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Electrochromic (EC) materials allow for dynamic tuning of optical properties via an applied electric field, presenting great potential in energy-efficient technologies, such as smart windows for effective light and temperature regulation. The precise control of precursor concentration has proven to be a powerful approach in tailoring the physicochemical properties of semiconducting metal oxides. In this study, we employed a one-step electrodeposition technique to fabricate tungsten oxide (WO3) thin films, systematically exploring how varying precursor concentrations influence the material's characteristics. X-ray diffraction analysis revealed significant changes in diffraction patterns, reflecting subtle structural modifications due to concentration variations. Additionally, scanning electron microscopy revealed significant changes in the microstructure, showing a progression from small nanogranules to larger agglomerations within the film matrix. The W-25 mM thin film delivered exceptional EC performance, efficiently accommodating lithium ions while showcasing superior EC properties. The optimized electrode, denoted as W-25 mM, showcased exceptional EC metrics, featuring the highest optical modulation at 82.66%, outstanding reversibility at 99%, and a notably high coloring efficiency of 83.01 cm2/C. These findings emphasize the importance of precursor concentration optimization in enhancing the EC properties of WO3 thin films, contributing to the advancement of high-performance, energy-efficient materials. [ABSTRACT FROM AUTHOR]

Electrochromic materials enable the precise control of their optical properties, making them essential for energy-saving applications such as smart windows. This study focuses on the synthesis of molybdenum-doped niobium oxide (Mo-Nb2O5) thin films using a one-step hydrothermal method to investigate the effect of Mo doping on the material's electrochromic performance. Mo incorporation led to distinct morphological changes and a transition from a compact granular structure to an anisotropic rod-like feature. Notably, the MN-3 (0.3% Mo) sample displayed an optimal electrochromic performance, achieving 77% optical modulation at 600 nm, a near-perfect reversibility of 99%, and a high coloration efficiency of 89 cm2/C. Additionally, MN-3 exhibited excellent cycling stability, with only 0.8% degradation over 5000 s. The MN-3 device also displayed impressive control over color switching, underscoring its potential for practical applications. These results highlight the significant impact of Mo doping on improving the structural and electrochromic properties of Nb2O5 thin films, offering improved ion intercalation and charge transport. This study underscores the potential of Mo-Nb2O5 for practical applications in energy-efficient technologies. [ABSTRACT FROM AUTHOR]

[Display omitted] • Delves into the design and synthesis of Nb 2 O 5 -TiO 2 bilayer thin films via hydrothermal method. • Intricate analysis of dual-band electrochromic energy storage through Nb 2 O 5 -TiO 2 bilayer nanoarchitectonics. • Investigate the influence of TiO 2 varying annealing temperature on overall electrochemical performance. • The objective of study is to regulate light and thermal dynamics while exhibiting superior charge storage. • The development of large-scale device boasting exceptional electrochromic energy storage characteristics. This paper introduces a proof of concept for a dual-band electrochromic (EC) device to modulate solar light transmission across visible and near-infrared regions selectively. EC materials based on ion insertion/extraction mechanisms also present the possibility for energy storage, widening its functionality to the supercapacitor platform. The bi-functional performance of dual-band radiation control and energy storage was achieved by exploiting two earth-abundant metal oxides that could absorb two different spectral regions when electrochemically charged. The bilayer structure was prepared using a one-step hydrothermal method, which produced Nb 2 O 5 -TiO 2 bilayer on fluorine-doped tin oxide (FTO) conducting glass substrates. The nano-dimensions of the active materials endorse the development of high-transparency thin film under open circuit conditions. The variations in the TiO 2 annealing temperature influence the crystallinity and surface morphology of the thin films, which influence the performance of dual-band EC energy storage. The well-optimized NT-500 sample facilitated exclusive electron-charge transport, producing excellent electrochemical performance in dual-band EC and energy storage. A large optical modulation of 80.4 % and 89.8 % at 600 nm and 800 nm (near-infrared) was achieved with an enhanced areal capacitance of 88.1 mF/cm2 and excellent cycling stability after continuous coloring/bleaching cycles for 18,000 s. This paper presents a prototype bi-functional device based on NT-500, which showed independent control and modulation of visible and near-infrared transmittance. Notably, the device retained excellent energy storage performance alongside its advanced optical functionalities. This bilayer nanostructure capitalizes on the inherent electrochemical properties of both materials and introduces novel features that can potentially revolutionize the platform of EC-energy storage. [ABSTRACT FROM AUTHOR]

The development of novel cathodic materials with tailored nanostructures is crucial for the advancement of electrochromic devices. In this study, we synthesized cobalt-doped titanium dioxide (Ti-Co) thin films using a facile hydrothermal method to investigate the effects of cobalt doping on their structural, morphological, and electrochromic properties. Comprehensive characterization techniques, including X-ray diffraction and Raman analysis, confirmed the highly crystalline nature of the Ti-Co thin films, with specific Raman bands indicating distinct modifications due to cobalt incorporation. The TiO2 nanorods, optimally doped with cobalt (TC-3), demonstrated enhanced charge transport and mobility, significantly improving the electrochromic performance. Among the various compositions studied, the TC-3 sample exhibited superior lithium-ion accommodation, achieving an optical modulation of 73.6% and a high coloration efficiency of 81.50 cm2/C. It also demonstrated excellent electrochromic stability, maintaining performance for up to 5000 s of coloring/bleaching cycles. These results confirm the beneficial impact of cobalt doping on the structural and functional properties of the host material. Furthermore, the practical effectiveness of the TC-3 thin film was validated through the fabrication of an electrochromic device, which showed efficient coloration and bleaching capabilities. This comprehensive research enhances the understanding and functionality of Ti-Co nanorod architectures, highlighting their promising potential for advanced electrochromic applications. [ABSTRACT FROM AUTHOR]

Electrochromic materials allow for precise control of their optical properties by applying an electric field, which has led to recent developments in energy-saving and indoor temperature control systems like smart windows. The selective incorporation of metal dopants is an effective technique for generating highly advanced semiconducting metal oxides with precisely customized physicochemical characteristics. In this report, we employed a one-step electrodeposition process to fabricate nickel-doped tungsten oxide (W–Ni) thin films, systematically probing the impact of nickel (Ni) doping on the collective material characteristics. Comprehensive X-ray diffraction research revealed significant changes in diffraction patterns, suggesting slight modifications in the structure caused by Ni doping. The scanning electron microscopy showed complex differences in the microstructure of the film, such as a dense surface, porosity, and clustering of nanogranules. The WNi-3% thin film doped at 3 wt. % exhibited excellent electrochromic performance by efficiently handling lithium ions and displaying favorable electrochromic properties. The improved electrode, WNi-3%, showed a maximum optical modulation of 81.90%, exceptional reversibility of 99.4%, and a high coloration efficiency of 75.12 cm2/C. These findings underscore the efficacy of Ni-doping in tailoring the electrochromic properties of nickel-doped tungsten oxide thin films, thereby advancing the frontiers of high-performance electrochromic materials for energy-efficient applications. [ABSTRACT FROM AUTHOR]

• One step hydrothermal method has been adapted to synthesize Nb2O5 thin films. • Orthorhombic 3D Nb2O5 nanospheres provided more active sites for Li+ ion diffusion. • Colored state Raman provides an intervalence charge transfer reaction mechanism. • Highest coloration efficiency with energy storage capacity. • Electrochromic supercapacitor devices have lightened up a red and yellow LED. The design and development of novel cathodic materials with suitable crystal structure and nanostructure is an essential basis for both electrochromism and electrochemical energy storage devices. In this study, Niobium oxide (Nb 2 O 5) thin films as high-performance cathodic materials were synthesized using a facile hydrothermal method. The influence of the precursor concentration on the structural, morphological, electrochromic, and energy storage properties was investigated successfully. The X-ray diffraction analysis confirmed the highly crystalline orthorhombic nature of Nb 2 O 5 thin films. Nanostructured Nb 2 O 5 nanospheres effectively improved the charge transportation and mobility of charge carriers. Nb 01 thin film most effectively accommodated lithium ions and facilitated the desired bifunctional performance. An electrochromic supercapacitor (ESC) of Nb 01 composition showed the highest optical modulation of (76.92%), excellent reversibility of (98%), high coloration efficiency (CE) (98.75 cm2 C−1), and high-energy storage capacity (93.33 C cm−2). The fully colored ESC devices (4 × 5 cm2) have lightened a red and yellow light-emitting diode (LED) which confirms the energy storage level with the color changing ability of the 3D Nb 2 O 5 nanospheres as a potential application in ESC. [Display omitted] [ABSTRACT FROM AUTHOR]