capacity retention of 96% after 500 cycles. Even a reversible specific capacity of 292 mAh g À1 can be achieved at a current density of 5 A g À1 and the capacity retention of 93% after 4000 cycles. A high coulombic efficiency stays nearly 100%. The electrochemical properties of the prepared cells measured in different folding states remain stable, indicating the devices are suitable for use as foldable energy storage devices.
“…The structural design of materials is the main factor affecting their properties. [16][17][18][19][20] Two-dimensional (2D) van der Waals heterostructures with the integrated advantages of two 2D nanomaterials are an emerging electrode material system in the field of energy storage. [21][22][23][24][25][26] It is worth noting that bismuth oxychloride (BiOCl) features a layered structure with [Cl-Bi-O-Bi-Cl] slices stacking through the weak van der Waals interaction among adjacent Cl layers.…”
The synergistic innovation from reasonable material design to electrolyte optimization is the key to improve the performance of anode materials for potassium ion batteries (PIBs). In this work, a two-dimensional...
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