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Hong Le Tam

Bio: Hong Le Tam is an academic researcher from Nanyang Technological University. The author has contributed to research in topics: Lithium. The author has an hindex of 2, co-authored 2 publications receiving 374 citations.
Topics: Lithium

Papers
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Journal ArticleDOI
TL;DR: A stirring hydrothermal process that enables the formation of elongated bending TiO2 -based nanotubes is presented, which can cycle over 10 000 times in half cells while retaining a relatively high capacity.
Abstract: A stirring hydrothermal process that enables the formation of elongated bending TiO2 -based nanotubes is presented. By making use of its bending nature, the elongated TiO2 (B) nanotubular crosslinked-network anode electrode can cycle over 10 000 times in half cells while retaining a relatively high capacity (114 mA h g(-1)) at an ultra-high rate of 25 C (8.4 A g(-1)).

390 citations


Cited by
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Journal ArticleDOI
TL;DR: This tutorial review presents the state-of-the-art developments in ultrafast charging LIBs by the rational design of materials, and several aspects of the intrinsic materials, materials engineering and processing, and electrode materials architecture design towards maximizing both ionic and electronic conductivity in the electrode with a short diffusion length.
Abstract: Rechargeable lithium-ion batteries (LIBs) are important electrochemical energy storage devices for consumer electronics and emerging electrical/hybrid vehicles. However, one of the formidable challenges is to develop ultrafast charging LIBs with the rate capability at least one order of magnitude (>10 C) higher than that of the currently commercialized LIBs. This tutorial review presents the state-of-the-art developments in ultrafast charging LIBs by the rational design of materials. First of all, fundamental electrochemistry and related ionic/electronic conduction theories identify that the rate capability of LIBs is kinetically limited by the sluggish solid-state diffusion process in electrode materials. Then, several aspects of the intrinsic materials, materials engineering and processing, and electrode materials architecture design towards maximizing both ionic and electronic conductivity in the electrode with a short diffusion length are deliberated. Finally, the future trends and perspectives for the ultrafast rechargeable LIBs are discussed. Continuous rapid progress in this area is essential and urgent to endow LIBs with ultrafast charging capability to meet huge demands in the near future.

804 citations

Journal ArticleDOI
TL;DR: In this article, the crystal structure of 1D TiO2 and the latest development on the fabrication of 2D and 3D 1DTiO2 nanostructured materials are reviewed.
Abstract: One-dimensional TiO2 (1D TiO2) nanomaterials with unique structural and functional properties have been extensively used in various fields including photocatalytic degradation of pollutants, photocatalytic CO2 reduction into energy fuels, water splitting, solar cells, supercapacitors and lithium-ion batteries. In the past few decades, 1D TiO2 nanostructured materials with a well-controlled size and morphology have been designed and synthesized. Compared to 0D and 2D nanostructures, more attention has been paid to 1D TiO2 nanostructures due to their high aspect ratio, large specific surface area, and excellent electronic or ionic charge transport properties. In this review, we present the crystal structure of TiO2 and the latest development on the fabrication of 1D TiO2 nanostructured materials. Besides, we will look into some critical engineering strategies that give rise to the excellent properties of 1D TiO2 nanostructures such as improved enlargement of the surface area, light absorption and efficient separation of electrons/holes that benefit their potential applications. Moreover, their corresponding environmental and energy applications are described and discussed. With the fast development of the current economy and technology, more and more effort will be put into endowing TiO2-based materials with advanced functionalities and other promising applications.

757 citations

Journal ArticleDOI
Xunliang Cheng1, Jian Pan1, Yang Zhao1, Meng Liao1, Huisheng Peng1 
TL;DR: GPEs with enhanced physicochemical properties and specified functionalities for the application in electrochemical energy storage have attracted worldwide attentions as discussed by the authors, and they are preferred due to their higher safety and adaptability to the design of flexible energy storage devices.
Abstract: With the booming development of flexible and wearable electronics, their safety issues and operation stabilities have attracted worldwide attentions. Compared with traditional liquid electrolytes, gel polymer electrolytes (GPEs) are preferred due to their higher safety and adaptability to the design of flexible energy storage devices. This review summarizes the recent progress of GPEs with enhanced physicochemical properties and specified functionalities for the application in electrochemical energy storage. Functional GPEs that are capable to achieve unity lithium-ion transference number and offer additional pseudocapacitance to the overall capacitance are carefully discussed. The smart GPEs with self-protection, thermotolerant, and self-healing abilities are particularly highlighted. To close, the future directions and remaining challenges of the GPEs for application in electrochemical energy storages are summarized to provide clues for the following development.

607 citations

Journal ArticleDOI
TL;DR: This review presents an overview of porous 1D nanostructure research, from the synthesis by bottom-up and top-down approaches with rational and controllable structures, to several important electrochemical energy storage applications including lithium-ion batteries, sodium-ion lithium-sulfur batteries, lithium-oxygen batteries and supercapacitors.
Abstract: Electrochemical energy storage technology is of critical importance for portable electronics, transportation and large-scale energy storage systems. There is a growing demand for energy storage devices with high energy and high power densities, long-term stability, safety and low cost. To achieve these requirements, novel design structures and high performance electrode materials are needed. Porous 1D nanomaterials which combine the advantages of 1D nanoarchitectures and porous structures have had a significant impact in the field of electrochemical energy storage. This review presents an overview of porous 1D nanostructure research, from the synthesis by bottom-up and top-down approaches with rational and controllable structures, to several important electrochemical energy storage applications including lithium-ion batteries, sodium-ion batteries, lithium-sulfur batteries, lithium-oxygen batteries and supercapacitors. Highlights of porous 1D nanostructures are described throughout the review and directions for future research in the field are discussed at the end.

582 citations

Journal ArticleDOI
TL;DR: This paper developed a versatile route to synthesize hollow TiO2/graphitic carbon (H-TiO/GC) spheres with superior electrochemical performance with high electrochemical reactivity and stability as an anode material for lithium ion batteries.
Abstract: Rational design and controllable synthesis of TiO2 based materials with unique microstructure, high reactivity, and excellent electrochemical performance for lithium ion batteries are crucially desired. In this paper, we developed a versatile route to synthesize hollow TiO2/graphitic carbon (H-TiO2/GC) spheres with superior electrochemical performance. The as-prepared mesoporous H-TiO2/GC hollow spheres present a high specific surface area (298 m2 g–1), a high pore volume (0.31 cm3 g–1), a large pore size (∼5 nm), well-defined hollow structure (monodispersed size of 600 nm and inner diameter of ∼400 nm, shell thickness of 100 nm), and small nanocrystals of anatase TiO2 (∼8 nm) conformably encapsulated in ultrathin graphitic carbon layers. As a result, the H-TiO2/GC hollow spheres achieve excellent electrochemical reactivity and stability as an anode material for lithium ion batteries. A high specific capacity of 137 mAh g–1 can be achieved up to 1000 cycles at a current density of 1 A g–1 (5 C). We believ...

501 citations