Yuliang Cao

Sodium ion insertion in hollow carbon nanowires for battery applications.

Hollow carbon nanowires (HCNWs) were prepared through pyrolyzation of a hollow polyaniline nanowire precursor. The HCNWs used as anode material for Na-ion batteries deliver a high reversible capacity of 251 mAh g(-1) and 82.2% capacity retention over 400 charge-discharge cycles between 1.2 and 0.01 V (vs Na(+)/Na) at a constant current of 50 mA g(-1) (0.2 C). Excellent cycling stability is also observed at an even higher charge-discharge rate. A high reversible capacity of 149 mAh g(-1) also can be obtained at a current rate of 500 mA g(-1) (2C). The good Na-ion insertion property is attributed to the short diffusion distance in the HCNWs and the large interlayer distance (0.37 nm) between the graphitic sheets, which agrees with the interlayered distance predicted by theoretical calculations to enable Na-ion insertion in carbon materials.

A Soft Approach to Encapsulate Sulfur: Polyaniline Nanotubes for Lithium‐Sulfur Batteries with Long Cycle Life

A novel vulcanized polyaniline nanotube/sulfur composite was prepared successfully via an in situ vulcanization process by heating a mixture of polyaniline nanotube and sulfur at 280 °C. The electrode could retain a discharge capacity of 837 mAh g(-1) after 100 cycles at a 0.1 C rate and manifested 76% capacity retention up to 500 cycles at a 1 C rate.

Reversible Sodium Ion Insertion in Single Crystalline Manganese Oxide Nanowires with Long Cycle Life

Single crystalline Na4Mn9O18 nanowires were synthesized via pyrolysis of polyacrylate salt precursors prepared by in-situ polymerization of the metal salts and acrylate acid, followed by calcinations at an appropriate temperature to achieve good crystalline structure and uniform nanowire morphology with an average diameter of 50 nm. The Na4Mn9O18 nanowires have shown a high, reversible, and near theoretical sodium ion insertion capacity (128 mA h g-1 at 0.1C), excellent long cyclability (77% capacity retention for 1000 cycles at 0.5 C), along with good rate capability. Good capacity and charge-discharge stability are also observed for full cell experiments using a pyrolyzed carbon as the anode, therefore demonstrating the potential of these materials for sodium-ion batteries for large scale energy storage. Furthermore, this research shows that a good crystallinity and small particles are required to enhance the Na-ion diffusion and increase the stability of the electrode materials for long charge-discharge cycles.

High Capacity and Rate Capability of Amorphous Phosphorus for Sodium Ion Batteries

Turning on your P/C: An amorphous phosphorus/carbon (a-P/C) composite was synthesized using simple mechanical ball milling of red phosphorus and conductive carbon powders. This material gave an extraordinarily high sodium ion storage capacity of 1764 mA h g(-1) (see graph) with a very high rate capability, showing great promise as a high capacity and high rate anode material for sodium ion batteries.

Sb–C nanofibers with long cycle life as an anode material for high-performance sodium-ion batteries

Sb–C nanofibers are synthesized successfully through a single-nozzle electrospinning technique and subsequent calcination. The structural and morphological characterizations reveal the uniform nanofiber structure with the Sb nanoparticles embedded homogeneously in the carbon nanofibers. Electrochemical experiments show that the Sb–C nanofiber electrode can deliver large reversible capacity (631 mA h g−1) at C/15, greatly improved rate capability (337 mA h g−1 at 5 C) and excellent cycling stability (90% capacity retention after 400 cycles). The superior electrochemical performances of the Sb–C nanofibers are due to the unique nanofiber structure and uniform distribution of Sb nanoparticles in carbon matrix, which provides a conductive and buffering matrix for effective release of mechanical stress caused by Na ion insertion/extraction and prevent the aggregation of the Sb nanoparticles.

Optimization of mesoporous carbon structures for lithium–sulfur battery applications

Mesoporous carbon (MC) with tunable pore sizes (22 nm, 12 nm, 7 nm, and 3 nm) and pore volumes (from 1.3 to 4.8 cm3 g−1) containing sulfur in the pores was studied as a mesoporous carbon–sulfur (MCS) composite electrode for lithium–sulfur (Li–S) batteries. Systematic investigation of these MCS composites reveals that MC with a larger pore volume can hold a higher maximum sulfur loading, but overall the battery performance is very similar for different MCS composites at full sulfur-filling conditions (i.e., the condition at which the sulfur loading approaches the maximum limit set by the pore volume of the individual MC and, therefore, the pores of each MC are fully filled by sulfur). For the same MC, partial sulfur-filling (i.e., the condition at which the sulfur loading is lower than the maximum limit and, therefore, the pores are only partially filled with sulfur) leads to an improved initial discharge capacity and cycle stability, probably because of improved electrical and ionic transport during electrochemical reactions. Based on this understanding, an MCS composite electrode using MC with a large pore volume, partial sulfur filling, and a novel surface modification was designed for Li–S batteries. An initial capacity of ∼1390 mA h g−1 (based on sulfur) and a capacity retention of ∼840 mA h g−1 over 100 cycles at a 0.1 C rate were obtained using MC (22 nm, 4.8 cm3 g−1) with 50 wt% sulfur loading and a commercially available Clevios P (poly(3,4-ethylenedioxythiophene)poly(styrenesulfonate) (PEDT/PSS)) coating.

Synergistic Na-Storage Reactions in Sn4P3 as a High-Capacity, Cycle-stable Anode of Na-Ion Batteries

Room-temperature Na-ion batteries have attracted great interest as a low cost and environmentally benign technology for large scale electric energy storage, however their development is hindered by the lack of suitable anodic host materials. In this paper, we described a green approach for the synthesis of Sn4P3/C nanocomposite and demonstrated its excellent Na-storage performance as a novel anode of Na-ion batteries. This Sn4P3/C anode can deliver a very high reversible capacity of 850 mA h g(-1) with a remarkable rate capability with 50% capacity output at 500 mA g(-1) and can also be cycled with 86% capacity retention over 150 cycles due to a synergistic Na-storage mechanism in the Sn4P3 anode, where the Sn nanoparticles act as electronic channels to enable electrochemical activation of the P component, while the elemental P and its sodiated product Na3P serve as a host matrix to alleviate the aggregation of the Sn particles during Na insertion reaction. This mechanism may offer a new approach to create high capacity and cycle-stable alloy anodes for Na-ion batteries and other electrochemical energy storage applications.

The mechanism of oxygen reduction on MnO2-catalyzed air cathode in alkaline solution

Abstract The mechanism of oxygen reduction at MnO2-catalyzed air cathode was investigated by measurements of polarization curves in wide OH− concentrations, oxygen pressures and using different crystalline MnO2 catalysts. It is found that the oxygen reduction at MnO2 catalyst is accompanied with the reduction of MnO2 and the catalytic activities of MnO2 is closely related to the electrochemical activities of MnO2. Based on the experimental determination of the reaction orders of OH−, O2 and the intermediate Mn3+ ion, we propose a chemical oxidation mechanism for the catalytic oxygen reduction, in which oxygen reduction proceeds through chemical oxidation of the discharge product of MnO2 rather than through a direct two-electron reduction. The rate expression derived from this mechanism can very well explain the observed polarization properties and the concentration dependence of oxygen reduction.

Hierarchical carbon framework wrapped Na3V2(PO4)3 as a superior high-rate and extended lifespan cathode for sodium-ion batteries.

Hierarchical carbon framework wrapped Na3 V2 (PO4 )3 (HCF-NVP) is successfully synthesized through chemical vapor deposition on pure Na3 V2 (PO4 )3 particles. Electrochemical experiments show that the HCF-NVP electrode can deliver a large reversible capacity (115 mA h g(-1) at 0.2 C), superior high-rate rate capability (38 mA h g(-1) at 500 C), and ultra-long cycling stability (54% capacity retention after 20 000 cycles).

Mesoporous Amorphous FePO4 Nanospheres as High-Performance Cathode Material for Sodium-Ion Batteries

FePO4 nanospheres are synthesized successfully through a simple chemically induced precipitation method. The nanospheres present a mesoporous amorphous structure. Electrochemical experiments show that the FePO4/C electrode demonstrates a high initial discharging capacity of 151 mAh g(-1) at 20 mA g(-1), stable cyclablilty (94% capacity retention ratio over 160 cycles), as well as high rate capability (44 mAh g(-1) at 1000 mA g(-1)) for Na-ion storage. The superior electrochemical performance of the FePO4/C nanocomposite is due to its particular mesoporous amorphous structure and close contact with the carbon framework, which significantly improve the ionic and electronic transport and intercalation kinetics of Na ions.