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The effect of NiO-Ni_(3)N interfaces in in-situ formed heterostructure ultrafine nanoparticles on enhanced polysulfide regulation in lithium-sulfur batteries

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Journal of Energy Chemistry 2022年第5期31卷 762-770页

作者： Jun Pu Zhenghua Wang Pan Xue Kaiping Zhu Jiachen Li Yagang Yao Key Laboratory of Functional Molecular Solids Ministry of EducationAnhui Provincial Engineering Laboratory for New-Energy Vehicle Battery Energy-Storage MaterialsCollege of Chemistry and Materials ScienceAnhui Normal UniversityWuhu 241002AnhuiChina National Laboratory of Solid State Microstructures College of Engineering and Applied SciencesJiangsu Key Laboratory of Artificial Functional MaterialsCollaborative Innovation Center of Advanced MicrostructuresNanjing UniversityNanjing 210093JiangsuChina School of Chemical Engineering Northwest UniversityXi’an 710069ShaanxiChina Division of Nanomaterials and Jiangxi Key Lab of Carbonene Materials Suzhou Institute of Nano-Tech and Nano-BionicsChinese Academy of SciencesNanchang 330200JiangxiChina

Inhibiting the “shuttle effect” of soluble polysulfides and improving reaction kinetics are the key factors necessary for further exploration of high-performance Li-S batteries. Herein, an effective interface engineering strategy is reported, wherein nitriding of an Ni-based precursor is controlled to enhance Li-S cell regulation. The resulting in-situ formed NiO-Ni_(3)N heterostructure interface not only has a stronger polysulfide adsorption effect than that of monomeric NiO or Ni_(3)N but also has a faster Li ion diffusion ability than a simple physical mixture. More importantly, this approach couples the respective advantages of NiO and Ni_(3)N to reduce polarization and facilitate electron transfer during polysulfide reactions and synergistically catalyze polysulfide conversion. In addition, ultrafine nanoparticles are thought to effectively improve the use of additive materials. In summary, Li-S batteries based on this NiO-Ni_(3)N heterostructure have the features of long cycle stability, rapid charging-discharging, and good performance under high sulfur loading.

关键词： NiO-Ni_(3)N heterostructure Interface effect ultrafine nanoparticles Li-S batteries Polysulfides

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Fabrication of ultrafine ZnFe2O4 nanoparticles for efficient photocatalytic reduction CO2 under visible light illumination

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Journal of Materials Science & Technology 2018年第12期34卷 2331-2336页

作者： Jun xiao Weiyi Yang Shuang Gao Caixia Sun Qi Li Environment Functional Materials Division Shenyang National Laboratory for Materials ScienceInstitute of Metal ResearchChinese Academy of SciencesShenyong 110016China University ofChineseAcademy of Sciences Beijing 100049China Division of Energy and Environment Graduate School of ShenzhenTsinghua UniversityShenzhen 518055China Key Laboratory of New Metallic Functional Materials and Advanced Surface Engineering in Universities of Shandong Qingdao Binhai UniversityQingdao 266555China School of Mechanical and Electronic Engineering Qingdao Binhai UniversityQingdao 266555China

A one-pot, solvent-thermal process was used to create the ultrafine ZnFe2O4nanoparticles photocatalyst.During the solvent-thermal process, the in situ self-forming NaCl not only served as a "cage" to confine the ion diffusion, but also acted as a microreactor for nanocrystallite growth. An average particle size of ～10 nm and a high-specific surface area of～112.9 m2/g were observed for the ultrafine ZnFe2O4nanoparticles Owing to the synergistic effect of ultrafine particle size, the full utilization of the visible light region and high conduction band(CB) position, ultrafine ZnFe2O4photocatalyst displayed an efficient photocatalytic CO2reduction under visible light illumination. Besides, the ultrafine ZnFe2O4photocatalyst showed high production selectivity for CH3CHO and C2H5OH generation in aqueous CO2/NaHCO3solution. This work may provide a new idea for the synthesis of new high-efficiency photocatalysts.

关键词： ultrafine nanoparticles Photocatalytic CO_2 reduction Visible light ZnFe_2O_4 photocatalyst In situ self-formed "cage"

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Preparation of ultrafine Ce-based oxide nanoparticles and their catalytic performances for diesel soot combustion

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Journal of Rare Earths 2014年第2期32卷 124-130页

作者：韦岳长赵震焦金庆刘坚段爱军姜桂元 State Key Laboratory of Heavy Oil Processing China University of Petroleum

The ultrafine Ce-based oxide nanoparticles with different element dopings （Zr, Y） were synthesized by the method of mi- cropores-diffused coprecipitation （MDC） using ammonia solution as the precipitation agent. The activities of the catalysts for soot oxidation were evaluated by the temperature-programmed oxidation （TPO） reaction. Ce-based oxides prepared in this study exhibited high catalytic activity for soot oxidation under tile condition of loose contact between soot particles and catalysts, and the catalytic ac- tivity ofultrafine Ce0.gZr0 iO2 nanoparticle for soot combustion was the highest, whose/＂10, Ts0 and Sco2m was 364, 442 ~C and 98.3%, respectively. All catalysts were systematically characterized by means of X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Brumauer-Emett-Teller （BET）, Fourier transform infrared spectroscopy （FT-IR） and UV-Vis diffuse reflectance spectroscopy （UV-Vis DRS）. It was indicated that the MDC method could prepare the ultrafine Ce-bascd oxide nanoparticles whose the crystal lattice were perfect, and the BET surface area and average crystal size of the ultrafine nanoparticles changed with the different element dopings （Zr, Y）. The H2-TPR measurements showed that the ultrafine Ce-based ox- ide nanoparticles with the doping-Zr cation could be favorable for improving the redox property of the catalysts.

关键词： ultrafine nanoparticles Ce-based oxides catalysts soot combustion micropores-diffused coprecipitation rare earths

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自还原法合成超小尺寸钯加氢催化剂

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Science China Materials 2023年第7期66卷 2708-2714页

作者：莫世广荆文彤张伟杰刘锟隆吴炳辉秦瑞轩郑南峰 State Key Laboratory for Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy Materialsand Engineering Research Center for Nano-Preparation Technology of Fujian ProvinceCollege of Chemistry and Chemical EngineeringXiamen UniversityXiamen 361005China Chemistry and Chemical Engineering Guangdong Laboratory Shantou 515031China Pen-Tung Sah Institute of Micro-Nano Science and Technology Xiamen UniversityXiamen 361005China

负载型超小尺寸金属纳米颗粒在多相催化过程中表现出优异的催化性能.虽然已经发展了一些合成方法,但仍缺少便捷地合成超小尺寸催化剂的方法.通常情况下,加氢金属催化剂往往需要经过高温还原过程.但过量的还原剂,如H2,会导致金属纳米颗... 详细信息

负载型超小尺寸金属纳米颗粒在多相催化过程中表现出优异的催化性能.虽然已经发展了一些合成方法,但仍缺少便捷地合成超小尺寸催化剂的方法.通常情况下,加氢金属催化剂往往需要经过高温还原过程.但过量的还原剂,如H2,会导致金属纳米颗粒的聚集.本研究利用含有有机配体的钯前驱体合成了金属氧化物负载的超小尺寸钯催化剂.在惰性气氛下,通过简单的煅烧即可得到尺寸均一、超小的Pd纳米颗粒(~1 nm).有机配体中的-CHx基团与氧化物载体的表面氧物种反应促进了Pd物种的还原.同时,反应过程中原位产生的CO和氧空位稳定了超小尺寸纳米颗粒.该方法所制备得到的催化剂具有较高的抗烧结能力、优异和稳定的催化加氢反应性能.

关键词： self-reduction organic ligand stoichiometric reduction ultrafine nanoparticles catalytic hydrogenation

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