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Indium tin oxide (ITO) film, which is the most commonly used transparent conductive film (TCF), has traditionally been believed to be transparent in the visible spectrum but to reflect infrared (IR) light beyond the plasma wavelength (λp). However, our theoretical analysis challenges this notion by demonstrating that an ultrathin ITO TCF that is thinner than the light's penetration depth can overcome the transmission barrier at λp. To validate the theoretical modeling, we have successfully fabricated ultrathin ITO films that, despite having λp ≈ 1 μm, remain transparent from 400 nm to 20 μm. This represents the broadest transparency range ever reported for any In2O3-based TCF. The 10-nm-thick ITO TCFs have high visible transmittance (91.0% at 550 nm), low resistivity (5 × 10−4 Ω cm), and good IR transmittance (averaging 60% over 1.35–18.35 μm). Their IR transparency facilitates radiative cooling of the underlying circuitry. When an operational resistor is enclosed by commercial ITO TCFs that are 140 nm thick, its temperature increases. However, using 10-nm-thick ITO TCFs instead of the commercial ones can completely avoid this temperature rise. Moreover, attaching a silver grid to a 10-nm-thick ITO TCF can reduce the effective sheet resistance to ∼10 Ω/□ at the expense of only ∼3% transmittance. This development paves the way for large-scale applications that require low sheet resistance and far-IR transparency. [ABSTRACT FROM AUTHOR]

Oxygen sensors, using organic-inorganic and all-inorganic lead halide perovskites, have demonstrated huge advantages in operating temperature, responding time, and reversing oxygen content detection. Nevertheless, the toxicity and instability issues hinder their wide application. In this work, for the first time, we report a sensitive fluorescence oxygen detector based on lead-free double perovskite Cs 2 AgBiBr 6 thin film. The sensor has a remarkable performance in terms of fast response time of ≈56 s, recovery time of ≈91 s, and a relatively low limit of detection (LOD) of 150 ppm. More importantly, the unencapsulated sensor still exhibits an obvious response at low oxygen concentrations after two-week storage in ambient, and the device also exhibits good humidity, light, and thermal stability. Consequently, the lead-free double perovskite (Cs 2 AgBiBr 6) will be promising environmentally friendly material in developing reversible, sensitive, high-efficiency, and stable perovskite oxygen sensors. [ABSTRACT FROM AUTHOR]