Ji Hyun Um

3D macroporous electrode and high-performance in lithium-ion batteries using SnO2 coated on Cu foam.

A three-dimensional porous architecture makes an attractive electrode structure, as it has an intrinsic structural integrity and an ability to buffer stress in lithium-ion batteries caused by the large volume changes in high-capacity anode materials during cycling. Here we report the first demonstration of a SnO2-coated macroporous Cu foam anode by employing a facile and scalable combination of directional freeze-casting and sol-gel coating processes. The three-dimensional interconnected anode is composed of aligned microscale channels separated by SnO2-coated Cu walls and much finer micrometer pores, adding to surface area and providing space for volume expansion of SnO2 coating layer. With this anode, we achieve a high reversible capacity of 750 mAh g−1 at current rate of 0.5 C after 50 cycles and an excellent rate capability of 590 mAh g−1 at 2 C, which is close to the best performance of Sn-based nanoscale material so far.

3D interconnected SnO2-coated Cu foam as a high-performance anode for lithium-ion battery applications

A SnO2-coated Cu foam with 3D interconnected scaffold was fabricated by a simple sol–gel method for use as a self-supporting anode for lithium-ion batteries. The binder- and carbon-free electrode integrated with a current collector exhibits a high reversible capacity, excellent rate capability, and stable cycle retention by preserving its structural integrity.

Porous V2O5/RGO/CNT hierarchical architecture as a cathode material: Emphasis on the contribution of surface lithium storage

A three dimensional vanadium pentoxide/reduced graphene oxide/carbon nanotube (3D V2O5/RGO/CNT) composite is synthesized by microwave-assisted hydrothermal method. The combination of 2D RGO and 1D CNT establishes continuous 3D conductive network, and most notably, the 1D CNT is designed to form hierarchically porous structure by penetrating into V2O5 microsphere assembly constituted of numerous V2O5 nanoparticles. The highly porous V2O5 microsphere enhances electrolyte contact and shortens Li+ diffusion path as a consequence of its developed surface area and mesoporosity. The successive phase transformations of 3D V2O5/RGO/CNT from α-phase to ε-, δ-, γ-, and ω-phase and its structural reversibility upon Li+ intercalation/de-intercalation are investigated by in situ XRD analysis, and the electronic and local structure reversibility around vanadium atom in 3D V2O5/RGO/CNT is observed by in situ XANES analysis. The 3D V2O5/RGO/CNT achieves a high capacity of 220 mAh g−1 at 1 C after 80 cycles and an excellent rate capability of 100 mAh g−1 even at a considerably high rate of 20 C. The porous 3D V2O5/RGO/CNT structure not only provides facile Li+ diffusion into bulk but contributes to surface Li+ storage as well, which enables the design of 3D V2O5/RGO/CNT composite to become a promising cathode architecture for high performance LIBs.

Soft Template Strategy to Synthesize Iron Oxide–Titania Yolk–Shell Nanoparticles as High‐Performance Anode Materials for Lithium‐Ion Battery Applications

Yolk-shell-structured nanoparticles with iron oxide core, void, and a titania shell configuration are prepared by a simple soft template method and used as the anode material for lithium ion batteries. The iron oxide-titania yolk-shell nanoparticles (IO@void@TNPs) exhibit a higher and more stable capacity than simply mixed nanoparticles of iron oxide and hollow titania because of the unique structure obtained by the perfect separation between iron oxide nanoparticles, in combination with the adequate internal void space provided by stable titania shells. Moreover, the structural effect of IO@void@TNPs clearly demonstrates that the capacity retention value after 50 cycles is approximately 4 times that for IONPs under harsh operating conditions, that is, when the temperature is increased to 80 °C.

Anode Design Based on Microscale Porous Scaffolds for Advanced Lithium Ion Batteries

Considering the increasing demands for advanced power sources, present-day lithium-ion batteries (LIBs) must provide a higher energy and power density and better cycling stability than conventional LIBs. This study suggests a promising electrode design solution to this problem using Cu, Co, and Ti scaffolds with a microscale porous structure synthesized via freeze-casting. Co3O4 and TiO2 layers are uniformly formed on the Co and Ti scaffolds, respectively, through a simple thermal heat-treatment process, and a SnO2 layer is formed on the Cu scaffold through electroless plating and thermal oxidation. This paper characterizes and evaluates the physical and electrochemical properties of the proposed electrodes using scanning electron microscopy, four-point probe and coin-cell tests to confirm the feasibility of their potential use in LIBs.

SnO2 nanotube arrays embedded in a carbon layer for high-performance lithium-ion battery applications

A facile strategy for preparing one-dimensional (1D) SnO2 nanotube arrays embedded in a carbon layer (C–SnO2 NTs) has been developed via a sol–gel method using polycarbonate (PC) as a template. The introduction of a carbon layer (carbonized from a PC membrane) at the top of SnO2 nanotube arrays results in the SnO2 nanotubes standing on the current collector and preserving their 1D structure without aggregation between each other, which enables their direct application to the anode of lithium-ion batteries. The binder- and carbon-free C–SnO2 NTs as a self-supporting anode exhibits a stable and high reversible capacity of 500 mA h g−1 at 0.1 A g−1 after 40 cycles. The improved Li ion storage and stable capability are attributed to the 1D hollow structure, alleviating the large volume changes of SnO2 and enhancing electron and Li ion diffusion transport in the nanotubes.

From grass to battery anode: agricultural biomass hemp-derived carbon for lithium storage

Biomass-derived carbon, as a low-cost material source, is an attractive choice to prepare carbon materials, thus providing an alternative to by-product and waste management. Herein, we report the preparation of carbon from hemp stem as a biomass precursor through a simple, low-cost, and environment-friendly method with using steam as the activating agent. The hemp-derived carbon with a hierarchically porous structure and a partial graphitization in amorphous domains was developed, and for the first time, it was applied as an anode material for lithium-ion battery. Natural hemp itself delivers a reversible capacity of 190 mA h g−1 at a rate of 300 mA g−1 after 100 cycles. Ball-milling of hemp-derived carbon is further designed to control the physical properties, and consequently, the capacity of milled hemp increases to 300 mA h g−1 along with excellent rate capability of 210 mA h g−1 even at 1.5 A g−1. The milled hemp with increased graphitization and well-developed meso-porosity is advantageous for lithium diffusion, thus enhancing electrochemical performance via both diffusion-controlled intercalation/deintercalation and surface-limited adsorption/desorption. This study not only demonstrates the application of hemp-derived carbon in energy storage devices, but also guides a desirable structural design for lithium storage and transport.

Revisiting Solid Electrolyte Interphase on the Carbonaceous Electrodes Using Soft X-ray Absorption Spectroscopy

It is widely accepted that solid electrolyte interphase (SEI) layer of carbonaceous material is formed by irreversible decomposition reaction of an electrolyte, and acts as a passivation layer to prevent further decomposition of the electrolyte, ensuring reliable operation of a Li-ion battery. On the other hand, recent studies have reported that some transition metal oxide anode materials undergo reversible decomposition of an organic electrolyte during cycling, which is completely different from carbonaceous anode materials. In this work, we revisit the electrochemical reaction of an electrolyte that produces SEI layer on the surface of carbonaceous anode materials using soft X-ray absorption spectroscopy. We discover that the reversible formation and decomposition of SEI layer are also able to occur on the carbonaceous materials in both Li- and Na-ion battery systems. These new findings on the unexpected behavior of SEI in the carbonaceous anode materials revealed by soft X-ray absorption spectroscopy would be highly helpful in more comprehensive understanding of the interfacial chemistry of carbonaceous anode materials in Li- and Na-ion batteries.