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具有可控表面缺陷的卤氧化铋半导体在光催化降解空气中甲苯方面的实际可行性。

The practical feasibility of bismuth oxyhalide semiconductors with controlled surface defects in photocatalytic degradation of toluene in air.

作者信息

Zhang Jinjian, Vikrant Kumar, Yeon Changho, Lee Chan-Woo, Kim Ki-Hyun

机构信息

Department of Civil and Environmental Engineering, Hanyang University, 222 Wangsimni-ro, Seoul 04763, Republic of Korea.

Energy AI & Computational Science Laboratory, Korea Institute of Energy Research, Daejeon 34129, Republic of Korea; Department of Materials Science and Engineering, Korea University, Seoul 02841, Republic of Korea.

出版信息

J Colloid Interface Sci. 2025 Apr;683(Pt 1):90-100. doi: 10.1016/j.jcis.2024.12.047. Epub 2024 Dec 9.

Abstract

The photocatalytic degradation (PCD) of toluene (as model aromatic volatile organic compound (VOC)) is studied using two-dimensional semiconductors (bismuth oxyhalides (BiOX (X = Cl and Br)) synthesized with surface defects (BiOX-R (R = reduction)) through a solvothermal-induced reduction process. The PCD efficiency of BiOCl-R against 5 ppm toluene (20 % relative humidity (RH)) is 98.6 % under ultraviolet light irradiation with the quantum yield and clean air delivery rate of 1.04E-03 molecules photon and 3 L/h, respectively. A combined evaluation of catalyst properties, experimental data, and density functional theory simulations consistently indicates that the formation of surface defects should promote the adsorption and activation of toluene, molecular oxygen (O), and water (HO) molecules. Meanwhile, the geometric and electronic structure of defective BiOX favorably generates superoxide anion (O) and hydroxyl (OH) radicals through electron (e)-assisted O activation and hole (h)-mediated HO oxidation, respectively. Notably, the BiOCl-R surface becomes more advantageous to reduce the reaction energy barrier in the ring-opening processes of intermediate forms like benzaldehyde and benzoic acid. Overall, the results of this study offer practical guidelines for the design of advanced photocatalysts with controlled surface defects for the efficient PCD of aromatic VOCs in air.

摘要

采用二维半导体(通过溶剂热诱导还原过程合成的具有表面缺陷的卤氧化铋(BiOX(X = Cl和Br),即BiOX-R(R = 还原)),研究了甲苯(作为典型的芳香族挥发性有机化合物(VOC))的光催化降解(PCD)。在紫外线照射下,BiOCl-R对5 ppm甲苯(相对湿度(RH)为20%)的PCD效率为98.6%,量子产率和清洁空气输送率分别为1.04E-03分子/光子和3 L/h。对催化剂性能、实验数据和密度泛函理论模拟的综合评估一致表明,表面缺陷的形成应促进甲苯、分子氧(O)和水分子(HO)的吸附和活化。同时,有缺陷的BiOX的几何和电子结构分别通过电子(e)辅助的O活化和空穴(h)介导的HO氧化,有利地生成超氧阴离子(O)和羟基(OH)自由基。值得注意的是,BiOCl-R表面在降低苯甲醛和苯甲酸等中间形式的开环过程中的反应能垒方面更具优势。总体而言,本研究结果为设计具有可控表面缺陷的先进光催化剂以实现空气中芳香族VOCs的高效PCD提供了实用指导。

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