Hao Ding

Bio: Hao Ding is an academic researcher from China University of Geosciences (Beijing). The author has contributed to research in topics: Composite number & Photocatalysis. The author has an hindex of 12, co-authored 46 publications receiving 461 citations.

Construction of urchin-like ZnIn2S4-Au-TiO2 heterostructure with enhanced activity for photocatalytic hydrogen evolution

Abstract: The ternary ZnIn2S4-Au-TiO2 Z-scheme heterostructure photocatalysts has been fabricated by selecting effectiveness Au NPs as a solid electron mediator, via a chemical-deposition process for water splitting under simulated solar light irradiation. The designed photocatalysts exhibit high surface area and wide light absorption range, which significantly enhance photocatalytic efficiency. At an optimal ratio of 24 wt% Au NPs and 60 wt% ZnIn2S4, the obtained ZnIn2S4-Au-TiO2 photocatalysts achieve the highest H2 production with the rate of 186.3 μmol g−1 h−1, and the O2 production rate is reached to 66.3 μmol g−1 h−1. It showed that the ZnIn2S4-Au-TiO2 composite structures exhibit significantly better photocatalytic activity than ZnIn2S4-TiO2 and Au-ZnIn2S4-TiO2 structure. Such an excellent performance should be attributed to the Au NPs in the Z-scheme system structure which favor to enhance the transfer rate of the photogenerated electrons and holes and remain strong redox ability of the photocatalysts. It is worth pointing out that the unique Z-scheme ZnIn2S4-Au-TiO2 heterostructure shows great solar activity toward water splitting into renewable hydrocarbon fuel.

Preparation of black-pearl reduced graphene oxide-sodium alginate hydrogel microspheres for adsorbing organic pollutants.

Abstract: The black-pearl reduced graphene oxide-sodium alginate (rGO-SA) hydrogel microspheres are prepared by the external emulsification and thermal reduction method, which are characterized by scanning electron microscope (SEM) and X-ray Diffraction (XRD). Sodium alginate (SA) serves as a template to form a 3D porous network structure, which can prevent the agglomeration and restacking of rGO sheets efficiently. The size of hydrogel microsphere can be controlled by adjusting the size of the liquid drop. The effects of rGO content (wt%), contact time, initial concentration of phenol, adsorption temperature and adsorption dose on the adsorption capacity of rGO-SA microspheres are investigated. The kinetics and isotherm data are well described by the pseudo-second-order kinetic model and the Langmuir equation, respectively. Thermodynamic results demonstrate the spontaneous and endothermic nature of adsorption. This rGO-SA microsphere exhibits the favorable adsorption performance for phenol, BPA and tetracycline. The rGO-SA microsphere might be a potential candidate for efficient adsorbents in water treatment.

The Preparation of TiO2 Film by the Sol-Gel Method and Evaluation of Its Self-Cleaning Property

Abstract: TiO2 sol was produced by the sol-gel method through the hydrolysis and the aging of tetrabutyl titanate and the TiO2 film was obtained by dipping and uniform lifting of the acid-treated and ultrasound-treated clean glass slides into the TiO2 sol followed by aging, drying, and calcination. The effect of the hydrolysis control agents to the formed sol was researched and the crystalline state, the morphology, and the photocatalytic properties of the products after calcination were characterized. The structural morphology, the contact angles before and after illumination, and the self-cleaning properties of the TiO2 film were characterized as well. The results showed that by using acetylacetone as the hydrolysis control agent, the formed TiO2 sol had relatively high stability. The product after the calcination of the TiO2 sol was of single anatase type with crystalline size of 18–20 nm and it could degrade nearly 100% of methylene blue after 90 min illumination. The formed TiO2 film is compact, continuous, smooth, and had the properties of super-hydrophilicity (after 30 min illumination due to its contact angle decreasing from 21° to nearly 0°) and anti-fogging capability, which indicated its excellent self-cleaning property.

g-C3N4-Based Heterostructured Photocatalysts

Abstract: Photocatalysis is considered as one of the promising routes to solve the energy and environmental crises by utilizing solar energy. Graphitic carbon nitride (g-C3N4) has attracted worldwide attention due to its visible-light activity, facile synthesis from low-cost materials, chemical stability, and unique layered structure. However, the pure g-C3N4 photocatalyst still suffers from its low separation efficiency of photogenerated charge carriers, which results in unsatisfactory photocatalytic activity. Recently, g-C3N4-based heterostructures have become research hotspots for their greatly enhanced charge carrier separation efficiency and photocatalytic performance. According to the different transfer mechanisms of photogenerated charge carriers between g-C3N4 and the coupled components, the g-C3N4-based heterostructured photocatalysts can be divided into the following categories: g-C3N4-based conventional type II heterojunction, g-C3N4-based Z-scheme heterojunction, g-C3N4-based p–n heterojunction, g-C3N4/metal heterostructure, and g-C3N4/carbon heterostructure. This review summarizes the recent significant progress on the design of g-C3N4-based heterostructured photocatalysts and their special separation/transfer mechanisms of photogenerated charge carriers. Moreover, their applications in environmental and energy fields, e.g., water splitting, carbon dioxide reduction, and degradation of pollutants, are also reviewed. Finally, some concluding remarks and perspectives on the challenges and opportunities for exploring advanced g-C3N4-based heterostructured photocatalysts are presented.

Photocatalytic hydrogen production using metal doped TiO2: A review of recent advances

Abstract: Hydrogen (H2) production via photocatalytic water splitting is one of the most promising technologies for clean solar energy conversion to emerge in recent decades. The achievement of energy production from water splitting would mean that we could use water as a fuel for future energy need. Among the various photocatalytic materials, titanium dioxide (TiO2) is the dominant and most widely studied because of its exceptional physico-chemical characteristics. Surface decoration of metal/non-metal on TiO2 nanoparticles is an outstanding technique to revamp its electronic properties and enrich the H2 production efficiency. Metal dopants play a vital role in separation of electron-hole pairs on the TiO2 surface during UV/visible/simulated solar light irradiation. In this paper, the basic principles, photocatalytic-reactor design, kinetics, key findings, and the mechanism of metal-doped TiO2 are comprehensively reviewed. We found that Langmuir-Hinshelwood kinetic model is commonly employed by the researchers to demonstrate the rate of H2 production. Copper (Cu), gold (Au) and platinum (Pt) are the most widely studied dopants for TiO2, owing to their superior work function. The metal dopants can amplify the H2 production efficiency of TiO2 through Schottky barrier formation, surface plasmon resonance (SPR), generation of gap states by interaction with TiO2 VB states. The recent advances and important consequences of 2D materials, perovskites, and other novel photocatalysts for H2 generation have also been reviewed.

Nitrogen-doped titanium dioxide (N-doped TiO2) for visible light photocatalysis

Abstract: TiO2 is an effective and well-known photocatalyst for water and air purification, but its practical applications in visible light-assisted chemical reactions are hindered mainly by its poor visible light absorption capacity. Nitrogen-doped TiO2 (N-doped TiO2) has attracted considerable attention as a photocatalyst, and rapid progress has been made in enhancing the photocatalytic efficiency of TiO2 under visible light irradiation. N-doped TiO2 exhibits broad absorption in the visible region, which can allow the utilization of a large part of the solar spectrum. This might be useful for environmental and energy applications, such as the photocatalytic degradation of organic pollutants, solar cells, sensors, and water splitting reactions. This review focuses on the major developments in the synthesis of N-doped TiO2 and its possible applications in the photocatalytic degradation of organic pollutants and environmental remediation under visible light irradiation.

The enhancement of photocatalytic hydrogen production via Ti3+ self-doping black TiO2/g-C3N4 hollow core-shell nano-heterojunction

Abstract: The Ti3+ self-doping B-TiO2/g-C3N4 hollow core-shell nano-heterojunction is synthesized via the continuous hydrothermal deposition and sculpture-reduction processes. The results of SEM, XRD, TEM, XPS and FT-IR imply that the B-TiO2/g-C3N4 hollow core-shell nanospheres have been prepared successfully. The photocatalytic activity of the B-TiO2/g-C3N4 nano-heterojunctions remarkably exhibits an enhancement of 18 times and 65 times than that of normal TiO2 and g-C3N4, respectively. Further, the photocatalytic process and the mechanism of the photocatalytic hydrogen production enhancement have been studied, which could be ascribed to the Ov-Ti3+ in the B-TiO2 and interface nano-heterojunction, that have been proved by the transient photocurrent, PL, EIS and Mott-Schottky plots.