The origin of potential rise during charging of Li-O2 batteries
When aprotic Li-O2 batteries recharge, the solid Li2O2 in the positive electrode is oxidized, which often exhibits a continuous or step increase in the charging potential as a function of the charging capacity, and its origin remains incompletely understood. Here, we report a model study of electro-...
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| Veröffentlicht in: | Science China. Chemistry 2017-12, Vol.60 (12), p.1527-1532 |
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| container_title | Science China. Chemistry |
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| creator | Guo, Limin Wang, Jiawei Ma, Shunchao Zhang, Yantao Wang, Erkang Peng, Zhangquan |
| description | When aprotic Li-O2 batteries recharge, the solid Li2O2 in the positive electrode is oxidized, which often exhibits a continuous or step increase in the charging potential as a function of the charging capacity, and its origin remains incompletely understood. Here, we report a model study of electro-oxidation of a Li2O2 film on an Au electrode using voltammetry coupled with in situ Raman spectroscopy. It was found that the charging reaction initializes at the positive electrodelLizO2 interface, instead of the previously presumed Li2O2 surface, and consists of two temporally and spatially separated Li2O2 oxidation processes, accounting for the potential rise during charging of Li-O2 batteries. Moreover, the electrode surface-initialized oxidation can disintegrate the Li2O2 film resulting in a loss of Li2O2 into electrolyte solution, which drastically decreases the charging efficiency and highlights the importance of using soluble electro-catalyst for the complete charging of Li-02 batteries. |
| doi_str_mv | 10.1007/s11426-017-9085-5 |
| format | Article |
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Here, we report a model study of electro-oxidation of a Li2O2 film on an Au electrode using voltammetry coupled with in situ Raman spectroscopy. It was found that the charging reaction initializes at the positive electrodelLizO2 interface, instead of the previously presumed Li2O2 surface, and consists of two temporally and spatially separated Li2O2 oxidation processes, accounting for the potential rise during charging of Li-O2 batteries. Moreover, the electrode surface-initialized oxidation can disintegrate the Li2O2 film resulting in a loss of Li2O2 into electrolyte solution, which drastically decreases the charging efficiency and highlights the importance of using soluble electro-catalyst for the complete charging of Li-02 batteries.</description><identifier>ISSN: 1674-7291</identifier><identifier>EISSN: 1869-1870</identifier><identifier>DOI: 10.1007/s11426-017-9085-5</identifier><language>eng</language><publisher>Beijing: Science China Press</publisher><subject>Charging ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Decomposition ; Efficiency ; Electrodes ; Electrolytes ; Metal air batteries ; Oxidation ; Raman spectroscopy ; Rechargeable batteries ; Voltammetry</subject><ispartof>Science China. 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Chemistry</title><addtitle>Sci. China Chem</addtitle><addtitle>SCIENCE CHINA Chemistry</addtitle><description>When aprotic Li-O2 batteries recharge, the solid Li2O2 in the positive electrode is oxidized, which often exhibits a continuous or step increase in the charging potential as a function of the charging capacity, and its origin remains incompletely understood. Here, we report a model study of electro-oxidation of a Li2O2 film on an Au electrode using voltammetry coupled with in situ Raman spectroscopy. It was found that the charging reaction initializes at the positive electrodelLizO2 interface, instead of the previously presumed Li2O2 surface, and consists of two temporally and spatially separated Li2O2 oxidation processes, accounting for the potential rise during charging of Li-O2 batteries. Moreover, the electrode surface-initialized oxidation can disintegrate the Li2O2 film resulting in a loss of Li2O2 into electrolyte solution, which drastically decreases the charging efficiency and highlights the importance of using soluble electro-catalyst for the complete charging of Li-02 batteries.</description><subject>Charging</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Decomposition</subject><subject>Efficiency</subject><subject>Electrodes</subject><subject>Electrolytes</subject><subject>Metal air batteries</subject><subject>Oxidation</subject><subject>Raman spectroscopy</subject><subject>Rechargeable batteries</subject><subject>Voltammetry</subject><issn>1674-7291</issn><issn>1869-1870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kD1PwzAQhi0EElXpD2CLYDb4nPhrQqjiS6rUpcyW49qpq5Kkdjrw73GUCjZuuRve9967B6FbIA9AiHhMABXlmIDAikiG2QWageQKgxTkMs9cVFhQBddokdKe5CpLQgWboafNzhVdDE1oi84XfTe4dgjmUMSQXLE9xdA2hd2Z2IxDVqwCXtOiNsPgYnDpBl15c0huce5z9Pn6slm-49X67WP5vMKWsnwRF8KVBJhn3lbSQAVbBV5AXavakq2xUDlBCKud4MZyryorqfWKc-eUdbyco_tpbx-748mlQe-7U2xzpM5_SaaoJFVWwaSysUspOq_7GL5M_NZA9IhKT6h0RqVHVJplD508qR-fdfFv83-mu3PQrmubY_b9JmXWBCQVtPwBqDV1kw</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Guo, Limin</creator><creator>Wang, Jiawei</creator><creator>Ma, Shunchao</creator><creator>Zhang, Yantao</creator><creator>Wang, Erkang</creator><creator>Peng, Zhangquan</creator><general>Science China Press</general><general>Springer Nature B.V</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FG</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>M2P</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20171201</creationdate><title>The origin of potential rise during charging of Li-O2 batteries</title><author>Guo, Limin ; 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Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Limin</au><au>Wang, Jiawei</au><au>Ma, Shunchao</au><au>Zhang, Yantao</au><au>Wang, Erkang</au><au>Peng, Zhangquan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The origin of potential rise during charging of Li-O2 batteries</atitle><jtitle>Science China. Chemistry</jtitle><stitle>Sci. China Chem</stitle><addtitle>SCIENCE CHINA Chemistry</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>60</volume><issue>12</issue><spage>1527</spage><epage>1532</epage><pages>1527-1532</pages><issn>1674-7291</issn><eissn>1869-1870</eissn><abstract>When aprotic Li-O2 batteries recharge, the solid Li2O2 in the positive electrode is oxidized, which often exhibits a continuous or step increase in the charging potential as a function of the charging capacity, and its origin remains incompletely understood. Here, we report a model study of electro-oxidation of a Li2O2 film on an Au electrode using voltammetry coupled with in situ Raman spectroscopy. It was found that the charging reaction initializes at the positive electrodelLizO2 interface, instead of the previously presumed Li2O2 surface, and consists of two temporally and spatially separated Li2O2 oxidation processes, accounting for the potential rise during charging of Li-O2 batteries. Moreover, the electrode surface-initialized oxidation can disintegrate the Li2O2 film resulting in a loss of Li2O2 into electrolyte solution, which drastically decreases the charging efficiency and highlights the importance of using soluble electro-catalyst for the complete charging of Li-02 batteries.</abstract><cop>Beijing</cop><pub>Science China Press</pub><doi>10.1007/s11426-017-9085-5</doi><tpages>6</tpages></addata></record> |
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| subjects | Charging Chemistry Chemistry and Materials Science Chemistry/Food Science Decomposition Efficiency Electrodes Electrolytes Metal air batteries Oxidation Raman spectroscopy Rechargeable batteries Voltammetry |
| title | The origin of potential rise during charging of Li-O2 batteries |
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