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室温下TiO/SiNWs p-n结催化剂上的光催化甲烷氧化反应。

Photocatalytic methane oxidation over a TiO/SiNWs p-n junction catalyst at room temperature.

作者信息

Ta Qui Thanh Hoai, Nguyen Luan Minh, Nguyen Ngoc Hoi, Nguyen Phan Khanh Thinh, Nguyen Dai Hai

机构信息

Institute of Chemical Technology, Vietnam Academy of Science and Technology, 1A TL29 Street, Thanh Loc Ward, District 12, Ho Chi Minh City 700000, Vietnam.

Graduate University of Science and Technology, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Street, Cau Giay District, Hanoi 100000, Vietnam.

出版信息

Beilstein J Nanotechnol. 2024 Sep 2;15:1132-1141. doi: 10.3762/bjnano.15.92. eCollection 2024.

Abstract

Rapid recombination of charge carriers in semiconductors is a main drawback for photocatalytic oxidative coupling of methane (OCM) reactions. Herein, we propose a novel catalyst by developing a p-n junction titania-silicon nanowires (TiO/SiNWs) heterostructure. The structure is fabricated by atomic layer deposition of TiO on p-type SiNWs. The TiO/SiNWs heterostructure exhibited an outstanding OCM performance under simulated solar light irradiation compared to the single components. This enhanced efficiency was attributed to the intrinsic electrical field formed between n-type TiO and p-type SiNWs, which forces generated charge carriers to move in opposite directions and suppresses charge recombination. Besides, surface morphology and optical properties of the the p-n TiO/SiNWs catalyst are also beneficial for the photocatalytic activity. It is expected that the results of this study will provide massive guidance in synthesizing an efficient photocatalyst for CH conversion under mild conditions.

摘要

半导体中电荷载流子的快速复合是甲烷光催化氧化偶联(OCM)反应的一个主要缺点。在此,我们通过开发一种p-n结二氧化钛-硅纳米线(TiO₂/SiNWs)异质结构来提出一种新型催化剂。该结构是通过在p型SiNWs上进行TiO₂的原子层沉积制备的。与单一组分相比,TiO₂/SiNWs异质结构在模拟太阳光照射下表现出优异的OCM性能。这种提高的效率归因于n型TiO₂和p型SiNWs之间形成的内建电场,它迫使产生的电荷载流子向相反方向移动并抑制电荷复合。此外,p-n TiO₂/SiNWs催化剂的表面形貌和光学性质也有利于光催化活性。预计这项研究的结果将为在温和条件下合成用于CH₄转化的高效光催化剂提供大量指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c5b/11403797/cd8660752eab/Beilstein_J_Nanotechnol-15-1132-g002.jpg

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