Electrochromism

About: Electrochromism is a research topic. Over the lifetime, 13097 publications have been published within this topic receiving 294637 citations.

Electric-field control of tri-state phase transformation with a selective dual-ion switch

Abstract: Materials can be transformed from one crystalline phase to another by using an electric field to control ion transfer, in a process that can be harnessed in applications such as batteries, smart windows and fuel cells. Increasing the number of transferrable ion species and of accessible crystalline phases could in principle greatly enrich material functionality. However, studies have so far focused mainly on the evolution and control of single ionic species (for example, oxygen, hydrogen or lithium ions). Here we describe the reversible and non-volatile electric-field control of dual-ion (oxygen and hydrogen) phase transformations, with associated electrochromic and magnetoelectric effects. We show that controlling the insertion and extraction of oxygen and hydrogen ions independently of each other can direct reversible phase transformations among three different material phases: the perovskite SrCoO3-δ (ref. 12), the brownmillerite SrCoO2.5 (ref. 13), and a hitherto-unexplored phase, HSrCoO2.5. By analysing the distinct optical absorption properties of these phases, we demonstrate selective manipulation of spectral transparency in the visible-light and infrared regions, revealing a dual-band electrochromic effect that could see application in smart windows. Moreover, the starkly different magnetic and electric properties of the three phases-HSrCoO2.5 is a weakly ferromagnetic insulator, SrCoO3-δ is a ferromagnetic metal, and SrCoO2.5 is an antiferromagnetic insulator-enable an unusual form of magnetoelectric coupling, allowing electric-field control of three different magnetic ground states. These findings open up opportunities for the electric-field control of multistate phase transformations with rich functionalities.

Fabrication of Ti3C2Tx MXene Transparent Thin Films with Tunable Optoelectronic Properties

Abstract: MXenes, a new class of 2D transition metal carbides and carbonitrides, show great promise in supercapacitors, Li-ion batteries, fuel cells, and sensor applications. A unique combination of their metallic conductivity, hydrophilic surface, and excellent mechanical properties renders them attractive for transparent conductive electrode application. Here, a simple, scalable method is proposed to fabricate transparent conductive thin films using delaminated Ti3C2 MXene flakes by spray coating. Homogenous films, 5–70 nm thick, are produced at ambient conditions over a large area as shown by scanning electron microscopy and atomic force microscopy. The sheet resistances (Rs) range from 0.5 to 8 kΩ sq−1 at 40% to 90% transmittance, respectively, which corresponds to figures of merit (the ratio of electronic to optical conductivities, σDC/σopt) around 0.5–0.7. Flexible, transparent, and conductive films are also produced and exhibit stable Rs values at up to 5 mm bend radii. Furthermore, the films' optoelectronic properties are tuned by chemical or electrochemical intercalation of cations. The films show reversible changes of transmittance in the UV–visible region during electrochemical intercalation/deintercalation of tetramethylammonium hydroxide. This work shows the potential of MXenes to be used as transparent conductors in electronic, electrochromic, and sensor applications.

Crystalline WO3 nanoparticles for highly improved electrochromic applications

Abstract: Electrochromic (EC) materials change their optical properties (darken/lighten) in the presence of a small electric potential difference, and are suitable for application in energy-efficient windows, antiglare automobile rear-view mirrors, sunroofs, displays, and hydrogen sensors. [1–4] The operation of conventional EC devices depends on the reversible electrochemical double injection of positive ions (H + ,L i + ,N a + ) and electrons into the host lattice of multivalent transition metal oxide materials, [5–10] with positive-ion insertion required to satisfy charge neutrality. However, diffusion of positive ions into the oxide layer is often slow, taking minutes to complete. Since the chemical diffusion coefficient of protons (DH+ )i s an order of magnitude larger than that of lithium ions (DLi+), EC systems based on proton electrolytes (e.g., aqueous H2SO4) are mandatory for display applications and preferred for other applications. Unfortunately, proton insertion currently results in rapid degradation of EC films. There are two important criteria for selecting an EC material. The first is the time constant of the ion-intercalation reaction, which is limited both by the diffusion coefficient and by the length of the diffusion path. While the former depends on the chemical structure and crystal structure of the metal oxide, the latter is determined by the material’s microstructure. [11] In the case of a nanoparticle, the smallest dimension is represented by the diffusion path length. Thus, designing a nanostructure with a small radius, while maintaining the proper crystal structure, is key to obtaining a material with fast insertion kinetics, enhanced durability, and superior performance. The second important criterion is coloration efficiency (CE), the change in optical density (OD) per unit inserted charge (Q), that is, CE= D(OD)/DQ. [12] A high CE provides

New Electrochromic Materials

Abstract: A number of inorganic and organic materials exhibit redox states (reduced and/or oxidised forms) with distinct UV-Visible (electronic) absorption bands. When electrochemical switching of these redox states gives rise to different colours (i.e. new or different visible region bands), the material is described as being electrochromic. By virtue of their numerous applications, both of academic and commercial interest, electrochromic materials are currently attracting a great deal of interest. This review provides an introduction to the major classes of electrochromic materials, namely transition metal oxides, Prussian blue systems, viologens, conducting polymers, transition metal and lanthanide coordination complexes and metallopolymers, and metal phthalocyanines. Examples of some new materials and of prototype and commercial electrochromic devices are cited.