The use of solar energy to catalyze the photo-driven processes has attracted tremendous attention from the scientific community because of its great potential to address energy and environmental is...

Perovskite Oxide Based Materials for Energy and Environment-Oriented Photocatalysis

Titanium dioxide nanomaterials: self-structural modifications.

An efficient binary Bi2Fe4O9/Bi2WO6 Z-scheme heterojunction was fabricated through a facile hydrothermal route. The obtained Bi2Fe4O9/Bi2WO6 displays high catalytic activity for rhodamine B (RhB) photodegradation, and 100% of RhB was photodegraded by Bi2Fe4O9 (7%)/Bi2WO6 within 90 min, which is much better than that by pure Bi2Fe4O9 and Bi2WO6. The effective photoinduced carrier separation, the broadened photoabsorption range, high oxidation capacity of hole, and the high reduction power of electron are in charge of the elevated catalytic activity because of the formed Z-scheme system. In addition, the effects such as pollutant concentration, pH, inorganic anions, and water sources exerted on photocatalytic performance were also investigated, and the results suggest that Bi2Fe4O9/Bi2WO6 still possesses a high photocatalytic performance. The free-radical trapping experiments and electron spin resonance spin-trapping technology disclose that hole (h+), hydroxy radical (•OH), and superoxide radical (•O2-) are cardinal active radicals in the catalytic system. In terms of the above experimental analysis, a possible photodegradation mechanism of the as-fabricated photocatalyst is thoroughly elucidated. In addition, the possible RhB photodegradation pathway is also raised in the light of the analysis of liquid chromatography-mass/mass spectrometry. In addition, Bi2Fe4O9/Bi2WO6 composite does not display dramatic reduction of the catalytic performance after five recycles. Thus, this study reveals that the as-obtained Bi2Fe4O9/Bi2WO6 catalyst has a great prospect for the environmental purification.

Facile Hydrothermal Synthesis of Z-Scheme Bi2Fe4O9/Bi2WO6 Heterojunction Photocatalyst with Enhanced Visible Light Photocatalytic Activity.

Solar-to-chemical energy conversion via heterogeneous photocatalysis is one of the sustainable approaches to tackle the growing environmental and energy challenges. Among various promising photocatalytic materials, plasmonic-driven photocatalysts feature prominent solar-driven surface plasmon resonance (SPR). Non-noble plasmonic metals (NNPMs)-based photocatalysts have been identified as a unique alternative to noble metal-based ones due to their advantages like earth-abundance, cost-effectiveness, and large-scale application capability. This review comprehensively summarizes the most recent advances in the synthesis, characterization, and properties of NNPMs-based photocatalysts. After introducing the fundamental principles of SPR, the attributes and functionalities of NNPMs in governing surface/interfacial photocatalytic processes are presented. Next, the utilization of NNPMs-based photocatalytic materials for the removal of pollutants, water splitting, CO2 reduction, and organic transformations is discussed. The review concludes with current challenges and perspectives in advancing the NNPMs-based photocatalysts, which are timely and important to plasmon-based photocatalysis, a truly interdisciplinary field across materials science, chemistry, and physics.

Non-Noble Plasmonic Metal-Based Photocatalysts.

Metasurfaces, two-dimensional equivalents of metamaterials, are engineered surfaces consisting of deep subwavelength features that have full control of the electromagnetic waves. Metasurfaces are not only being applied to the current devices throughout the electromagnetic spectrum from microwave to optics but also inspiring many new thrilling applications such as programmable on-demand optics and photonics in future. In order to overcome the limits imposed by passive metasurfaces, extensive researches have been put on utilizing different materials and mechanisms to design active metasurfaces. In this paper, we review the recent progress in tunable and reconfigurable metasurfaces and metadevices through the different active materials deployed together with the different control mechanisms including electrical, thermal, optical, mechanical, and magnetic, and provide the perspective for their future development for applications.

/pdf/tunable-and-reconfigurable-metasurfaces-and-metadevices-383g1l09dq.pdf

Tunable and reconfigurable metasurfaces and metadevices

Pure BiFeO3, Bi2Fe4O9, and BiFeO3/Bi2Fe4O9 heterostructure nanofibers were successfully synthesized by a facile wet chemical process followed by an electrospinning technique. Compared with the pure BiFeO3 and Bi2Fe4O9 nanofibers, the introduction of Bi2Fe4O9 in the BiFeO3 makes its absorption edge red shift to absorb much more visible light, and improves its separation efficiency of photogenerated carrier. Besides, the as-obtained BiFeO3/Bi2Fe4O9 nanofibers exhibit higher photocatalytic activity in both the degradation of Rhodamine B and H2 evolution from water under visible-light irradiation. The BiFeO3/Bi2Fe4O9 nanofibers exhibited about 2.7 times and 2.0 times higher H2 evolution than that of pure BiFeO3 and pure Bi2Fe4O9 samples, respectively. The possible photoreactive mechanism of the BiFeO3/Bi2Fe4O9 nanofibers was carefully investigated according to the results of photocatalytic and photoelectric performance, and a Z-scheme mechanism was proposed. Such BiFeO3/Bi2Fe4O9 heterostructure and its compos...

Facial Synthesis and Photoreaction Mechanism of BiFeO3/Bi2Fe4O9 Heterojunction Nanofibers

Self-doping TiO2 has recently attracted considerable attention for its high photocatalytic activity under visible-light irradiation. However, the literature reported synthetic methods until now were very time-consuming. In this study, we establish a quick and facile method for obtaining self-doping TiO2 with the use of directly treated commercial P25 at a desired temperature for only 5 min through spark plasma sintering technology. With the using of this method, the modified P25 samples exhibit significantly high photoelectric and photocatalytic performance. Furthermore, the sample prepared at 600°C exhibits the optimum catalytic activity. The photodegradation and H2 evolution rates of this samples are significantly higher than those of unmodified P25 sample under visible-light irradiation. The physical origin of the visible-light absorption for the modified P25 samples is investigated in detail according to their structural, optical, and electronic properties. This work will provide a quick and facile method for the large-scale synthesis of visible-light driven photocatalyst for practical applications.

/pdf/quick-and-facile-preparation-of-visible-light-driven-tio2-53unq56zyo.pdf

Quick and facile preparation of visible light-driven TiO2 photocatalyst with high absorption and photocatalytic activity.

(Mo + N) codoped TiO2 for enhanced visible-light photoactivity

Photocatalytic degradation of methylene blue over BiVO4/BiPO4/rGO heterojunctions and their artificial neural network model

Decrease in the dielectric loss of CaCu3Ti4O12 at high frequency by Ru doping

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