ABSTRACT
Reversible electrochemical mirror (REM) electrochromic devices with electrochemical tunability in multiple optical states are exciting alternatives to conventional electrochromic smart windows. Electrochromic devices are studied extensively, yet widespread adoptions have not been achieved due to problems associated with durability, switching speed, limited options on optical states, and cost. In this study, a REM electrochromic device based on CuSn alloy is developed, which offers highly reversible switching between transparent, greyish-blue, and mirror states via reversible electrodeposition and dissolution. The alloying element, Sn acts as an electrochemical mediator, which facilitates the electrodeposition and dissolution of Cu. The CuSn-based REM device shows superior cycling stability for 2400 cycles (transmittance mode) and 1000 cycles (reflectance mode). The electrodeposited CuSn alloy film is resistant to surface oxidation in ambient air, with a 2.9% difference in reflectance at 2000 nm after 3 days. In addition, the alloy film exhibits excellent NIR reflectance property with thermal modulation of 18.5 °C at a high temperature of 180 °C. The REM device with zero power consumption maintains its mirror state for at least 100 min, making it a promising candidate for energy-efficient applications.
ABSTRACT
In this communication, we facily fabricated nanostructured CoP particles (150 to 200 nm) on carbon fiber paper (CFP) for hydrogen evolution reaction (HER) by a simple two-step process via a green route. In the first step, crystalline Co3O4 nanocubes (150-200 nm) were loaded on CFP through a hydrothermal process at low temperature (120 °C). Interestingly, crystalline Co3O4 nanocubes with a size 150-200 nm exhibited different growth mechanisms in contrast to the crystalline Co3O4 nanocubes with a size <100 nm reported earlier. In the second step, these crystalline Co3O4 nanocubes were converted to catalytically active CoP particles through chemical vapor deposition (CVD) phosphorization (denoted as CoP/CFP-H). Remarkably, CoP/CFP-H exhibited a low Tafel slope of 49.7 mV/dec and only required overpotentials of 128.1, 144.4, and 190.8 mV to drive geometric current densities of -10, -20, and -100 mA cm-2, respectively. Besides, the CoP/CFP-H also demonstrated an excellent durability in an acidic environment under 2000 sweeps at a high scan rate (100 mV s-1) and a 24 h chronopotentiometry testing. For comparison, CoP was also fabricated through the electrodeposition method, followed by CVD phosphorization (denoted as CoP/CFP-E). It was found that the latter had exhibited inferior activity compared to CoP/CFP-H. The good performances of CoP/CFP-H are essentially due to the rational designs of electrode: (i) the applications of highly HER active CoP electrocatalyst, (ii) the intimate contact of nanostructured CoP on carbon fibers, and (iii) the large electrochemical surface area at electrocatalyst/electrolyte interface due to the large retaining of particles features after phosphorization. Notably, the intermediate Co3O4/CFP can serve as a platform to develop other cobalt-based functional materials.
