Sushama M. Nikam, Suhas H. Sutar, Shubham D. Jituri, Akbar I. Inamdar and Sarfraj H. Mujawar
{"title":"Cobalt phosphate nanorod bundles for efficient supercapacitor and oxygen evolution reaction applications and their temperature dependence†","authors":"Sushama M. Nikam, Suhas H. Sutar, Shubham D. Jituri, Akbar I. Inamdar and Sarfraj H. Mujawar","doi":"10.1039/D4NJ03712J","DOIUrl":null,"url":null,"abstract":"<p >Developing highly stable, low-cost, and efficient electrode materials for supercapacitor and oxygen evolution reactions is a challenging issue in energy storage and generation technology to meet the demand for sustainable and clean energy. Herein, cobalt phosphates in comparison with cobalt oxides were synthesized using a successive ionic layer adsorption and reaction (SILAR) method on a nickel foam substrate with different crystallization temperatures, and their supercapacitor and oxygen evolution reaction performances were studied. The nanorod bundles of cobalt phosphate electrodes prepared at 150 °C delivered an excellent specific charge storage capacity of 1512 F g<small><sup>−1</sup></small> (681 C g<small><sup>−1</sup></small>) at a current density of 5 mA cm<small><sup>−2</sup></small>, which is higher than that of cobalt oxide (1103.9 F g<small><sup>−1</sup></small> (496 C g<small><sup>−1</sup></small>)). They are highly stable for more than 2000 charge–discharge cycles with a coulombic efficiency of 93%. Furthermore, the same electrodes exhibited enhanced electrocatalytic behaviour for the oxygen evolution reaction (OER) with an overpotential of 359 mV at a current density of 30 mA cm<small><sup>−2</sup></small>, lowest Tafel slope of 60 mV dec<small><sup>−1</sup></small> and stability of 20 hours. Enhanced reaction kinetics are attributed to the high electrochemical surface area with a <em>C</em><small><sub>dl</sub></small> of 594 μF and improved electronic conductivity. The above results indicated that cobalt phosphate is one of the most efficient electrode materials for the OER and supercapacitors.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 45","pages":" 19113-19124"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/nj/d4nj03712j","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Developing highly stable, low-cost, and efficient electrode materials for supercapacitor and oxygen evolution reactions is a challenging issue in energy storage and generation technology to meet the demand for sustainable and clean energy. Herein, cobalt phosphates in comparison with cobalt oxides were synthesized using a successive ionic layer adsorption and reaction (SILAR) method on a nickel foam substrate with different crystallization temperatures, and their supercapacitor and oxygen evolution reaction performances were studied. The nanorod bundles of cobalt phosphate electrodes prepared at 150 °C delivered an excellent specific charge storage capacity of 1512 F g−1 (681 C g−1) at a current density of 5 mA cm−2, which is higher than that of cobalt oxide (1103.9 F g−1 (496 C g−1)). They are highly stable for more than 2000 charge–discharge cycles with a coulombic efficiency of 93%. Furthermore, the same electrodes exhibited enhanced electrocatalytic behaviour for the oxygen evolution reaction (OER) with an overpotential of 359 mV at a current density of 30 mA cm−2, lowest Tafel slope of 60 mV dec−1 and stability of 20 hours. Enhanced reaction kinetics are attributed to the high electrochemical surface area with a Cdl of 594 μF and improved electronic conductivity. The above results indicated that cobalt phosphate is one of the most efficient electrode materials for the OER and supercapacitors.
为满足可持续清洁能源的需求,开发高稳定性、低成本、高效率的超级电容器和氧进化反应电极材料是储能和发电技术领域的一项挑战性课题。本文采用连续离子层吸附和反应(SILAR)方法,在不同结晶温度的泡沫镍基底上合成了磷化钴和氧化钴,并研究了它们的超级电容器和氧进化反应性能。在 150 °C 下制备的磷酸钴电极纳米棒束在 5 mA cm-2 的电流密度下具有 1512 F g-1 (681 C g-1)的优异比电荷存储容量,高于氧化钴(1103.9 F g-1(496 C g-1))。它们在 2000 多个充放电循环中都非常稳定,库仑效率高达 93%。此外,这些电极在氧进化反应(OER)中表现出更强的电催化性能,在电流密度为 30 mA cm-2 时,过电位为 359 mV,最低塔菲尔斜率为 60 mV dec-1,稳定性达 20 小时。反应动力学的增强归功于高电化学表面积(Cdl 为 594 μF)和更高的电子传导性。上述结果表明,磷酸钴是 OER 和超级电容器最有效的电极材料之一。