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In this paper, sulfonic groups functionalized annealed bio-based carbon microspheres loaded polytetrafluoroethylene (A-BCMSs-SO3H@PTFE) fibers with high activity, high stability, and easy regeneration were successfully fabricated by a simple method using low-cost raw materials. The characterization results showed that the annealed biomass carbon microspheres derived from waste Camellia oleifera shells were evenly distributed on the polytetrafluoroethylene fibers and the sulfonic groups can be successfully loaded on the surface of annealed biomass carbon microspheres by room temperature sulfonation. Subsequently, the as-prepared A-BCMSs-SO3H@PTFE fibers were applied to the acid-catalyzed synthesis of liquid biofuel 5-ethoxymethylfurfural. The catalytic experiment results indicated that the annealing temperature and time during catalyst preparation have a significant effect on the activity and selectivity of A-BCMSs-SO3H@PTFE fibers. The results of catalytic reaction kinetics showed that the yield of 5-ethoxymethylfurfural can reach more than 60% after 72 h of acid-catalyzed reaction. The stability test showed that the as-prepared A-BCMSs-SO3H@PTFE fibers still maintained a stable acid catalytic activity after four recycles.

Polymeric materials are promising candidates as photocatalysts for environmental purification, however their catalytic performance are still unsatisfactory mainly due to the strong Coulomb interactions between electron and hole that leads to fast charge recombination. Herein, taking graphitic carbon nitride as an example, we verify that installing carbon nitride nanosheets with nitrogen vacancy could break the intrinsic electronic state distribution, forming energy disordered interfaces around the vacancies with the energy difference as large as 0.35 eV. Such a large energy difference is found energetic enough to overcome the strong Coulomb interactions between electron and hole for hot electron and hole generation, as a result showing high electron-hole separation efficiency. Benefited from these advantages, the as prepared material shows remarkable photocatalytic performance toward organic pollutants degradation. The improved catalytic performance is originated from the promoted exciton dissociation that leads to ultra high hydroxyl radical generation. This study offers a new understanding of the excitonic effects for designing advanced polymeric photocatalyst for energy and environment related applications.