ABSTRACT
Thermochromic smart windows with rational modulation in indoor temperature and brightness draw considerable interest in reducing building energy consumption, which remains a huge challenge to meet the comfortable responsive temperature and the wide transmittance modulation range from visible to near-infrared (NIR) light for their practical application. Herein, a novel thermochromic Ni(II) organometallic of [(C2 H5 )2 NH2 ]2 NiCl4 for smart windows is rationally designed and synthesized via an inexpensive mechanochemistry method, which processes a low phase-transition temperature of 46.3 °C for the reversible color evolution from transparent to blue with a tunable visible transmittance from 90.5% to 72.1%. Furthermore, cesium tungsten bronze (CWO) and antimony tin oxide (ATO) with excellent NIR absorption in 750-1500 and 1500-2600 nm are introduced in the [(C2 H5 )2 NH2 ]2 NiCl4 -based smart windows, realizing a broadband sunlight modulation of a 27% visible light modulation and more than 90% of NIR shielding ability. Impressively, these smart windows demonstrate stable and reversible thermochromic cycles at room temperature. Compared with the conventional windows in the field tests, these smart windows can significantly reduce the indoor temperature by 16.1 °C, which is promising for next-generation energy-saving buildings.
ABSTRACT
A series of novel transition metal ion-substituted Zn1-xAxWO4 (A = Co, Mn, and Fe, 0 < x ≤ 0.1) inorganic pigments with blue, yellow, brown, and pale green colors have been prepared by a solution combustion method and exhibit extremely high near-infrared reflectance (R > 85%). X-ray energy-dispersive spectroscopy analysis makes it clear that transition metal ions have already been incorporated into the host ZnWO4 lattice and do not change the lattice's initial wolframite structure. The optical absorption spectrum in the UV region of the ZnWO4 pigment calcined at 800 °C for 3 h is a ligand-to-metal charge transfer from O 2p nonbonding orbits to antibonding W 5d orbits. On account of the doping Co2+ (3d7), Mn2+ (3d5), and Fe3+ (3d5) transition metal ions, these chromophore ions have occupied the distorted octahedral site of Zn2+, leading to d-d transition and metal-to-metal charge transfer from the occupied 3d orbits of A2+ to unoccupied W 5d orbits in UV and visible ranges and generating some bright colors. Significantly, these inorganic pigments are also endowed with excellent thermal and chemical stability and are conducive to harsh working conditions. All of the analysis results have offered some design strategies for various colorful inorganic pigments with high near-infrared reflectance.