<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0872-1904</journal-id>
<journal-title><![CDATA[Portugaliae Electrochimica Acta]]></journal-title>
<abbrev-journal-title><![CDATA[Port. Electrochim. Acta]]></abbrev-journal-title>
<issn>0872-1904</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Electroquímica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0872-19042007000300004</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Cyclic Voltammetric Investigation on the Catalysis of Electrodeposited Manganese Oxide on the Electrochemical Reduction of Oxygen (ORR) in Room Temperature Ionic Liquids (RTILs) of 1-Ethyl-3-Methylimidazolium Tetrafluorobroate (EMIBF4) on Glass Carbon (GC) Electrode]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ding]]></surname>
<given-names><![CDATA[K.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Wang]]></surname>
<given-names><![CDATA[Q.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Zhao]]></surname>
<given-names><![CDATA[M.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hebei Teacher’s University Chemistry College ]]></institution>
<addr-line><![CDATA[Shijiazhuang ]]></addr-line>
<country>P. R . China</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Teacher’s University Huihua College ]]></institution>
<addr-line><![CDATA[Shijiazhuang ]]></addr-line>
<country>P. R . China</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Tokyo Institute of Technology Interdisciplinary Graduate School of Science and Engineering Department of Electronic Chemistry]]></institution>
<addr-line><![CDATA[Yokohama ]]></addr-line>
<country>Japan</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2007</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2007</year>
</pub-date>
<volume>25</volume>
<numero>3</numero>
<fpage>335</fpage>
<lpage>348</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0872-19042007000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0872-19042007000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0872-19042007000300004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[In this preliminary work, for the first time, the electrochemical oxygen reduction reaction (ORR) was investigated using cyclic voltammetry (CV) on the electrodeposited manganese oxide (MnOx)-modified glass carbon electrode (MnOx-GC) at room temperature ionic liquids (RTILs) of EMIBF4, i.e., 1-ethyl-3-methylimidazolium tetrafluorobroate (EMIBF4). The results demonstrated that, after being modified by MnOx on GC, the reduction peak current of oxygen was increased to some extent, while the oxidation peak current, corresponding to the oxidation of superoxide anion, O2-, was attenuated in some degree, suggesting that MnOx catalyzed ORR in RTILs of EMIBF4, which is consistent with the results obtained in aqueous solution. To accelerate the electron transfer rate, multi-walled carbon nanotubes (MWCNTs) were modified on GC, and then MnOx was electrodeposited onto the MWCNTs-modified GC electrode to give rise to the MnOx /MWCNTs-modified GC electrode; consequently, the improved standard rate constant, &#954;s,originated from the modified MWCNTs, along with the modification of electrodeposited MnOx, showed us a satisfactory electrocatalysis for ORR in RTILs of EMIBF4. In addition, not only for the MnOx-modified GC but also for the MnOx/ MWCNTs-modified GC, there is a novel small oxidation peak appearing at -0.2 V vs. solid Ag/AgCl, implying that the catalysis of MnOx for ORR in EMIBF4 is somewhat different from that observed in aqueous solution, though the exact interpretation is not achieved in this preliminary work. Initiating the catalysis of MnOx on ORR in RTILs is the main contribution of this work. Further discussions are in progress.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[manganese oxide (MnOx)]]></kwd>
<kwd lng="en"><![CDATA[multi-walled carbon nanotubes (MWCNTs)]]></kwd>
<kwd lng="en"><![CDATA[room temperature ionic liquids (RTILs)]]></kwd>
<kwd lng="en"><![CDATA[electrochemical oxygen reduction reaction (ORR)]]></kwd>
<kwd lng="en"><![CDATA[glass carbon (GC) electrode]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="center"><b>Cyclic Voltammetric Investigation on the Catalysis of Electrodeposited    Manganese Oxide on the Electrochemical Reduction of Oxygen (ORR) in Room Temperature    Ionic Liquids (RTILs) of 1-Ethyl-3-Methylimidazolium Tetrafluorobroate (EMIBF<sub>4</sub>)    on Glass Carbon (GC) Electrode</b></p>     <p align="center"><b >&nbsp;K. Ding,<i><sup>a,c,</sup></i><a href="#1">*</a><a name="top1"></a>Q. Wang<i><sup>a</sup></i>    and M. Zhao<i><sup>b</sup></i></b></p>     <p align="center">&nbsp;</p>     <p align="center"><sup>a</sup>ChemistryCollege, Hebei Teacher’s University, Shijiazhuang    050016, P. R . China</p>     <p align="center"><sup>b</sup>Huihua College, Teacher’s University, Shijiazhuang    050091, P. R . China</p>     <p align="center"><sup>c</sup>Department of Electronic Chemistry, Interdisciplinary    Graduate School of Science and Engineering, Tokyo Institute of Technology, Midori-ku,    Yokohama 226-8502, Japan</p>     <p align="center">&nbsp;</p>     <p align="center">&nbsp;</p>      <p><b >Abstract</b></p>      <p>In this preliminary work, for the first time, the electrochemical oxygen reduction reaction (ORR) was investigated using cyclic voltammetry (CV) on the electrodeposited manganese oxide (MnO<sub>x</sub>)-modified glass carbon electrode (MnO<sub>x</sub>-GC) at room temperature ionic liquids (RTILs) of EMIBF<sub>4</sub>, i.e., 1-ethyl-3-methylimidazolium tetrafluorobroate (EMIBF<sub>4</sub>). The results demonstrated that, after being modified by MnO<sub>x</sub> on GC, the reduction peak current of oxygen was increased to some extent, while the oxidation peak current, corresponding to the oxidation of superoxide anion, O<sub>2</sub><sup>-</sup>, was attenuated in some degree, suggesting that MnO<sub>x</sub>catalyzed ORR in RTILs of EMIBF<sub>4</sub>, which is consistent with the results obtained in aqueous solution. To accelerate the electron transfer rate, multi-walled carbon nanotubes (MWCNTs) were modified on GC, and then MnO<sub>x</sub> was electrodeposited onto the MWCNTs-modified GC electrode to give rise to the MnO<sub>x</sub> /MWCNTs–modified GC electrode; consequently, the improved standard rate constant, &#954;<sub>s</sub>,originated from the modified MWCNTs, along with the modification of electrodeposited MnO<sub>x</sub>, showed us a satisfactory electrocatalysis for ORR in RTILs of EMIBF<sub>4</sub>. In addition, not only for the MnO<sub>x</sub>-modified GC but also for the MnO<sub>x</sub>/ MWCNTs-modified GC, there is a novel small oxidation peak appearing at –0.2 V <i>vs</i>. solid Ag/AgCl, implying that the catalysis of MnO<sub>x</sub> for ORR in EMIBF<sub>4</sub> is somewhat different from that observed in aqueous solution, though the exact interpretation is not achieved in this preliminary work. Initiating the catalysis of MnO<sub>x</sub>on ORR in RTILs is the main contribution of this work. Further discussions are in progress.</p>      ]]></body>
<body><![CDATA[<p>&nbsp;</p>      <p><b ><i>Keywords: </i></b>manganese oxide (MnO<sub>x</sub>), multi-walled carbon nanotubes (MWCNTs), room temperature ionic liquids (RTILs), electrochemical oxygen reduction reaction (ORR), glass carbon (GC) electrode.</p>      <p>&nbsp;</p>      <p>&nbsp;</p>      <p>Texto disponível em PDF</p>      <p>Full text only in PDF format</p>      <p>&nbsp;</p>     <p>&nbsp;</p>      <p><b >References</b></p>      <!-- ref --><p>1.  P. Zoltowski, D.M. Drazic, L. Vorkapic,<i> J. Appl. Electrochem.</i> 3 (1973) 271.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000022&pid=S0872-1904200700030000400001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2.  J.P. Brenet, <i>J. Power Sources 4</i> (1979) 183.</p>      <p>3.  K. Matsuki, H. Kamada, <i>Electrochim. Acta </i>31 (1986) 13.</p>      <p>4.  L. Mao, D. Zhang, T. Sotomura, K. Nakatsu, N. Koshiba, T. Ohsaka, <i>Electrochim. Acta</i> 48 (2003) 1015.</p>      <p>5.  T. Welton, <i>Chem. Rev.</i> 99 (1999) 2071.</p>      <p>6.  R.M. Lau, F. Rantwijl, K.R. Seddon, R.A. Sheldon, <i>Org. Lett.</i> 2 (2000) 189.</p>      <p>7.   M.T. Carter, C.L. Hussey, S.K.D Strubinger, R.A. Osteryong, <i>Inorg. Chem.</i>30 (1991) 1149.</p>      <p>8.   I.M Alnashef, M.L. Leonard, M.C. Kittle, M.A. Matthews, W. Weidner, <i>Electrochem. Solid-State Lett. </i>4 (2001) D16.</p>      <p>9.   D. Zhang, T. Okajima, F. Matsumoto, T. Ohsaka, <i>J. Electrochem. Soc.,</i> 151 (2004) D31. </p>      <p>10.  L. Mao, T. Sotomura, K. Nakatsu, N. Koshiba, D. Zhang, T. Ohsaka, <i>J. Electrochem. Soc.</i> 149 (2002) A504.</p>      <p>11.  M. Wu, G.A. Snook, G.Z. Chen, D.J. Fray, <i>Electrochem. Commun.</i>6 (2004) 499.</p>      ]]></body>
<body><![CDATA[<p>12.  J.N. Barisci, G.G. Wallace, D.R. Macfarlane, R.H. Baughman, <i>Electrochem. Commun.</i>6(2004) 22.</p>      <p>13.  J.S. Ye, Y. Wen, W.D. Zhang, L.M. Gan, G.Q. Xu, F.S. Sheu, <i>Electrochem. Commun.</i> 6 (2004) 66.</p>      <p>14.  W. Chen, J. Zhao, J.Y. Lee, Z. Liu, <i>Mater. Chem. Phys.</i> 91 (2005) 124.</p>      <p>15.  Z.P. Guo, Z.W. Zhao, H.K. Liu, S.X. Dou, <i>Carbon</i> 43 (2005) 1392.</p>      <p>16.  B.M. Quinn, C. Dekker, S.G. Lemay, <i>J. Am. </i><i>Chem. Soc.</i> 127 (2005) 6146.</p>      <p>17.  M.J. Park, J.K. Lee, B.S. Lee, Y.W. Lee, I.S. Choi, S. Lee, <i>Chem. Mater.</i> 18 (2006) 1546.</p>      <p>18.  R.G. Evans, O.V. Klymenko, S.A. Saddoughi, C. Hardacre, R.G. Compton, <i>J. Phys. </i><i>Chem. B</i>. 108 (2004) 7878.</p>      <p>19.  N.K. Beck, B. Steiger, G.G. Scherer, A. Wokaun, <i>Fuel Cells</i>6 (2006) 26.</p>      <p>20.  A. Vanella, C.D. Giacomo, V. Sorrenti, A. Russo, C. Castorina, A. Campisi, M. Renis, J.R. Perez-Polo, <i>Neurochem. Res.</i> 18 (1993) 1337.</p>      <p>21.  H.A. Kontos, E.P. Wei, <i>J. Neurosurg</i>. 64 (1986) 803.</p>      ]]></body>
<body><![CDATA[<p>22.  C. Hu, S. Yuan and S. Hu, <i>Electrochim. Acta</i> 51 (2006) 3013. </p>      <p>23.  D. Zhang, T. Sotomura, T. Ohsaka, <i>Chem. Lett. </i>35 (2006)520.</p>      <p>24.  M. Wu, G.A. Snook, G.Z. Chen, D.J. Fray, <i>Electrochem. </i><i>Commun.</i> 6 (2004) 499.</p>      <p>25.  D.T. Sawyer, G. Jr. Chiericato, C.T. Angelis, E.J. Jr. Nannl, T. Tsuchiya, <i>Anal. Chem. </i>54 (1982) 1720.</p>      <p>26.  R.S. Nicholson, <i>Anal. Chem.</i> 37 (1965) 1351.</p>      <p>27.  Y. Katayama, H. Onodera, M. Yamagata, T. Miura, <i>J. Electrochem. Soc.</i> 151 (2004) A59.</p>      <p>28.  Y. Chen, M.L. Zhang, Z.H. Shi, <i>J. Electrochem. </i><i>Soc.</i> 152 (2005) A1272.</p>      <p>29.  F. Zhao, X. Wu, M. Wang, Y. Liu, L. Gao, S. Dong, <i>Anal. Chem.</i> 76 (2004) 4960.</p>      <p>30. P. Yu, Y. Lin, L. Xiang, L. Su, J. Zhang, L. Mao, <i>Langmuir</i> 21 (2005) 9000.</p>      <p>31.  V.H. Crespi, M.L. Cohen, A. Rubio, <i>Phys. Rev. Lett.</i> 79 (1997) 2093.</p>      ]]></body>
<body><![CDATA[<p>32.  P.J. Britto, K.S.V. Santhanam, A. Rubio, J.A. Alonso, P.M. Ajayan, <i>Adv. Mater.</i> 11 (1999) 154.</p>         <p>&nbsp;</p>     <p>&nbsp;</p>     <p><a name="1"></a><a href="#top1">*</a> Corresponding author. E-mail address:    <a href="mailto:dkeqiang@263.net">dkeqiang@263.net</a></p>       ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zoltowski]]></surname>
<given-names><![CDATA[P.]]></given-names>
</name>
<name>
<surname><![CDATA[Drazic]]></surname>
<given-names><![CDATA[D.M.]]></given-names>
</name>
<name>
<surname><![CDATA[Vorkapic]]></surname>
<given-names><![CDATA[L.]]></given-names>
</name>
</person-group>
<source><![CDATA[J. Appl. Electrochem]]></source>
<year>1973</year>
<volume>3</volume>
<page-range>271</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
