2017
DOI: 10.1016/j.ensm.2016.12.005
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Recent progress in rational design of anode materials for high-performance Na-ion batteries

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Cited by 213 publications
(108 citation statements)
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“…Due to the large abundance and low cost of sodium resources and similar chemical/electrochemical properties to established lithium‐ion batteries (LIBs), room temperature sodium‐ion batteries (SIBs) emerge as a potential technology for grid‐scale energy storage . A large number of materials, such as transition metal oxides, phosphates, ferrocyanides, metal alloys, and hard carbon, have been investigated and have shown acceptable electrochemical performance, and some reviews have summarized recent developments in electrodes for SIBs . However, due to the higher molar weight of the Na element and more positive standard electrochemical potential of Na/Na + (compared to Li/Li + ), SIBs exhibit lower energy densities than LIBs.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the large abundance and low cost of sodium resources and similar chemical/electrochemical properties to established lithium‐ion batteries (LIBs), room temperature sodium‐ion batteries (SIBs) emerge as a potential technology for grid‐scale energy storage . A large number of materials, such as transition metal oxides, phosphates, ferrocyanides, metal alloys, and hard carbon, have been investigated and have shown acceptable electrochemical performance, and some reviews have summarized recent developments in electrodes for SIBs . However, due to the higher molar weight of the Na element and more positive standard electrochemical potential of Na/Na + (compared to Li/Li + ), SIBs exhibit lower energy densities than LIBs.…”
Section: Introductionmentioning
confidence: 99%
“…The accumulation of the SEI layer,w hich not only increased the electrode resistance but also decreased the number of electroactives ites, led to the capacity fading.I nc ontrast, the adhesive and dispersant nature of NaCMC, [11] when mixed with NaPAA, improved the wetting and spreading of the binder on the active particles urface. [16,70,71] Figure S11c ompares the surfacea ppearances of the electrodes after 300 charge-discharge cycles.F or the PVDF electrode, some of the Cu substrate was exposed (owing to the detachment of the active material layer), whereas the NaCMC/NaPAA electrode retained the bestm echanical integrity.T he corresponding electrode morphologies examined using SEM are shown in Figure 6. After 150 cycles,t he capacity retentionr atios were 56 %, 64 %, 66 %, and 73 %f or the PVDF,N aCMC, NaPAA, and NaCMC/NaPAA electrodes, respectively.T he decreased durability at ah igh sodiation-desodiation rate suggested that the electrode volume expansion/shrinkage, rather than other parasitic reactions, was mainly responsible for the capacity decay.Agood binder,e ven thoughi ta ccountsf or only as mall portion of the electrode, plays as ignificant role in cycling stability, especially under high-rate operation.…”
Section: Resultsmentioning
confidence: 99%
“…All in all, through nanostructure engineering and hybridization with conductive materials, the obtained composites often show better electrochemical performance compared to bulk electrodes and pure nanostructured electrodes in terms of rate capability and cycling stability. The improvement in performance is very limited, however, for the engineered composites of metal oxides and phosphides . The reversible capacities of the oxides and phosphides discussed above are still much lower than their theoretical capacities.…”
Section: Strategies Toward High Rate Capability and Stable Cycling Pementioning
confidence: 99%