Advanced fuel cell based on Perovskite La-SrTiO3 semiconductor as the electrolyte with superoxide-ion conduction

A solid oxide fuel cell’s (SOFC) performance is largely determined by the ionic-conducting electrolyte. A novel approach is presented for using the semiconductor perovskite LaR0.25RSrR0.75RTiOR3R (LST) as the electrolyte by creating surface superionic conduction, and the authors show that the LST electrolyte can deliver superior power density, 908.2 mW·cmP-2P at just 550 °C. The prepared LST materials formed a heterostructure including an insulating core and a super ionic conducting surface layer. The rapid ion transport along the surfaces or grain boundaries was identified as the primary means of oxygen ion conduction. The fuel cell-induced phase transition was observed from the insulating LST to a super OP2-P conductivity of 0.221 S·cmP-1P at 550 °C, leading to excellent current and power outputs

DataSheet_1_Photodegradation of biobased polymer blends in seawater: A major source of microplastics in the marine environment.docx

IntroductionBiobased polymer blends have been recommended as an eco-friendly solution to abate plastic pollution in the environment. However, the formation of microplastics (MPs) by photodegradation of biobased polymer blends in the marine environment is still not well understood. In this study, we investigated the formation of MPs and the changes in the physicochemical properties of three types of biobased polymer blends after photodegradation in seawater.MethodsThe investigated materials included non-biodegradable polyethylene/ thermoplastic starch blends (PE/TPS) and polypropylene/thermoplastic starch blends (PP/TPS), as well as biodegradable polylactic acid/poly (butylene adipate-co-terephthalate)/thermoplastic starch blends (PLA/PBAT/TPS). The control groups were the corresponding neat polymers, including polyethylene (PE), polypropylene (PP), and polylactic acid (PLA).ResultsThe size distribution of the pristine and aged MPs indicated that the polymer blends were more likely to produce small-sized particles after photodegradation due to their poorer mechanical properties and lower resistance to UV irradiation than the neat polymers. Noticeable surface morphology alterations, including cracks, holes, and pits, were observed for polymer blends after photodegradation, while neat polymers were relatively resistant. After photodegradation, the attenuated total reflection Fourier transformed infrared spectroscopy (ATR-FTIR) spectrum of the polymer blends showed a significant decrease in the characteristic bands of thermoplastic starch (TPS), indicating depletion of their starch fractions. The C1s spectra of the polymer blends demonstrated that the aged MPs contained fewer -OH groups than the pristine MPs, further confirming the photodegradation of TPS. The molecular weight distribution curve of the polymer blends shifted significantly towards low molecular weight, suggesting the occurrence of chain scission during photodegradation. These results indicate that the polymer blends have a higher degree of photodegradation than neat polymers, and thereby generate more small-sized MPs than neat polymers. Photodegradation caused changes in the contact angle and surface charge of MPs derived from biobased polymer blends, which may affect the vector effects of MPs on any coexisting pollutants.DiscussionIn summary, polymer blends may pose a higher risk to the marine environment than neat polymers, and caution should be taken in promoting biobased polymer blends.</p