WS2-intercalated Ti3C2Tx MXene/TiO2-stacked hybrid structure as an excellent sonophotocatalyst for tetracycline degradation and nitrogen fixation

被引:18
作者
Ranjith, Kugalur Shanmugam [1 ]
Ghoreishian, Seyed Majid [2 ]
Umapathi, Reddicherla [3 ]
Raju, Ganji Seeta Rama [1 ]
Lee, Hyun Uk [4 ]
Huh, Yun Suk [3 ]
Han, Young-Kyu [1 ]
机构
[1] Dongguk Univ Seoul, Dept Energy & Mat Engn, Seoul 04620, South Korea
[2] Univ South Carolina, Dept Chem Engn, Columbia, SC USA
[3] Inha Univ, Nano Bio High Tech Mat Res Ctr, Dept Biol Sci & Bioengn, Incheon 22212, South Korea
[4] Korea Basic Sci Inst, Div Mat Anal & Res, Daejeon 34133, South Korea
基金
新加坡国家研究基金会;
关键词
MXene; Transition metal dichalcogenide; Sonophotocatalysis; N; 2; fixation; Interfacial contact; NANOSTRUCTURES; HETEROJUNCTION; COMPOSITES;
D O I
10.1016/j.ultsonch.2023.106623
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Designing a heterostructure nanoscale catalytic site to facilitate N2 adsorption and photogenerated electron transfer would maximize the potential for photocatalytic activity and N2 reduction reactions. Herein, we have explored the interfacial TiO2 nanograins between the Ti3C2Tx MXene-WS2 heterostructure and addressed the beneficial active sites to expand the effective charge transfer rate and promote sonophotocatalytic N2 fixation. Benefiting from the interfacial contact and dual heterostructure interface maximizes the photogenerated carrier separation between WS2 and MXene/TiO2. The sonophotocatalytic activity of the MXene@TiO2/WS2 hybrid, which was assessed by examining the photoreduction of N2 with ultrasonic irradiation, was much higher than that of either sonocatalytic and photocatalytic activity because of the synergistic sonocatalytic effect under photoirradiation. The Schottky junction between the MXene and TiO2 on the hybrid MXene/TiO2-WS2 hetero-structure resulted in the sonophotocatalytic performance through effective charge transfer, which is 1.47 and 1.24 times greater than MXene-WS2 for nitrogen fixation and pollutant degradation, respectively. Under the sonophotocatalytic process, the MXene/TiO2-WS2 heterostructure exhibits a decomposition efficiency of 98.9 % over tetracycline in 90 min, which is 5.46, 1.73, and 1.10 times greater than those of sonolysis, sonocatalysis, and photocatalysis, respectively. The production rate of NH3 on MXene/TiO2-WS2 reached 526 mu mol g-1 h-1, which is 3.17, 3.61, and 1.47 times higher than that of MXene, WS2, and MXene-WS2, respectively. The hybridized structure of MXene-WS2 with interfacial surface oxidized TiO2 nanograins minimizes the band potential and improves photocarrier use efficiency, contributing directly to the remarkable catalytic performance towards N2 photo fixation under visible irradiation under ultrasonic irradiation. This report provides the strategic outcome for the mass carrier transfer rate and reveals a high conversion efficiency in the hybridized heterostructure.
引用
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页数:13
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