Photocatalytic reduction of CO2 over Ti3+ self-doped TiO2-based nanomaterials

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F24%3A10255698" target="_blank" >RIV/61989100:27710/24:10255698 - isvavai.cz</a>

Alternative codes found

RIV/61989100:27360/24:10255698 RIV/61989100:27640/24:10255698 RIV/61989592:15640/24:73624731 RIV/70883521:28110/24:63578878

Result on the web

<a href="https://www.sciencedirect.com/science/article/pii/S2212982024000362#ab0015" target="_blank" >https://www.sciencedirect.com/science/article/pii/S2212982024000362#ab0015</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.jcou.2024.102701" target="_blank" >10.1016/j.jcou.2024.102701</a>

Result language

angličtina

Original language name

Photocatalytic reduction of CO2 over Ti3+ self-doped TiO2-based nanomaterials

Original language description

In this study, we explored the photocatalytic efficacy of Ti3+-doped TiO2-based photocatalysts for CO2 reduction. The Ti3+ self-doped photocatalysts were synthesized using a straightforward chemical reduction with sodium borohydride (NaBH4). Our investigation aimed to elucidate the intricate interplay between the synthesis process and the quantity of NaBH4 reductant on the physical-chemical and photocatalytic attributes of the defective TiO2-based photocatalysts. We explored three different commercially available TiO2 materials labeled P25, (S)TiO2, and KRONOClean7050, which were reduced (2 g of TiO2) with 0.75 and 1.5 g of NaBH4. The reduction with 0.75 g of NaBH4 led to a significant decrease of photocatalytic activity in all three cases. It was caused by clogging of the photocatalysts surface by sodium ions which resulted in the surface recombination of charge carriers. Oppositely, the reduction with 1.5 g of NaBH4, led to an increase of the photocatalytic activity with superior performance of KRONOClean7050. The comprehensive characterization of all the samples explained this superior performance of KC7050_RED_1.5 sample. Importantly, it did not contain any amorphous phase and the crystal size was two times higher compared to other 2 samples reduced by 1.5 g of NaBH4. In the addition to higher crystallinity, the formation of a disordered TiO2MINUS SIGN x layer, enriched with Ti3+ defects and oxygen vacancies, was confirmed. These structural features enhance the light absorption and mitigate undesired recombination of photogenerated charge carriers. These results would trigger farther investigation of defect engineering towards enhancement of the efficiency of metal oxide photocatalysts. (C) 2024 The Authors

Czech name

—

Czech description

—

Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

10403 - Physical chemistry

Project

<a href="/en/project/GF21-24268K" target="_blank" >GF21-24268K: CO2 transformation to valuable chemicals by catalytic and photocatalytic ways over highly active materials</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2024

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Journal of CO2 Utilization

ISSN

2212-9820

e-ISSN

2212-9839

Volume of the periodical

80

Issue of the periodical within the volume

february

Country of publishing house

GB - UNITED KINGDOM

Number of pages

13

Pages from-to

nestránkováno

UT code for WoS article

001185145900001

EID of the result in the Scopus database

2-s2.0-85185288451