钴镍氧化物纳米笼上的双贵金属助催化剂促进光催化氧化脱硫

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Catalysis Pub Date : 2025-07-01 Epub Date: 2025-04-01 DOI:10.1016/j.jcat.2025.116120
Xinyu Zhao , Dongxiao Wang , Caiwei Deng , Hao Niu , Huawei Yang , Lixia Yang , Liangjiu Bai , Kun Yin , Donglei Wei , Hou Chen
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引用次数: 0

摘要

光催化好氧氧化脱硫(PAODS)作为一种可持续的燃料脱硫方法受到广泛关注,但目前报道的光催化剂仍存在硫化物转化动力学缓慢的问题。本文提出了一种MoOx和NiCoP共同修饰的CoNiO2空心纳米笼(MoOx/P-CoNiO2)催化剂,用于促进PAODS反应。该光催化剂在氧化二苯并噻吩(DBT)中表现出良好的光催化活性,质量活性比为10.4 mmol g−1 h−1,具有良好的重复性。MoOx和NiCoP作为双助催化剂的战略性加入,通过促进有效的电荷分离、增强活性氧(ROS)的产生以及为氧化难降解硫化合物提供活性位点,显著提高了光催化效率。在实际柴油脱硫试验中,该催化剂将硫含量从559.3 ppm降至10 ppm以下,满足了最严格的运输柴油标准,突出了其在工业环境中深度脱硫的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Dual noble-metal-free cocatalysts on cobalt nickel oxide nanocages for boosting photocatalytic oxidation desulfurization
Photocatalytic aerobic oxidative desulfurization (PAODS) has attracted widespread attention as a sustainable fuel desulfurization method, but the photocatalysts reported so far still suffer from slow sulfide conversion kinetics. Here we propose a MoOx and NiCoP co-decorated on CoNiO2 hollow nanocage (MoOx/P-CoNiO2) catalyst for boosting the PAODS reactions. The photocatalyst exhibits remarkable photocatalytic activity in oxidizing dibenzothiophene (DBT), attaining a mass activity ratio of 10.4 mmol g−1 h−1 and exhibiting excellent repeatability. The strategic incorporation of MoOx and NiCoP as dual cocatalysts significantly improved photocatalytic efficiency by facilitating efficient charge separation, enhancing the production of reactive oxygen species (ROS), and providing active sites for oxidizing refractory sulfur compounds. In real diesel desulfurization tests, the catalyst reduced sulfur content from 559.3 ppm to below 10 ppm, meeting the most stringent transportation diesel standards, highlighting its practical applicability for deep desulfurization in industrial settings.
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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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