The vacancy defects of semiconductor photocatalysts play key roles in enhancing their photocatalytic CO reduction activity. In this work, CeO was chosen as a model catalyst and oxygen vacancies were introduced on its surface by a facile and mild oxalic acid treatment followed by moderate heating in N. Such a treatment resulted in a much increased ratio of Ce/Ce in CeO, and the oxygen vacancy-enriched CeO showed remarkably enhanced photocatalytic activity in CO reduction, with CO being the dominant reduction product, whose yield was about 8 times that on the pristine CeO. In situ FT-IR spectra showed that the abundant oxygen vacancies substantially improved the CO adsorption/activation on the surface of CeO, which facilitated the subsequent reduction of CO. However, the carbonates strongly adsorbed on the photocatalyst surface might be the main obstacle to maintaining the high CO reduction activity and stability of CeO with O vacancies.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d0nr00717jDOI Listing

Publication Analysis

Top Keywords

oxygen vacancies
12
reduction activity
8
ceo
7
reduction
5
mild generation
4
surface
4
generation surface
4
oxygen
4
surface oxygen
4
vacancies
4

Similar Publications

Carboxylated cellulose nanocrystals mediated flower-like zinc oxide for antimicrobial without activation of light.

J Colloid Interface Sci

April 2025

State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640, China. Electronic address:

Conventional light-driven antimicrobial strategies of zinc oxide (ZnO) are limited by inadequate illumination in dark environments. In this study, carboxylated cellulose nanocrystals (MCNC) mediated flower-like ZnO (C@Z) with self-promoted reactive oxygen species release under dark is fabricated. The adsorption of Zn ions on MCNC prompts the growth of ZnO along the (002) crystal plane, forming a flower-like hybrid with superior dispersibility and oxygen vacancies compared to MCNC-free ZnO, which exposes the (100) plane.

View Article and Find Full Text PDF

The development of electrode materials for aqueous ammonium-ion supercapacitors (NH-SCs) has garnered significant attention in recent years. Poor intrinsic conductivity, sluggish electron transfer and ion diffusion kinetics, as well as structural degradation of vanadium oxides during the electrochemical process, pose significant challenges for their efficient ammonium-ion storage. In this work, to address the above issues, the core-shell VO·nHO@poly(3,4-ethylenedioxithiophene) composite (denoted as VOH@PEDOT) is designed and prepared by a simple agitation method to boost the ammonium-ion storage of VO·nHO (VOH).

View Article and Find Full Text PDF

Porous Single-Crystalline Rare Earth Phosphates Monolith to Enhance Catalytic Activity and Durability.

Molecules

January 2025

Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China.

Rare earth phosphate (XPO) is an extremely important rare earth compound. It can exhibit excellent activity and stability in catalytic applications by modifying its inherent properties. Porous single-crystalline (PSC) PrPO and SmPO with a large surface area consist of ordered lattices and disordered interconnected pores, resulting in activity similar to nanocrystals and stability resembling bulk crystals.

View Article and Find Full Text PDF

With growing environmental concerns and the need for sustainable energy, multifunctional materials that can simultaneously address water treatment and clean energy production are in high demand. In this study, we developed a cost-effective method to synthesize zinc oxide (ZnO) nanowires via the anodic oxidation of zinc foil. By carefully controlling the anodization time, we optimized the Zn/ZnO-5 min electrode to achieve impressive dual-function performance in terms of effective photoelectrocatalysis for water splitting and waste water treatment.

View Article and Find Full Text PDF

The influence of Mg doping in α-AlO crystals is investigated in this article by first-principles calculations and formation energies, density of states, and computed absorption spectra. Three models related to Mg substituting for Al doping structures were constructed, as well as spinel structure models with varying aluminum-magnesium ratios. The formation energy calculations confirmed the rationality of the MgV model, which means that Mg substitutional doping incorporating oxygen vacancies is most likely to form in crystals.

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!