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In this work, shape manipulation in porous CeO2 nanofibers was successfully achieved by a simple electrospinning technology with high quality and high reproducibility. By simply tuning the electric field strength during electrospinning, the diameter of as-spun nanofibers composed of Ce(acac)3 and polyvinylpyrrolidone can be precisely controlled. As a result, the morphology of nanofibers can change from columnar to celery-like and belt-like structure. The formation mechanism of this intriguing diameter-dependent morphology can be assigned to the gradient evaporation of solvent across the nanofiber. After calcination at 500 °C, porous CeO2 nanofibers were obtained, showing unusually observed celery-like or belt-like morphologies. These intriguing CeO2 nanofibers exhibited good thermal stability in terms of phase structures and morphologies up to 700 °C. The fibrous CeO2 mats were active toward soot combustion with decreased activation energy, compared with commercial samples. Among three kinds of shapes, the fibrous CeO2 mats made of columnar-like nanofibers were endowed with the lowest activation energy of 120.1 kJ/mol, due to the most effective contact between soot and CeO2 surface, regardless a loose contact mode. [ABSTRACT FROM AUTHOR]

Metal sintering poses significant challenges for developing reliable catalytic systems toward high-temperature reactions, particularly those based on metal clusters with sizes below 3 nm. In this work, electrospun dual-oxide fibril-in-tubes consisting of CeO 2 and Al 2 O 3 are rationally designed in an all-in-one manner, to stabilize 2.3 nm Pt clusters with a Tammann temperature (sintering onset temperature) lower than 250 °C. The abundant pores and channels effectively stabilize the Pt clusters physically, while the strong support, CeO 2 , with high adhesion, pins Pt clusters firmly, and the adjacent weak support, Al 2 O 3 , with low adhesion, provides energy barriers to prevent the clusters and emitted Pt atom(s) from moving across the support. Therefore, the ultra-close 2.3 nm Pt clusters, featuring an average nearest neighboring distance of only 2.1 nm, were carefully stabilized against sintering at temperatures exceeding 750 °C, even in oxidative and steam-containing environments. In addition, this catalytic system can efficiently and durably serve in diesel combustion, a high-temperature exothermic reaction, showing no activity decline after 5 cycles. This work provides a comprehensive understanding of sinter-resistant catalytic systems, and presents new insights for the development of advanced nanocatalysts., Competing Interests: The authors declare no competing interests., (This journal is © The Royal Society of Chemistry.)

Photothermal heating and photocatalytic treatment are two solar-driven water processing approaches by harnessing NIR and UV-vis light, respectively, which can fully utilize solar energy if integrated. However, it remains a challenge to achieve high performance in both approaches when integrated in a material due to uncontrollable heat diffusion. Here, we report a demonstration of heat confinement on photothermal sites and fluid cooling on photocatalysis sites at the nanoscale, within a well-designed heat and fluid confinement nanofiber reactor. Photothermal and photocatalytic nanostructures were alternatively aligned in electrospun nanofibers for on-demand nanofluidic thermal management as well as easy folding into 3D structures with enhanced light utilization and mass transfer. Such a design showed simultaneously high photothermal evaporation rate (2.59 kg m -2 h -1 , exceeding the limit rate) and efficient photocatalytic upcycling of microplastics pollutant into valued products. Enabled by controlled photothermal heating, the valued main product (i.e., methyl acetate) can be evaporated out with 100% selectivity by in situ separation., Competing Interests: Competing interests statement:The authors declare no competing interest.