11 research outputs found
Lightweight Reduced Graphene Oxide@MoS<sub>2</sub> Interlayer as Polysulfide Barrier for High-Performance Lithium–Sulfur Batteries
The
further development of lithium–sulfur (Li–S) batteries
is limited by the fact that the soluble polysulfide leads to the shuttle
effect, thereby reducing the cycle stability and cycle life of the
batteries. To address this issue, here a thin and lightweight (8 μm
and 0.24 mg cm<sup>–2</sup>) reduced graphene oxide@MoS<sub>2</sub> (rGO@MoS<sub>2</sub>) interlayer between the cathode and
the commercial separator is developed as a polysulfide barrier. The
rGO plays the roles of both a polysulfide physical barrier and an
additional current collector, while MoS<sub>2</sub> has a high chemical
adsorption for polysulfides. The experiments demonstrate that the
Li–S cell constructed with an rGO@MoS<sub>2</sub>-coated separator
shows a high reversible capacity of 1122 mAh g<sup>–1</sup> at 0.2 C, a low capacity fading rate of 0.116% for 500 cycles at
1 C, and an outstanding rate performance (615 mAh g<sup>–1</sup> at 2 C). Such an interlayer is expected to be ideal for lithium–sulfur
battery applications because of its excellent electrochemical performance
and simple synthesis process
Metallurgy Inspired Formation of Homogeneous Al<sub>2</sub>O<sub>3</sub> Coating Layer To Improve the Electrochemical Properties of LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> Cathode Material
Inspired by the metallurgical
process of aluminum production, a
controllable and cost-effective Al<sub>2</sub>O<sub>3</sub> coating
strategy is introduced to improve the surface stability of LiNi<sub>0.8</sub>Co<sub>0.1</sub>ÂMn<sub>0.1</sub>O<sub>2</sub>. The
CO<sub>2</sub> is introduced to NaAlO<sub>2</sub> aqueous solution
to generate a weak basic condition that is able to decrease the deposition
rate of AlÂ(OH)<sub>3</sub> and is beneficial to the uniform coating
of AlÂ(OH)<sub>3</sub> on the surface of commercial Ni<sub>0.8</sub>Co<sub>0.1</sub>ÂMn<sub>0.1</sub>(OH)<sub>2</sub> precursor.
The electrochemical performance of Al<sub>2</sub>O<sub>3</sub>-coated
LiNi<sub>0.8</sub>Co<sub>0.1</sub>ÂMn<sub>0.1</sub>O<sub>2</sub> is improved at both ordinary cutoff voltage of 4.3 V and elevated
cutoff voltage of 4.5 V. With the optimized Al<sub>2</sub>O<sub>3</sub> coating amount (1%), the capacity retention of the material after
60 cycles increases from 90% to 99% at 2.8–4.3 V and from 86%
to 99% at 2.8–4.5 V, respectively. The Al<sub>2</sub>O<sub>3</sub>-coated sample also delivers a better rate capability, maintaining
117 and 131 mA h g<sup>–1</sup> in the voltage ranges 2.8–4.3
and 2.8 V–4.5 V at the current density of 5 C, respectively.
The enhanced properties of as-prepared Al<sub>2</sub>O<sub>3</sub>-coated LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> are due to the Al<sub>2</sub>O<sub>3</sub> coating layer building
up a favorable interface, preventing the direct contact between the
active material and electrolyte and promoting Li<sup>+</sup> transmission
at the interface
- Changes of CEIFI, aggregation activity, HSR, CD62P expression and PS externalization in platelets during 7-day storage at 22 ± 2°C.
<p>Data are the mean ± S.D. *<i>P</i> <0.05 as compared with platelets stored for 1 day.</p
The difference in cytosolic esterase-induced fluorescence with CMFDA between resting and activated human platelets.
<p>The activity of cytosolic esterase-induced fluorescence reaction is visualized with CMFDA. The fluorescence of resting platelets was clearly visible in laser confocal microscopy, whereas activated platelets release no or little fluorescence. A, C: Resting platelets; B, D: Activated platelets (activated by 100μM ADP); A, B: green fluorescence; C, D: bright field.</p
The change of cytosolic esterase-induced fluorescence activity in platelets during 7-day storage at 22 ± 2°C.
<p>The activity of cytosolic esterase-induced fluorescence in platelets is measured with CMFDA. *<i>P</i> <0.05 as compared with platelets stored for 1 day.</p
CD62P expression percentage on membrane of platelets during 7-day storage at 22± 2°C.
<p>A: Mouse IgG1 κ Iso control. B: platelets stored for 1 day. C: platelets stored for 3 days. D: platelets stored for 5 days. E: platelets stored for 7 days.</p
PS externalization of platelets during 7-day storage at 22 ± 2°C.
<p>A: platelets stored for 1 day. B: platelets stored for 3 days. C: platelets stored for 5 days. D: platelets stored for 7 days.</p
Correlation of platelet CEIFI with functional parameters of platelets during 7-day storage.
<p>A: Correlation to the ADP-induced aggregation activity, r = 0.9813. B: Correlation to the HSR activity, r = 0.9848. C: Correlation to the expression percentage of CD62P on platelet membrane, r = -0.9945. D: Correlation to the PS externalization percentage, r = -0.9847.</p
Aggregation curves of platelets during 7-day storage at 22 ± 2°C.
<p>A: platelets stored for 1 day. B: platelets stored for 3 days. C: platelets stored for 5 days. D: platelets stored for 7 days.</p
HSR curves of platelets during 7-day storage at 22± 2°C.
<p>A: platelets stored for 1 day. B: platelets stored for 3 days. C: platelets stored for 5 days. D: platelets stored for 7 days.</p