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dc.contributor.authorWang, Tianshuai
dc.contributor.authorLegut, Dominik
dc.contributor.authorFan, Yanchen
dc.contributor.authorQin, Jian
dc.contributor.authorLi, Xifei
dc.contributor.authorZhang, Qianfan
dc.date.accessioned2020-10-15T12:05:38Z
dc.date.available2020-10-15T12:05:38Z
dc.date.issued2020
dc.identifier.citationNano Letters. 2020, vol. 20, issue 8, p. 6199-6205.cs
dc.identifier.issn1530-6984
dc.identifier.issn1530-6992
dc.identifier.urihttp://hdl.handle.net/10084/142326
dc.description.abstractHeterostructure engineering is one of the most promising modification strategies toward improving sluggish kinetics for the anode of sodium ion batteries (SIBs). Herein, we report a systemic investigation on the different types of heterostructure interfaces' effects of discharging products (Na2O, Na2S, Na2Se) on the rate performance. First-principle calculations reveal that the Na2S/Na2Se interface possesses the lowest diffusion energy barrier (0.39 eV) of Na among three kinds of interface structures (Na2O/Na2S, Na2O/Na2Se, and Na2S/Na2Se) due to its smallest recorded interface deformation, similar electronegativity, and lattice constant. The experimental evidence confirms that the metal sulfide/metal selenide (SnS/SnSe2) hierarchical anode exhibits outstanding rate performance, where the normalized capacity at 10 A g(-1) compared to 0.1 A g(-1) is 45.6%. The proposed design strategy in this work is helpful to design high rate performance anodes for advanced battery systems.cs
dc.language.isoencs
dc.publisherAmerican Chemical Societycs
dc.relation.ispartofseriesNano Letterscs
dc.relation.urihttp://doi.org/10.1021/acs.nanolett.0c02595cs
dc.rightsCopyright © 2020, American Chemical Societycs
dc.subjectfast diffusion channelcs
dc.subjectheterostructures anode materialscs
dc.subjectmetal sulfide/metal selenidecs
dc.subjectsodium ion batteriescs
dc.titleBuilding fast diffusion channel by constructing metal sulfide/metal selenide heterostructures for high-performance sodium ion batteries anodecs
dc.typearticlecs
dc.identifier.doi10.1021/acs.nanolett.0c02595
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume20cs
dc.description.issue8cs
dc.description.lastpage6205cs
dc.description.firstpage6199cs
dc.identifier.wos000562935200085


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