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      Nanostructured inorganic electrochromic materials for light applications

      1 , 1 , 1 , 1
      Nanophotonics
      Walter de Gruyter GmbH

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          Abstract

          Electrochromism, an emerging energy conversion technology, has attracted immense interest due to its various applications including bistable displays, optical filters, variable optical attenuators, optical switches, and energy-efficient smart windows. Currently, the major drawback for the development of electrochromism is the slow switching speed, especially in inorganic electrochromic materials. The slow switching speed is mainly attributed to slow reaction kinetics of the dense inorganic electrochromic films. As such, an efficient design of nanostructured electrochromic materials is a key strategy to attain a rapid switching speed for their real-world applications. In this review article, we summarize the classifications of electrochromic materials, including inorganic materials (e.g., transition metal oxides, Prussian blue, and polyoxometalates), organic materials (e.g., polymers, covalent organic frameworks, and viologens), inorganic-organic hybrids, and plasmonic materials. We also discuss the electrochromic properties and synthesis methods for various nanostructured inorganic electrochromic materials depending on structure/morphology engineering, doping techniques, and crystal phase design. Finally, we outline the major challenges to be solved and discuss the outlooks and our perspectives for the development of high-performance nanostructured electrochromic materials.

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          2D metal carbides and nitrides (MXenes) for energy storage

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            Copper hexacyanoferrate battery electrodes with long cycle life and high power.

            Short-term transients, including those related to wind and solar sources, present challenges to the electrical grid. Stationary energy storage systems that can operate for many cycles, at high power, with high round-trip energy efficiency, and at low cost are required. Existing energy storage technologies cannot satisfy these requirements. Here we show that crystalline nanoparticles of copper hexacyanoferrate, which has an ultra-low strain open framework structure, can be operated as a battery electrode in inexpensive aqueous electrolytes. After 40,000 deep discharge cycles at a 17 C rate, 83% of the original capacity of copper hexacyanoferrate is retained. Even at a very high cycling rate of 83 C, two thirds of its maximum discharge capacity is observed. At modest current densities, round-trip energy efficiencies of 99% can be achieved. The low-cost, scalable, room-temperature co-precipitation synthesis and excellent electrode performance of copper hexacyanoferrate make it attractive for large-scale energy storage systems.
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              Electrochromics for smart windows: Oxide-based thin films and devices

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                Author and article information

                Contributors
                Journal
                Nanophotonics
                Walter de Gruyter GmbH
                2192-8614
                2192-8606
                December 11 2020
                November 20 2020
                January 02 2021
                December 11 2020
                November 20 2020
                January 02 2021
                : 10
                : 2
                : 825-850
                Affiliations
                [1 ]Department of Electrical and Computer Engineering , Ultrafast Optics and Nanophotonics Laboratory, University of Alberta , Edmonton , Alberta , T6G 2V4 , Canada
                Article
                10.1515/nanoph-2020-0474
                ea69c494-bb60-4b84-bbab-dd47fb816c92
                © 2021

                http://creativecommons.org/licenses/by/4.0

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