Moqing Wu

Bio: Moqing Wu is an academic researcher from Tianjin University. The author has contributed to research in topics: Wetting & Water splitting. The author has an hindex of 11, co-authored 15 publications receiving 635 citations.

Rational construction of oxygen vacancies onto tungsten trioxide to improve visible light photocatalytic water oxidation reaction

Abstract: Defect engineering is a promising strategy to enhance light absorption and charge separation of photocatalysts. Herein, we simply tailor the quantity and distribution of oxygen vacancies, as one of typical defects, on surface or bulk of thermal-treated WO3 in the different H2 concentration. The quantity of bulk oxygen vacancies on WO3 consistently rises with the increased H2 concentration, while that of surface oxygen vacancies presents a volcano-type variation. The sample of WO3-H20, thermal-pretreated in 20% H2, contains the largest amount of surface oxygen vacancies. Our results show that both surface and bulk oxygen vacancies on WO3 can promote the visible light photocatalytic activity in water splitting, however, in different ways. Bulk oxygen vacancies mainly promote the visible light harvesting and slightly restrain the electrons and holes recombination by narrowing band gap energy (Eg), while surface oxygen vacancies significantly increase the charge-carriers separation efficiency by lowering valence band edge (VBE). Compared with the light absorption, the separation of electrons and holes is more critical in photocatalytic oxygen evolution over WO3, revealing the more decisive role of surface oxygen vacancies than bulk oxygen vacancies. Expectedly, WO3-H20 shows the highest charge-carriers separation efficiency and visible light photocatalytic performance. Our work provides a new insight into designing of efficient defect-engineered semiconductors for the related solar light utilization processes.

Insights into the Effects of Surface/Bulk Defects on Photocatalytic Hydrogen Evolution over TiO2 with Exposed {001} Facets

Abstract: This paper describes the effects of defect distribution on energy band structure and the subsequent photocatalytic activity over TiO2 with exposed {001} facets as the model catalyst. Our results show that only surface oxygen vacancies (Vo’s) and Ti3+ centers in TiO2 can be induced by hydrogenation treatment, whereas the generation of bulk Vo’s and Ti3+ species depends on the thermal treatment in nitrogen. Both the surface and bulk defects in TiO2 can promote the separation of electron-hole pairs, enhance the light absorption, and increase the donor density. The presence of surface and bulk defects in TiO2 can not change the valence band maximum, but determine the conduction band minimum. Surface defects in TiO2 induce a tail of conduction band located above the H+/H2 redox potential, which benefits the photocatalytic performance. However, bulk defects in TiO2 generate a band tail below the H+/H2 potential, which inhibits hydrogen production. Thus, the change of band gap structure by defects is the major factor to determine the photocatalytic activity of TiO2 for hydrogen evolution. It is a new insight into the rational design and controllable synthesis of defect-engineered materials for various catalytic processes.

In Situ Formation of Disorder-Engineered TiO2(B)-Anatase Heterophase Junction for Enhanced Photocatalytic Hydrogen Evolution

Abstract: Hydrogenation of semiconductors is an efficient way to increase their photocatalytic activity by forming disorder-engineered structures. Herein, we report a facile hydrogenation process of TiO2(B) nanobelts to in situ generate TiO2(B)-anatase heterophase junction with a disordered surface shell. The catalyst exhibits an excellent performance for photocatalytic hydrogen evolution under the simulated solar light irradiation (∼580 μmol h(-1), 0.02 g photocatalyst). The atomically well-matched heterophase junction, along with the disorder-engineered surface shell, promotes the separation of electron-hole and inhibits their recombination. This strategy can be further employed to design other disorder-engineered composite photocatalysts for solar energy utilization.

Hydrogenated Cagelike Titania Hollow Spherical Photocatalysts for Hydrogen Evolution under Simulated Solar Light Irradiation

Abstract: We synthesized the hydrogenated cagelike TiO2 hollow spheres through a facile sacrificial template method. After the hydrogenation treatment, the disordered surface layer and cagelike pores were generated on the shell of the hollow spheres. The spheres exhibit a high hydrogen evolution rate of 212.7 ± 10.6 μmol h–1 (20 mg) under the simulated solar light irradiation, which is ∼12 times higher than the hydrogenated TiO2 solid spheres and is ∼9 times higher than the original TiO2 hollow spheres. The high activity results from the unique architectures and hydrogenation. Both the multiple reflection that was improved by the cagelike hollow structures and the red shift of the absorption edge that was induced by hydrogenation can enhance the ultraviolet and visible light absorption. In addition, the high concentration of oxygen vacancies, as well as the hydrogenated disordered surface layer, can improve the efficiency for migration and separation of generated charge carriers.

Hollow Nanostructures for Photocatalysis: Advantages and Challenges.

Abstract: Photocatalysis for solar-driven reactions promises a bright future in addressing energy and environmental challenges. The performance of photocatalysis is highly dependent on the design of photocatalysts, which can be rationally tailored to achieve efficient light harvesting, promoted charge separation and transport, and accelerated surface reactions. Due to its unique feature, semiconductors with hollow structure offer many advantages in photocatalyst design including improved light scattering and harvesting, reduced distance for charge migration and directed charge separation, and abundant surface reactive sites of the shells. Herein, the relationship between hollow nanostructures and their photocatalytic performance are discussed. The advantages of hollow nanostructures are summarized as: 1) enhancement in the light harvesting through light scattering and slow photon effects; 2) suppression of charge recombination by reducing charge transfer distance and directing separation of charge carriers; and 3) acceleration of the surface reactions by increasing accessible surface areas for separating the redox reactions spatially. Toward the end of the review, some insights into the key challenges and perspectives of hollow structured photocatalysts are also discussed, with a good hope to shed light on further promoting the rapid progress of this dynamic research field.

One‐dimensional TiO2 Nanotube Photocatalysts for Solar Water Splitting

Abstract: Hydrogen production from water splitting by photo/photoelectron-catalytic process is a promising route to solve both fossil fuel depletion and environmental pollution at the same time. Titanium dioxide (TiO2) nanotubes have attracted much interest due to their large specific surface area and highly ordered structure, which has led to promising potential applications in photocatalytic degradation, photoreduction of CO2, water splitting, supercapacitors, dye-sensitized solar cells, lithium-ion batteries and biomedical devices. Nanotubes can be fabricated via facile hydrothermal method, solvothermal method, template technique and electrochemical anodic oxidation. In this report, we provide a comprehensive review on recent progress of the synthesis and modification of TiO2 nanotubes to be used for photo/photoelectro-catalytic water splitting. The future development of TiO2 nanotubes is also discussed.

Tuning defects in oxides at room temperature by lithium reduction.

Abstract: Defects can greatly influence the properties of oxide materials; however, facile defect engineering of oxides at room temperature remains challenging. The generation of defects in oxides is difficult to control by conventional chemical reduction methods that usually require high temperatures and are time consuming. Here, we develop a facile room-temperature lithium reduction strategy to implant defects into a series of oxide nanoparticles including titanium dioxide (TiO2), zinc oxide (ZnO), tin dioxide (SnO2), and cerium dioxide (CeO2). Our lithium reduction strategy shows advantages including all-room-temperature processing, controllability, time efficiency, versatility and scalability. As a potential application, the photocatalytic hydrogen evolution performance of defective TiO2 is examined. The hydrogen evolution rate increases up to 41.8 mmol g−1 h−1 under one solar light irradiation, which is ~3 times higher than that of the pristine nanoparticles. The strategy of tuning defect oxides used in this work may be beneficial for many other related applications. Defective oxides are attractive for energy conversion and storage applications, but it remains challenging to implant defects in oxides under mild conditions. Here, the authors develop a versatile lithium reduction strategy to engineer the defects of oxides at room temperature leading to enhanced photocatalytic properties.