2021
DOI: 10.1002/aenm.202102342
|View full text |Cite
|
Sign up to set email alerts
|

Liquid Phase‐Induced Solid Solution Phase Mechanisms for Highly Stable and Ultrafast Energy Storage

Abstract: Phase transitions induce large changes of the lattice parameters, and thus have negative effects on the electrochemical energy storage of electrode materials. In contrast, solid solution phase energy storage mechanisms can ensure smaller shrinkage/expansion of the structure, and therefore better cyclability and fast reaction kinetics of the electrode materials. In this work, the liquid phase is found to control the energy storage mechanisms of K2.55Zn3.08[Fe(CN)6]2·0.28H2O (KZnHCF). Via in situ characterizatio… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
6
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 12 publications
(5 citation statements)
references
References 43 publications
0
6
0
Order By: Relevance
“…[96][97][98] Figure 4e shows that the initial discharge capacity of 549.5 mAh g −1 is delivered at 1 A g −1 in the first cy-cle, and 401.1 mAh g −1 of discharge capacity can be achieved after cycling for 650 cycles, presenting good cyclic stability of the I 2 @MBene-Br cathode within 0.4-2.1 V, which are mainly attributed to the strong adsorption of iodine species by the layered MBene-Br host with ordered metal vacancies and the high reversibility of Br − /Br 0 in the MBene-Br skeleton. [40] As illustrated in Figure 4f, the I 2 @MBene-Br cathode displays a recorded specific energy of 485.8 Wh kg −1 at the specific power of 899.7 W kg −1 and a recorded specific power of 6007.7 W kg −1 at the specific energy of 180.2 Wh kg −1 , superior to the state of the art of aqueous Zn||I 2 batteries [57,60,66,75,77,88,90,[99][100][101][102][103] and most aqueous Zn||PBA (Prussian Blue analogs), [104][105][106] Zn||V 2 O 5 , [107][108][109][110][111] Zn||MnO 2 [112] and Zn||organic [113] battery systems.…”
Section: Resultsmentioning
confidence: 99%
“…[96][97][98] Figure 4e shows that the initial discharge capacity of 549.5 mAh g −1 is delivered at 1 A g −1 in the first cy-cle, and 401.1 mAh g −1 of discharge capacity can be achieved after cycling for 650 cycles, presenting good cyclic stability of the I 2 @MBene-Br cathode within 0.4-2.1 V, which are mainly attributed to the strong adsorption of iodine species by the layered MBene-Br host with ordered metal vacancies and the high reversibility of Br − /Br 0 in the MBene-Br skeleton. [40] As illustrated in Figure 4f, the I 2 @MBene-Br cathode displays a recorded specific energy of 485.8 Wh kg −1 at the specific power of 899.7 W kg −1 and a recorded specific power of 6007.7 W kg −1 at the specific energy of 180.2 Wh kg −1 , superior to the state of the art of aqueous Zn||I 2 batteries [57,60,66,75,77,88,90,[99][100][101][102][103] and most aqueous Zn||PBA (Prussian Blue analogs), [104][105][106] Zn||V 2 O 5 , [107][108][109][110][111] Zn||MnO 2 [112] and Zn||organic [113] battery systems.…”
Section: Resultsmentioning
confidence: 99%
“…In the charging process, [Fe(II)(CN) 6 ] 4+ in the KFeMnHCF skeleton was converted to [Fe(III)(CN) 6 ] 3+ with a larger radius, causing the lattice expansion, and vice versa [12b] . This reversible evolution means that the KZnHCF electrode underwent a solid‐solution ion (de)intercalation mechanism, [14b] which was also confirmed by X‐ray photoelectron spectroscopy (XPS) for the KFeMnHCF cathode after the 20 th cycle (Figure 3e–g). Until the battery was charged to 200 mAh g −1 (stage 3), the gradually increased peak of Cl 2p represents the Cl − intercalation (Figure 3e).…”
Section: Resultsmentioning
confidence: 99%
“…Impressively, the achieved energy density of the PBI//Zn battery surpasses the corresponding values of the PB//Zn batteries, carbon materials, and MOFs at all power rates. [26,41,42,44,[46][47][48][49][50][51][52][53]…”
Section: Resultsmentioning
confidence: 99%