A template-assisted method for synthesizing TiO2 nanoparticles and Ni/ TiO2 nanocomposites for urea electrooxidation

被引:4
作者
Mohamed, Ibrahim M. A. [1 ]
Shehata, Aboelhasan G. [1 ]
Al-Anazi, Abdulaziz [2 ]
Khairy, Mohamed [1 ]
Newair, Emad F. [1 ,3 ]
机构
[1] Sohag Univ, Fac Sci, Chem Dept, Sohag 82524, Egypt
[2] King Saud Univ, Coll Engn, Dept Chem Engn, POB 800, Riyadh 11421, Saudi Arabia
[3] Damanhour Univ, Fac Sci, Chem Dept, Damanhour 22511, Egypt
关键词
TiO2; Anatase; Ni/TiO2; Electrochemistry; NiOOH; Urea oxidation; OXIDATION; NANOFIBERS; MECHANISM; BEHAVIOR; UV;
D O I
10.1016/j.matchemphys.2024.129112
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The exploration of electrocatalytic urea -assisted wastewater treatment as a method for sustainable energy generation presents a compelling approach within the domain of green chemistry. In this context, titanium dioxide (TiO2) and nickel -doped TiO2 (Ni@TiO2) nanocomposites were developed through an innovative organic template -assisted synthesis strategy. These were denoted as m-TiO2-org and Ni@m-TiO2-org, respectively, to create cost-effective and high-performance electrodes for urea electrooxidation in urea -based fuel cells. The structural and chemical properties of the fabricated m-TiO2-org and Ni@m-TiO2-org materials were meticulously analyzed using a suite of physicochemical characterization techniques, including Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA), and Energy -Dispersive X-ray Spectroscopy (EDX). These investigations revealed that both m-TiO2-org and Ni@m-TiO2-org materials predominantly consisted of irregular monolithic microparticles formed through the aggregation of spherical nanoparticles, with diameters ranging from 8.16 nm to 13.1 nm. Subsequent evaluations of these TiO2-based materials as electrocatalysts for urea electrooxidation demonstrated their efficacy, as evidenced by voltammetric and electrochemical impedance spectroscopy measurements. Notably, the Ni@m-TiO2-org variant exhibited enhanced electrochemical performance, attributed to the presence of Ni2+ sites. These sites facilitated electrochemical activation and the formation of active NiOOH sites, leading to a significant increase in the current density (0.78 mA/cm2 at 1.523 V vs. the Reversible Hydrogen Electrode (RHE)), as a fiftyfold enhancement compared to mTiO2-org@Glassy Carbon Electrode (GCE) under similar conditions (3 M KOH containing 3 M urea), with a Tafel slope of 33 mV/decade. This research not only elucidates the potential of TiO2-based nanocomposites in the electrooxidation of urea but also heralds the development of innovative electrode materials for commercial electrochemical cells, marking a significant advancement in the field of electrocatalysis and sustainable energy technology.
引用
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页数:12
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