In the Raman effect, incident light is inelastically scattered from a sample and shifted in frequency by the energy of its characteristic molecular vibrations. Since its discovery in 1927, the effect has attracted attention from a basic research point of view as well as a powerful spectroscopic technique with many practical applications. The advent of laser light sources with monochromatic photons at high flux densities was a milestone in the history of Raman spectroscopy and resulted in dramatically improved scattering signals (for a general overview of modern Raman spectroscopy, see refs 1-5). In addition to this so-called spontaneous or incoherent Raman scattering, the development of lasers also opened the field of stimulated or coherent Raman spectroscopies, in which molecular vibrations are coherently excited. Whereas the intensity of spontaneous Raman scattering depends linearly on the number of probed molecules, the coherent Raman signal is proportional to the square of this number (for an overview, see refs 6 and 7). Coherent Raman techniques can provide interesting new opportunities such as vibrational imaging of biological samples,8 but they have not yet advanced the field of ultrasensitive trace detection. Therefore, in the following article, we shall focus on the spontaneous Raman effect, in the following simply called Raman scattering. Today, laser photons over a wide range of frequencies from the near-ultraviolet to the near-infrared region are used in Raman scattering studies, allowing selection of optimum excitation conditions for each sample. By choosing wavelengths which excite appropriate electronic transitions, resonance Raman studies of selected components of a sample or parts of a molecule can be performed.9 In the past few years, the range of excitation wavelengths has been extended to the near-infrared (NIR) region, in which background fluorescence is reduced and photoinduced degradation from the sample is diminished. High-intensity NIR diode lasers are easily available, making this region attractive for compact, low cost Raman instrumentation. Further, the development of low noise, high quantum efficiency multichannel detectors (chargecoupled device (CCD) arrays), combined with highthroughput single-stage spectrographs used in combination with holographic laser rejection filters, has led to high-sensitivity Raman spectrometers (for an overview on state-of-the-art NIR Raman systems, see ref 10). As we shall show in section 2, the nearinfrared region also has special importance for ultrasensitive Raman spectroscopy at the singlemolecule level. As with optical spectroscopy, the Raman effect can be applied noninvasively under ambient conditions in almost every environment. Measuring a Raman spectrum does not require special sample preparation techniques, in contrast with infrared absorption spectroscopy. Optical fiber probes for bringing excitation laser light to the sample and transporting scattered light to the spectrograph enable remote detection of Raman signals. Furthermore, the spatial and temporal resolution of Raman scattering are determined by the spot size and pulse length, respectively, of the excitation laser. By using a confocal microscope, Raman signals from femtoliter volumes (∼1 μm3) can by observed, enabling spatially resolved measurements in chromosomes and cells.11 Techniques such as multichannel Hadamard transform Raman microscopy12,13 or confocal scanning Fourier transform Raman microscopy14 allow generation of high-resolution Raman images of a sample. Recently, Raman spectroscopy was performed using near-field optical microscopy.15-17 Such techniques overcome the diffraction limit and allow volumes significantly smaller than the cube of the wavelength to be investigated. In the time domain, Raman spectra can be measured on the picosecond time scale, providing information on short-lived species such as excited 2957 Chem. Rev. 1999, 99, 2957−2975

Ultrasensitive Chemical Analysis by Raman Spectroscopy

Limit of detection. A closer look at the IUPAC definition

Preface.- Contributors.- List of Abbreviations.- Section 1: Basic Principles: Introduction.-Sources of Heavy Metals and Metalloids in Soils.- Chemistry of Heavy Metals and Metalloids in Soils.- Methods for the Determination of Heavy Metals and Metalloids in Soils.- Effects of Heavy Metals and Metalloids on Soil Organisms.- Soil-Plant Relationships of Heavy Metals and Metalloids.- Heavy Metals and Metalloids as Micronutrients for Plants and Animals.-Critical Loads of Heavy Metals for Soils.- Section 2: Key Heavy Metals And Metalloids: Arsenic.- Cadmium.- Chromium and Nickel.- Cobalt and Manganese.- Copper.-Lead.- Mercury.- Selenium.- Zinc.- Section 3: Other Heavy Metals And Metalloids Of Potential Environmental Significance: Antimony.- Barium.- Gold.- Molybdenum.- Silver.- Thallium.- Tin.- Tungsten.- Uranium.- Vanadium.- Glossary of Specialized Terms.- Index.

Heavy metals in soils : trace metals and metalloids in soils and their bioavailability

The current status of the use of nanoparticles for photothermal treatments is reviewed in detail. The different families of heating nanoparticles are described paying special attention to the physical mechanisms at the root of the light-to-heat conversion processes. The heating efficiencies and spectral working ranges are listed and compared. The most important results obtained in both in vivo and in vitro nanoparticle assisted photothermal treatments are summarized. The advantages and disadvantages of the different heating nanoparticles are discussed.

Nanoparticles for photothermal therapies.

On the basis of different types of experiments, the authors develop implicitly the model of surface-enhanced Raman scattering (SERS) of adsorbates on metal surfaces. The long-range enhancement by resonances of the macroscopic laser and Stokes field is separated quantitatively from the metal electron-mediated resonance Raman effect. The latter mechanism proceeds by increased electron-photon coupling at an atomically rough surface and by temporary charge transfer to orbitals of the adsorbates. This model can account for the chemical specificity and vibrational selectivity of SERS and (partly) for the SERS specificity of the various metals.

https://iopscience.iop.org/article/10.1088/0953-8984/4/5/001/pdf

Surface-enhanced Raman scattering

The “super stars” of analytical atomic spectrometry are electrothermal atomization-atomic absorption spectrometry (ETA-AAS), inductively coupled plasma-atomic emission spectrometry (ICP-AES) and inductively coupled plasma-mass spectrometry (ICP-MS). Many other atomic spectrometric methods have been used to determine levels of elements present in solid, liquid and gaseous samples, but in most cases these other methods are inferior to the big three super star methods. The other atomic methods include glow discharge emission, absorption and mass spectrometric methods, laser excited fluorescence emission and ionization methods, and flame and microwave plasma emission and mass spectrometric methods. These “lesser” methods will be compared to the “super star” methods based on a number of figures of merit, including detection power, selectivity, multi-element capability, cost, applications, and “age” of the methods. The “age” of the method will be determined by a modification of the well-known Laitinen “Seven Ages of an Analytical Method”
				(H.A. Laitinen, Anal. Chem., 1973, 45, 2305). Calculations will show that certain methods are capable of single atom detection, including several atomic absorption methods, as well as laser atomic ionization and fluorescence methods. The comparison of methods will indicate why the “super stars” of atomic spectrometric methods will continue to retain their status and what must be done for the lesser atomic methods to approach “super star” status. Certainly most of the lesser atomic spectrometric methods will have a limited place in the analytical arena. Because of the wide current interest and research activity, special emphasis will be placed on the technique of laser induced breakdown spectrometry (LIBS). Its current status and future developments will therefore be reviewed.

Comparing several atomic spectrometric methods to the super stars: special emphasis on laser induced breakdown spectrometry, LIBS, a future super star

The objective of this work is to develop a novel laserexcited spectrometric method to reliably detect a single molecule in a flowing stream which is confined in a capillary. An argon ion-pumped Ti-sapphire laser tuned to a rubidium atomic transition line at 780.023 nm is used to excite the fluorescence of IR140 molecules in a capillary. A focused laser beam illuminates the whole capillary inner diameter to achieve near unity spatial probing efficiency. A rubidium metal vapor filter, based on the resonance absorption of an atomic metal vapor, absorbs the laser specular scatter from the capillary while passing the molecular fluorescence

Laser-induced fluorescence detection of a single molecule in a capillary

Line broadening mechanisms in the low pressure laser-induced plasma

On the usefulness of a duplicating mirror to evaluate self-absorption effects in laser induced breakdown spectroscopy

Materials analysis and characterization can provide important information as evidence in legal proceedings. The potential of laser induced breakdown spectroscopy (LIBS) for the discrimination of glass fragments for forensic applications is presented here. The proposed method is based on the fact that glass materials can be characterized by their unique spectral fingerprint. Taking advantage of the multielement detection capability and minimal to no sample preparation of LIBS, we compared glass spectra from car windows using linear and rank correlation methods. Linear correlation combined with the use of a spectral mask, which eliminates some high-intensity emission lines from the major elements present in glass, provides effective identification and discrimination at a 95% confidence level.

James D. Winefordner

Papers

Comparing several atomic spectrometric methods to the super stars: special emphasis on laser induced breakdown spectrometry, LIBS, a future super star

Laser-induced fluorescence detection of a single molecule in a capillary

Line broadening mechanisms in the low pressure laser-induced plasma

On the usefulness of a duplicating mirror to evaluate self-absorption effects in laser induced breakdown spectroscopy

Laser induced breakdown spectroscopy as a tool for discrimination of glass for forensic applications.