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π-conjugated chromophore functionalized high-nuclearity titanium-oxo clusters containing structural unit of anatase for photocatalytic selective oxidation of sulfides

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Rare Metals 2024年第4期43卷 1736-1746页

作者： Ling-Rong Liao Dong-Chun Zheng Pin-Xi Ou Qi-Xin Zhao Wei-Min Xuan Qi Zheng State Key laboratory for Modification of Chemical Fibers and Polymer Materials&College of Materials Science and Engineering Donghua UniversityShanghai201620China State Key laboratory for Modification of Chemical Fibers and Polymer Materials and College of Chemistry and Chemical Engineering Donghua UniversityShanghai 201620China

N-doping has significant influence in manipulating the properties of TiO_(2),and this has stimulated the development of N-donor-functionalized titanium-oxo clusters(TOCs)as molecular models to study the structure-property ***,the structural type and photoresponsive application are still limited for such TOCs,especially regarding the high-nuclearity TOCs that contain structure unit of TiO_(2)for ***,we showed the synthesis of a series of high-nuclearity TOCs 1-3 compounds usingπ-conjugated 1,10-phenanthroline(phen)as chromophore and N-donor functional *** 1 features cocrystal structure composed of one[Ti_(26)]~(2+)and half[Ti_(22)]~(2+),which renders it as the first cocrystallized TOC containing two positively charged species and phen-functionalized TOC showing the highest nuclearity up to 37 Ti *** adjusting the synthetic conditions,the individual{Ti_(22)}and{Ti_(26)}clusters can also be isolated as Compounds 2 and 3,*** core structure of{Ti_(22)}is mainly constructed from four lacunary{Ti_(4)}derived from pentagonal{Ti(Ti)_5}unit,while{Ti_(26)}is built from four complete{Ti(Ti)_5}***,a{Ti_8O_(14)}structure unit of anatase TiO_(2)can be identified in{Ti_(26)}.Based on the unique structural features and proper photophysical and photochemical properties of Compounds 1-3,they are applied for photocatalytic *** to the presence of anatase structure unit in{Ti_(26)}and the synergistic effect from{Ti_(22)}and{Ti_(26)},the catalytic performance presents in the order of Compound 1>Compound 3>Compound *** work provides excellent models to understand the structureproperty relationship from the perspective of cocrystallization and Ti-O binding model and will further promote the application of TOCs as functional catalysts for organic transformation.

关键词： Titanium-oxo cluster Molecular model of anatase TiO_(2) High nuclearity π-conjugated chromophore Photocatalytic sulfoxidation

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KLVFF peptide functionalized nanoparticles capture Aβ_(42) by co-assembly for decreasing cytotoxicity

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Chinese Chemical Letters 2018年第12期29卷 1811-1814页

作者： Peipei Yang Chao Yang Kuo Zhang Lei Wang Hao Wang cas Center for Excellence in Nanoscience CAS Key Laboratory for Biomedical Effects of Nanomaterials and NanosafetyNational Center for Nanoscience and Technology (NCNST)

The accumulation of extracellular senile plagues of amyloid β-proteins(Aβ) in the patient brain is one of most important facture in Alzheimer’s disease(AD), which is resulted from abnormal self-assembly of Aβpeptide. Nanoparticles show greatly potential for therapeutic studies due to the sophisticated surface which can mimic the functionality of protein. Herein, we design the bis(pyrene)-Lys-Leu-Val-Phe-PheGly-poly ethylene glycol(BP-KLVFFGPEG) based nanoparticles, which capture Aβthrough recognition and co-assembly of KLVFF. The resulting co-assemblies show different morphologies, such as large aggregates, nanoparticles and nanofibers corresponding to the different length chain of PEG, leading to different capture efficiencies. The co-assembly strategy shows a decrease of cytotoxicity, potentially for AD treatment.

关键词： Co-assembly Morphology Capture Nanoparticles Aβ

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LiOH-mediated crystallization regulating strategy enhancing electrochemical performance and structural stability of SiO anodes for lithium-ion batteries

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Nano Research 2024年第9期17卷 8174-8183页

作者： Zhengqiu He Zewen Xu Yu Long Jiexin Zhu Hao Yang Kuo Chen Qiang Zhou Ning Cao Xiaobo Wang Juan Wang Xiaojie Tan Litao Wang Luhai Wang Shengbao He Mengdi Zhang Han Hu Mingbo Wu State Key laboratory of Heavy Oil Processing College of Chemistry and Chemical EngineeringChina University of Petroleum(East China)Qingdao 266580China Department of Chemistry National University of Singapore3 Science Drive 3Singapore 117543Singapore School of Chemical Sciences University of AucklandAuckland 1010New Zealand Petrochemical Research Institute Petro China Company Ltd.Beijing 102206China

Silicon monoxide(SiO)is widely recognized as a promising anode material for next-generation lithium-ion *** to its metastable amorphous structure,SiO exhibits a highly complex degree of crystallization at the microscopic level,which significantly influences its electrochemical *** a consequence,accurately regulating the crystallization of SiO,and further establishing the relationship between crystallinity and electrochemical performance are very critical for SiO *** this article,carbon-coated SiO materials with different crystallinity degrees were synthesized using lithium hydroxide monohydrate(LiOH·H_(2)O)as a structural modifier to reveal this ***,moderate amount of LiOH·H_(2)O addition results in the forming of an oxygen-rich shell,which effectively inhibits the inward migration of oxygen atoms on the SiO surface and suppresses volume ***,the crystallinity of SiO will gradually enhance and the crystalline phase appears with increasing the amount of LiOH·H_(2)O,which will generate a deteriorative Li+diffusion *** balancing the above two contradictions,a mass fraction of 1%LiOH·H_(2)O for the additive yielded SiO@C-1,characterized by optimal ***@C-1 demonstrates exceptional long-cycle stability with 74.8%capacity retention after 500 cycles at 1 A·g^(-1).Furthermore,it achieves a capacity retention of 52.2%even at a high density of 5 A·g^(-1).This study first reveals the relationship between SiO crystallinity and electrochemical performance,which efficiently guides the design of high-performance SiO anodes.

关键词： lithium-ion batteries SiO anodes crystallinity regulation high rate long life

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互花米草有利于我国海岸带蓝碳功能提升

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Science Bulletin 2024年第12期69卷 1991-2000页

作者：张靖凡毛德华刘纪化陈雅萍 Matthew Kirwan Christian Sanders 周金戈卢哲覃国铭黄幸运李慧焉恒琦焦念志苏纪兰王法明 Guangdong Key laboratory of Applied Botany Xiaoliang Research Station of Tropical Coastal Ecosystemsthe CAS Engineering Laboratory for Ecological Restoration of Island and Coastal EcosystemsSouth China Botanical GardenChinese Academy of SciencesGuangzhou 510650China University of Chinese Academy of Sciences Beijing 100049China South China national Botanical Garden Chinese Academy of SciencesGuangzhou 510650China Key laboratory of Wetland Ecology and Environment Northeast Institute of Geography and AgroecologyChinese Academy of SciencesChangchun 130102China Marine Research Institute Shandong UniversityQingdao 266237China School of Ecology Shenzhen Campus of Sun Yat-sen UniversityShenzhen 518107China Virginia Institute of Marine Science Gloucester PointVA 23062USA national Marine Science Centre School of EnvironmentScience and EngineeringSouthern Cross UniversityCoffs HarbourNSW 2450Australia Guangdong Eco-engineering Polytechnic Guangzhou 510520China Carbon Neutral Innovation Research Center and Fujian Key laboratory of Marine Carbon Sequestration Xiamen UniversityXiamen 361005China Second Institute of Oceanography State Oceanic AdministrationHangzhou 310012China Southern Marine Science and Engineering Guangdong laboratory(Zhuhai) Zhuhai 519082China School of Ecology and Environment Hainan UniversityHaikou 570228China

Spartina alterniflora has rapidly and extensively encroached on China's coastline over the past *** the coastal areas invaded by ***,at most 93%are ***,the effect of *** invasion on soil organic carbon(SOC)stocks of coastal mudflats has not been systematically studied on a national ***,we quantified the nationwide changes in SOC stocks in coastal mudflats associated with *** invasion between 1990 and *** found that *** invasion significantly enhanced SOC stocks in coastal ***,the benefit of *** invasion of coastal SOC stock may be weakened by continuing human *** found that *** invading mudflats added 2.3 Tg SOC stocks to China's coastal blue carbon,while 1.78 Tg SOC stocks were lost mainly due to human activities,resulted in a net SOC stock gain of 0.52 Tg *** findings overturned the traditionally thought that *** invasion would reduce ecosystem services by highlighting that the historical invasion of *** has broadly and consistently enhanced blue carbon stock in coastal China.

关键词： Spartina alterniflora invasion Mudflats China coastal wetland Blue carbon sequestration

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The Burden of Hypertension-Related Chronic Kidney Disease—China,2010–2019

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China CDC weekly 2024年第14期6卷 282-288页

作者： Youyuan Bu Yueru Liu Maigeng Zhou Peng Yin Kejun Liu Yamin Bai Xuancheng Lu Chinese Center for Disease Control and Prevention BeijingChina national Center for Chronic and Non-Communicable Disease Control and Prevention Chinese Center For Disease Control and PreventionBeijingChina China national Health Development Research Center BeijingChina

What is already known about this topic?The global burden of chronic kidney disease(CKD)is on the *** is added by this report?In 2019,5.58 million individuals in China were affected by CKD related to hypertension,leading to 70,260 fatalities and 1.69 million disability-adjusted life years(DALYs).The most affected groups were men,older individuals,and residents of western *** the period from 2010–2019,the age-standardized prevalence rate(ASPR)remained constant,and the agestandardized mortality rate(ASMR)and agestandardized DALY rate(ASDR)showed a decreasing ***,there was an increase in the number of cases,deaths,and DALYs associated with this *** are the implications for public health practice?Hypertension significantly contributes to the burden of CKD;therefore,raising awareness and implementing early screening measures are essential.

关键词： Kidney mortality burden

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Step-edge-guided nucleation and growth mode transition of α-Ga_(2)O_(3) heteroepitaxy on vicinal sapphire

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Chinese Physics B 2024年第8期33卷 397-403页

作者：郝景刚张彦芳张贻俊徐科韩根全叶建东 Test&Analysis Platform Suzhou Institute of Nano-Tech and Nano-BionicsChinese Academy of SciencesSuzhou 215123China School of Electronic Science and Engineering Nanjing UniversityNanjing 210023China Wuxi Institute of Technology Wuxi 214121China School of Microelectronics Xidian UniversityXi'an 710071China Suzhou national laboratory for Materials Science Jiangsu Institute of Advanced SemiconductorsSuzhou 215123China

Controlling the epitaxial growth mode of semiconductor layers is crucial for optimizing material properties and device *** this work,the growth mode ofα-Ga_(2)O_(3) heteroepitaxial layers was modulated by tuning miscut angles(θ)from 0°to 7°off the(1010)direction of sapphire(0002)*** flat sapphire surfaces,the growth undergoes a typical three-dimensional(3D)growth mode due to the random nucleation on wide substrate terraces,as evidenced by the hillock morphology and high dislocation *** the miscut angle increases toθ=5°,the terrace width of sapphire substrate is comparable to the distance between neighboring nuclei,and consequently,the nucleation is guided by terrace edges,which energetically facilitates the growth mode transition into the desirable two-dimensional(2D)coherent ***,the mean surface roughness decreases to only 0.62 nm,accompanied by a significant reduction in screw and edge dislocations to 0.16×10^(7) cm^(-2)and 3.58×10^(9) cm^(-2),***,the further increment of miscut angles toθ=7°shrink the terrace width less than nucleation distance,and the step-bunching growth mode is *** this circumstance,the misfit strain is released in the initial growth stage,resulting in surface morphology degradation and increased dislocation densities.

关键词： growth mode miscut angle crystalline quality surface morphology

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Effect of TiO_(2) addition on microstructures and properties of Mgo-Cao refractory aggregates

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Journal of Iron and Steel Research International 2024年第6期31卷 1547-1554页

作者： Shuai Zhang Jing-ran Wang Yuan-gao Li Feng-you Li Wen Yan Hui-ying Shi The State Key laboratory of Refractories and Metallurgy Wuhan University of Science and TechnologyWuhan 430081HubeiChina Joint International Research laboratory of Refractories and Metallurgy Wuhan 430081HubeiChina Shanxi Luweibao Taigang Refractory Co. Ltd.Taiyuan 030003ShanxiChina

MgO-CaO(40 wt.%CaO)refractory aggregates were prepared using the calcined dolomite and light-burned magnesia fine powder as raw materials and TiO_(2) as *** effect of TiO_(2) on their phase composition,microstructures and properties was investigated by X-ray diffraction and scanning electron *** properties such as bulk density,apparent porosity,relative aggregate tube strength and hydration resistance were also *** results showed that the CaTiO_(3) generated by the reaction between CaO and TiO_(2) was distributed around the CaO grain boundaries and intermittently distributed with MgO,which formed an isolation layer around CaO and greatly improved the hydration ***,the introduction of TiO_(2) promoted sintering and increased the grain size,further improving the strengths and hydration resistance of the *** addition,the most significant enhancement in the hydration resistance and strengths of the samples was achieved when 1.0-2.0 wt.%TiO_(2) was *** this case,the relative strength of aggregate increased from 33.3% to 37.3%-43.1%,and the mass gain after the hydration test decreased from 3.13% to 1.26%-1.45%.

关键词： MgO-CaO refractory aggregate TiO_(2)addition Phase composition Microstructure Hydration resistance

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Toluene Processed All-Polymer Solar Cells with 18% Efficiency and Enhanced Stability Enabled by Solid Additive:Comparison Between Sequential-Processing and Blend-casting

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Energy & Environmental Materials 2024年第4期7卷 247-254页

作者： Guoping Zhang Chaoyue Zhao Liangxiang Zhu Lihong Wang Wenzhao Xiong Huawei Hu Qing Bai Yaping Wang Chen Xie Peng You He Yan Dan Wu Tao Yang Mingxia Qiu Shunpu Li Guangye Zhang College of New Materials and New Energies Shenzhen Technology University Department of Chemistry and Hong Kong Branch of Chinese national Engineering Research Center for Tissue Restoration and Reconstruction The Hong Kong University of Science and Technology State Key laboratory for Modification of Chemical Fibers and Polymer Materials Center for Advanced Low-dimension Materials College of Materials Science and Engineering Donghua University Julong College Shenzhen Technology University

The emergence of polymerized small molecule acceptors (PSMAs) has significantly improved the performance of all-polymer solar cells (all-PSCs).However,the pace of device engineering lacks behind that of materials deve... 详细信息

关键词： all-polymers solar cells sequential processing solid additive

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Anion-induced electrolyte chemistry enables high energy density primary battery for ultralow-temperature conditions

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Science China Chemistry 2024年

作者： Zi-Hang Xue Hao-Jie Liang Yong-Li Heng Jia-Lin Yang Edison Huixiang Ang Hong-Yan Lü Hong Yu Dong-Mei Dai Dai-Huo Liu Chuan-Yu Zheng Wei Guo Xing-Long Wu Department of Chemistry Northeast Normal University MOE Key laboratory for UV Light-Emitting Materials and Technology Northeast Normal University Natural Sciences and Science Education National Institute of Education Nanyang Technological University State Key laboratory of Solidification Processing Center of Advanced Lubrication and Seal Materials Northwestern Polytechnical University School of Chemistry and Chemical Engineering Henan Normal University Key laboratory of Organo-Pharmaceutical Chemistry of Jiangxi Province Gannan Normal University

Lithium/fluorinated-carbon（Li/CFx） primary batteries are widely used in defense and military fields due to their stable discharge plateau, low self-discharge rate, and adaptability across a wide temperature range. However, enhancing their overall energy density and discharge capacity at low temperatures remains a critical challenge. Herein, we report a strategically designed LiBF4-based sulfite/carboxylate electrolyte, where the anion-involved solvation structure significantly enhances electrochemical kinetics by reducing the desolvation barrier. Simultaneously, it introduces a radical reaction mechanism that contributes to additional capacity. As a result, the Li/CFxprimary batteries with this formulated electrolyte deliver a specific capacity of 2,257.15 mAh g-1at 25 °C. More importantly, when operating at -40 °C, the batteries exhibit an exceptionally high discharge capacity of 1,549.4 m Ah g-1and an energy density of 2,868.6 Wh kg-1. Even at -60 °C, the Li/CFxcells achieve a specific capacity of 444.3 mAh g-1and an energy density of 821.8 Wh kg-1at 0.1 C, significantly outperforming previously reported organic-based liquid electrolytes. This work offers a viable strategy for enhancing the specific capacity and energy density of primary batteries in extreme environments, providing valuable insights for future developments.

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Organic Synthesis through Radical Innovation:Frustrated Radical Pairs

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Chinese Journal of Chemistry 2024年第10期42卷 1157-1160页

作者： Zhibin Hu Zengrui Cheng Ning Jiao State Key laboratory of Natural and Biomimetic Drugs School of Pharmaceutical SciencesPeking UniversityBeijing 100191China Shanghai Key laboratory of Green Chemistry and Chemical Processes East China Normal UniversityShanghai 200062China

Frustrated Lewis Pairs(FLPs)represent a unique class of interactions in Lewis acid-base chemistry,driven by spatial hindrance or incongruent orbital energy levels that hinder the formation of effective coordination *** have received significant attention for their application in activating small molecules and facilitating organic synthesis *** developments have led to the emergence of Frustrated Radical Pairs(FRPs)as an extension of the radical *** are formed from FLPs through Single Electron Transfer(SET)and exhibit the ability to activate a variety of chemical *** research on FLPs is well-established,investigations into FRPs in organic reactions remain *** review highlights the current state of FRPs in organic synthesis,delves into mechanistic insights,explores their potential,and underscores the challenges in this emerging field.

关键词： Radicals Frustrated Lewis Pairs Frustrated Radical Pairs Methodology and reactions Reaction mechanisms

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