Bandal Harshad A, Kim Hern
Department of Energy Science and Technology, Environmental Waste Recycle Institute, Myongji University, Yongin, Gyeonggi-do 17058, Republic of Korea.
Department of Energy Science and Technology, Environmental Waste Recycle Institute, Myongji University, Yongin, Gyeonggi-do 17058, Republic of Korea.
J Colloid Interface Sci. 2022 Dec;627:1030-1038. doi: 10.1016/j.jcis.2022.07.104. Epub 2022 Jul 21.
Substituting water oxidation half of water splitting with anodic oxidation of urea can reduce the cost of H production and provide an avenue for treating urea-rich wastewater. However, developing an efficient and stable electrocatalyst is necessary to overcome the indolent kinetics of the urea oxidation reaction (UOR). Accordingly, we have used the Schikorr reaction to deposit FeO particles on the nickel foam (FeO/NF). Results from the various analysis indicated that under the operational conditions, FeO underwent surface reconstruction to produce a heterolayered structure wherein a catalytically active FeOOH layer encased a conducting FeO. FeO/NF outperformed RuO as a UOR catalyst and delivered a current density of 10 50 and 100 mA cm at low applied potentials of 1.38 1.42 and 1.46 V, respectively, with a Tafel slope of 28 mV dec. At the applied potential of 1.4 V, FeO/NF demonstrated a turnover frequency (TOF) of 2.8 × 10 s, highlighting its superior intrinsic activity. In addition, a symmetrical urea electrolyzer constructed using FeO/NF produced the current density of 10 mA cm at a cell voltage of 1.54 V.
用尿素的阳极氧化替代水分解中的析氧半反应可以降低制氢成本,并为处理富含尿素的废水提供一条途径。然而,开发一种高效且稳定的电催化剂对于克服尿素氧化反应(UOR)缓慢的动力学是必要的。因此,我们利用施科反应在泡沫镍上沉积FeO颗粒(FeO/NF)。各种分析结果表明,在操作条件下,FeO经历表面重构以产生一种异质层结构,其中催化活性的FeOOH层包裹着导电的FeO。作为UOR催化剂,FeO/NF的性能优于RuO,在分别为1.38、1.42和1.46 V的低施加电位下,电流密度分别为10、50和100 mA cm,塔菲尔斜率为28 mV dec。在1.4 V的施加电位下,FeO/NF的周转频率(TOF)为2.8×10 s,突出了其优异的本征活性。此外,使用FeO/NF构建的对称尿素电解槽在1.54 V的电池电压下产生了10 mA cm的电流密度。