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Effect of yttrium on catalytic performance of Y-doped TiO_(2) catalysts for propane dehydrogenation

Journal of Rare Earths 2024年第5期42卷 962-971,I0005页

作者： Liyu Hou Liming Xia Ruipeng Zhou Jianmei Li Renjie Li Zhen Zhao Guimei Yuan Aijun Duan State Key Laboratory of Heavy Oil Processing China University of PetroleumBeijing102249China Institute of catalysis for Energy and Environment College of Chemistry and Chemical EngineeringShenyang Normal UniversityShenyang110034China

Defective bulk catalysts based on TiO_(2) have superior catalytic performance for propane dehydrogenation(PDH).The oxygen vacancy concentration and the number of active sites on the catalyst surface can be effectively tuned by doping metal in TiO_(2).Herein,yttrium(Y)-doped titanium dioxide(nY/TiO_(x))catalysts were in-situ synthesized via the coprecipitation method to study the effect of rare earth metal Y doping on the structure of TiO_(2) and the catalytic performance for *** results demonstrate that Ydoped TiO_(2) exhibits higher catalytic activity,propylene selectivity and stability than bare TiO_(2).Full characterizations with X-ray diffraction(XRD),high-resolution transmission electron microscope(HRTEM),X-ray photoelectron spectroscopy(XPS),infrared spectroscopy of pyridine adsorption(Py-IR),temperature-programmed desorption of ammonia(NH_(3)-TPD),H_(2) temperature-programmed reduction(H_2-TPR),and Raman techniques on these catalysts reveal that Y^(3+)can enter TiO_(2) lattice,and the lattice stability of the catalyst can be enhanced by replacing Ti^(4+)to form Y-O-Ti ***,the introduction of an appropriate amount of Y can obviously promote the PDH reaction by adjusting the acidity of the catalyst,improving the release capacity of TiO_(2) lattice oxygen and increasing the formation of active ***,excessive Y doping will lead to pore clogging,and the exposure of active sites will be reduced,resulting in the degradation of catalytic performance.

关键词： Propane dehydrogenation Anatase Lattice defects Coordinatively unsaturated Ti cations Oxygen vacancy Rare earths

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Modification, application and expansion of electrode materials based on cobalt telluride

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Journal of Energy chemistry 2024年第10期97卷 710-737页

作者： Huilin Fan Yao Dai Xiaoyun Xue Runguo Zheng Yuan Wang Hamidreza Arandiyan Zhiyuan Wang Zongping Shao Hongyu Sun Yanguo Liu School of Materials Science and Engineering Northeastern University School of Resources and Materials Northeastern University at Qinhuangdao Key Laboratory of Dielectric and Electrolyte Functional Material Hebei Province Northeastern University at Qinhuangdao Department of Chemical Engineering The University of Melbourne centre for Advanced Materials and Industrial chemistry (CAMIC) School of Science RMIT University Laboratory of Advanced catalysis for Sustainability School of Chemistry University of Sydney WA School of Mines: Minerals Energy and Chemical Engineering Curtin University

Metal(Li,Na,K,Al)-ion batteries and lithium-sulfur and lithium-tellurium batteries are gaining recognition for their eco-friendly characteristics,substantial energy density,and sustainable ***,the overall performance of rechargeable batteries heavily depends on their electrode *** metal tellurides have recently gained significant attention due to their high electrical conductivity and *** telluride has received the most extensive research due to its catalytic activity,unique magnetic properties,and diverse composition and crystal ***,its limited conductivity and significant volume variation contribute to electrode structural deterioration and rapid capacity *** review comprehensively summarizes recent advances in rational design and synthesis of modified cobalt telluride-based electrodes,encompassing defect engineering(Te vacancies,cation vacancies,heterointerfaces,and homogeneous interfaces) and composite engineering(derived carbon from precursors,carbon fibers,Mxene,graphene nanosheets,etc.).Particularly,the intricate evolution mechanisms of the conversion reaction process during cycling are ***,these modified strategies applied to other transitional metal tellurides,such as iron telluride,nickel telluride,zinc telluride,copper telluride,molybdenum telluride,etc.,are also thoroughly ***,their application extends to emerging aqueous zinc-ion ***,potential challenges and prospects are discussed to further propel the development of transition metal tellurides electrode materials for next-generation rechargeable batteries.

关键词： Rechargeable batteries Transition metal tellurides Cobalt telluride Defect engineering Composite engineering

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Enhanced photocatalytic nitrogen fixation performance via in situ constructing BiO_(2-x)/NaNbO_(3) heterojunction

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Chinese Journal of Chemical Engineering 2024年第5期69卷 92-100页

作者： Jiayu Zhang Zhihao Zeng Lin Yue Chunran Zhao Xin Hu Leihong Zhao Xiuwen Wang Yiming He Key Laboratory of the Ministry of Education for Advanced catalysis Materials College of Chemistry and Materials ScienceZhejiang Normal UniversityJinhua 321004China Heilongjiang Provincial Key Laboratory of Surface Active Agent and Auxiliary School of Chemistry and Chemistry EngineeringQiqihar UniversityQiqihar 161006China Department of Materials Science and Engineering Zhejiang Normal UniversityJinhua 321004China

The fabrication of heterojunction catalysts is an effective strategy to enhance charge separation efficiency,thereby boosting the performance of *** this study,BiO_(2-x)nanosheets were synthesized through a hydrothermal process and loaded onto NaNbO_(3) microcube to construct a series of BiO_(2-x)/NaNbO_(3) heterojunctions for photocatalytic N_(2) *** indicated that 2.5%BiO_(2-x)/NaNbO_(3) had the highest photocatalytic *** NH_(3) production rate under simulated solar light reached 406.4μmol·L^(-1)·g^(-1)·h^(-1),which reaches 2.6 and 3.8 times that of NaNbO_(3) and BiO_(2-x),***_(2-x)nanosheets primarily act as electron trappers to enhance the separation efficiency of charge *** strong interaction between BiO_(2-x)and NaNbO_(3) facilitates the electron migration between ***,the abundant oxygen vacancies in BiO_(2-x)nanosheets may facilitate the adsorption and activation of N_(2),which may be another possible reason of the high photocatalytic activity of the BiO_(2-x)/NaNbO_(3).This study may offer new insights for the development of semiconductor materials in photocatalytic nitrogen fixation.

关键词： Catalyst Solar energy Hydrothermal BiO_(2-x)/NaNbO_(3) Photocatalytic N_(2)-fixation

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Research progress on preparation of cerium-based oxide catalysts with specific morphology and their application for purification of diesel engine exhaust

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Journal of Rare Earths 2024年第7期42卷 1187-1216,I0001页

作者： Chunlei Zhang Siyu Gao Di Yu Shengran Zhou Lanyi Wang Xuehua Yu Zhen Zhao Institute of catalysis for Energy and Environment College of Chemistry and Chemical EngineeringShenyang Normal UniversityShenyang110034China State Key Laboratory of Heavy Oil Processing China University of PetroleumBejing102249China

The elimination of pollutants from diesel exhaust has received widespread research attention as they cause serious air pollution and pose a threat to human *** post-treatment technology is one of the most effective and universal technologies to treat diesel exhaust *** design and development of efficient and low-cost catalysts is the key factor to realize the wide application of catalytic post-treatment ***(Ce)-based oxides with specific morphologies are widely used to eliminate pollutants in diesel vehicle exhaust due to their unique physical and chemical properties,such as high catalytic activity,low cost and *** this review,the preparation methods of Cebased oxide materials with specific morphologies,such as nanoparticles,nanocubes,nanorods,nanofibers,and multi-stage pores,are introduced in detail,and the research progress on using these catalysts for the removal of carbon monoxide,hydrocarbons,soot particles,nitrogen oxides,and other pollutants from diesel exhaust is reviewed in ***,the unresolved issues associated with using Ce-based oxide catalysts with a specific morphology to catalytically remove pollutants from diesel exhaust are highlighted,and future application prospects and development directions are discussed.

关键词： Ce-based oxide catalysts Dies elexhaust pollutants Specific morphology Catalytic purification Rare earths

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一种快速响应的光致变色SCC-MOF用于光开关和信息加密

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Science China Materials 2024年第2期67卷 698-704页

作者：宋玙潘张佳妮王俊如李恺袁迎雪李波臧双全 Henan Key Laboratory of Crystalline Molecular Functional Materials Henan International Joint Laboratory of Tumor Theranostical Cluster MaterialsGreen Catalysis Centerand College of ChemistryZhengzhou UniversityZhengzhou 450001China College of chemistry and Pharmaceutical Engineering Nanyang Normal UniversityNanyang 473061China

由于银硫簇的不稳定性和有限的刺激响应特性,构建新型的具有光开关性质的银-硫簇基金属有机框架(SCC-MOF)面临着重大挑战.基于此,本文设计并合成了一种新型光致变色的SCC-MOF(Ag_(12)-BMPTC),该材料利用二芳基乙烯配体和银硫簇前驱体通... 详细信息

由于银硫簇的不稳定性和有限的刺激响应特性,构建新型的具有光开关性质的银-硫簇基金属有机框架(SCC-MOF)面临着重大挑战.基于此,本文设计并合成了一种新型光致变色的SCC-MOF(Ag_(12)-BMPTC),该材料利用二芳基乙烯配体和银硫簇前驱体通过溶剂缓慢挥发而得到.Ag_(12)-BMPTC在365和500 nm光照射下表现出优异的可逆光响应特性.此外,这种光开关性质为其在信息加密和手性开关方面提供了潜在应用.本研究不仅扩大了SCC-MOF的种类,而且为设计和合成新型光致变色材料提供了新的思路和潜在应用.

关键词： silver nanoclusters metal-organic frameworks photochromism diarylethene information encryption

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Mechanisms of isomerization and hydration reactions of typicalβ-diketone at the air-droplet interface

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Journal of Environmental Sciences 2024年第7期141卷 225-234页

作者： Yuemeng Ji Weiyong Luo Qiuju Shi Xiaohui Ma Ziqi Wu Weina Zhang Yanpeng Gao Taicheng An Guangdong-Hong Kong-Macao Joint Laboratory for Contaminants Exposure and Health Guangdong Key Laboratory of Environmental Catalysis and Health Risk ControlInstitute Environmental Health and Pollution ControlGuangdong University of TechnologyGuangzhou 510006China Guangzhou Key Laboratory of Environmental catalysis and Pollution Control Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of EducationSchool of Environmental Science and EngineeringGuangdong University of TechnologyGuangzhou 510006China

Acetylacetone(AcAc)is a typical class ofβ-diketones with broad industrial applications due to the property of the keto-enol isomers,but its isomerization and chemical reactions at the air-droplet interface are still ***,using combined molecular dynamics and quantum chemistry methods,the heterogeneous chemistry of AcAc at the air-droplet interface was investigated,including the attraction of AcAc isomers by the droplets,the distribution of isomers at the air-droplet interface,and the hydration reactions of isomers at the air-droplet *** results reveal that the preferential orientation of two AcAc isomers(keto-and enol-AcAc)to accumulate and accommodate at the acidic air-droplet *** isomerization of two AcAc isomers at the acidic air-droplet interface is more favorable than that at the neutral air-droplet interface because the“water bridge”structure is destroyed by H_(3)O^(+),especially for the isomerization from keto-Ac Ac to *** the acidic air-droplet interface,the carbonyl or hydroxyl O-atoms of two AcAc isomers display an energetical preference to ***-diol is the dominant products to accumulate at the air-droplet interface,and excessive keto-diol can enter the droplet interior to engage in the *** photooxidation reaction of AcAc will increase the acidity of the air-droplet interface,which indirectly facilitate the uptake and formation of more *** results provide an insight into the heterogeneous chemistry ofβ-diketones and their influence on the environment.

关键词： Acetylacetone Air-droplet interface Theoretical simulation Isomerization Hydration reaction mechanism

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Relay C（sp）-H bond trifluoromethylthiolation and amidation by visible light photoredox catalysis

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Science China chemistry 2024年

作者： Junheng Liu Suqi Yang Shunruo Yao Chengjian Zhu Yong Liu Weipeng Li Jin Xie State Key Laboratory of Coordination chemistry Jiangsu Key Laboratory of Advanced Organic Materials Chemistry and Biomedicine Innovation Center (ChemBIC) School of Chemistry and Chemical Engineering Nanjing University green catalysis Center College of Chemistry Zhengzhou University State Key Laboratory of Organometallic chemistry Shanghai Institute of Organic Chemistry Nanjing Bready Advanced Materials Technology Co. Ltd. State Key Laboratory of Natural Medicines China Pharmaceutical University

Selective functionalization of C（sp3）–H bonds is a straightforward and practical method to construct complex molecule skeletons. In this field, direct transformation of unactivated C（sp3）–H bonds into C（sp3）–SCF3architectures is still a great *** report a highly selective trifluoromethylthiolation of unactivated aliphatic C（sp3）–H bonds by combination of proton-coupled electron transfer（PCET） and hydrogen atom transfer（HAT） strategy. A wide range of structurally diverse alkyl trifluoromethyl sulfides are obtained. Furthermore, the use of two different photocatalysts can realize an unprecedented trifluoromethylthiolation and amidation cascade of different C（sp3）–H bonds. It can afford a good access to bifunctionalized molecules in synthetically useful yields.

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Light sheet microscope scanning of biointegrated microlasers for localized refractive index sensing

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Photonics Research 2024年第8期12卷 1673-1680页

作者： ROSS C.COWIE MARCEL SCHUBERT SUPA School of Physics and AstronomyUniversity of St Andrews Humboldt centre for Nano and Biophotonics Department of ChemistryUniversity of Cologne

Whispering gallery mode (WGM) microlasers are highly sensitive to localized refractive index changes allowing to link their emission spectrum to various chemical, mechanical, or physical stimuli. Microlasers recently found applications in biological studies within single cells, in three-dimensional samples such as multicellular spheroids,or in vivo. However, detailed studies of biological samples also need to account for the structural heterogeneity of tissues and live animals, therefore requiring a combination of high-resolution microscopy and laser ***,we design and construct a light sheet fluorescence microscope with a coupled spectrometer for use in microlaser studies for combined high-resolution, high-speed imaging and WGM spectral analysis. The light sheet illumination profile and the decoupled geometry of excitation and emission hereby directly affect the lasing and sensing properties, mainly through geometric constraints and by light coupling effects. We demonstrate the basic working principle of microlaser spectroscopy under light sheet excitation and measure the absolute refractive index within agarose and in zebrafish tail muscle tissue. We further analyze the light coupling conditions that lead to the occurrence of two separate oscillation planes. These so-called cross modes can be scanned around the entire microlaser surface, which allows to estimate a surface-averaged refractive index profile of the microlaser environment.

关键词： High speed imaging Light sheet fluorescence microscopy Refractive index Scanning microscopy Second harmonic generation Solid state lasers

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Strain-promoted S-arylation and alkenylation of sulfinamides using arynes and cyclic alkynes

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Science China chemistry 2024年第3期67卷 928-935页

作者： Xi Zou Boming Shen Gao-lin Li Qian Liang Yanhua Ouyang Binghe Yang Peiyuan Yu Bing Gao State Key Laboratory of Chemo/Bio-Sensing and Chemometrics College of Chemistry and Chemical EngineeringInstitute of Chemical Biology and NanomedicineHunan UniversityChangsha 410082China Department of chemistry and Shenzhen Grubbs Institute Guangdong Provincial Key Laboratory of CatalysisSouthern University of Science and TechnologyShenzhen 518055China

The conversion of commercially available chiral sulfinamides into pharmaceutically useful chiral sulfoximines via direct SIVfunctionalization is synthetically attractive but challenging due to the competitive reaction of N-functionalization. Herein, we disclose a novel strain-release strategy to access stereospecific and chemoselective SIV-arylation and alkenylation of sulfinamides using arynes and strained cyclic alkynes. This method tolerates an unprecedented chemical diversity of functional groups attached to the nitrogen center(N-R). The origin of the high SIV-selectivity is elucidated by density functional theory calculations, suggesting a stepwise mechanism for the aryne substrates and a concerted mechanism for the cyclic alkynes.

关键词： arylation alkenylation sulfoximines sulfinamides arynes

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Enabling heterogeneous catalysis to achieve carbon neutrality: Directional catalytic conversion of CO_(2) into carboxylic acids

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Carbon Energy 2024年第3期6卷 1-35页

作者： Xiaofei Zhang Wenhuan Huang Le Yu Max García-Melchor Dingsheng Wang Linjie Zhi Huabin Zhang KAUST catalysis Center(KCC) King Abdullah University of Science and Technology(KAUST)ThuwalSaudi Arabia Key Laboratory of Chemical Additives for China National Light Industry College of Chemistry and Chemical EngineeringShaanxi University of Science and TechnologyXi'anChina State Key Lab of Organic-Inorganic Composites Beijing University of Chemical TechnologyBeijingChina School of chemistry CRANN and AMBERResearch CentresTrinity College DublinCollege GreenDublinIreland Department of chemistry Tsinghua UniversityBeijingChina Advanced Chemical Engineering and Energy Materials Research Center China University of Petroleum(East China)QingdaoChina

The increase in anthropogenic carbon dioxide(CO_(2))emissions has exacerbated the deterioration of the global environment,which should be controlled to achieve carbon *** to the core goal of achieving carbon neutrality is the utilization of CO_(2) under economic and sustainable ***,the strong need for carbon neutrality has led to a proliferation of studies on the direct conversion of CO_(2) into carboxylic acids,which can effectively alleviate CO_(2) emissions and create high-value *** purpose of this review is to present the application prospects of carboxylic acids and the basic principles of CO_(2) conversion into carboxylic acids through photo-,electric-,and thermal *** attention is focused on the regulation strategy of the activity of abundant catalysts at the molecular level,inspiring the preparation of high-performance *** addition,theoretical calculations,advanced technologies,and numerous typical examples are introduced to elaborate on the corresponding process and influencing factors of catalytic ***,challenges and prospects are provided for the future development of this *** is hoped that this review will contribute to a deeper understanding of the conversion of CO_(2) into carboxylic acids and inspire more innovative breakthroughs.

关键词： carbon neutrality carboxylic acids CO_(2)conversion heterogeneous catalyst in situ technology

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