In-situ construction of TiO polymorphic junction nanoarrays without cocatalyst for boosting photocatalytic hydrogen generation.

J Colloid Interface Sci

Key Laboratory of Interface Science and Engineering in Advanced Materials (Taiyuan University of Technology), Ministry of Education, Taiyuan 030024, PR China; College of Materials Science and Engineering, Taiyuan University of Technology, Taiyuan 030024, PR China. Electronic address:

Published: January 2024

There are significant challenges in developing technologies for high-yield photocatalytic hydrogen production reactions. Current photocatalytic materials face three key problems: low utilization of light, rapid recombination of photogenerated electron-hole pairs, and a limited number of active sites during photocatalytic reactions. As a result, these materials only improve one or two of the three steps involved in photocatalytic hydrogen production reactions. Consequently, achieving simultaneous multifunctional synergy to enhance the efficiency of all three processes is difficult. Here, we report an in situ dissolution-recrystallisation approach to design and fabricate a three-dimensional TiO rutile/anatase (AE-TiO) array photocatalytic material for photocatalytic hydrolysis applications. It is shown that the unique 3D nanoarray structure and in situ fabrication of the AE-TiO homojunction with synergistic effects among the components lead to an increase in light harvesting efficiency, charge transport separation efficiency and surface active sites, which remarkably improve the photocatalytic hydrolysis performance. The prepared AE-TiO homojunction materials realizes a maximal photoactivity of 4 μmol cm·h, which is 39 times larger than that of pure TiO rutile nanorods.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jcis.2023.09.198DOI Listing

Publication Analysis

Top Keywords

photocatalytic hydrogen
12
photocatalytic
8
hydrogen production
8
production reactions
8
active sites
8
photocatalytic hydrolysis
8
ae-tio homojunction
8
in-situ construction
4
construction tio
4
tio polymorphic
4

Similar Publications

Hydrogen evolution from water, catalyzed by solar energy, is a promising yet challenging endeavor. Small-sized catalysts usually exhibit high utilization and high performance in the hydrogen evolution field. However, the high surface energy tends to make them aggregate.

View Article and Find Full Text PDF

Photocatalytic methane oxidation under mild conditions using single-atom catalysts remains an advanced technology. In this work, gold single atoms (Au SAs) were introduced onto TiO nanostructures using a simple method. The resulting performance demonstrated effective conversion of methane into H and C products at room temperature.

View Article and Find Full Text PDF

Development of Triphenylamine Derived Photosensitizers for Efficient Hydrogen Evolution from Water.

Chemistry

January 2025

The Hong Kong Polytechnic University, Department of Applied Biology and Chemical Technology, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Hom, Hong Kong (P.R. China), 000000, Hong Kong, HONG KONG.

A series of new (donor)₂-donor-π-acceptor (D2-D-π-A) and (acceptor)₂-donor-π-acceptor (A2-D-π-A) organic photosensitizers based on the framework of (Z)-2-cyano-3-(5-(4-(diphenylamino)phenyl)thiophen-2-yl)acrylic acid have been synthesized and characterized. By incorporating groups with different electron-donating or withdrawing abilities, such as dibenzothiophene (DBT), dibenzofuran (DBF), and triazine (TA), into the triphenylamine segment, their photophysical properties have been regulated.  Theoretical calculations were used to explore how various donor-acceptor combinations influence their hydrogen production performance.

View Article and Find Full Text PDF

Pairing photocatalytic 1,2,3,4-tetrahydroisoquinoline semi-dehydrogenation reaction (THIQ-SDR) with two-electron oxygen reduction reaction (2e- ORR) is a green solar to chemical strategy by simultaneously utilizing the photo-excited electrons and holes. However, it is still short of high-efficiency photocatalyst to drive two reactions above. In the present work, crystalline pyrene-thiourea/urea covalent organic frameworks (COF-Py-S and -O) were synthesized and demonstrated as high-performance metal-free photocatalysts.

View Article and Find Full Text PDF

Structural Isomerism of {Ag14}10+ Nanocluster Encapsulated by Bowl-like Polyoxometalates.

Angew Chem Int Ed Engl

January 2025

Beijing Institute of Technology, School of Chemistry and Chemical Engineering, 8th Liangxiang East Road, Room 829, Eco-Industrial Building, Beijing, 102488, Beijing, CHINA.

The structural isomerism of atomically precise nanoclusters provides a preeminent theoretical model to investigate the structure-property relationships. Herein, we synthesized three bowl-like polyoxometalate (POM)-encapsulated Ag nanoclusters (denoted as {Ag14(Sb3W30)2}-1, {Ag14(Sb3W30)2}-1a, and {Ag14(Sb3W30)2}-2) via a facile one-pot solvothermal approach. Among them, for the first time, an unprecedented isomeric {Ag14}10+ nanoclusters are obtained in polyoxoanions {Ag14(Sb3W30)2}-1 and {Ag14(Sb3W30)2}-2, which should be probably induced by the different distribution of coordinating O atoms in two isomeric bowl-like {Sb3W30} ligands.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!