Inversion of two-flux and four-flux radiative transfer models for determining scattering and absorption coefficients for a suspended particle device.

Intrinsic and extrinsic scattering and absorption coefficients of a suspended particle device (SPD) smart window sample at dark and clear appearance states-without and with applied electrical voltage, respectively-were determined by means of the Maheu, Letoulouzan, and Gouesbet four-flux (intrinsic) and Kubelka-Munk two-flux (extrinsic) radiative transfer models, respectively. Extrinsic values were obtained from fitting to the two-flux model taking into account the predominantly forward scattering of the SPD. As an approximation, the Fresnel reflection coefficients were integrated out to the critical angle of total internal reflection in order to compute diffuse interface reflectances.

Setup for simultaneous electrochemical and color impedance measurements of electrochromic films: Theory, assessment, and test measurement.

Combined frequency-resolved techniques are suitable to study electrochromic (EC) materials. We present an experimental setup for simultaneous electrochemical and color impedance studies of EC systems in transmission mode and estimate its frequency-dependent uncertainty by measuring the background noise. We define the frequency-dependent variables that are relevant to the combined measurement scheme, and a special emphasis is given to the complex optical capacitance and the complex differential coloration efficiency, which provide the relation between the electrical and optical responses.

A novel phase function describing light scattering of layers containing colloidal nanospheres.

Light scattering from small particles exhibit unique angular scattering distributions, which are strongly dependent on the radius to wavelength ratio as well as the refractive index contrast between the particles and the surrounding medium. As the concentration of the particles increases, multiple scattering becomes important. This complicates the description of the angular scattering patterns, and in many cases one has to resort to empirical phase functions.

Electrochromic WO thin films attain unprecedented durability by potentiostatic pretreatment.

Electrochromic windows and glass facades are able to impart energy efficiency jointly with indoor comfort and convenience. Long-term durability is essential for practical implementation of this technology and has recently attracted broad interest. Here we show that a simple potentiostatic pretreatment of sputter-deposited thin films of amorphous WO-the most widely studied electrochromic material-can yield unprecedented durability for charge exchange and optical modulation under harsh electrochemical cycling in a Li-ion-conducting electrolyte and effectively evades harmful trapping of Li.

Electrochemical Rejuvenation of Anodically Coloring Electrochromic Nickel Oxide Thin Films.

Nickel oxide thin films are of major importance as anodically coloring components in electrochromic smart windows with applications in energy-efficient buildings. However, the optical performance of these films degrades upon extended electrochemical cycling, which has hampered their implementation. Here, we use a potentiostatic treatment to rejuvenate degraded nickel oxide thin films immersed in electrolytes of LiClO in propylene carbonate.

Galvanostatic Rejuvenation of Electrochromic WO Thin Films: Ion Trapping and Detrapping Observed by Optical Measurements and by Time-of-Flight Secondary Ion Mass Spectrometry.

Electrochromic (EC) smart windows are able to decrease our energy footprint while enhancing indoor comfort and convenience. However, the limited durability of these windows, as well as their cost, result in hampered market introduction. Here, we investigate thin films of the most widely studied EC material, WO.

Degradation Dynamics for Electrochromic WO Films under Extended Charge Insertion and Extraction: Unveiling Physicochemical Mechanisms.

Degradation of electrochromic thin films under extended charge insertion and extraction is a technically important phenomenon for which no in-depth understanding is currently on hand. Here, we report on an explorative study of sputter-deposited WO films in a Li-ion-conducting electrolyte by use of cyclic voltammetry, in situ optical transmittance, and impedance spectroscopy. A cycling-dependent decrease of the charge capacity could be accurately modeled by a power-law function, and impedance spectroscopy gave evidence for anomalous diffusion as well as a higher charge-transfer resistance during deintercalation than during intercalation.

Eliminating Electrochromic Degradation in Amorphous TiO2 through Li-Ion Detrapping.

The quest for superior and low-cost electrochromic (EC) thin films, for applications in smart windows, remains strong because of their large importance for energy-efficient buildings. Although the development of new EC materials for improved devices is important, diminishing or reversing degradation is another key issue, and electrical rejuvenation of degraded EC materials can offer new opportunities. Here we demonstrate that cathodically coloring EC thin films of TiO2, which normally suffer from ion-trapping-induced degradation of charge capacity and optical modulation upon extensive electrochemical cycling, can recover their initial EC performance by a rejuvenation procedure involving Li(+) ion detrapping.

Galvanostatic Ion Detrapping Rejuvenates Oxide Thin Films.

Ion trapping under charge insertion-extraction is well-known to degrade the electrochemical performance of oxides. Galvanostatic treatment was recently shown capable to rejuvenate the oxide, but the detailed mechanism remained uncertain. Here we report on amorphous electrochromic (EC) WO3 thin films prepared by sputtering and electrochemically cycled in a lithium-containing electrolyte under conditions leading to severe loss of charge exchange capacity and optical modulation span.

Sustainable Rejuvenation of Electrochromic WO3 Films.

Devices relying on ion transport normally suffer from a decline of their long-term performance due to irreversible ion accumulation in the host material, and this effect may severely curtail the operational lifetime of the device. In this work, we demonstrate that degraded electrochromic WO3 films can sustainably regain their initial performance through galvanostatic detrapping of Li(+) ions. The rejuvenated films displayed degradation features similar to those of the as-prepared films, thus indicating that the detrapping process is effectively reversible so that long-term performance degradation can be successfully avoided.

Eliminating degradation and uncovering ion-trapping dynamics in electrochromic WO3 thin films.

There is keen interest in the use of amorphous WO3 thin films as cathodic electrodes in transmittance-modulating electrochromic devices. However, these films suffer from ion-trapping-induced degradation of optical modulation and reversibility on extended Li(+)-ion exchange. Here, we demonstrate that ion-trapping-induced degradation, which is commonly believed to be irreversible, can be successfully eliminated by constant-current-driven de-trapping; that is, WO3 films can be rejuvenated and regain their initial highly reversible electrochromic performance.

Strongly improved electrochemical cycling durability by adding iridium to electrochromic nickel oxide films.

Anodically colored nickel oxide (NiO) thin films are of much interest as counter electrodes in tungsten oxide based electrochromic devices such as "smart windows" for energy-efficient buildings. However, NiO films are prone to suffering severe charge density degradation upon prolonged electrochemical cycling, which can lead to insufficient device lifetime. Therefore, a means to improve the durability of NiO-based films is an important challenge at present.

Low-frequency dielectric properties of three bentonites at different adsorbed water states.

Three bentonites of varying smectite content were investigated by dielectric spectroscopy in the frequency range 10(-4) to 10(6) Hz after storage at well-defined humidities. The identification of relaxation processes from complex permittivity measurements was difficult, since conductivity effects were superimposed on the underlying relaxations. Relaxation peaks revealed by the dissipation factor indicated the occurrence of interfacial processes between 10(2) and 10(6) Hz.

Electronic and optical properties of nanocrystalline WO₃ thin films studied by optical spectroscopy and density functional calculations.

The optical and electronic properties of nanocrystalline WO3 thin films prepared by reactive dc magnetron sputtering at different total pressures (Ptot) were studied by optical spectroscopy and density functional theory (DFT) calculations. Monoclinic films prepared at low Ptot show absorption in the near infrared due to polarons, which is attributed to a strained film structure. Analysis of the optical data yields band-gap energies Eg ≈ 3.

Spectrally selective reflector surfaces for heat reduction in concentrator solar cells: modeling and applications of TiO₂:Nb-based thin films.

The energy conversion efficiency of a conventional pn junction solar cell decreases as the temperature increases, and this may eventually lead to failures in the photovoltaic system, especially if it uses concentrated solar radiation. In this work, we show that spectrally selective reflector (SSR) surfaces can be important for reducing the heat buildup on passively cooled solar cells. We outline a computational scheme for optimizing DC magnetron-sputtered TiO₂:Nb-based SSRs tailored for silicon solar cells and find good agreement of the reflectance with an experimental realization of the optimal SSR.

New probe of the electronic structure of amorphous materials.

Here we show that electrochemical equilibrium voltage curves of amorphous WO3 and TiO2 coatings exhibit fine structure in striking agreement with the density of states in the conduction bands, as obtained by ab initio calculations for the crystalline counterparts. We suggest that localization of the band states is essential for observing the electronic structure. Our highly sensitive electrochemical method opens new vistas for studying the electronic structure of nonmetallic disordered materials that can be intercalated with an ionic species.

Coupled multipolar interactions in small-particle metallic clusters.

We propose a new formalism for computing the optical properties of small clusters of particles. It is a generalization of the coupled dipole-dipole particle-interaction model and allows one in principle to take into account all multipolar interactions in the long-wavelength limit. The method is illustrated by computations of the optical properties of N = 6 particle clusters for different multipolar approximations.