SERS谱峰强度比与电位的关系

ＳＥＲＳ谱峰强度比与电位的关系顾仁敖，吴芸，乔专虹，姚建林（苏州大学化学系２１５００６）田中群，李五湖（厦门大学化学系３６１００５）ＴｈｅＤｅｐｅｎｄｅｎｃｅｏｆＴｈｅＳＥＲＳＩｎｔｅｎｓｉｔｉｅｓＲａｔｅｏｎＴｈｅＰｏｔｅｎｔｉａｌ￥ＧｕＲｅｎａｏ...     

SERS谱峰强度随电位的变化

ＳＥＲＳ谱峰强度随电位的变化顾仁敖，吴芸，乔专虹（苏州大学化学系２１５００６）田中群，李五湖（厦门大学化学系３６１００５）ＴｈｅＤｅｐｅｎｄｅｎｃｅｏｆＴｈｅＳＥＲＳＩｎｔｅｎｓｉｔｉｅｓｏｎＴｈｅｐｏｔｅｎｔｉａｌ￥ＧｕＲｅｎａｏ；ＷｕＹｕｎａｎｄ...     

SERS技术研究电化学中的共吸附

ＳＥＲＳ技术研究电化学中的共吸附顾仁敖（苏州大学化学系苏州２１５００６）ＳＥＲＳＳｔｕｄｉｅｓｏｎＥｌｅｃｔｒｏｃｈｅｍｉｃａｌＣｏａｄｓｏｒｐｔｉｏｎＧｕＲｅｎａｏ（ＤｅｐａｒｔｍｅｎｔＣｈｅｍｉｓｔｒｙ，ＳｕｚｈｏｕＵｎｉｖｅｒｓｉｔｙＳｕｚｈｏ...     

SERS技术研究不同酸度下TU与ClO_4~-在金电极上的共吸附

ＳＥＲＳ技术研究不同酸度下ＴＵ与ＣｌＯ－４在金电极上的共吸附姚建林袁亚仙曹佩根顾仁敖（苏州大学化学系苏州２１５００６）田中群（厦门大学化学系固体表面物理化学国家重点实验室厦门３６１００５）ＳＥＲＳＳｔｕｄｉｅｓｏｎＣｏａｄｓｏｒｐｔｉｏｎｏｆＴ...     

两种新卟啉的FT－SERS光谱

两种新卟啉的ＦＴ－ＳＥＲＳ光谱周光明，盛蓉生，徐知三，王霆，熊亚，王小华，曾云鹗（武汉大学化学系武汉大学分析测试中心武汉４３００７２）（北京Ｂｒｕｋｅｒ公司北京１００８７１）ＦＴ－ＳＥＲＳＳｐｅｃｔｒａｏｆＴｗｏＮｏｖｅｌＰｏｒｐｈｙｒｉｎｓ￥Ｚｈｏ...     

电极/水溶液界面的SERS研究Ⅰ.Cu/1.0M的Na_2SO_4和NaCl溶液体系

电极／水溶液界面的ＳＥＲＳ研究Ⅰ．Ｃｕ／１．０Ｍ的Ｎａ２ＳＯ４和ＮａＣｌ溶液体系陈燕霞黄开启田中群（厦门大学化学系固体表面物理化学国家重点实验室物理化学研究所厦门３６１００５）ＳＥＲＳＳｔｕｄｉｅｓｏｆＥｌｅｃｔｒｏｄｅ／ＥｌｅｃｔｒｏｌｙｔｅＳｏ...     

电极/水溶液界面的SERS研究Ⅱ.Ag/MgSo_4体系——一种可能的检测界面pH值的方法

电极／水溶液界面的ＳＥＲＳ研究Ⅱ．Ａｇ／ＭｇＳｏ４体系——一种可能的检测界面ｐＨ值的方法陈燕霞黄开启田中群（厦门大学化学系固体表面物理化学国家重点实验室物理化学研究所厦门３６１００５）ＳＥＲＳＳｔｕｄｉｅｓｏｆＥｌｅｃｔｒｏｄｅ／Ｅｌｅｃｔｒｏｌｙ...     

结晶紫分子的近红外傅里叶变换表面增强拉曼研究

结晶紫分子的近红外傅里叶变换表面增强拉曼研究李勤，张敏，林书煌，张崇起（首都师范大学物理系，化学系，综合所，物理系北京１０００３７）ＴｈｅＮＩＲ－ＦＴ－ＳＥＲＳｏｆＣｒｙｓｔａｌＶｉｏｌｅｔＡｄｓｏｒｂｅｄｂｙＳｉｌｖｅｒＣｏｌｌｏｉｄ￥ＬｉＱｉｎ；...     

水杨酸分子NIR－FT－SERS与VIS－SERS的比较研究

水杨酸分子ＮＩＲ－ＦＴ－ＳＥＲＳ与ＶＩＳ－ＳＥＲＳ的比较研究方炎，汪媛，胡凤霞（首都师范大学实验中心，首都师范大学综合所北京１０００３７）ＴｈｅＣｏｍｐａｒｉｓｏｎｏｆＶＩＳ－ＳＥＲＳｔｏＮＩＲ－ＦＴ－ＳＥＲＳｏｆＭｏｌｅｃｕｌｅｓＡｄｓｏｒｂｅｄｏ...     

ELECTRON MOMENTUM SPECTRA OF EXCITED He(2~1S) AND He(2~3S)

ＥＬＥＣＴＲＯＮＭＯＭＥＮＴＵＭＳＰＥＣＴＲＡＯＦＥＸＣＩＴＥＤＨｅ（２１Ｓ）ＡＮＤＨｅ（２３Ｓ）ＣｈｅｎＺｈａｎｇｊｉｎＳｈｉＱｉｃｕｎＣｈｅｎＪｉＸｕＫｅｚｕｎＤｅｐａｒｔｍｅｎｔｏｆＭｏｄｅｒｎＰｈｙｓｉｃｓ，ＵｎｉｖｅｒｓｉｔｙｏｆＳｃｉｅｎ...     

The role of surface electronic states in surface enhanced raman scattering

The dependence of the surface enchanced Raman scattering (SERS) intensity on the electrode potential is considered in terms of the nonresonant adiabatic charge-transfer mechanism. Surface electronic states of a substrate metal are proposed to be responsible for the observed potential dependence of the SERS signal. The contribution of surface states to the nonlinear metal polarizability was found from electroreflectance spectra of silver single-crystals. Good agreement between the measured and calculated potential behaviour of the SERS signal was found for pyridine absorbed on the silver electrode.     

SERS imaging of silver coated nanostructured Al and Al2O3 substrates. The effect of nanostructure

The last few years have witnessed rapid development of highly ordered and reproducible surface‐enhanced Raman scattering (SERS) nanostructured substrates for their potential medical and analytical application such as biosensing and bioimaging. In this work, 5‐nm silver films deposited on nanostructured Al and Al₂O₃ templates are investigated as substrates for SERS. The chosen templates show different honeycomb nanostructures with two sets of dimension, i.e. pore diameter of ca. 25 and 50 nm and interpore distance of ca. 56 and 100 nm. The SERS imaging results reveal that the signal of the probe molecule (4‐thiazolidinone‐2‐thione) is distributed inhomogeneously on the substrate surface, and this fact is correlated with the morphology of nanostructures determined by atomic force microscopy. The variation of SERS intensity among the substrates is strongly correlated with the shape and size of potential SERS‐active sites, e.g. nanocups and nanopores. The strongest SERS response is found for the Ag/Al₂O₃ template anodized in sulfuric acid, which represents the nanopore array with the smallest dimensions (e.g. pore diameter, interpore distance etc.). Furthermore, depending on size and nanostructure shape, changes in the adsorption mechanism of the probe molecule are observed. Copyright © 2014 John Wiley & Sons, Ltd.     

咪唑在铜电极上吸附行为的SERS研究

咪唑在铜电极上吸附行为的ＳＥＲＳ研究张传飞，徐知三，旷富贵，王小华，刘海林（武汉大学分析测试中心武汉４３００７２）（武汉大学环境科学系武汉４３００７２）ＳｔｕｄｙｏｎＴｈｅＡｄｓｏｒｐｔｉｏｎＢｅｈａｖｉｏｕｒｏｆＩｍｉｄａｚｏｌｅｏｎＣｏｐｐｅｒＥ...     

Biocompatible gold/silver nanostars for surface‐enhanced Raman scattering

Raman‐enhancing properties of chitosan (CS)‐coated gold/silver nanostars (Au/AgNSs) were demonstrated by using them as a surface‐enhanced Raman scattering (SERS) probe. Based on the energy‐dispersive X‐ray spectroscopy element distribution maps and highly enhanced SERS spectra, we suggest that the incorporation of silver into the NS tips leads to a stronger SERS behavior. The SERS spectra of the proteins adsorbed on the NS surface greatly differ from their respective Raman spectra in both the band positions and relative intensities, indicating that the protein molecules penetrate through the CS coating layer and interact closely with the NS surface. Raman and SERS spectra of Chlamydia trachomatis protease/proteasomelike activity factor are reported for the first time, demonstrating the potential of these NSs for the development of a diagnosis method for Chlamydia based on SERS. The results showed a good SERS performance of the Au/AgNSs and their potential for SERS detection of biomolecules. Copyright © 2016 John Wiley & Sons, Ltd.     

N-甲基咪唑与2,2'-联吡啶在铜表面共吸附的SERS研究

采用电化学现场表面增强拉曼光谱(SERS)分别研究了非水体系中N-甲基咪唑(NMIM),2,2’-联吡啶(2,2-’bipy)在铜电极表面的吸附行为以及两者的共吸附行为。结果表明在非水体系中,NMIM可在很宽的电位区间内稳定地吸附在金属表面,而2,2-’bipy在一个相对较窄的电位区间内能稳定地吸附在金属表面。当两者共存时存在竞争吸附和共吸附行为,较负的电位下主要以NMIM吸附为主,在略偏负的电位区间内以2,2-’bipy吸附为主,而正电位区间两者在金属表面共吸附,NMIM倾斜吸附在金属表面,而2,2’-bipy以顺式结构垂直吸附在金属表面。     

吡啶－碘电子转移复合物的表面增强拉曼光谱（SERS）研究

吡啶－碘电子转移复合物的表面增强拉曼光谱（ＳＥＲＳ）研究马树国，吴国祯（清华大学物理系北京１０００８４）ＴｈｅＳｕｒｆａｃｅＥｎｈａｎｃｅｄＲａｍａｎＳｔｕｄｙｏｆＴｈｅｃｈａｒｇｅＴｒａｎｓｆｅｒＣｏｍｐｌｅｘｏｆＰｙｒｉｄｉｎｅ－Ｉｏｄｉｎｅｏｎ...     

铜纳米线阵列的表面增强拉曼光谱和AFM研究

通过以有序的多孔氧化铝为模板,利用交流电在孔中沉积金属铜,并以此作为ＳＥＲＳ活性基底。原子力显微镜（ＡＦＭ）研究了氧化铝溶解过程中铜纳米线形貌,共焦显微拉曼则研究表面吸附ＳＣＮ 的ＳＥＲＳ光谱的变化。结果表明：铜纳米线表面ＳＥＲＳ强度和纳米金属在表面直立的高度有关;而其频率和直立的高度无关。ＳＣＮ 吸附在纳米线上比普通电化学粗糙的电极表面ＳＥＲＳ强度高,说明纳米线（点）有望成为一种活性高,稳定性好的ＳＥＲＳ基底。     

Improving SERS uniformity by isolating hot spots in gold rod-in-shell nanoparticles

Surface-enhanced Raman scattering (SERS) tags show ultrasensitivity and multiplexing abilities due to strong and characteristic Raman signals and therefore can be utilized as optical labeling agents similar to fluorescent dyes and quantum dots for biosensing and bioimaging. However, SERS tags have the difficulty to realize quantitative analysis due to the uniformity and reproducibility issue. In this work, we have reported on a new type of SERS tag called Au rod-in-shell (RIS) gap-enhanced Raman tag (GERT). With the high-resolution transmission electron microscopy (TEM) and optical absorbance measurements, we have demonstrated the subnanometer sized gap junctions inside the RIS GERTs. SERS measurements and FDTD calculations show that the core–shell subnanometer gap geometry in the RIS GERTs not only generates strong SERS hot spots but also isolates SERS hot spots by Au shells to avoid the influence when the particle aggregates form, therefore showing better SERS uniformity and stronger SERS intensity than normal Au nanorods. Those RIS NPs exhibit great potential as the labeling agents for SERS-based bioimaging and biosensing applications.     

Label‐free optical detection of type II diabetes based on surface‐enhanced Raman spectroscopy and multivariate analysis

Surface‐enhanced Raman scattering (SERS) spectroscopy was first employed to detect oxyhemoglobin (OxyHb, the common type of hemoglobin) variation in type II diabetic development without using exogenous reagents. Using silver nanoparticles as SERS‐active substrate, high‐quality SERS spectra are obtained from blood OxyHb samples of 49 diabetic patients and 40 healthy volunteers. Tentative assignment of the observed SERS bands indicates specific structural changes of OxyHb molecule in diabetes, including heme transformation and globin variation. Furthermore, partial least squares and principal component analysis combined with linear discriminate analysis diagnostic algorithms are employed to analyze and classify the SERS spectra acquired from diabetic and healthy OxyHb, yielding the diagnostic accuracies of 90.0% and 95.5%, respectively. This exploratory work suggests that the silver nanoparticles‐based OxyHb SERS method in combination with multivariate statistical analysis has great potential for the label‐free detection of type II diabetes. Copyright © 2014 John Wiley & Sons, Ltd.