2018
DOI: 10.1016/j.mtener.2018.09.013
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Metal-organic framework-derived Co0.85Se nanoparticles in N-doped carbon as a high-rate and long-lifespan anode material for potassium ion batteries

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Cited by 112 publications
(53 citation statements)
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“…The peaks emerging from 0.90 to 0.41 V in the first cathodic scan correspond to the insertion of K + ions into the Co-Fe selenides to form the K x (Co 0.5 Fe 0.5 ) y Se z product and SEI layers, followed by the formation of metallic Co and Fe nanoparticles as well as K 2 Se. [39][40][41] These results are in good agreement with the ex situ analysis data. Furthermore, the strong reversible peak at approximately 0.01 V can be attributed to the K + storage in the carbon.…”
Section: Resultssupporting
confidence: 89%
“…The peaks emerging from 0.90 to 0.41 V in the first cathodic scan correspond to the insertion of K + ions into the Co-Fe selenides to form the K x (Co 0.5 Fe 0.5 ) y Se z product and SEI layers, followed by the formation of metallic Co and Fe nanoparticles as well as K 2 Se. [39][40][41] These results are in good agreement with the ex situ analysis data. Furthermore, the strong reversible peak at approximately 0.01 V can be attributed to the K + storage in the carbon.…”
Section: Resultssupporting
confidence: 89%
“…Therefore, as presented in the Ragone plot (Figure S15, Supporting Information), the CoSeS@C/G has overwhelming higher rate capability than other reported cobalt selenide‐base anodes for LIB. [ 9,11,35,53–55 ]…”
Section: Resultsmentioning
confidence: 99%
“…Cobalt selenides, as to their larger deintercalation interstitial distance and weaker ion bonds of CoSe compared with the cobalt oxides/sulfides, have been deemed as one of the most promising candidate for utilization in alkali‐ion batteries. [ 7–9 ] However, during the insertion/extraction process of alkali ion, cobalt selenides present the deficient diffusion kinetics and mediocre capacity, which is derived from the unacceptable electronic/ionic conductivity, resulting in the unsatisfactory electrochemical performance. [ 10 ] It is confirmed that tailoring chemical composition through doping into the crystal lattice, is an efficient approach to enhance the intrinsic conductivity of the target material by adjusting its electronic structure in wide ranges.…”
Section: Introductionmentioning
confidence: 99%
“…The peak 1 can be caused by the intercalation of K ion to ZnSe. Subsequently, the peak 1 shifts to ≈0.63 V, which can be attributed to the conversion reaction with Se translating into K 2 Se after the first cycle . The peak 2 vanishes in the subsequent cycles, which can be attributed to some irreversible reactions and the formation of solid‐electrolyte interphase (SEI) film .…”
Section: Resultsmentioning
confidence: 99%