Liu Yang, Chen Ziliang, Jia Huaxian, Xu Hongbin, Liu Miao, Wu Renbing
Department of Materials Science , Fudan University , Shanghai 200433 , P.R. China.
Department of Chemistry , Fudan University , Shanghai 200433 , P.R. China.
ACS Nano. 2019 May 28;13(5):6113-6124. doi: 10.1021/acsnano.9b02928. Epub 2019 May 13.
Transition metal chalcogenides (TMCs) have been investigated as promising anodes for high-performance lithium-ion batteries, but they usually suffer from poor conductivity and large volume variation, thus leading to unsatisfactory performance. Although nanostructure engineering and hybridization with conductive materials have been proposed to address this concern, a better performance toward practical device applications is still highly desired. Herein, we report an iron-doping-induced structural phase transition from pyrite-type (cubic) to marcasite-type (orthorhombic) phases in porous carbon/rGO-coupled CoSe. The dual-carbon-confined orthorhombic CoSe ( o-Fe CoSe@NC@rGO) composites exhibit dramatically enhanced lithium storage performance (920 mAh g after 1000 cycles at 1.0 A g) over cubic CoSe-based composites ( c-CoSe@NC@rGO). The combined experimental studies and density functional theory calculations reveal that this doping-induced structural phase transformation strategy could create a favorable electronic structure and ensure a rapid charge transfer. These results demonstrate that the phase-transformation engineering may provide another opportunity in the design of high-performance TMC-based electrodes.
过渡金属硫族化合物(TMCs)已被研究作为高性能锂离子电池的有前景的负极材料,但它们通常存在导电性差和体积变化大的问题,从而导致性能不尽人意。尽管已经提出了纳米结构工程和与导电材料杂化来解决这一问题,但对于实际器件应用而言,仍非常需要更好的性能。在此,我们报道了在多孔碳/rGO耦合的CoSe中,铁掺杂诱导的从黄铁矿型(立方)到白铁矿型(正交)相的结构相变。双碳限制的正交CoSe(o-Fe CoSe@NC@rGO)复合材料相较于立方CoSe基复合材料(c-CoSe@NC@rGO),展现出显著增强的锂存储性能(在1.0 A g下循环1000次后为920 mAh g)。结合实验研究和密度泛函理论计算表明,这种掺杂诱导的结构相变策略可以创造有利的电子结构并确保快速的电荷转移。这些结果表明,相变工程可能为设计高性能的基于TMC的电极提供另一个机会。