Polymers with excellent dielectric properties are strongly desired for pulsed power film capacitors. However, the adverse coupling between the dielectric constant and breakdown strength greatly limits the energy storage capability of polymers. In this work, we report an easily operated method to solve this problem via sputtering the interface of bilayer polymer films with ultralow content of gold nanoparticles. Interestingly, the gold nanoparticles can effectively block the movement of charge carriers because of the Coulomb blocking effect, yielding significantly enhanced breakdown strength. Meanwhile, the gold nanoparticles can act as electrodes to form numerous equivalent microcapacitors, resulting in an obviously enhanced dielectric constant. Impressively, the polymer film with merely 0.01 vol % gold nanoparticles exhibits an obvious dielectric constant and breakdown strength, which are 129 and 131% that of the pristine polymer film, respectively. Consequently, a high energy density which is 176% of that of the pristine polymer film is achieved, and a high efficiency of 79.2% is maintained. Moreover, this process can be well combined with the production process of commercial dielectric polymer films, which is beneficial for mass production. This work offers an easily operated way to improve the dielectric capacitive energy storage properties of polymers, which could also be applicable to other materials, such as ceramics and composites.

The Yungang Grottoes, with over 1500 years of history, have been subjected to air pollution since the last century. Field investigations have indicated that acid gases, particularly sulfur dioxide (SO2), have accumulated on the surface of the sculptures and caused various types of decay that reduce their artistic value. To shed new light on the gas–stone interaction process, artificially accelerated weathering was performed on local sandstone in the laboratory. In a specially developed test device, fresh specimens were exposed to gaseous SO2 under different relative humidity and temperature conditions. The physical, mineralogical, and chemical changes of Yungang sandstone were evaluated conjointly using destructive and non-destructive methods. The results show that after weathering, the luminosity of all specimens changed, with a slight alteration in hue toward yellow. The weight increased to various degrees during the aging cycles, which depended on both the accumulation of matter and the detachment of particles. Higher relative humidity and cyclic temperature fluctuations favored the dissolution of carbonates and the hydrolysis of feldspar in sandstone. The concentration of ions, especially dissolved Ca2+ and SO42-, increased considerably over time in the near-surface region of the specimens. A trace of newly formed gypsum was detected in some specimens at the end of the test. Knowing the synergistic impact of different climatic variables will make it possible to identify the mechanisms of the deterioration of sandstone in complex environments.

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