Hu Jun, Wang Bo, Yu Qiyao, Zhang Di, Zhang Yanghuan, Li Ying, Wang Wei Alex
Department of Functional Material Research, Central Iron and Steel Research Institute, Beijing 100081, People's Republic of China.
Nanotechnology. 2020 Sep 25;31(39):395403. doi: 10.1088/1361-6528/ab9578. Epub 2020 May 21.
Transition metal selenides (TMS), on account of their relatively high theoretical capacity, unique electrical properties, easy compositing and low cost, are considered to be a candidate anode material for potassium-ion batteries. However, the cycling stability of TMS is unsatisfactory owing to the large intercalation/deintercalation of K ions. Herein, a CoSe/N-doped carbon porous frame (CoSe@NC) is successfully synthesized through a simple mixing and sintering approach and displays excellent potassium storage performance. Plentiful C-N bonds in the precursor can induce the formation of homogeneous N-doped carbon matrix and C-N-Co bonds, thus endowing robust structure and high electronic conductivity for superior cycling stability. Therefore, the unique porous nanoframe suppresses volume expansion and provides more diffusion paths for K ions. After 1000 cycles at 50 mA g, a high capacity of 311.3 mA h g is acquired. When the current density increases to 500 mA g, the CoSe@NC can still maintain a capacity of 184.5 mA h g after 1000 cycles. The high performance, easy compositing and low cost of the CoSe@NC make it a favorable material for application in KIBs.
过渡金属硒化物(TMS)由于其相对较高的理论容量、独特的电学性质、易于复合且成本较低,被认为是钾离子电池的候选负极材料。然而,由于钾离子的大量嵌入/脱出,TMS的循环稳定性并不理想。在此,通过一种简单的混合烧结方法成功合成了CoSe/N掺杂碳多孔框架(CoSe@NC),其展现出优异的储钾性能。前驱体中丰富的C-N键可诱导形成均匀的N掺杂碳基体和C-N-Co键,从而赋予其坚固的结构和高电子导电性,以实现卓越的循环稳定性。因此,独特的多孔纳米框架抑制了体积膨胀,并为钾离子提供了更多的扩散路径。在50 mA g的电流密度下循环1000次后,获得了311.3 mA h g的高容量。当电流密度增加到500 mA g时,CoSe@NC在1000次循环后仍能保持184.5 mA h g的容量。CoSe@NC的高性能、易于复合及低成本使其成为钾离子电池应用的理想材料。