The phase of BiFeO (BFO) as well as its domain configuration can be tuned by strain engineering. Phase change may greatly influence the properties of the polarization field and hence charge separation. However, the photoelectrochemical properties of different BFO phases have rarely been addressed. Here, the photoelectrochemical study of tetragonal (T-) and rhombohedral (R-) phase BFO films was conducted under visible light illumination. The photocurrent density of R-BFO is 5 times that of T-BFO. A ferroelectric domain study shows that T-BFO features single domain structure in contrast to the polydomain structure of R-BFO. Higher charge separation efficiency is achieved in R-BFO, dominated by the domain walls as conducting pathways for efficient charge separation and transfer. This work provides a fundamental understanding of the photoelectrochemical properties of T- and R-BFO, offering valuable insights for the development of BFO-based materials for solar energy conversion.
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http://dx.doi.org/10.1021/acs.jpclett.4c01245 | DOI Listing |
Bioelectrochemistry
January 2025
School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, People's Republic of China; Key Laboratory for Polymeric Composite & Functional Materials of Ministry of Education, School of Chemistry, Sun Yat-sen University, Guangzhou 510275, People's Republic of China.
Highly stable calcium ion selective electrodes (Ca-ISEs) were developed by drop-casting a layer of poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT: PSS) as an ion-to-electron transfer layer onto Au electrode. The conductive PEDOT: PSS ink was prepared using a metastable liquid-liquid contact (MLLC) doping method, which induced phase separation, removed excess PSS, and significantly enhanced charge transfer kinetics and conductivity. The resulting Ca-ISEs exhibited excellent electrochemical performance.
View Article and Find Full Text PDFACS Nano
January 2025
WA School of Mines: Minerals, Energy and Chemical Engineering, Curtin University, Perth, WA 6102, Australia.
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.
View Article and Find Full Text PDFLangmuir
January 2025
Heilongjiang Provincial Key Laboratory of CO2 Resource Utilization and Energy Catalytic Materials, School of Material Science and Chemical Engineering, Harbin University of Science and Technology, Harbin 150040, China.
Constructing wide and narrow band gap heterogeneous semiconductors is a method to improve the activity of photocatalysts. In this paper, CMS/ZnO heterojunctions were prepared by solvothermal loading of ZnO particles on the surface of CuMoS nanosheets. The photocatalytic H precipitation rate is about 545 μmol·g·h, which is 6.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Nuclear Waste Disposal Research & Analysis Department, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States.
Fluid-silica interfaces are ubiquitous in chemistry, occurring in both natural geochemical environments and practical applications ranging from separations to catalysis. Simulations of these interfaces have been, and continue to be, a significant avenue for understanding their behavior. A constraining factor, however, is the availability of accurate force fields.
View Article and Find Full Text PDFSmall
January 2025
MOE International Joint Laboratory of Materials Microstructure, Institute for New Energy Materials and Low Carbon Technologies, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin, 300384, China.
The photocatalytic activity of lead-free perovskite heterostructures currently suffers from low efficiency due to the lack of active sites and the inadequate photogenerated carrier separation, the latter of which is hindered by slow charge transfer at the heterostructure interfaces. Herein, a facile strategy is reported for the construction of lead-free halide-perovskite-based heterostructure with swift interfacial charge transfer, achieved through direct partial conversion of 2D antimony oxybromide SbOBr to generate CsSbBr/SbOBr heterostructure. Compared to the traditional electrostatic self-assembly method, this approach endows the CsSbBr/SbOBr heterostructure with a tightly interconnected interface through in situ partial conversion, significantly accelerating interfacial charge transfer and thereby enhancing the separation efficiency of photogenerated carriers.
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