Materials 2023, 16, 1081. https://doi.org/10.3390/ma16031081 www.mdpi.com/journal/materials
Review
Advanced Photocatalysts for CO2 Conversion by Severe Plastic
Deformation (SPD)
Saeid Akrami
1,
*, Tatsumi Ishihara
2,3,4
, Masayoshi Fuji
1,5
and Kaveh Edalati
2,3,
*
1
Department of Life Science and Applied Chemistry, Nagoya Institute of Technology,
Tajimi 507-0071, Japan
2
WPI International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University,
Fukuoka 819-0395, Japan
3
Mitsui Chemicals, Inc.—Carbon Neutral Research Center (MCI-CNRC), Kyushu University,
Fukuoka 819-0395, Japan
4
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, Fukuoka 819-0395, Japan
5
Advanced Ceramics Research Center, Nagoya Institute of Technology, Tajimi 507-0071, Japan
* Correspondence: saeidakrami91@gmail.com (S.A.); kaveh.edalati@kyudai.jp (K.E.);
Tel.: +81-572-24-8110 (S.A.); +81-82-802-6744 (K.E.)
Abstract: Excessive CO2 emission from fossil fuel usage has resulted in global warming and
environmental crises. To solve this problem, the photocatalytic conversion of CO2 to CO or useful
components is a new strategy that has received significant attention. The main challenge in this
regard is exploring photocatalysts with high efficiency for CO2 photoreduction. Severe plastic
deformation (SPD) through the high-pressure torsion (HPT) process has been effectively used in
recent years to develop novel active catalysts for CO2 conversion. These active photocatalysts have
been designed based on four main strategies: (i) oxygen vacancy and strain engineering, (ii)
stabilization of high-pressure phases, (iii) synthesis of defective high-entropy oxides, and (iv)
synthesis of low-bandgap high-entropy oxynitrides. These strategies can enhance the photocatalytic
efficiency compared with conventional and benchmark photocatalysts by improving CO2
adsorption, increasing light absorbance, aligning the band structure, narrowing the bandgap,
accelerating the charge carrier migration, suppressing the recombination rate of electrons and holes,
and providing active sites for photocatalytic reactions. This article reviews recent progress in the
application of SPD to develop functional ceramics for photocatalytic CO2 conversion.
Keywords: functional properties; ultrafine-grained (UFG) materials; nanostructured materials;
photocatalytic CO2 conversion; high-pressure torsion (HPT); oxygen vacancies; high-pressure
phases; high-entropy ceramics
1. Introduction
Nowadays, environmental crises, especially global warming caused by CO2 emission
from burning fossil fuels and humankind activities, are considered one of the most
significant challenges in the world. Reduction of CO2 to reactive CO gas or useful
components and fuels, such as CH4 and CH3OH, using photocatalysts is one of the clean
and new strategies, which is developing rapidly [1–3]. In photocatalytic CO2 conversion,
excited electrons transfer from the valence band to the conduction band of the
photocatalysts by solar irradiation and contribute to the reduction of CO2 to form
desirable products, as shown in Figure 1a [3]. To perform these reduction reactions, some
thermodynamic and kinetic conditions should be provided. From the viewpoint of
thermodynamics, the standard potential of the reduction and oxidation reactions should
be between the valence band and the conduction band of the photocatalyst [3,4]. On the
other hand, from the kinetic viewpoint, the electrons should absorb the light, transfer to
the conduction band, migrate to the surface of the photocatalyst, and take part in the
Citation: Akrami, S.; Ishihara, T.;
Fuji, M.; Edalati, K. Advanced
Photocatalysts for CO2 Conversion
by Severe Plastic Deformation (SPD).
Materials 2023, 16, 1081.
https://doi.org/10.3390/ma16031081
Academic Editor: Ovidiu Oprea
Received: 31 December 2022
Revised: 22 January 2023
Accepted: 24 January 2023
Published: 26 January 2023
Copyright: © 2023 by the authors.
Licensee MDPI, Basel, Switzerland.
This article is an open access article
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conditions of the Creative Commons
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(https://creativecommons.org/license
s/by/4.0/).