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| 1 | Growth mechanism of CsPbBr3 perovskite nanocrystals by a co-precipitation method in a CSTR system显示文摘A co-precipitation method based on supersaturated recrystallization in a continuous stirred-tank reactor(CSTR)system was applied to un cover the growth mecha nism of CsPbBr3 perovskite nano crystals(NCs).The reacti on rate can be controlled by changi ng the reaction conditions in this CSTR system,which helps us to observe importa nt intermediate stages to gain in sight into the growth mecha nism of these NCs.The effects of the temperature,concentrations of the ligands(oleylamine and oleic acid),and precursor concerttrations during the growth process of CsPbBr3 NCs were discussed in detail.Further,the growth mechanism of CsPbBr3 NCs was investigated in terms of the dynamics and thermodynamics on the basis of experimental results.The growth mechanism is a useful guide to large-scale synthesis.The synthesized CsPbBr3 NCs were employed for fabrication of both white light-emitting diodes and quantum-dot light-emitting diodes to test their photoelectric properties;the results show that CsPbBr3 NCs show great promise for optoelectronics applications. | Jibin Zhang Lianwei Fan Junli Li Xiangfu Liu Rongwen Wang Lei Wang Guoli Tu | 2019 | Nano Research2019，12，1： | 3 |
| 2 | A Clicked Tetrathiafulvalene-oxyquinoline Dyad as an Optical and Electrochemical Zn2+ Probe显示文摘一篇小说点按 tetrathiafulvalene 衍生物 3 生二个 8-oxyquinoline 组通过光、电气化学的变化为 Zn2+ 的选择察觉被综合。Zn2+ 和 Cd2+ 的增加在荧光紧张导致了一个重要变化,它对从 oxyquinoline 和 1,2,3-triazole 戒指的提高 chelation 的荧光效果可归因。3 的电气化学的潜力测试的另外的金属阳离子相对那些向更积极的价值面对 Zn2+ 被转移。 | Zhao,Bangtun Liu,Lianwei Li,Xiaochuan Qu,Guirong | 2012 | Chinese Journal of Chemistry2012，30，2： | 2 |
| 3 | Frequent Itemset Mining of User’s Multi-Attribute under Local Differential Privacy显示文摘Frequent itemset mining is an essential problem in data mining and plays a key role in many data mining applications.However,users’personal privacy will be leaked in the mining process.In recent years,application of local differential privacy protection models to mine frequent itemsets is a relatively reliable and secure protection method.Local differential privacy means that users first perturb the original data and then send these data to the aggregator,preventing the aggregator from revealing the user’s private information.We propose a novel framework that implements frequent itemset mining under local differential privacy and is applicable to user’s multi-attribute.The main technique has bitmap encoding for converting the user’s original data into a binary string.It also includes how to choose the best perturbation algorithm for varying user attributes,and uses the frequent pattern tree(FP-tree)algorithm to mine frequent itemsets.Finally,we incorporate the threshold random response(TRR)algorithm in the framework and compare it with the existing algorithms,and demonstrate that the TRR algorithm has higher accuracy for mining frequent itemsets. | Haijiang Liu Lianwei Cui Xuebin Ma Celimuge Wu | 2020 | Computers, Materials & Continua2020，，10： | 1 |
| 4 | A novel model to determine the dipeptides responsible for optimum temperature in F/10 xylanase显示文摘 | Liu Lianwei Wang Mingli Shao Weilan | 2005 | Process Biochemistry2005，40，3： | 1 |
| 5 | A-site Cation Defects(Ba_(0.5)Sr_(0.5))_(1-x)Co_(0.8)Fe_(0.2)O_(3-δ)Perovskites as Active Oxygen Evolution Reaction Catalyst in Alkaline Electrolyte显示文摘Main observation and conclusion Perovskites(Ba_(0.5)Sr_(0.5))_(1-x)Co_(0.8)Fe_(0.2)O_(3-δ)(x=0.02,0.05,0.1 denoted as BSCF-0.98,BSCF-0.95,BSCF-0.9,respectively)with A-site cation defects are synthesized by simple and efficient sol-gel method and are proved to have better OER catalytic effect than the well-known(Ba_(0.5)Sr_(0.5))_(1-x)Co_(0.8)Fe_(0.2)O_(3-δ)(BSCF)oxides.BSCF-0.95 exhibits the best OER catalytic activity in the series perovskite.The current density of BSCF-0.95 is about 56%higher than that of BSCF oxide at a potential of 1.7 V.The experimental studies have shown that compared with BSCF,BSCF-0.95 oxide has a larger electrochemical surface area(ECSA),a higher content of O_(2)^(2–)species related to surface oxygen vacancies,and faster charge transfer rate,which may be the factors for the enhancement of OER activity.The theoretical calculation results prove that the center positions of the O 2p-band of perovskite with A-site cation defects are closer to the Fermi level than BSCF oxide,which agrees with the OER performance trend of the material. | Lulu Tang Yifei Rao Lianwei Wei Hui Zheng Huimin Liu Wenhua Zhang Kaibin Tang | 2021 | Chinese Journal of Chemistry2021，39，10： | 0 |
| 6 | Iridium-Doped 10H-Phase Perovskite BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3-δ)as an Efficient Oxygen Evolution Reaction Catalyst显示文摘Designing low-cost and high-performance catalysts of electrocatalytic oxygen evolution reaction(OER)has always been one of the hot topics in current research.Hexagonal perovskite materials show great application potential in this field.Here,we synthesized 5%Iridium(Ir)-doped hexagonal phase perovskite BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3–δ)(BCFI).Using the Rietveld method to refine the structure,combining with the spherical aberration corrected high-angle annular dark-field scanning transmission electron microscopy(HAADF-STEM)atomic imaging,we found that BCFI is a ten-layer hexagonal(10H)structure,which belongs to the Purn:x-wiley:1001604X:media:cjoc202200200:cjoc202200200-math-0001m2 space group.In addition,BCFI shows excellent OER catalytic effect and good stability in 1 mol/L KOH solution,and the overpotential reaches 294 mV at a current density of 10 mA cm^(–2).The reduction of Cobalt(Co)valence state induced by Ir doping significantly enhances the OER activity of BCFI.Meanwhile,density functional theory(DFT)calculations show that the 2p-band center of oxygen(O)in BCFI is closer to the Fermi level than that in undoped BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3–δ)(BCF),which is beneficial to the OER.This work reveals a novel 10H-BCFI material with excellent OER performance,and provides a basis for the design of hexagonal perovskite materials in OER and other energy conversion fields. | Huimin Liu Qinxin Luo Jiaping Hu Lianwei Wei Wanqun Zhang Hui Zheng Shusheng Wu Kaibin Tang | 2022 | Chinese Journal of Chemistry2022，40，19： | 0 |
| 7 | Synchronous Variations in Abundance and Distribution of Ommastrephes bartramii and Dosidicus gigas in the Pacific Ocean显示文摘An analysis was performed in this study to investigate synchronous fluctuations in abundance and distribution of Om-mastrephes bartramii in the Northwest Pacific Ocean and Dosidicus gigas in the Southeast Pacific Ocean.The impacts of two Niño indices and regional water surface temperature on the two squids during 2006-2015 were evaluated,which possibly can explain the observed synchronicity.Catch per unit effort(CPUE)and the latitudinal gravity centers(LATG)of fishing effort were used to indi-cate squid abundance and distribution,respectively.The results indicated that both the CPUE and LATG showed highly interannual variations and synchronous fluctuation with significant negative associations between the two squid species from September to No-vember.Strong positive cross-correlations with 2-month lag was found between sea surface temperature(SST)anomaly in the Niño 3.4 and Niño 1+2 regions,which have significant linkage with the SST on the fishing ground of O.bartramii and D.gigas,respec-tively.Moreover,the proportion of favorable-SST area(PFSST)and the latitudinal location of the optimal SST for O.bartramii and D.gigas were positively correlated with the CPUE and LATG,respectively.Increased O.bartramii PFSST clearly corresponded to decreased D.gigas PFSST in phase as well as the latitudinal location of the optimal SST from September to November over 2006-2015.Our findings suggest that synchronous changes in abundance and distribution of the two squids were due to simultaneous variations in the PFSST and the latitudinal location of the optimal SST front which were affected by the SSTA changes in the Niño 3.4 and Niño 1+2 regions. | YU Wei CHEN Xinjun LIU Lianwei | 2021 | Journal of Ocean University of China2021，20，3： | 0 |
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