2014
DOI: 10.1039/c3cc47607c
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High rate sodium ion insertion into core–shell nanoparticles of Prussian blue analogues

Abstract: We demonstrate that core-shell nanoparticles consisting of two different Prussian blue analogues, one high capacity and the other robust, can provide enhanced rate capability as cathode materials in sodium-ion batteries.

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Cited by 97 publications
(56 citation statements)
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“…Advance in cathode materials is of great importance in accelerating the commercialization of SIBs due to their relatively low capacity value [4,5] and poor rate capability [5,6] compared with the anode counterparts [7][8][9]. Nickel hexacyanoferrate (NiHCF), a compound with [10], the PB analogues have attracted growing interests owing to the advantages of the rigid open framework for Na-ion diffusion, the tunable composition, the non-toxicity and the low cost [11][12][13][14][15][16][17]. Therein, iron hexacyanferrate (FeHCF) is under most investigation due to its two-electron-redox processes and the corresponding high theoretical capacity of ~170 mAh g -1 (based on Na 2 FeFe(CN) 6 ) [13,[18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…Advance in cathode materials is of great importance in accelerating the commercialization of SIBs due to their relatively low capacity value [4,5] and poor rate capability [5,6] compared with the anode counterparts [7][8][9]. Nickel hexacyanoferrate (NiHCF), a compound with [10], the PB analogues have attracted growing interests owing to the advantages of the rigid open framework for Na-ion diffusion, the tunable composition, the non-toxicity and the low cost [11][12][13][14][15][16][17]. Therein, iron hexacyanferrate (FeHCF) is under most investigation due to its two-electron-redox processes and the corresponding high theoretical capacity of ~170 mAh g -1 (based on Na 2 FeFe(CN) 6 ) [13,[18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…[ 238 ] The family of alkali-ion-defi cient cubic AM II Fe III (CN) 6 (A = Na or K) compounds requires a presodiation process to be combined with conventional Na-free anodes; otherwise, the electrode operation undergoes only one electron transfer with Fe 3+ /Fe 2+ redox couples, resulting in a low capacity below 70 mA h g −1 . [239][240][241][242][243] The Na-rich compound, Na 1.72 MnFe(CN) 6 , was successfully synthesized by Wang et al [ 229 ] This electrode delivers a capacity of 130 mA h g −1 with a high average voltage of 3.4 V involving Mn 2+ /Mn 3+ and Fe 2+ /Fe 3+ redox reactions. The high Na concentration in the structure induces a structural transition from cubic to rhombohedral symmetry with cooperative Na displacement along the [ 111 ] direction.…”
Section: (16 Of 38)mentioning
confidence: 99%
“…Other Na x MFe(CN) 6 (M = Co, Ni, Cu, Ti) hexacyanoferrates have also been investigated [145][146][147]. The Na 2 CoFe(CN) 6 sample delivered a high reversible capacity of 150 mAh g −1 with two distinguishable potential plateaus at 3.8 and 3.2 V (Fig.…”
Section: Ferrocyanide Materialsmentioning
confidence: 99%