RESUMO
Graphite is considered to be the most auspicious anode candidate for potassium ion batteries. However, the inferior rate performances and cycling stability restrict its practical applications. Few studies have investigated the modulating the graphitization degree of graphitic materials. Herein, a nitrogen-doped carbon-coated carbon fiber composite with tunable graphitization (CNF@NC) through etching growth, in-situ oxidative polymerization, and subsequent carbonization process is reported. The prepared CNF@NC with abundant electrochemical active sites and a rapid K+/electron transfer pathway, can effectively shorten the K+ transfer distance and promote the rapid insertion/removal of K+. Amorphous domains and short-range curved graphite layers can provide ample mitigation spaces for K+ storage, alleviating the volume expansion of the highly graphitized CNF during repeated K+ insertion/de-intercalation. As expected, the CNF@NC-5 electrode presents a high initial coulombic efficiency (ICE) of 69.3%, an unprecedented reversible volumetric capacity of 510.2 mA h cm-3 at 0.1 A g-1 after 100 cycles with the mass-capacity of 294.9 mA h g-1. The K+ storage mechanism and reaction kinetic analysis are studied by combining in-situ analysis and first-principles calculation. It manifests that the K+ storage mechanism in CNF@NC-5 is an adsorption-insertion-insertion mechanism (i.e., the "1+2" model). The solid electrolyte interphase (SEI) film forming is also detected.
RESUMO
Potassium-ion batteries (PIBs) have become the desirable alternatives for lithium-ion batteries (LIBs) originating from abundant reserves and appropriate redox potential, while the considerable radius size of K+ leading to poor reaction kinetics and huge volume expansion limits the practical application of PIBs. Hybridization of transition-metal phosphides and carbon substrates can effectively optimize the obstacles of poor conductivity, sluggish kinetics, and huge volume variation. Thus, the peapod-like structural MxPy@BNCNTs (M = Fe, Co, and Ni) composites as anode materials for PIBs were synthesized through a facile strategy. Notably, the unique architecture of B/N codoped carbon nanotube array as fast ion/electron transfer pathways effectively improves the electronic conductivity of composites. The MxPy nanoparticles (NPs) are encapsulated in BNCNTs with an amorphous carbon layer (5-10 nm), which discernibly alleviate the volume changes during potassiation/depotassiation. In conclusion, the composites show a commendable cycling performance, possessing reversible capacities of 111, 152, and 122 mA h g-1 after 1000 cycles at 1.0 A g-1 with a negligible capacity loss for FeP@BNCNT, CoP/Co2P@BNCNT, and Ni2P@BNCNT electrodes, respectively. Especially, after 1000 cycles at 2.0 A g-1, the CoP/Co2P@BNCNT electrode still possesses a capacity of 87.9 mA h g-1, demonstrating excellent rate performance and long-term life. This work may offer an innovative and viable route to construct a stable architecture for solving the issue of poor stability of TMP-based anodes at a high current density.
RESUMO
Constructing bimetallic sulfide components are considered to be a promising and efficient lithium storage materials. Nonetheless, preparation routes of rational structures that have abundant hierarchical interfaces or phase boundaries bimetallic sulfide are still a problem to over come. In this work, a novel hierarchical nanostructure of bimetal sulfide CoS-MoS2 nanorods are synthesized successfully by in-situ self-growth means at the hydrothermal conditions. Subsequently, we loaded it to the carbon matrix (CoS-MoS2@rGO) forming a three-dimensional structures with the help of freeze drying technology. This well-designed hierarchical structure could created a stable heterogeneous contact surface, which guarantees rapid Li+ ions diffusion and facilitates charge transfer at the heterointerface. Which can maintain capacity of 776 mAh/g over 800 cycles at 1 A/g. On the other hand, it shows an excellent rate capability of 464 mAg h-1 at 5 A/g. From the perspective of electrochemical kinetics, we analyze and explore the reason about the improved lithium storage performance. Furthermore, to insight into the relationship between matter and phase conversion, the in-situ X-ray diffraction characterization is executed. The strategy of rationally designing hierarchical heterostructures will shed light on outstanding electrochemical performance in energy storage applications.
RESUMO
Nowadays with the increasing demand for lithium-ion batteries (LIBs), the high-capacity silicon anode is becoming a promising electrode material. However, the huge expansion of silicon during long cycling remains a significant challenge. Herein, a functional double layer Si-based multi-component structure Si@void C@TiO2 was designed as anode material for lithium-ion batteries. This structure has a void space inside and a double shell composed of carbon layer and crystalline TiO2 outside, which not only takes effective in improving electric conductivity of the Si electrode material, but also maintains the structural stability and integrity of the electrode. The layers impede the electrolyte from contacting with Si, contributing to forming a stable SEI film and providing high Coulombic efficiency. Therefore, the Si@void C@TiO2 electrode provides a high reversible capacity of 1251 mA h g-1, and stable long cycling with a capacity of 668 mA h g-1 over 500 cycles at a current density of 100 mA g-1, and 98% average Coulombic efficiency, making this potential superior material Si-based multi-component anode a high-performance electrode material for Li-ion batteries.
