Development and Application of Mesoporous Nanocomposite Materials Based on Crystalline Metal
Oxide Materials
Based on an original concept, the ETRI-AIST has succeeded in synthesizing crystalline-glass mesoporous nanocomposite TiO2-P2O5 (Fig. 1), consisting of a crystalline phase and an amorphous phase and based on crystalline metal oxide equipped with 3D regular-aligned nano-channel structures, by adding a trace amount of an organic metal compound, trimethyl phosphoric acid, PO(OC2H5)3 to the synthetic process of metal oxide through the conventional template method. Moreover, the CGMN materials based on multiple crystalline metal oxide afforded with electron conductivity (TiO2-P2O5-CuO and TiO2-P2O5-SnO2) have been successfully synthesized by doping conductive cupric oxide (CuO) and stannic oxide (SnO2) into the three dimensional glass network in the framework of CGMN, AIST Press Release, February 4, 2004.
The ETRI-AIST has demonstrated that using the CGMN materials based on crystalline metal oxide for the negative electrode of lithium rechargeable battery facilitates the transport of lithium ion (Li+) and electrolyte solution into the interior of electrode through the oriented nano-channel construction of 5 nm size, and the adsorption of lithium ion (Li+) on enormous surface area of nano-channels realizes the super-capacitor features, allowing to keep the energy density as high as the level of the conventional lithium rechargeable battery and to upgrade the power density by two orders of magnitude or more. Additionally, it has been confirmed that providing electron conductivity to the framework constituting TiO2-P2O5 nano-channels will effectively upgrade the discharge-recharge characteristics.
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Fig. 1 Transmission electron microgram of micro-crystalline TiO2-P2O5 nano-porous powder with 3D construction |
Battery Performance of Mesoporous Nanoconposite Material Based on Crystalline Metal Oxide
(TiO2-P2O5)
With the CGMN material based on crystalline metal oxide (TiO2-P2O5) used for the negative electrode of lithium rechargeable battery, the performance of the battery was evaluated. We only take TiO2 as active materials because both the specific capacities of pure AB and pure P2O5 are too small to be measured at a current density of 10A/g. Theoretically, the maximum capacity of anatase TiO2 is 165 mAh/g. It was demonstrated, however, that the new material could have much greater capacity than the theoretical maximum, for the constant current charge-discharge at 0.1 A/g current density, and could reach the capacity limit of reversible charge-discharge, 370 mAh/g (black line in Fig. 2). This data cannot be accounted for by the insertion/extraction process of lithium ion (Li+) into anatase TiO2, suggesting chemical adsorption and desorption of Li+ at the surface of nano-channels in the composite material (TiO2-P2O5). The mechanism of super-capacitor feature seems to be attributed to the chemical adsorption and desorption. The newly developed material is characterized by much higher energy density than that of the conventional anatase scheme, owing to simultaneous implementation of redox capacity and adsorption capacity.
In addition to drastic increase of the capacity (or energy density), the power density is also upgraded by two orders of magnitude or more. With the current density (or power density) for charge-discharge increased by two orders of magnitude from 0.1 A/g to 10 A/g, the charge-discharge capacity density (energy density) is kept as high as 270 mAh/g (red line in Fig. 2). The cycle performance, that is, durability for repeated charge-discharge operation cycles, is also improved significantly, keeping the capacity for charge-discharge with 10 A/g current density, 190 mAh/g after 200 cycles, and 160 mAh/g even after 800 cycles.
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Fig. 2 The 2nd cycle charge-discharge profiles of TiO2-P2O5 CGMN in the potential range from 1.0 V to 4.0 V (vs. Li+/Li) with current densities 0.1 A/g, 0.5 A/g, 2 A/g and 10 A/g on the basis of active TiO2. |
Battery Performance of Mesoporous Nanocomposite Materials Based on Multiple
Crystalline Metal Oxide (TiO2-P2O5-CuO and TiO2-P2O5-SnO2)
Furthermore, the battery performance of the CGMN materials based on multiple crystalline metal oxides (TiO2-P2O5-CuO and TiO2-P2O5-SnO2) doped with electron conductive functional substance CuO or SnO2 into the three dimensional glass P2O5 network in the framework of CGMN, was evaluated. It was confirmed that the high charge-discharge capacity density (or energy density) was maintained owing to the improved electron conductivity. For instance, with current density 20 A/g, the charge-discharge capacity density of TiO2-P2O5 was 60 mAh/g (green line in Fig. 3 bottom), and that of two composites with electron conduction path was: 190 mAh/g for TiO2-P2O5-CuO (blue line in Fig. 3 bottom), and 265 mAh/g for TiO2-P2O5-SnO2 (red line in Fig. 3 bottom). Even with still higher current density 50 A/g, the newly developed materials (TiO2-P2O5-SnO2) held as high capacity as 130 mAh/g (black line in Fig. 3 top).
When the CGMN material based on crystalline metal oxide is used as the negative electrode, and combined with 4V-class anode materials to build a practical battery, it may be claimed that the goal of EV storage device development has been achieved with this material, in consideration of weight of electrolyte solution and casing, in respect to both energy density and power density, as compared to other storage devices. The development goal has been set to increase by an order of magnitude or more in energy density (from 1 Wh/kg) and in power density (from 1 kW/kg), assuming that the electric double layer capacitor is applied to EV (Fig. 4).
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Fig. 3 The charge-discharge profiles of TiO2-P2O5 CGMN, TiO2-P2O5-SnO2 CGMN and TiO2-P2O5-CuO CGMN at 20A/g. The specific capacities 65mAh/g of TiO2-P2O5 CGMN at 20A/g is considerably improved to 195mAh/g and 270mAh/g for TiO2-P2O5-SnO2 and TiO2-P2O5-CuO, respectively. The inset shows that the specific capacities of TiO2-P2O5-SnO2 CGMN under current densities of 10A/g, 20A/g and 50A/g were 230mAh/g, 195mAh/g and 178mAh/g, respectively. |
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| Fig. 4 A Regone plot shows the position of the power and energy density of CGMN as energy storage devise comparing with EDLC, Capacitor, a traditional rechargeable lithium battery, and the PNGV target. |