| Literature DB >> 32286055 |
Zhanpeng Li1, Ning Sun1,2, Razium Ali Soomro1,2, Zhaoruxin Guan1, Li Ma1, Mingchi Jiang1, Qizhen Zhu1, Bin Xu1.
Abstract
Graphite is an attractive anode with high capacity and low cost for potassium ion batteries (PIBs) but suffers from poor cycle performance due to the large interlayer expansion during the potassiation/depotassiation process. Here, we propose structurally engineered hollow graphitized carbon nanocages (HGCNs) as efficient anode materials for PIBs. The HGCNs were synthesized using a one-pot, self-template and self-graphitization approach where direct pyrolysis of nickel citrate converts citrate chains into carbon-shell and simultaneously reduces Ni2+ to form a Ni metal core. This nickel core serves as not only a hard-template to create hollow-cage structure but also a catalyst to facilitate the graphitization of the carbon-shell. The HGCNs synthesized at 1000 °C (HGCN-1000), with its highly graphitized carbon-cage and developed porosity, exhibited an impressive K-storage capacity of 402.2 mAh g-1 at a current density of 30 mA g-1. The synergic combination of hollow morphology with graphitized carbon layers configured a stable structure capable of enduring extreme deformation, endowing HGCN-1000 a robust cyclic stability with a capacity retention of 95.9% over 2000 cycles at 1 A g-1. The proposed strategy provides an efficient route to combat the bottleneck cycling instability issue of graphitic carbon with hollow-graphitized carbon nanocages as promising anode materials for PIBs.Keywords: anode; graphitized carbon; hollow nanocages; potassium-ion batteries; structural engineering
Year: 2020 PMID: 32286055 DOI: 10.1021/acsnano.0c01150
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881