Poly(vinylidene fluoride) (PVDF) has been made radiation-resistant through a nanocomposite (NC) route. The bombardment of high-energy swift heavy ions (SHI) on PVDF and its NCs with layered silicate has been studied in a range of fluences. The degradation of PVDF after SHI irradiation is suppressed radically in NCs. PVDF forms an intercalated nanostructure in the presence of nanoclay and, further, the ion fluence raises the extent of intercalation. The crystallinity and the heat of fusion of pristine PVDF have drastically been reduced after SHI irradiation, while there are relatively small changes in NCs even at higher fluences. The metastable piezoelectric beta form of PVDF gets stabilized by the presence of layered silicate, and the structure is retained upon SHI irradiation. The clay platelets act as nucleating agents, and SHI irradiation causes two crystallization temperatures for the samples exposed to high fluences. The damages created on the surface and bulk of PVDF and its NC films upon SHI irradiation have been measured quantitatively by using atomic force microscopy. The pitting dimensions and degradation are enhanced significantly beyond 10(11) ions/cm(2) fluence for pristine PVDF, which limits the use of PVDF for any ion irradiation application. The degradation is considerably suppressed in NCs, providing a suitable high-energy radiation-resistant thermoplastic polymer.

We demonstrate a highly selective and reversible NO resistive gas sensor using vertically aligned MoS (VA-MoS) flake networks. We synthesized horizontally and vertically aligned MoS flakes on SiO/Si substrate using a kinetically controlled rapid growth CVD process. Uniformly interconnected MoS flakes and their orientation were confirmed by scanning electron microscopy, x-ray diffraction, Raman spectroscopy and x-ray photoelectron spectroscopy. The VA-MoS gas sensor showed two times higher response to NO compared to horizontally aligned MoS at room temperature. Moreover, the sensors exhibited a dramatically improved complete recovery upon NO exposure at its low optimum operating temperatures (100 °C). In addition, the sensing performance of the sensors was investigated with exposure to various gases such as NH, CO, H, CH and HS. It was observed that high response to gas directly correlates with the strong interaction of gas molecules on edge sites of the VA-MoS. The VA-MoS gas sensor exhibited high response with good reversibility and selectivity towards NO as a result of the high aspect ratio as well as high adsorption energy on exposed edge sites.

Poly(vinylidene fluoride-co-hexafluoropropylene) (HFP) nanocomposites with layered silicate have been synthesized via the melt extrusion route. The intriguing nanostructure, crystalline structure, morphology, and thermal and mechanical properties of the nanocomposites have been studied and compared critically with pristine polymer. HFP forms intercalated or partially exfoliated nanostructure (or both) in the presence of nanoclay, depending on its concentration. The bombardment of high-energy swift, heavy ions (SHI) on HFP and its nanocomposites has been explored in a wide range of fluence. The nanoclay induces the piezoelectric beta-phase in bulk HFP, and the structure remains intact upon SHI irradiation. SHI irradiation degrades pure polymer, but the degradation is suppressed radically in nanocomposites. The heat of fusion of pristine HFP has drastically been reduced upon SHI irradiation, whereas there are relatively minute changes in nanocomposites. The coarsening on the surface and bulk of HFP and its nanocomposite films upon SHI irradiation has been measured quantitatively by using atomic force microscopy. The degradation has been considerably suppressed in nanocomposites through cross-linking of polymer chains, providing a suitable high-energy, radiation-resistant polymeric material. A mechanism for this behavior originating from the swelling test and gel fraction (chemical cross-linking) as a result of SHI irradiation has been illustrated.