TY - JOUR
T1 - Creation of Piezoelectricity in Quadruple Perovskite Oxides by Harnessing Cation Defects and Their Application in Piezo-Photocatalysis
AU - Wang, Kai
AU - Guo, Xiangyu
AU - Han, Chen
AU - Liu, Lihong
AU - Wang, Zhiliang
AU - Thomsen, Lars
AU - Chen, Peng
AU - Shao, Zongping
AU - Wang, Xudong
AU - Xie, Fang
AU - Liu, Gang
AU - Wang, Lianzhou
AU - Liu, Shaomin
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/1/28
Y1 - 2025/1/28
N2 - Quadruple perovskite oxides have received extensive attention in electronics and catalysis, owing to their cation-ordering structure and intriguing physical properties. However, their repertoires still remain limited. In particular, piezoelectricity from quadruple perovskites has been rarely reported due to the frustrated symmetry-breaking transition in A-site-ordered perovskite structures, disabling their piezoelectric applications. Herein, we report a feasible strategy to achieve piezoelectricity in CaCu3Ti4O12 (CCTO) quadruple perovskite via cation defect engineering, specifically through a thermal-driven selective cation exsolution strategy to introduce Cu vacancies. The introduction of Cu point defects in CCTO locally destabilizes the constrained tilted TiO6 octahedra framework, relaxing the octahedral tilting and inducing structural heterogeneity which, in turn, disrupts the high symmetry of the pristine cubic phase. As a result, the defective CCTO with localized asymmetry exhibits intense polarization and a robust piezoelectricity of 7 pC N-1. The created piezoelectricity is further validated by its application as a piezo-photocatalyst, enabling efficient charge separation and transfer with a 2.5-times increment in the lifetime of photoexcitations. This enhancement leads to a 3.86- and 31-fold increase in the production of hydrogen peroxide and reactive oxygen species compared with individual piezocatalysis and photocatalysis, respectively. This study establishes a pathway to engineer piezoelectricity in quadruple perovskites, potentially unlocking a wide range of applications in modern microelectronics beyond the demonstrated piezo-photocatalysis.
AB - Quadruple perovskite oxides have received extensive attention in electronics and catalysis, owing to their cation-ordering structure and intriguing physical properties. However, their repertoires still remain limited. In particular, piezoelectricity from quadruple perovskites has been rarely reported due to the frustrated symmetry-breaking transition in A-site-ordered perovskite structures, disabling their piezoelectric applications. Herein, we report a feasible strategy to achieve piezoelectricity in CaCu3Ti4O12 (CCTO) quadruple perovskite via cation defect engineering, specifically through a thermal-driven selective cation exsolution strategy to introduce Cu vacancies. The introduction of Cu point defects in CCTO locally destabilizes the constrained tilted TiO6 octahedra framework, relaxing the octahedral tilting and inducing structural heterogeneity which, in turn, disrupts the high symmetry of the pristine cubic phase. As a result, the defective CCTO with localized asymmetry exhibits intense polarization and a robust piezoelectricity of 7 pC N-1. The created piezoelectricity is further validated by its application as a piezo-photocatalyst, enabling efficient charge separation and transfer with a 2.5-times increment in the lifetime of photoexcitations. This enhancement leads to a 3.86- and 31-fold increase in the production of hydrogen peroxide and reactive oxygen species compared with individual piezocatalysis and photocatalysis, respectively. This study establishes a pathway to engineer piezoelectricity in quadruple perovskites, potentially unlocking a wide range of applications in modern microelectronics beyond the demonstrated piezo-photocatalysis.
KW - cation defect
KW - hydrogen peroxide
KW - piezo-photocatalysis
KW - piezoelectricity
KW - polarization
KW - quadruple perovskite oxide
UR - http://www.scopus.com/inward/record.url?scp=85215663090&partnerID=8YFLogxK
U2 - 10.1021/acsnano.4c14974
DO - 10.1021/acsnano.4c14974
M3 - 文章
AN - SCOPUS:85215663090
SN - 1936-0851
VL - 19
SP - 3818
EP - 3829
JO - ACS Nano
JF - ACS Nano
IS - 3
ER -