JP6167127B2 - Electrode and electrochemical element - Google Patents
Electrode and electrochemical element Download PDFInfo
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
Description
本発明は、金属酸化物の製造方法、電極、及び電気化学素子に関する。 The present invention relates to a method for producing a metal oxide, an electrode, and an electrochemical element.
従来より、加水分解反応、酸化反応、重合反応、縮合反応等、液相反応において金属酸化物、金属水酸化物などの不溶性生成物を生成する反応方法が知られているが、このような反応方法としては、ゾル−ゲル法が代表的である。しかしながら、このゾル−ゲル法は金属塩の加水分解反応、重縮合反応等によるものであり反応速度は遅く、均一な生成物を得ることができない。その問題点を解決する方法として、触媒を用いて反応を促進する方法が知られている。このほか、反応性のよい反応物を用いたり（特許文献１）、撹拌方法を改善した例（特許文献２）がある。
さらに、このような液相反応によって生成される水酸化金属水和物が電気エネルギー貯蔵素子として用いられる試みがある（特許文献３）
Conventionally, there are known reaction methods for producing insoluble products such as metal oxides and metal hydroxides in liquid phase reactions such as hydrolysis reactions, oxidation reactions, polymerization reactions and condensation reactions. As a method, a sol-gel method is representative. However, this sol-gel method is based on a hydrolysis reaction, polycondensation reaction, etc. of a metal salt, and the reaction rate is slow, so that a uniform product cannot be obtained. As a method for solving the problem, a method of promoting a reaction using a catalyst is known. In addition, there are examples in which reactants having good reactivity are used (Patent Document 1) and the stirring method is improved (Patent Document 2).
Furthermore, there is an attempt to use a metal hydroxide hydrate produced by such a liquid phase reaction as an electric energy storage element (Patent Document 3).
しかしながら、このような方法によっても反応を促進することができず、結果として均一な生成物を得ることができないという問題点があった。また、電気エネルギー貯蔵素子として好適なナノ粒子とすることができないという問題点があった。そこで、本発明は、従来にない液相反応において反応を促進する方法を用いて作成した金属酸化物ナノ粒子を高分散担持したカーボン、このカーボンを含有する電極材料、この電極材料を用いた電極及び電気化学素子を提供することを目的とする。 However, there is a problem that the reaction cannot be promoted even by such a method, and as a result, a uniform product cannot be obtained. Moreover, there existed a problem that it could not be set as a suitable nanoparticle as an electrical energy storage element. Accordingly, the present invention provides a carbon in which metal oxide nanoparticles prepared using a method for promoting a reaction in an unprecedented liquid phase reaction are highly dispersed and supported, an electrode material containing the carbon, and an electrode using the electrode material And it aims at providing an electrochemical element.
本発明の金属酸化物ナノ粒子を担持したカーボン材料、このカーボン材料を含有する電極、及びこの電極を用いた電気化学素子を作製するための反応方法は、化学反応の過程で、旋回する反応器内で反応物にずり応力と遠心力を加えて化学反応を促進することを特徴としている。この反応方法においては、反応物にずり応力と遠心力の双方の機械的エネルギーが同時に加えられることによって、このエネルギーが化学エネルギーに転化することによるものと思われるが、従来にない速度で化学反応を促進させることができる。 A carbon material carrying metal oxide nanoparticles of the present invention, an electrode containing the carbon material, and a reaction method for producing an electrochemical device using the electrode are a reactor that swirls in the course of a chemical reaction. It is characterized in that a chemical reaction is promoted by applying shear stress and centrifugal force to the reactant. In this reaction method, mechanical energy of both shear stress and centrifugal force is applied to the reactant at the same time, which seems to be due to the conversion of this energy into chemical energy. Can be promoted.
さらに、この反応は、旋回する反応器内で反応物を含む薄膜を生成し、この薄膜にずり応力と遠心力を加えることによって、薄膜内の反応物に大きなずり応力と遠心力が加わり、さらに化学反応を促進することができる。 In addition, this reaction produces a thin film containing the reactants in a swirling reactor, and by applying shear stress and centrifugal force to the thin film, large shear stress and centrifugal force are applied to the reactants in the thin film. Can promote chemical reactions.
そして、このような化学反応を促進させるには、外筒と内筒の同心円筒からなり、内筒の側面に貫通孔を備えるとともに、外筒の開口部にせき板を配置してなる反応器において、内筒の旋回による遠心力によって内筒内の反応物を内筒の貫通孔を通じて外筒の内壁面に移動させ、外筒の内壁面に反応物を含む薄膜を生成するとともに、この薄膜にずり応力と遠心力を加えることによって実現することができる。 And in order to promote such a chemical reaction, the reactor which consists of a concentric cylinder of an outer cylinder and an inner cylinder, is equipped with a through-hole in the side surface of an inner cylinder, and arrange | positions a dam plate at the opening part of an outer cylinder In this, the reactant in the inner cylinder is moved to the inner wall surface of the outer cylinder through the through-hole of the inner cylinder by centrifugal force due to the turning of the inner cylinder, and a thin film containing the reactant is generated on the inner wall surface of the outer cylinder. This can be realized by applying shear stress and centrifugal force.
ここで、薄膜の厚みを５ｍｍ以下とすることによって、この反応方法の効果を高めることができる。この場合、反応器の内筒内の反応物に加えられる遠心力を１５００Ｎ（ｋｇｍｓ-2）以上とすることによって、本発明の反応方法の効果を高めることができる。また、この化学反応は金属塩の加水分解反応または縮合反応に用いることができる。以上の化学反応によって、金属酸化物ナノ粒子を形成することができる。 Here, the effect of this reaction method can be enhanced by setting the thickness of the thin film to 5 mm or less. In this case, the effect of the reaction method of the present invention can be enhanced by setting the centrifugal force applied to the reactant in the inner cylinder of the reactor to 1500 N (kgms-2) or more. Moreover, this chemical reaction can be used for the hydrolysis reaction or condensation reaction of a metal salt. Metal oxide nanoparticles can be formed by the above chemical reaction.
本発明のカーボンは、化学反応の過程で、旋回する反応器内で反応物にずり応力と遠心力を加えて生成した金属酸化物ナノ粒子と、旋回する反応器内でずり応力と遠心力を加えて分散したカーボン材料とからなり、金属酸化物ナノ粒子を高分散担持させたカーボンであることを特徴としている。このような金属酸化物ナノ粒子を高分散担持させたカーボンは、金属酸化物ナノ粒子の生成とともにこの金属酸化物ナノ粒子とカーボン材料が均一分散され、反応終了とともにカーボン材料の表面に金属酸化物ナノ粒子を高分散担持させた状態となって形成される。このカーボンは前述した反応方法によって、反応物とカーボン材料を混合した状態で、反応させると同時に分散させることによって作成することができる。 The carbon of the present invention is produced by applying shear stress and centrifugal force to a reactant in a swirling reactor in the course of a chemical reaction, and generating shear stress and centrifugal force in the swirling reactor. In addition, the carbon material is characterized by being composed of a dispersed carbon material and having a highly dispersed support of metal oxide nanoparticles. The carbon in which such metal oxide nanoparticles are supported in a highly dispersed state is uniformly dispersed as the metal oxide nanoparticles are generated and the metal oxide nanoparticles and the carbon material are dispersed. Nanoparticles are formed in a highly dispersed state. This carbon can be produced by the reaction method described above and by reacting and dispersing in the mixed state of the reactant and the carbon material.
このカーボンは電気化学素子用電極材料として用いることができる。この電極はナノ化しているため、比表面積が格段に拡大しているので、リチウムイオンの貯蔵電極として用いた場合には出力特性が向上し、プロトンの貯蔵電極として用いた場合には容量特性が向上する。したがって、この電極を用いることによって、高出力、高容量特性を有する電気化学素子を得ることができる。 This carbon can be used as an electrode material for electrochemical devices. Since this electrode is nano-sized, the specific surface area is greatly expanded, so that the output characteristics are improved when used as a lithium ion storage electrode, and the capacity characteristics when used as a proton storage electrode. improves. Therefore, by using this electrode, an electrochemical element having high output and high capacity characteristics can be obtained.
以上のように、前記の化学反応方法は、ずり応力と遠心力の双方が同時に反応物に加えられることによって、この機械的エネルギーが反応に必要な化学エネルギーに転化することによるものと思われるが、従来にない速度で化学反応が進行する。この方法を金属塩の加水分解、縮合反応に適用することによって、反応が瞬時に進行して本発明でカーボン材料に担持させる金属酸化物ナノ粒子を生成することができる。 As described above, the chemical reaction method seems to be due to the fact that both mechanical stress and centrifugal force are simultaneously applied to the reaction material, whereby this mechanical energy is converted into chemical energy necessary for the reaction. The chemical reaction proceeds at an unprecedented rate. By applying this method to the hydrolysis and condensation reactions of metal salts, the reaction can proceed instantaneously to produce metal oxide nanoparticles supported on the carbon material in the present invention.
さらに、この化学反応過程で、反応物にカーボン材料を添加することにすることによって、金属酸化物ナノ粒子を高分散担持させたカーボンを得ることができ、このカーボンを電極として用いることによって、高出力、高容量特性を有する電気化学素子を実現すことができる。 In addition, by adding a carbon material to the reactant in the chemical reaction process, it is possible to obtain carbon in which metal oxide nanoparticles are supported in a highly dispersed state. An electrochemical element having output and high capacity characteristics can be realized.
以下に本発明の金属酸化物ナノ粒子を担持したカーボンを製造するための化学反応方法について、さらに詳細に説明する。
この化学反応方法は、例えば図１に示すような反応器を用いて行うことができる。図１に示すように、反応器は開口部にせき板１−２を有する外筒１と貫通孔２−１を有し旋回する内筒２からなる。この反応器の内筒内部に反応物を投入し、内筒を旋回することによってその遠心力で内筒内部の反応物が内筒の貫通孔を通って外筒の内壁１−３に移動する。この時反応物は内筒の遠心力によって外筒の内壁に衝突し、薄膜状となって内壁の上部へずり上がる。この状態では反応物には内壁との間のずり応力と内筒からの遠心力の双方が同時に加わり、薄膜状の反応物に大きな機械的エネルギーが加わることになる。この機械的なエネルギーが反応に必要な化学エネルギー、いわゆる活性化エネルギーに転化するものと思われるが、短時間で反応が進行する。
The chemical reaction method for producing carbon carrying the metal oxide nanoparticles of the present invention will be described in more detail below.
This chemical reaction method can be performed, for example, using a reactor as shown in FIG. As shown in FIG. 1, the reactor includes an outer cylinder 1 having a cough plate 1-2 at an opening and an inner cylinder 2 having a through hole 2-1 and swirling. By putting the reactant into the inner cylinder of the reactor and turning the inner cylinder, the reactant inside the inner cylinder moves to the inner wall 1-3 of the outer cylinder through the through hole of the inner cylinder by the centrifugal force. . At this time, the reaction product collides with the inner wall of the outer cylinder by the centrifugal force of the inner cylinder, and forms a thin film and slides up to the upper part of the inner wall. In this state, both the shear stress between the inner wall and the centrifugal force from the inner cylinder are simultaneously applied to the reactant, and a large mechanical energy is applied to the thin-film reactant. This mechanical energy seems to be converted into chemical energy required for the reaction, so-called activation energy, but the reaction proceeds in a short time.
この反応において、薄膜状であると反応物に加えられる機械的エネルギーは大きなものとなるため、薄膜の厚みは５ｍｍ以下、好ましくは２．５ｍｍ以下、さらに好ましくは１．０ｍｍ以下である。なお、薄膜の厚みはせき板の幅、反応液の量によって設定することができる。 In this reaction, since the mechanical energy applied to the reaction product is large when it is in the form of a thin film, the thickness of the thin film is 5 mm or less, preferably 2.5 mm or less, more preferably 1.0 mm or less. The thickness of the thin film can be set according to the width of the dam plate and the amount of the reaction solution.
この反応方法は反応物に加えられるずり応力と遠心力の機械的エネルギーによって実現できるものと考えられるが、このずり応力と遠心力は内筒内の反応物に加えられる遠心力によって生じる。したがって、本発明に必要な内筒内の反応物に加えられる遠心力は１５００Ｎ（ｋｇｍｓ-2）以上、好ましくは７００００Ｎ（ｋｇｍｓ-2）以上、さらに好ましくは２７００００Ｎ（ｋｇｍｓ-2）以上である。 This reaction method is considered to be realized by the mechanical energy of the shear stress and the centrifugal force applied to the reactant, but the shear stress and the centrifugal force are generated by the centrifugal force applied to the reactant in the inner cylinder. Thus, the centrifugal force applied to the reactants in the inner cylinder necessary for the present invention is 1500 N (kgms -2) or more, preferably 70000N (kgms -2) or more, more preferably 270000N (kgms -2) or more.
以上の本発明の反応方法は液相反応であれば、加水分解反応、酸化反応、重合反応、縮合反応等様々な反応に適用することができる。 As long as the reaction method of the present invention is a liquid phase reaction, it can be applied to various reactions such as a hydrolysis reaction, an oxidation reaction, a polymerization reaction, and a condensation reaction.
なかでも、従来ゾル−ゲル法で行われていた金属塩の加水分解反応、縮合反応よる金属酸化物の生成に適用することによって、均一な金属酸化物ナノ粒子を形成することができる。 Among these, uniform metal oxide nanoparticles can be formed by applying to the metal salt hydrolysis reaction and condensation reaction conventionally performed by the sol-gel method.
金属酸化物の金属としては、Li, Al, Si, P, B, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Nb, Mo, Ru, Pb, Ag, Cd, In, Sn, Sb, W, Ce等を挙げることができる。酸化物としては、例えばMxOz、AxMyOz、Mx(DO4)y、AxMy(DO4)z（M:金属元素 A：アルカリ金属又はランタノイド元素 D: Be, B, Si, P, Ge等 ）で表される酸化物であり、これらの固溶体とすることもできる。 Metal oxides include Li, Al, Si, P, B, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Nb, Mo, Ru, Pb, Ag, Cd, In, Sn, Sb, W, Ce, etc. can be mentioned. Examples of oxide M x O z, A x M y O z, M x (DO 4) y, A x M y (DO 4) z (M: metal element A: alkali metal or a lanthanoid element D: Be , B, Si, P, Ge, etc.), and these solid solutions can also be used.
以上の金属酸化物ナノ粒子は電気化学素子用電極に好適な活物質として作用する。すなわち、ナノ粒子化することによって比表面積が格段に拡大して、出力特性、容量特性が向上する。 The above metal oxide nanoparticles act as an active material suitable for an electrode for an electrochemical device. That is, by making nanoparticles, the specific surface area is greatly expanded, and the output characteristics and capacity characteristics are improved.
さらに、このような金属塩の加水分解反応、縮合反応よる金属酸化物の生成反応において、反応過程でカーボン材料を加えることによって、金属酸化物ナノ粒子を高分散担持させたカーボンを得ることができる。すなわち、図１の反応器の内筒の内部に金属塩とカーボン材料を投入して、内筒を旋回して金属塩とカーボン材料を混合、分散する。さらに内筒を旋回させながら水酸化ナトリウムなどの触媒を投入して加水分解、縮合反応を進行させ、金属酸化物を生成するとともに、この金属酸化物とカーボン材料を分散状態で、混合する。反応終了とともに、金属酸化物ナノ粒子を高分散担持させたカーボンを形成することができる。 Furthermore, in such a metal salt hydrolysis reaction and metal oxide formation reaction by a condensation reaction, by adding a carbon material during the reaction process, carbon in which metal oxide nanoparticles are supported in a highly dispersed state can be obtained. . That is, the metal salt and the carbon material are put into the inner cylinder of the reactor shown in FIG. 1, and the inner cylinder is turned to mix and disperse the metal salt and the carbon material. Furthermore, while rotating the inner cylinder, a catalyst such as sodium hydroxide is added to cause hydrolysis and condensation reactions to proceed to produce a metal oxide, and the metal oxide and the carbon material are mixed in a dispersed state. Along with the completion of the reaction, carbon in which metal oxide nanoparticles are supported in a highly dispersed state can be formed.
ここで用いるカーボン材料としては、ケッチェンブラック、アセチレンブラック等のカーボンブラック、カーボンナノチューブ、カーボンナノホーン、無定形炭素、炭素繊維、天然黒鉛、人造黒鉛、活性炭、メソポーラス炭素等を挙げることができ、これらの複合材を用いることもできる。 Examples of the carbon material used here include carbon black such as ketjen black, acetylene black, carbon nanotube, carbon nanohorn, amorphous carbon, carbon fiber, natural graphite, artificial graphite, activated carbon, mesoporous carbon, etc. These composite materials can also be used.
以上の金属酸化物ナノ粒子を高分散担持させたカーボンは場合によっては焼成して、バインダーと混錬、成型し、電気化学素子の電極、すなわち電気エネルギー貯蔵用電極とすることができるが、この電極は高出力特性、高容量特性を示す。 The carbon in which the above metal oxide nanoparticles are supported in a highly dispersed state may be calcined in some cases, kneaded with a binder, and molded to form an electrode for an electrochemical element, that is, an electrode for storing electrical energy. The electrode exhibits high output characteristics and high capacity characteristics.
ここで、この電極を用いることができる電気化学素子は、リチウムイオンを含有する電解液を用いる電気化学キャパシタ、電池、水系の電解液を用いる電気化学キャパシタ、電池である。すなわち、本発明の電極は、リチウムイオン、プロトンのレドックス反応を行うことができる。さらに金属種および酸化還元電位の異なる対極の選択によって、負極、正極として作動する。したがって、リチウムイオンを含有する電解液または水系の電解液を用い、対極として活性炭、リチウムがレドックス反応するカーボン、プロトンがレドックス反応する高分子、さらにはリチウムまたはプロトンがレドックス反応する金属酸化物を用いることによって、電気化学キャパシタ、電池を構成することができる。 Here, the electrochemical element which can use this electrode is an electrochemical capacitor using an electrolyte containing lithium ions, a battery, an electrochemical capacitor using an aqueous electrolyte, and a battery. That is, the electrode of the present invention can perform a redox reaction of lithium ions and protons. Furthermore, it operates as a negative electrode and a positive electrode by selecting a counter electrode with different metal species and redox potential. Therefore, an electrolytic solution containing lithium ions or an aqueous electrolytic solution is used, and activated carbon, carbon in which lithium is redox-reacted, polymer in which proton is redox-reactive, and metal oxide in which lithium or proton is redox-reactive are used as a counter electrode. Thus, an electrochemical capacitor and a battery can be configured.
以下に実施例により本発明をさらに具体的に説明する。 The present invention will be described more specifically with reference to the following examples.
（実施例１）
旋回反応器の中に40mlのイソプロピルアルコール、1.25ｇのチタンテトラブトキシド、1gのケッチェンブラック（ケッチェン・ブラック・インターナショナル社製、商品名：ケッチェンブラックＥＣ６００ＪＤ、空隙率７８Ｖｏｌ．％、一次粒子径４０ｎｍ、平均二次粒径３３７．８ｎｍ）を加え、反応器の中でこれらを撹拌した。さらに、1gの水を添加して、６６,０００Ｎ（ｋｇｍｓ-2）の遠心力で１０分間、内筒を旋回して外筒の内壁に反応物の薄膜を形成するとともに、反応物にずり応力と遠心力を加えて化学反応を促進させ、酸化チタニウムナノ粒子を高分散担持させたケッチェンブラックを得た。
Example 1
In a swirl reactor, 40 ml of isopropyl alcohol, 1.25 g of titanium tetrabutoxide, 1 g of ketjen black (manufactured by ketjen black international, trade name: ketjen black EC600JD, porosity 78 Vol.%, Primary particle size 40 nm , Average secondary particle size 337.8 nm) was added and they were stirred in the reactor. Furthermore, 1 g of water was added and the inner cylinder was swirled for 10 minutes with a centrifugal force of 66,000 N (kgms −2 ) to form a thin film of the reactant on the inner wall of the outer cylinder, and shear stress on the reactant The chemical reaction was promoted by applying a centrifugal force to obtain ketjen black carrying titanium oxide nanoparticles in a highly dispersed manner.
得られた酸化チタニウムナノ粒子を高分散担持させたケッチェンブラックをフィルターフォルダーに通してろ過し、１００℃で６時間乾燥することにより、酸化チタニウムのナノ粒子がケッチェンブラックの内表面に高分散担持している構造体を得た。図２にこの構造体のＴＥＭ像を示す。図２においては、一次粒子径１〜１０ｎｍの酸化チタニウムナノ粒子がケッチェンブラックに高分散担持していることが分かる。 The obtained Ketjen black carrying highly dispersed titanium oxide nanoparticles is filtered through a filter folder and dried at 100 ° C. for 6 hours, so that the titanium oxide nanoparticles are highly dispersed on the inner surface of the Ketjen black. A supported structure was obtained. FIG. 2 shows a TEM image of this structure. In FIG. 2, it can be seen that titanium oxide nanoparticles having a primary particle diameter of 1 to 10 nm are highly dispersed and supported on ketjen black.
（実施例２）
ケッチェンブラックに変えて、１ｇのカーボンナノチューブ（株式会社ジェムコ製）を用いて、実施例１と同様にして、酸化チタニウムナノ粒子を高分散担持させたカーボンナノチューブを得た。酸化チタニウムナノ粒子の一次粒子径は１〜１０ｎｍであった。
(Example 2)
Instead of ketjen black, 1 g of carbon nanotubes (manufactured by Gemco Co., Ltd.) was used to obtain carbon nanotubes in which titanium oxide nanoparticles were supported in a highly dispersed manner in the same manner as in Example 1. The primary particle diameter of the titanium oxide nanoparticles was 1 to 10 nm.
（実施例３）
イソプロピルアルコール、チタンテトラブトキシド、ケッチェンブラックに変えて、40mlの水、1.965ｇの塩化ルテニウム、1ｇのカーボンナノチューブ（株式会社ジェムコ製）を用いて、実施例１と同様にして、酸化ルテニウムナノ粒子を高分散担持させたカーボンナノチューブを得た。図３にこの構造体のＴＥＭ像を示す。図３においては、一次粒子径１〜１０ｎｍの酸化ルテニウムナノ粒子がケッチェンブラックに高分散担持していることが分かる。
(Example 3)
Instead of isopropyl alcohol, titanium tetrabutoxide, and ketjen black, 40 ml of water, 1.965 g of ruthenium chloride, and 1 g of carbon nanotubes (manufactured by Gemco) were used in the same manner as in Example 1 to obtain ruthenium oxide nanoparticles. A carbon nanotube carrying highly dispersed particles was obtained. FIG. 3 shows a TEM image of this structure. In FIG. 3, it can be seen that ruthenium oxide nanoparticles having a primary particle diameter of 1 to 10 nm are highly dispersed and supported on ketjen black.
（比較例）
従来のゾル−ゲル法によって、すなわち本発明の化学反応を行わず、実施例１と同様にして、酸化チタニウム粒子が担持したケッチェンブラックを得た。酸化チタニウム粒子の一次粒子径は１０〜５０ｎｍであった。
(Comparative example)
A ketjen black carrying titanium oxide particles was obtained by a conventional sol-gel method, that is, without carrying out the chemical reaction of the present invention and in the same manner as in Example 1. The primary particle diameter of the titanium oxide particles was 10 to 50 nm.
以上の結果から、比較例では１０〜５０ｎｍにまで粒子成長して反応が終了しているが、実施例は１〜１０ｎｍ粒子成長した時点で反応が終了しており、本発明の反応方法によって従来にない液相反応の促進が実現されていることが明らかである。 From the above results, in the comparative example, the particles were grown to 10 to 50 nm and the reaction was completed. However, in the examples, the reaction was completed when the particles were grown to 1 to 10 nm, and the reaction method of the present invention was conventionally used. It is clear that the acceleration of the liquid phase reaction that is not present is realized.
実施例１、２、比較例で得られたサンプルについて400℃窒素雰囲気で12時間熱処理を行なった。熱処理したサンプルはバインダーと混合した後成形し、SUSメッシュに圧着することによって電極とした。この電極を真空乾燥した後、対極には金属リチウムを用い、電解液には1MLiPF6/EC-DEC(1:1vol%)を用いてセルを作製し、充放電挙動及びレート特性を調べた。結果を図４及び図５に示す。 The samples obtained in Examples 1 and 2 and Comparative Example were heat-treated in a nitrogen atmosphere at 400 ° C. for 12 hours. The heat-treated sample was mixed with a binder, molded, and pressed onto a SUS mesh to form an electrode. After this electrode was vacuum dried, a cell was fabricated using metallic lithium as the counter electrode and 1MLiPF6 / EC-DEC (1: 1 vol%) as the electrolyte, and the charge / discharge behavior and rate characteristics were examined. The results are shown in FIGS.
図４から、実施例１、実施例２の電極は、1.75〜2.0Ｖ付近にプラトーを持つ。これはTi(III)からTi(IV)の酸化還元に対応しており、この電極が電気化学素子用エネルギー貯蔵酸化物複合電極として作動できることを示している。 From FIG. 4, the electrodes of Examples 1 and 2 have a plateau in the vicinity of 1.75 to 2.0V. This corresponds to the oxidation-reduction of Ti (III) to Ti (IV), indicating that this electrode can operate as an energy storage oxide composite electrode for electrochemical devices.
図５から、実施例１、実施例２の電極は、比較例１と比べ高い電流においても高い容量保持率を示しており、高出力電気化学素子用電極として有効である。 From FIG. 5, the electrodes of Example 1 and Example 2 show a high capacity retention even at a higher current than that of Comparative Example 1, and are effective as electrodes for high-power electrochemical devices.
１…外筒
１−２…せき板
１−３…内壁
２…内筒
２−１…貫通孔
DESCRIPTION OF SYMBOLS 1 ... Outer cylinder 1-2 ... Baffle 1-3 ... Inner wall 2 ... Inner cylinder 2-1 ... Through-hole
Claims (2)
内部に空隙部を有する、ケッチェンブラック、カーボンナノチューブ、カーボンナノホーン、活性炭、メソポーラス炭素またはこれら２種以上の複合材のいずれかのカーボンと、
を有し、
前記金属酸化物が前記カーボンの内表面に担持されていることを特徴とする電極。 M x O z , A x M y O z , M x (DO 4 ) y , or A x M y (DO 4 ) z (where M: metal element (excluding ruthenium), A: alkali metal or lanthanoid element D: Be, B, Si, P, or Ge), and a metal oxide having a primary particle diameter of 1 to 10 nm ,
Ketjen black, carbon nanotubes, carbon nanohorns, activated carbon, mesoporous carbon, or any of these two or more composite materials having voids inside,
Have
An electrode, wherein the metal oxide is supported on the inner surface of the carbon .
An electrochemical device using the electrode according to claim 1.
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| JP3601124B2 (en) * | 1995-09-22 | 2004-12-15 | 株式会社デンソー | A positive electrode active material of a secondary battery using a non-aqueous solution, and a positive electrode. |
| JP4297533B2 (en) * | 1998-10-13 | 2009-07-15 | ホソカワミクロン株式会社 | Method for producing lithium ion battery material |
| JP4923372B2 (en) * | 2001-09-25 | 2012-04-25 | セイコーエプソン株式会社 | Method for producing spherical oxide particles |
| JP2005129507A (en) * | 2003-10-02 | 2005-05-19 | Jfe Chemical Corp | Graphitic powder for fuel cell separator, and fuel cell separator |
| JP2005174655A (en) * | 2003-12-09 | 2005-06-30 | Toyota Motor Corp | Lithium battery |
| JP2005169315A (en) * | 2003-12-12 | 2005-06-30 | Hosokawa Funtai Gijutsu Kenkyusho:Kk | Method of producing compound powder |
| US7468224B2 (en) * | 2004-03-16 | 2008-12-23 | Toyota Motor Engineering & Manufacturing North America, Inc. | Battery having improved positive electrode and method of manufacturing the same |
| JP4765077B2 (en) * | 2004-06-11 | 2011-09-07 | 国立大学法人東京農工大学 | Ruthenium oxide encapsulated nanocarbon composite structure |
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