ABSTRACT
The development of anode materials with high theoretical capacity and cycling stability is very important for the electrochemical performance of lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs). Herein, SnSe/NC hollow nanospheres with different crystal orientations were prepared by regulating the high-temperature selenization of the PDA@SnO2 precursor for lithium/sodium storage. In SnSe/NC hollow nanospheres, the physical buffering and chemical bonding of the nitrogen carbon matrix and SnSe nanoparticles could inhibit volume expansion and polyselenide loss, thus maintaining long-term structural stability. More importantly, electrochemical tests and DFT calculations show that the diffusion energy barrier of Li+/Na+ is significantly reduced at the SnSe (400) rather than the usual (111) facet, which is conducive to the uniformity of ion insertion into SnSe, thus effectively enhancing the reaction kinetics and reversibility of lithium/sodium storage. Therefore, SnSe/NC hollow nanospheres with rich SnSe (400) and good dispersion formed at 550 °C delivered the best reversible specific capacity and rate performance. After a long period of 900 cycles, the capacity retention of lithium/sodium ion batteries is close to 84.88% and 77.05%, respectively. Our findings provide valuable insights into the design of metal selenides for advanced LIBs/SIBs.
ABSTRACT
Tin-based anode materials with high theoretical specific capacity are subject to huge volume expansion and poor reaction reversibility, leading to degradation of battery performance. Herein, the steric-hindrance effect and self-sacrificing template behavior of polydopamine were firstly developed to induce the formation of hollow nanospheres assembled by ultrafine SnO2 quantum dots (SnO2-QDs) and nitrogen-doped carbon (NC), containing residual polydopamine (PDA) cores. The PDA@SnO2-QDs/NC hollow nanospheres could effectively accommodate the volume expansion and maintain structural stability. More importantly, the PDA core could capture oxygen free radicals produced by the charge/discharge process and be involved in the evolution of the SEI layer, achieving enhanced electrochemical reaction kinetics. The optimized PDA@SnO2-QDs/NC anode shows a specific capacity of 898 mAh g-1 after 300 cycles at 0.3 A g-1, and scarcely capacity attenuation after 1500 cycles at 1 A g-1. The long-cyclic life is up to 3000 cycles at 3 A g-1. Even after 200 cycles, the anode in the PDA@SnO2-QDs/NC||LFP full battery gives a reversible capacity of 489 mAh g-1 at 0.3 A g-1, with a capacity retention of 77 %. This work casts new light on tin-based anode materials and interface optimization.
