This paper presents a pyroelectric approach for the synthesis of metal−BaTiO 3 hybrid nanoparticles (NPs) and demonstrates the enhanced performance on the degradation of dye solution using such hybrid NPs. During the synthesis process, rapid temperature oscillation accelerated the electron generation at the surface of pyroelectric barium titanate (BTO) NPs that were dispersed in either aqueous or nonaqueous solutions. These generated electrons were used to reduce the metal salts on the surface of BTO NPs without the need for a reducing reagent. The Au− BTO hybrid NPs synthesized by such approach showed higher pyrocatalytic degradation efficiency for dye solution than the physically mixed solutions of Au NPs and BTO NPs. Compared to conventional processes, this pyrocatalytic approach without the need for additional reducing reagents not only offers an alternative strategy for the synthesis of metal−pyroelectric hybrid materials but also opens a new way to harvest thermal energy for efficient pyrocatalysis process.

Solar-driven interfacial evaporation, as one of the most effective ways to convert and utilize solar energy, has attracted lot of interest recently. Most of the previous research studies, however, mainly focused on nonpatterned solar absorbers by improving the structural and chemical characteristics of the solar absorbers used in the interfacial evaporation systems. In this work, we investigated the influence of patterned surface on the evaporation performance of solar absorbers. The patterned surfaces studied, which include black patterns and white patterns, were achieved by selectively printing carbon black on the air-laid paper. Such a design leads to the lateral temperature differences between adjacent patterns of the solar absorber under solar illumination. The temperature differences result in the lateral heat and mass transfer between those patterns, which can effectively accelerate solar-driven vapor generation. With similar patterns and same coverage of carbon black, the increase in the circumference of the surface patterns leads to the increase in the evaporation performance. Additionally, we found that the evaporation performance can be optimized through the design of surface patterns, which demonstrates the potential in reducing the usage of the light-absorbing materials in the solar absorber. The findings in this work not only expand the understanding of the interfacial evaporation systems but also offer additional guidelines in designing interfacial evaporation systems.

This paper reports the highly efficient pyroelectric nanomaterial-based catalytic degradation of waste dye under rapid temperature oscillation, which was achieved by periodical solar irradiation on a porous pyroelectric membrane that was floating at the liquid/air interface. Such a membrane consists of the light-to-heat conversion carbon black film as the top layer and the porous poly(vinylidene difluoride) (PVDF) film embedded with pyroelectric barium titanate (BaTiO) nanoparticles (BTO NPs) as the bottom layer. By using an optical chopper, solar light can be modulated to periodically irradiate on the floating membrane. Because of the photothermal effect and low thermal conductivity of the PVDF polymer, the generated heat is localized at the surface of the membrane and substantially increases the surface temperature within a short period of time. When the solar light is blocked by the chopper, interfacial evaporation through the porous membrane along with convective air cooling and radiative cooling leads to heat dissipation, and then the temperature of the membrane is rapidly decreased. Such an efficient thermal cycle results in a substantial rate of temperature change of the membrane, which enhances its pyroelectric capability and subsequent pyro-catalysis. In contrast, the efficiency of pyro-catalysis through the dispersed BTO NP solution is about 4 times lower than that of the BTO composite membrane. With the large heat capacity of the aqueous solution and inevitable thermal loss because of bulk heating, the rate of temperature change of the BTO NP solution is much smaller than that of the BTO composite membrane and thus results in a relatively small pyro-catalytic capability. Furthermore, the reusability and transferability of this newly developed composite membrane make it amenable to practical use in treating contaminated water. The findings in our report not only offer a new design strategy for efficient solar-enabled pyro-catalysis but also pave a new way to rationally harvest solar-thermal energy in nature for various applications that involve pyroelectric materials.