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Enhanced Solar Photothermal Catalysis over Solution Plasma Activated TiO2.

ABSTRACT: Colored wide-bandgap semiconductor oxides with abundant mid-gap states have long been regarded as promising visible light responsive photocatalysts. However, their catalytic activities are hampered by charge recombination at deep level defects, which constitutes the critical challenge to practical applications of these oxide photocatalysts. To address the challenge, a strategy is proposed here that includes creating shallow-level defects above the deep-level defects and thermal activating the migration of trapped electrons out of the deep-level defects via these shallow defects. A simple and scalable solution plasma processing (SPP) technique is developed to process the presynthesized yellow TiO2 with numerous oxygen vacancies (Ov), which incorporates hydrogen dopants into the TiO2 lattice and creates shallow-level defects above deep level of Ov, meanwhile retaining the original visible absorption of the colored TiO2. At elevated temperature, the SPP-treated TiO2 exhibits a 300 times higher conversion rate for CO2 reduction under solar light irradiation and a 7.5 times higher removal rate of acetaldehyde under UV light irradiation, suggesting the effectiveness of the proposed strategy to enhance the photoactivity of colored wide-bandgap oxides for energy and environmental applications.

SUBMITTER: Yu F

PROVIDER: S-EPMC7435248 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Enhanced Solar Photothermal Catalysis over Solution Plasma Activated TiO<sub>2</sub>.

Yu Fei F Wang Changhua C Li Yingying Y Ma He H Wang Rui R Liu Yichun Y Suzuki Norihiro N Terashima Chiaki C Ohtani Bunsho B Ochiai Tsuyoshi T Fujishima Akira A Zhang Xintong X

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20200611 16

Colored wide-bandgap semiconductor oxides with abundant mid-gap states have long been regarded as promising visible light responsive photocatalysts. However, their catalytic activities are hampered by charge recombination at deep level defects, which constitutes the critical challenge to practical applications of these oxide photocatalysts. To address the challenge, a strategy is proposed here that includes creating shallow-level defects above the deep-level defects and thermal activating the mi ...[more]

PMID: 32832348

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Project description:In this work, we propose a hybrid and unique process combining solar irradiation and post-plasma catalysis (PPC) for the effective oxidation of toluene over a highly active and stable MnO2/GFF (bifunctional graphene fin foam) catalyst. The bifunctional GFF, serving as both the catalyst support and light absorber, is decorated with MnO2 nanofins, forming a hierarchical fin-on-fin structure. The results show that the MnO2/GFF catalyst can effectively capture and convert renewable solar energy into heat (absorption of >95%), leading to a temperature rise (55.6 °C) of the catalyst bed under solar irradiation (1 sun, light intensity 1000 W m-2). The catalyst weight (9.8 mg) used in this work was significantly lower (10-100 times lower) than that used in previous studies (usually 100-1000 mg). Introducing solar energy into the typical PPC process via solar thermal conversion significantly enhances the conversion of toluene and CO2 selectivity by 36-63%, reaching ?93% for toluene conversion and ?83% for CO2 selectivity at a specific input energy of ?350 J L-1, thus remarkably reducing the energy consumption of the plasma-catalytic gas cleaning process. The energy efficiency for toluene conversion in the solar-enhanced post-plasma catalytic (SEPPC) process reaches up to 12.7 g kWh-1, ?57% higher than that using the PPC process without solar irradiation (8.1 g kWh-1), whereas the energy consumption of the SEPPC process is reduced by 35-52%. Moreover, the MnO2/GFF catalyst exhibits an excellent self-cleaning capability induced by solar irradiation, demonstrating a superior long-term catalytic stability of 72 h at 1 sun, significantly better than that reported in previous works. The prominent synergistic effect of solar irradiation and PPC with a synergistic capacity of ?42% can be mainly attributed to the solar-induced thermal effect on the catalyst bed, boosting ozone decomposition (an almost triple enhancement from ?0.18 gO3 g-1 h-1 for PPC to ?0.52 gO3 g-1 h-1 for SEPPC) to generate more oxidative species (e.g., O radicals) and enhancing the catalytic oxidation on the catalyst surfaces, as well as the self-cleaning capacity of the catalyst at elevated temperatures driven by solar irradiation. This work opens a rational route to use abundant, renewable solar power to achieve high-performance and energy-efficient removal of volatile organic compounds.

Dataset Information

Enhanced Solar Photothermal Catalysis over Solution Plasma Activated TiO2.

Publications

Enhanced Solar Photothermal Catalysis over Solution Plasma Activated TiO<sub>2</sub>.

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