Sodium diffusion in hard carbon studied by small- and wide-angle neutron scattering and muon spin relaxation

大石 一城*; 五十嵐 大輔*; 多々良 涼一*; 河村 幸彦*; 廣井 孝介  ; 鈴木 淳市*; 梅垣 いづみ*; 西村 昇一郎*; 幸田 章宏*; 駒場 慎一*; 杉山 純*

Oishi, Kazuki*; Igarashi, Daisuke*; Tatara, Ryoichi*; Kawamura, Yukihiko*; Hiroi, Kosuke; Suzuki, Junichi*; Umegaki, Izumi*; Nishimura, Shoichiro*; Koda, Akihiro*; Komaba, Shinichi*; Sugiyama, Jun*

Hard carbon is the most common anode material for Na-ion battery. The structure of the hard carbon and the dynamics of Na-ion in hard carbon were studied with small- and wide- angle neutron scattering and muon spin relaxation technique. The neutron scattering revealed the increase of interlayer distance between graphenes and decrease of the size of nanopores with increasing sodium intercalation in hard carbon. The muon spin relaxation revealed that a systematic increase in the field fluctuation rate with increasing temperature evidenced a thermally activated sodium diffusion. Assuming the two-dimensional diffusion of Na-ion in the graphene layers, the self-diffusion coefficient of Na-ion was estimated to be 2.610 cm/s at 310 K, with a thermal activation energy of 39(7) meV.