Weihan Li

Amorphous Red Phosphorus Embedded in Highly Ordered Mesoporous Carbon with Superior Lithium and Sodium Storage Capacity

Red phosphorus (P) have been considered as one of the most promising anode material for both lithium-ion batteries (LIBs) and (NIBs), because of its high theoretical capacity. However, natural insulating property and the large volume expansion of red P during cycling lead to poor cyclability and low rate performance, which prevents its practical application. Here, we significantly improves both lithium storage and sodium storage performance of red P by confining nanosized amorphous red P into the mesoporous carbon matrix (P@CMK-3) using a vaporization-condensation-conversion process. The P@CMK-3 shows a high reversible specific capacity of ∼ 2250 mA h g(-1) based on the mass of red P at 0.25 C (∼ 971 mA h g(-1) based on the composite), excellent rate performance of 1598 and 624 mA h g(-1) based on the mass of red P at 6.1 and 12 C, respectively (562 and 228 mA h g(-1) based on the mass of the composite at 6.1 and 12 C, respectively) and significantly enhanced cycle life of 1150 mA h g(-1) based on the mass of red P at 5 C (500 mA h g(-1) based on the mass of the composite) after 1000 cycles for LIBs. For Na ions, it also displays a reversible capacity of 1020 mA h g(-1) based on the mass of red P (370 mA h g(-1) based on the mass of the composite) after 210 cycles at 5C. The significantly improved electrochemical performance could be attributed to the unique structure that combines a variety of advantages: easy access of electrolyte to the open channel structure, short transport path of ions through carbon toward the red P, and high ionic and electronic conductivity.

Confined Amorphous Red Phosphorus in MOF-Derived N-Doped Microporous Carbon as a Superior Anode for Sodium-Ion Battery

Red phosphorus (P) has attracted intense attention as promising anode material for high-energy density sodium-ion batteries (NIBs), owing to its high sodium storage theoretical capacity (2595 mAh g-1 ). Nevertheless, natural insulating property and large volume variation of red P during cycling result in extremely low electrochemical activity, leading to poor electrochemical performance. Herein, the authors demonstrate a rational strategy to improve sodium storage performance of red P by confining nanosized amorphous red P into zeolitic imidazolate framework-8 (ZIF-8) -derived nitrogen-doped microporous carbon matrix (denoted as P@N-MPC). When used as anode for NIBs, the P@N-MPC composite displays a high reversible specific capacity of ≈600 mAh g-1 at 0.15 A g-1 and improved rate capacity (≈450 mAh g-1 at 1 A g-1 after 1000 cycles with an extremely low capacity fading rate of 0.02% per cycle). The superior sodium storage performance of the P@N-MPC is mainly attributed to the novel structure. The N-doped porous carbon with sub-1 nm micropore facilitates the rapid diffusion of organic electrolyte ions and improves the conductivity of the encapsulated red P. Furthermore, the porous carbon matrix can buffer the volume change of red P during repeat sodiation/desodiation process, keeping the structure intact after long cycle life.

A General Strategy to Fabricate Carbon-Coated 3D Porous Interconnected Metal Sulfides: Case Study of SnS/C Nanocomposite for High-Performance Lithium and Sodium Ion Batteries.

Transition metal sulfides have a great potential for energy storage due to the pronouncedly higher capacity (owing to conversion to metal or even alloy) than traditional insertion electrode materials. However, the poor cycling stability still limits the development and application in lithium and sodium ion batteries. Here, taking SnS as a model material, a novel general strategy is proposed to fabricate a 3D porous interconnected metal sulfide/carbon nanocomposite by the electrostatic spray deposition technique without adding any expensive carbonaceous materials such as graphene or carbon nanotube. In this way, small nanorods of SnS are generated with sizes of ≈10–20 nm embedded in amorphous carbon and self‐assembled into a 3D porous interconnected nanocomposite. The SnS:C is directly deposited on the Ti foil as a current collector and neither conductive additives nor binder are needed for battery assembly. Such electrodes exhibit a high reversible capacity, high rate capability, and long cycling stability for both lithium and sodium storage.

FeS@C on Carbon Cloth as Flexible Electrode for Both Lithium and Sodium Storage

Flexible and self-supported carbon-coated FeS on carbon cloth films (denoted as FeS@C/carbon cloth) is prepared by a facial hydrothermal method combined with a carbonization treatment. The FeS@C/carbon cloth could be directly used as electrodes for Li-ion batteries (LIBs) and sodium-ion batteries (NIBs). The synthetic effects of the structure, highly electron-conductive of carbon cloth, porous structure for electrolyte access, and uniform carbon shell on FeS surface to accommodate the volume change lead to improved cyclability and rate capability. For lithium storage, the FeS@C/carbon cloth electrode delivers a high discharge capacity of 420 mAh g(-1) even after 100 cycles at a current density of 0.15 C and 370 mAh g(-1)at a high current density of 7.5 C (1 C = 609 mA g(-1). When used for sodium storage, it keeps a reversible capacity of 365 mAh g(-1)after 100 cycles at 0.15 C. Similar process can be utilized for the formation of various cathode and anode composites on carbon cloth for flexible energy storage devices.

Superior Sodium Storage in 3D Interconnected Nitrogen and Oxygen Dual-Doped Carbon Network

Carbonaceous materials have attracted immense interest as anode materials for Na-ion batteries (NIBs) because of their good chemical, thermal stabilities, as well as high Na-storage capacity. However, the carbonaceous materials as anodes for NIBs still suffer from the lower rate capability and poor cycle life. An N,O-dual doped carbon (denoted as NOC) network is designed and synthesized, which is greatly favorable for sodium storage. It exhibits high specific capacity and ultralong cycling stability, delivering a capacity of 545 mAh g(-1) at 100 mA g(-1) after 100 cycles and retaining a capacity of 240 mAh g(-1) at 2 A g(-1) after 2000 cycles. The NOC composite with 3D well-defined porosity and N,O-dual doped induces active sites, contributing to the enhanced sodium storage. In addition, the NOC is synthesized through a facile solution process, which can be easily extended to the preparation of many other N,O-dual doped carbonaceous materials for wide applications in catalysis, energy storage, and solar cells.

Carbon‐Coated Germanium Nanowires on Carbon Nanofibers as Self‐Supported Electrodes for Flexible Lithium‐Ion Batteries

A hybrid structure with carbon-coated germanium nanowires grown on the surface of carbon nanofibers is fabricated using an in situ vapor-liquid-solid process. It is used as a self-supported and flexible anode for Li-ion batteries.

Engineering nanostructured electrode materials for high performance sodium ion batteries: a case study of a 3D porous interconnected WS2/C nanocomposite

Much attention is being paid to sodium ion batteries (SIBs) in view of the abundance of sodium sources and the cost issues. Layered transition metal dichalcogenides (such as MoS2 and WS2) have great potential to be used as anode materials for sodium storage owing to their high capacity. However, they still suffer from low rate capability and poor cycling stability. Compared to MoS2, WS2 has been scarcely studied in view of sodium storage. Here, we report, for the first time, a 3D porous interconnected WS2/C nanocomposite prepared by an electrostatic spray deposition (ESD) technique, which is composed of nano-0D WS2, nano-1D CNTs and nano-2D reduced graphene oxide. Such a nanocomposite shows excellent rate performance and long cycling stability, demonstrating great potential for its use as a sodium anode. Moreover, this strategy can be applied to other electrode materials for both lithium and sodium batteries.

Sb Nanoparticles Encapsulated in a Reticular Amorphous Carbon Network for Enhanced Sodium Storage

Sb nanoparticles encapsulated in 3D reticular carbon network (denoted Sb@3D RCN) film are prepared by the electrostatic spray deposition technique followed by a heat treatment. When used as a binder-free anode for a Na-ion battery, it shows excellent long-life cyclability. The unique reticular, porous, and core-shell structure of Sb@3D RCN contributes significantly to the excellent sodium storage performance.

N-doped porous hollow carbon nanofibers fabricated using electrospun polymer templates and their sodium storage properties

N-doped hollow porous carbon nanofibers (P-HCNFs) were prepared through pyrolyzation of hollow polypyrrole (PPy) nanofibers fabricated using electrospun polycaprolactone (PCL) nanofibers as a sacrificial template. When used as anode material for NIBs, P-HCNFs exhibit a reversible capacity of 160 mA h g−1 after 100 cycles at a current density of 0.05 A g−1. An improved rate capability is also obtained at even higher charge–discharge rates. When cycled at a current density of 2 A g−1, the electrode can still show a reversible capacity of 80 mA h g−1. The N-doped sites, one-dimensional nanotube structure, and functionalized surface of P-HCNFs are capable of rapidly and reversibly accommodating sodium ions through surface adsorption and redox reactions. Therefore, P-HCNF is a promising anode material for next-generation NIBs.

Membranes of MnO Beading in Carbon Nanofibers as Flexible Anodes for High-Performance Lithium-Ion Batteries

Freestanding yet flexible membranes of MnO/carbon nanofibers are successfully fabricated through incorporating MnO2 nanowires into polymer solution by a facile electrospinning technique. During the stabilization and carbonization processes of the as-spun membranes, MnO2 nanowires are transformed to MnO nanoparticles coincided with a conversion of the polymer from an amorphous state to a graphitic structure of carbon nanofibers. The hybrids consist of isolated MnO nanoparticles beading in the porous carbon and demonstrate superior performance when being used as a binder-free anode for lithium-ion batteries. With an optimized amount of MnO (34.6 wt%), the anode exhibits a reversible capacity of as high as 987.3 mAh g−1 after 150 discharge/charge cycles at 0.1 A g−1, a good rate capability (406.1 mAh g−1 at 3  A g−1) and an excellent cycling performance (655 mAh g−1 over 280 cycles at 0.5 A g−1). Furthermore, the hybrid anode maintains a good electrochemical performance at bending state as a flexible electrode.