Alex G. Lambert

Bio: Alex G. Lambert is an academic researcher from University of Cambridge. The author has contributed to research in topics: Dielectric & Monolayer. The author has an hindex of 4, co-authored 4 publications receiving 672 citations.

Implementing the Theory of Sum Frequency Generation Vibrational Spectroscopy: A Tutorial Review

Abstract: The interfacial regions between bulk media, although often comprising only a fraction of the material present, are frequently the site of reactions and phenomena that dominate the macroscopic properties of the entire system. Spectroscopic investigations of such interfaces are often hampered by the lack of surface specificity of most available techniques. Sum frequency generation vibrational spectroscopy (SFS) is a non‐linear optical technique which provides vibrational spectra of molecules solely at interfaces. The spectra may be analysed to provide the polar orientation, molecular conformation, and average tilt angle of the adsorbate to the surface normal. This article is aimed at newcomers to the field of SFS, and via a tutorial approach will present and develop the general sum frequency equations and then demonstrate how the fundamental theory elucidates the important experimental properties of SFS.

Interference Effects in Sum Frequency Spectra from Monolayers on Composite Dielectric/Metal Substrates

Abstract: A theoretical model has been developed to describe the generation of Sum Frequency (SF) light from a monolayer film adsorbed to the surface of a dielectric and metal composite substrate. This type of substrate provides enhanced SF signals from the monolayer without modifying the intrinsic (hydrophilic) properties of the dielectric surface. The fundamental equations of both resonant and nonresonant SF generation have been extended from a single interface to encompass the two displaced sources, the air/dielectric interface at which the monolayer film is located, and the dielectric/metal interface. The model describes the coherent addition of three separate SF signals which coherently interfere with each other, thereby affecting the line-shape observed in the net SF spectrum. Representative calculations have been made for a highly ordered monolayer of an aliphatic hydrocarbon molecule, adsorbed on a dielectric with the optical properties of mica, which is itself in contact with a metal modeled to resemble go...

Enhanced Sum Frequency Generation from a Monolayer Adsorbed on a Composite Dielectric/Metal Substrate

Abstract: A composite dielectric/metal substrate, consisting of a thin mica sheet backed with a gold film, has been employed to enhance the intensity of sum frequency vibrational spectroscopy (SFS) signals arising from model monolayers of octadecylsiloxane (ODS) adsorbed at the mica/air interface. In addition to enhanced intensities in comparison to SF spectra of ODS on mica sheets without gold backing, resonant line profiles were found to vary as a function of the thickness of the mica component of the composite substrate. This experimental result concurs with a recent theoretical study of the composite substrate which showed that interference between SF signals arising from the ODS monolayer and from the displaced gold surface results in variations in the resonant phase of the SF vibrational mode. The interference phase/thickness effect has been investigated for several composite samples, each containing a series of steps of well-defined mica thicknesses. A periodic relationship between the mica thickness and the...

Quantitative spectral and orientational analysis in surface sum frequency generation vibrational spectroscopy (SFG-VS)

Abstract: Sum frequency generation vibrational spectroscopy (SFG-VS) has been proven to be a uniquely effective spectroscopic technique in the investigation of molecular structure and conformations, as well as the dynamics of molecular interfaces. However, the ability to apply SFG-VS to complex molecular interfaces has been limited by the ability to abstract quantitative information from SFG-VS experiments. In this review, we try to make assessments of the limitations, issues and techniques as well as methodologies in quantitative orientational and spectral analysis with SFG-VS. Based on these assessments, we also try to summarize recent developments in methodologies on quantitative orientational and spectral analysis in SFG-VS, and their applications to detailed analysis of SFG-VS data of various vapour/neat liquid interfaces. A rigorous formulation of the polarization null angle (PNA) method is given for accurate determination of the orientational parameter D = ⟨cos θ ⟩/⟨cos3 θ⟩, and comparison between the PNA me...

Protons and Hydroxide Ions in Aqueous Systems

Abstract: Understanding the structure and dynamics of water's constituent ions, proton and hydroxide, has been a subject of numerous experimental and theoretical studies over the last century. Besides their obvious importance in acid-base chemistry, these ions play an important role in numerous applications ranging from enzyme catalysis to environmental chemistry. Despite a long history of research, many fundamental issues regarding their properties continue to be an active area of research. Here, we provide a review of the experimental and theoretical advances made in the last several decades in understanding the structure, dynamics, and transport of the proton and hydroxide ions in different aqueous environments, ranging from water clusters to the bulk liquid and its interfaces with hydrophobic surfaces. The propensity of these ions to accumulate at hydrophobic surfaces has been a subject of intense debate, and we highlight the open issues and challenges in this area. Biological applications reviewed include proton transport along the hydration layer of various membranes and through channel proteins, problems that are at the core of cellular bioenergetics.

In situ analytical techniques for battery interface analysis

Abstract: Lithium-ion batteries, simply known as lithium batteries, are distinct among high energy density charge-storage devices. The power delivery of batteries depends upon the electrochemical performances and the stability of the electrode, electrolytes and their interface. Interfacial phenomena of the electrode/electrolyte involve lithium dendrite formation, electrolyte degradation and gas evolution, and a semi-solid protective layer formation at the electrode–electrolyte interface, also known as the solid–electrolyte interface (SEI). The SEI protects electrodes from further exfoliation or corrosion and suppresses lithium dendrite formation, which are crucial needs for enhancing the cell performance. This review covers the compositional, structural and morphological aspects of SEI, both artificially and naturally formed, and metallic dendrites using in situ/in operando cells and various in situ analytical tools. Critical challenges and the historical legacy in the development of in situ/in operando electrochemical cells with some reports on state-of-the-art progress are particularly highlighted. The present compilation pinpoints the emerging research opportunities in advancing this field and concludes on the future directions and strategies for in situ/in operando analysis.

Interfacial water structure associated with phospholipid membranes studied by phase-sensitive vibrational sum frequency generation spectroscopy.

Abstract: Phase-sensitive vibrational sum frequency generation is employed to investigate the water structure at phospholipid/water interfaces. Interfacial water molecules are oriented preferentially by the electrostatic potential imposed by the phospholipids and have, on average, their dipole pointing toward the phospholipid tails for all phospholipids studied, dipalmitoyl phosphocholine (DPPC), dipalmitoyl phosphoethanolamine (DPPE), dipalmitoyl phosphate (DPPA), dipalmitoyl phosphoglycerol (DPPG), and dipalmitoyl phospho-l-serine (DPPS). Zwitterionic DPPC and DPPE reveal weaker water orienting capability relative to net negative DPPA, DPPG, and DPPS. Binding of calcium cations to the lipid phosphate group reduces ordering of the water molecules.