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Adv. Mater. 2010, XX, 1¨C5

ÎÄÕÂÌâÄ¿£ºLithium Iron Borates as High-Capacity Battery Electrodes

×÷ÕߣºAtsuo Yamada , * Nobuyuki Iwane , Yu Harada , Shin-ichi Nishimura , Yukinori Koyama , and Isao Tanaka £¨À´×Ô¶«¾©´óѧ£¬ ¶«¾©¹¤Òµ´óѧ£¬¾©¶¼´óѧ£©

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ÅðËáÌúï®Ïà±ÈÁ×ËáÌú﮵ÄÓÅÊÆÔÚÓÚ£º ¸ü¸ßµÄ±ÈÈÝÁ¿£¨~220mAh/g£©£¬ ¸üºÃµÄµ¼µçÐÔ£¨µçµ¼ÂÊ~3.9¡Á10^{− 7} S/cm£©£¬ ¼«Ð¡µÄÌå»ý±ä»¯ÂÊ£¨~2%£©¡£

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Highly reversible and large capacity ( > 190 mAh/g) charge-discharge reaction of Li x FeBO 3 with negligible volume change. (a) Charge-discharge curves of Li x FeBO 3 up to 20 cycles measured at room temperature under C/20 rate. Upon charging, voltage was kept at 4.5 V until the current decays down to the value  corresponding to 1 mA/g. (b) Discharge capacity under various current densities. Inset shows excellent cycle life. (c) Shift of the diffraction peak upon lithium extraction. (d) Overall change in lattice dimensions as a function of lithium content x , in Li x FeBO 3 . (e) Very small volume change in Li x FeBO 3 of ca. − 2% (0.15 < x < 1) as compared with those of other typical intercalation compounds, Li x FePO 4 (0 < x < 1, − 6.5%), Li x MnPO4 (0 < x < 1, − 10%), Li x Mn 2 O 4 (0 < x < 1.0, − 7.3%) and Li x CoO 2 (0.5 < x < 1, + 1.9%)

ÎÄÕÂÖÐÖÆ±¸µÃµ½µÄµç³Ø±ÈÈÝÁ¿Îª190mAh/g£¬ ³äµç/·ÅµçЧÂÊ´ïµ½ÁË98%£¬ ²Ù×÷µçѹΪ3V£¬ÁíÍâÖµµÃ×¢ÒâµÄÊÇ£¬ ÕâÒ»µç³ØÔÚ2C·Åµç20´ÎÒÔºó£¬ ÈÝÁ¿»¹Äܱ£³Ö75%ÒÔÉÏ£¨ÓÐЩµÍ£¬µ«ÊÇÕâÒ»²ÄÁÏ»¹´¦ÓÚʵÑé½×¶Î£¬Ç±Á¦»¹ÊǺܴóµÄ£©¡£

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µç³ØµÄ¹¹ÔìΪ£ºA 2032-type coin cell was fabricated using lithium metal as an anode, 1 M solution of LiPF6 in 3:7 EC/DEC as an electrolyte, and polypropylene film as a separator.

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×îºó£¬Í¨¹ý¼õС²ÄÁÏ¿ÅÁ£´óСÒÔ¼°ÐγÉ̼»¯ÎïµÈ·½·¨µÄÓÅ»¯£¬ ÔÚ2C¸ßËÙÂʷŵçÏ£¬²ÉÓÃÅðËáï®×÷ΪÒõ¼«»îÐÔ²ÄÁÏµÄµç³ØÈÝÁ¿»¹Äܱ£³Ö80%£¬ ÇÒÑ­»·ÖÐÔì³ÉµÄÈÝÁ¿Ëðʧ¼¸ºõ¿ÉÒÔºöÂÔ¡£¶øÇÒͨ¹ýÀíÂÛ¼ÆËã¿ÉÒÔ·¢ÏÖ£¬ ʵÏÖ220mAh/gµÄÀíÂÛ±ÈÈÝÁ¿£¬ ÊÇûÓÐÈÈÁ¦Ñ§ÏÞÖÆµÄ¡£

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Electrochemical Tests : A 2032 type coin cell was used for the chargedischarging test with a TOSCAT-3100 battery tester (Toyo System) at 25 ¡ã C. For an open circuit voltage measurement, the cell was discharged galvanostatically at C/20 rate at 25 ¡ã C under an anodic current rate of 150 ¦Ì A for 6 minutes, which corresponds to ca . 0.5%  of the theoretical capacity. The open circuit voltage at 25 ¡ã C was measured after 30 hours. Again, the cell was charged under a anodic current of 150 ¦Ì A for 6  minutes. These procedures were repeated several times until the open circuit voltage at 25 ¡ã C reaches at ca . 3.7 V.
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