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In-situ electrochemical surface-enhanced Raman spectroscopy in metal/polyelectrolyte interfaces 被引量:1
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作者 li-wen wu Mo-Li Huang +1 位作者 Yun-Xiao Yang Yi-Fan Huang 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第11期2820-2825,共6页
Polyelectrolyte becomes more and more popular in electrocatalysis.The understanding of electrode/polyelectrolyte interfaces at the molecular level is important for guiding further the polyelectrolyte-based electrocata... Polyelectrolyte becomes more and more popular in electrocatalysis.The understanding of electrode/polyelectrolyte interfaces at the molecular level is important for guiding further the polyelectrolyte-based electrocatalysis.Herein,we demonstrate an in-situ surface-enhanced Raman spectroscopic method by using a three-electrode spectroelectrochemical cell towards characterizing the electrode/polyelectrolyte interfaces.The Ag/AgCl and Ag/Ag_(2)O electrodes are used as the reference electrode in the acidic and the alkaline systems,respectively.The working electrode is made of a transparent carbon thin film which loads the electrocatalysts.The applications of this method are demonstrated through the in-situ characterizations of the p-methylthiophenol adsorbed on the Au and Pt and the electrochemical oxidation of Au on polyelectrolyte membranes.The potential-dependent spectral features of these two systems show that this method is a powerful tool for investigating the electrode/polyelectrolyte interfaces in electrocatalysis. 展开更多
关键词 POLYELECTROLYTE In-situ electrochemical characterization Surface-enhanced Raman spectroscopy Three-electrode cell Au oxidation
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应用镍超微电极的电化学表面增强拉曼光谱技术研究 被引量:1
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作者 吴丽文 王玮 黄逸凡 《电化学》 CAS CSCD 北大核心 2021年第2期208-215,共8页
镍(Ni)电极在电化学中应用广泛。原位表征Ni电极表面的吸附物种有益于帮助理解电极反应历程、指导发展高效电催化剂。应用超微电极作为工作电极的电化学表面增强拉曼光谱技术结合了超微电极表面的传质特性和分子水平的高灵敏度表征,是研... 镍(Ni)电极在电化学中应用广泛。原位表征Ni电极表面的吸附物种有益于帮助理解电极反应历程、指导发展高效电催化剂。应用超微电极作为工作电极的电化学表面增强拉曼光谱技术结合了超微电极表面的传质特性和分子水平的高灵敏度表征,是研究Ni电化学的有力手段。本文所述的研究工作通过在金(Au)超微电极表面电吸附具有SERS活性的Au纳米粒子并恒电流沉积金属Ni薄层,制备并表征了具有SERS活性的Ni超微电极。在氢氧化钠溶液中的循环伏安实验和以4-甲基苯硫酚分子作为探针分子的SERS实验结果表明,沉积速率和沉积电量是影响超微电极表面Ni的覆盖度和SERS活性的关键因素。在吸附了直径为55 nm Au纳米粒子的、直径为10μm Au的超微电极表面,以100μA·cm^(-2)电流密度电沉积厚度约为5个原子层Ni的条件下,可获得Ni覆盖完好的、具有最强SERS活性的Ni超微电极。 展开更多
关键词 超微电极 表面增强拉曼光谱 电沉积
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Classification,metallogenesis and exploration of silver deposits in Daxing’anling of Inner Mongolia and its adjacent areas
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作者 Biao Jiang Deng-hong Wang +12 位作者 Yu-chuan Chen Tong Zhang Xiu-lang Pu Wen-wen Ma Yan Wang Guang wu li-wen wu Tong Zhang Xue-jiao Li Jie Yan Yu-shan Zuo Hong-jun Sun Zhi-yuan Li 《China Geology》 CAS 2022年第4期595-613,共19页
By the end of 2020,83 silver deposits(or ore occurrences),including four super-large-scale deposits,nine large-scale deposits,33 medium-scale deposits and 37 small-scale deposits or ore occurrences,have been proved.Th... By the end of 2020,83 silver deposits(or ore occurrences),including four super-large-scale deposits,nine large-scale deposits,33 medium-scale deposits and 37 small-scale deposits or ore occurrences,have been proved.The amount of silver metal exceeds 86000 t with average grade of 100 g/t,which makes Daxing’anling region one of the the most important silver ore belt in China.However,the metallogenic characteristics and metallogenesis need to be clarified.The silver deposits in the study area are classified into three main types,which are magmatic hydrothermal vein type,continental volcano-subvolcanic type and skarn type,respectively.The supergiant deposits include the Shuangjianzishan deposit(silver metal amount of 15214 t with average grade of 138 g/t),the Baiyinchagandongshan deposit(silver metal amount of 9446 t with average grade of 187 g/t),the Huaobaote deposit(silver metal amount of 6852 t with average grade of 170 g/t),and the Fuxingtun deposit(silver metal amount of 5240 t with average grade of 196 g/t).The silver deposits are mainly distributed in the central and south of the Daxing’anling area,and mainly formed in the Yanshanian period.The silver polymetallic deposits in the Daxinganling area are significantly controlled by regional faults and the junction zone of volcanic rock basins and their margins.The north-east trending deep faults are the most important ore-controlling structures in this area.The distribution of silver polymetallic deposits along the main faults is obvious,and the intersection area of multiple groups of faults often form important mine catchments.The Permian is the most important ore-bearing formation in this area,but some important silver polymetallic deposits occur in Mesozoic volcanic basins or pre-Mesozoic strata.The magmatic rocks related to mineralization are mainly intermediate acidic or acidic intrusions,intermediate acidic lavas,pyroclastic rocks,and small intrusions of ultra-shallow or shallow facies of the Yanshanian Period.The mineralization element combination is mainly determined by the elemental geochemical background of surrounding rocks or source layers.In addition,the type of deposit,the distance from the mineralization center,and the degree of differentiation of ore-forming rock mass are also important influence factors.The article analyzes the prospecting prospects of each silver deposit type in the study area,discusses the relationship between mineralization center and deep prospecting,and proposes that porphyry silver deposits should be paid attention to.In the prospecting and exploration of silver deposits,comprehensive evaluation and multi-target prospecting need to be strengthened because silver can coexist or be associated with a variety of metals. 展开更多
关键词 Silver deposit Deposit type Porphyry silver deposit Supergiant silver deposit METALLOGENESIS Mineral exploration engineering Prospecting direction Daxing’anling Inner Mongolia
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Spatio-temporal Expression Study of Phosphorylated 70-kDa Ribosomal S6 Kinase (p70S6k) in Mesial Temporal Lobe Epilepsy
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作者 Xiao-liang Xing Long-ze Sha +3 位作者 Yuan Yao Yan Shen li-wen wu Qi Xu 《Chinese Medical Sciences Journal》 CAS CSCD 2012年第1期7-10,共4页
Objective To determine the spatio-temporal expression of p70S6k activation in hippocampus in mesial temporal lobe epilepsy. Methods Temporal lobe epilepsy model was established by stereotaxically unilateral and intrah... Objective To determine the spatio-temporal expression of p70S6k activation in hippocampus in mesial temporal lobe epilepsy. Methods Temporal lobe epilepsy model was established by stereotaxically unilateral and intrahip-pocampal injection of kainite acid (KA) in adult male C57BL/6 mice. Latent and chronic epileptogenesis were represented by mice 5 days after KA injection (n=5) and mice 5 weeks after KA injection (n=8), respectively. Control mice (n=5) were injected with saline. Immunohistochemical assays were performed on brain sections of the mice. Results Hippocampus both ipsilateral and contralateral to the KA injection displayed significantly up-regulated pS6 immunoreactivity in dispersed granule cells in 5-day and 5-week model mice. Conclusion The activation of p70S6k is mainly located in the dentate gyrus in KA-induced mouse model of temporal lobe epilepsy, indicating that the activation may be related with the disperse degree and hypertrophy of granule cells. 展开更多
关键词 mesial temporal lobe epilepsy P70S6K kainate acid IMMUNOREACTIVITY
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Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of China 被引量:5
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作者 Li-Hong Liao Chen Chen +9 位作者 Jing Peng li-wen wu Fang He Li-Fen Yang Ci-Liu Zhang Guo-Li Wang Pan Peng Yu-Ping Ma Pu Miao Fei Yin 《Chinese Medical Journal》 SCIE CAS CSCD 2019年第13期1533-1540,共8页
Background:Advanced technology has become a valuable tool in etiological studies of intellectual disability/global developmental delay(ID/GDD).The present study investigated the role of genetic analysis to confirm the... Background:Advanced technology has become a valuable tool in etiological studies of intellectual disability/global developmental delay(ID/GDD).The present study investigated the role of genetic analysis to confirm the etiology in ID/GDD patients where the cause of the disease was uncertain in central China.Methods:We evaluated 1051 ID/GDD children aged 6 months to 18 years from March 2009 to April 2017.Data concerning basic clinical manifestations were collected,and the method of etiology confirmation was recorded.Genome-wide copy number variations(CNVs)detection and high-throughput sequencing of exons in the targeted regions was performed to identify genetically-based etiologies.We compared the incidence of different methods used to confirm ID/GDD etiology among groups with differing degrees of ID/GDD using the Chi-square or Fisher exact probability test.Results:We recruited 1051 children with mild(367,34.9%),moderate(301,28.6%),severe(310,29.5%),and profoundly severe(73,6.9%)ID/GDD.The main causes of ID/GDD in the children assessed were perinatal factors,such as acquired brain injury,as well as single gene imbalance and chromosomal gene mutation.We identified karyotype and/or CNVs variation in 46/96(47.9%)of cases in severe ID/GDD patients,which was significantly higher than those with mild and moderate ID/GDD of 34/96(35.4%)and 15/96(15.6%),respectively.A total of 331/536(61.8%)patients with clear etiology have undergone genetic analysis while 262/515(50.9%)patients with unclear etiology have undergone genetic analysis(x^2=12.645,P<0.001).Gene structure variation via karyotype analysis and CNV detection increased the proportion of children with confirmed etiology from 51.0%to 56.3%,and second-generation high-throughput sequencing dramatically increased this to 78.9%.Ten novel mutations were detected,recessive mutations in X-linked genes(ATPase copper transporting alpha and bromodomain and WD repeat domain containing 3)and dominant de novo heterozygous mutations in X-linked genes(cyclin-dependent kinase like 5,protocadherin 19,IQ motif and Sec7 domain 2,and methyl-CpG binding protein 2)were reported in the study.Conclusions:The present study indicates that genetic analysis is an effective method to increase the proportion of confirmed etiology in ID/GDD children and is highly recommended,especially in ID/GDD children with uncertain etiology. 展开更多
关键词 INTELLECTUAL DISABILITY Global DEVELOPMENTAL delay CHILDREN Gene analysis ETIOLOGY
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