著者
Quanyi LIU Qian ZHU Wentian ZHU Xiaoying YI
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.90, no.8, pp.087003, 2022-08-05 (Released:2022-08-05)
参考文献数
31
被引用文献数
1 5

With the improvement of lithium-ion batteries in civil aviation transportation, the thermal safety of lithium-ion batteries can not be ignored. Especially in a battery pack, the thermal runaway of batteries can spread from cell to cell, resulting in catastrophic hazards. This work focuses on the experimental setup and analysis of the experimental parameters of lithium-ion batteries with different thicknesses of aerogel felt to study the blocking effect of barrier materials on thermal runaway propagation of lithium-ion batteries in civil aviation transport. The aerogel felt was selected as the barrier material and a series of experiments were carried out with different thicknesses of 1 mm, 3 mm, and 6 mm. The results demonstrated that the increase of aerogel felt thickness exhibited excellent performance in delaying lithium-ion battery thermal runaway. Additionally, a simplified thermal model of thermal runaway propagation was proposed to explain the thermal runaway propagation in the battery to adjacent batteries. These results provide valuable suggestions and enlightenment for the aviation safety transportation of lithium-ion batteries.
著者
Quanyi LIU Qian ZHU Wentian ZHU Xiaoying YI Xu HAN
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.90, no.8, pp.087004, 2022-08-05 (Released:2022-08-05)
参考文献数
21
被引用文献数
1 5

To better understand the thermal runaway characteristics of lithium-ion batteries in civil aviation transportation environments, an experimental platform for the fire and explosion of lithium-ion batteries was designed and built. The 18650 NCM lithium-ion battery was selected as the test sample to study the influence of different initial pressures on the thermal runaway characteristics of the lithium-ion battery pack in a confined space. The results showed that, under 61 kPa, the initial thermal runaway triggering time is longer, the initial thermal runaway temperature is higher, and the explosion pressure and TNT equivalent are lower than that under 96 kPa. The mass loss increased with the increase of pressure and the number of batteries. In addition, the initial thermal runaway triggering time and temperature are affected by the number of batteries. These results could provide some support for civil aviation transportation safety.
著者
宮代 一 小林 陽 中村 龍哉 関 志朗 三田 裕一 宇佐美 章
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.74, no.4, pp.321-325, 2006-04-05 (Released:2012-03-20)
参考文献数
23
被引用文献数
2 4

Olivine structured LiFePO4 cathode is the promising cathode active material for lithium secondary batteries due to its low cost and quite excellent reversibility. On the other hand, lithium polymer secondary batteries (LPBs) have been studied for the purpose of large-scaled batteries (for example, electric power load leveling). In this study, we prepared LPBs using the LiFePO4 cathode. By measuring the charge-discharge properties and electrochemical impedance spectroscopy, basic properties were investigated compared with the LPBs using the 4V-class LiCoO2 cathode.
著者
嘉藤 徹
出版者
公益社団法人 電気化学会
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.75, no.3, pp.283-289, 2007-03-05 (Released:2012-03-20)
参考文献数
30
被引用文献数
1
著者
Igseon GU Takuya ISHIDA Tetsu TATSUMA
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.90, no.7, pp.077006, 2022-07-09 (Released:2022-07-09)
参考文献数
40
被引用文献数
2

Chiral plasmonic nanostructures attract much attention because of their potential applications to advanced optical materials and enantioselective sensors. However, the latter has been fabricated on the basis of top-down methods, which take time and cost. Here we developed a one-step method for preparation of chiral gold nanostructures immobilized on an electrode by a simple electrodeposition in the presence of L- or D-cysteine. Opposite circular dichroism (CD) spectra were obtained by using L- or D-cysteine, while achiral structures were deposited for racemic cysteine or in the absence of cysteine. The chirality was attributed to geometries of the nanostructures. Chiral gold nanostructures electrodeposited in the presence of L-cysteine gave higher CD signals to (S)-enantiomer than those to (R)-enantiomer of 1,2-propanediol, and vice versa. TiO2-coated electrodes were also used as a substrate for the electrodeposition of chiral nanostructures, so that the chiral plasmonic electrodes would be employed for optoelectronic and photoelectrochemical applications.
著者
Ryoichi TATARA Yukihiro OKAMOTO Yosuke UGATA Kazuhide UENO Masayoshi WATANABE Kaoru DOKKO
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.89, no.6, pp.590-596, 2021-11-05 (Released:2021-11-05)
参考文献数
43
被引用文献数
3

The performance of a sodium-ion (Na) battery is significantly influenced by its electrolyte characteristics. In particular, the transport properties of the electrolyte have considerable effects on the discharge rate capability. During discharging of a Na battery at high current densities, a concentration gradient of Na salt develops because both cations and anions are mobile in the liquid electrolyte. Concentration polarization can be suppressed by increasing the Na+ transference number (tNa+) of the electrolyte. This study demonstrates that highly concentrated NaN(SO2F)2 dissolved in 3-methylsulfolane (MSL) exhibits a high tNa+ value of >0.6 under anion-blocking conditions. Raman spectroscopy revealed that Na+ ions formed complexes with MSL and anions in the electrolyte. Na+ ions exchange ligands dynamically and move faster than the ligands, resulting in a high tNa+. The high tNa+ enables a high-rate discharge of the Na battery, despite the low ionic conductivity of the highly concentrated electrolyte.
著者
Hiroyuki UEDA Katsuhiko NISHIYAMA Soichiro YOSHIMOTO
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.86, no.5, pp.217-219, 2018-09-05 (Released:2018-09-05)
参考文献数
22
被引用文献数
5 8

The electrochemical behavior and specific adsorption of an ionic liquid, 1-butyl-3-methylimidazolium iodide, on a Au(111) electrode surface were investigated via voltammetric analyses, X-ray photoelectron spectroscopy (XPS), and scanning tunneling microscopy (STM). The electrochemical potential window and the reductive desorption of I adatoms were evaluated using voltammetric techniques. The XPS and STM results supported the specific adsorption of I adatoms on Au(111). Furthermore, high-resolution STM images revealed the formation of characteristic nanostructured rings consisting of imidazolium cations on I adatoms for the first time.
著者
Yuto NAKAMURA Yasushi SATO Naoki SHIDA Mahito ATOBE
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
pp.21-00053, (Released:2021-05-12)
参考文献数
27
被引用文献数
1

In this study, we report one step electrochemical trimerization of catechol to 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) for the first time. Electrochemical trimerization was demonstrated in a flow microreactor, which offers advantages for reaction screening owing to short reaction time and small reaction scale, as well as avoiding the further oxidation of HHTP. The use of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as a solvent was essential for the efficient production of HHTP. Computational simulation, pKa calculation, and electrochemical measurements gave some important insights into the mechanism of the electrochemical oxidation of catechol in HFIP.
著者
Kazunari MIYAZAKI Yidan DING Hiroki MUROYAMA Toshiaki MATSUI Koichi EGUCHI
出版者
The Electrochemical Society of Japan
雑誌
Electrochemistry (ISSN:13443542)
巻号頁・発行日
vol.88, no.1, pp.28-33, 2020-01-05 (Released:2020-01-05)
参考文献数
33
被引用文献数
1 9

In this study, the applicability of Ba(Ce,Co,Y)O3−δ (BCCY) for a cathode of proton-conducting ceramic fuel cells was investigated. The electrical conductivity and transference number of BCCY were significantly affected by a cobalt content in the oxide. It was found that this material showed a mixed conduction of proton, oxide ion, and electron. The addition of cobalt into Ba(Ce,Y)O3−δ mainly increased the electronic conductivity of materials. Composite electrodes with an optimum composition of La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF)–BaCe0.7Co0.2Y0.1O3−δ (50:50 wt.%) exhibited lower polarization for the symmetrical cell test with a BaCe0.8Y0.2O3−δ electrolyte in 6.5% humidified oxygen atmosphere, as compared with La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF) itself and LSCF–BaCe0.9Y0.1O3−δ (50:50 wt.%) composite electrodes. The power generation test was performed at 600°C–700°C using a BaCe0.8Y0.2O3−δ electrolyte-supported single cell employing a LSCF–BaCe0.7Co0.2Y0.1O3−δ (50:50 wt.%) composite cathode, upon feeding 3% humidified hydrogen and pure oxygen to the anode and cathode, respectively. The cell with a LSCF–BaCe0.7Co0.2Y0.1O3−δ (50:50 wt.%) composite cathode exhibited much higher performance than that with a LSCF electrode. Consequently, the introduction of cobalt into Ba(Ce,Y)O3−δ was an effective strategy for an improvement in an oxygen reduction reaction activity of a cathode material.