Tailoring lanthanide doping in perovskite CaTiO3 for luminescence applications
Literature Information
Bo Tai, Weikang Wu, Feng Wang, Shan Guan, Wei Guo, Yunhao Lu, Shengyuan A. Yang
Perovskite oxide materials have been attracting significant attention due to their rich physical and chemical properties. With its proven stability and bio-compatibility, we suggest the lanthanide-doped perovskite to be a promising material for biological luminescence applications. Here, taking CaTiO3 as a concrete example, we systematically investigate its doping properties using first-principles computational methods. We determine the conditions allowing the growth of CaTiO3 against various competing phases. We obtain the formation energies of various intrinsic point defects in the material. The doping configuration and the charge state of the lanthanide dopants are determined. We find that for heavier elements in the lanthanide family, the substitution at the Ca site is favored under p-type growth conditions and tends to be trivalent, whereas the substitution at the Ti site is favored under n-type growth conditions and tends to be divalent. And for lighter elements in the family, the substitution at the Ca site is more favored for most cases and the dopant is more likely to be trivalent. By tuning the growth conditions, one could control the valence state of the lanthanide dopant, which in turn controls the luminescence spectra. We collect and identify the emission peaks in the infrared biological window, based on which possible doping schemes are suggested for bio-labeling and imaging applications.
Recommended Journals
Related Literature
In situ phosphonium-containing Lewis base-catalyzed 1,6-cyanation reaction: a facile way to obtain α-diaryl and α-triaryl acetonitriles
Yuan Chen, Xiaoyu Ren, Yumeng Guo, Bing Yi, Hongkui Zhang, Guowei Gao, Tianli Wang
DOI: 10.1039/D1QO01501J
Synthesis and biochemical evaluation of two novel N-hydroxyalkylated cyclosporin A analogs
Viktoria Kahlert, Oliver Ohlenschläger, Jelena Melesina, Christian Lücke
DOI: 10.1039/C8OB00980E
Figure-eight arylene ethynylene macrocycles: facile synthesis and specific binding behavior toward Hg2+
Hui Nie, Qian-Hui Li, Siqi Zhang, Chuan-Ming Wang, Wen-Hui Lin, Ke Deng, Li-Jin Shu, Qing-Dao Zeng, Jun-Hua Wan
DOI: 10.1039/D1QO00812A
Correction: 2-Aroylquinoline-5,8-diones as potent anticancer agents displaying tubulin and heat shock protein 90 (HSP90) inhibition
Kunal Nepali, Sunil Kumar, Hsiang-Ling Huang, Fei-Chiao Kuo, Cheng-Hsin Lee, Ching-Chuan Kuo, Teng-Kuang Yeh, Yu-Hsuan Li, Jang-Yang Chang, Jing-Ping Liou, Hsueh-Yun Lee
DOI: 10.1039/C8OB90080A
Synthesis of N-indolated amino acids or peptides from 2-alkynylanilines via a dearomatization process
Weilian Qiu, Weiyi Wang, Yin Liu, Renhua Fan
DOI: 10.1039/D1QO01257F
Highly regioselective, electrophile induced cyclizations of 2-(prop-1-ynyl)benzamides
Bhavani Shankar Chinta, Harikrishna Sanapa, Kamala Prasad Vasikarla, Beeraiah Baire
DOI: 10.1039/C8OB00434J
Intramolecular iron-catalyzed transannulation of furans with O-acetyl oximes: synthesis of functionalized pyrroles
Anton S. Makarov, Alexander A. Fadeev, Maxim G. Uchuskin
DOI: 10.1039/D1QO01281A
Water-promoted regio-selective trifluoromethylation of vinyl conjugated diazoacetates
Xinxin Han, Xin Liu, Yueyun Bao, Hunahuan Song, Yu-Rou Zhao, Xiaoying Wang, Junjie Zhang, Le Liu, Xin-Hua Duan, Jinbo Hu, Mingyou Hu
DOI: 10.1039/D1QO01654G
A transition-metal-free, base-promoted annulation/ring-cleavage/ring-reconstruction cascade reaction: a facile access to N-protection free indole-indenones
Na Luo, Zhen-Wei Sun, Xing-Xin Xu, Xiao-Qiang Hu, Feng-Cheng Jia
DOI: 10.1039/D1QO01280K
Nickel-catalyzed electrochemical reductive relay cross-coupling of alkyl halides with alkyl carboxylic acids
Cong Ma, Dong Liu, Hui Qiu, Bin Cheng, Tian-Sheng Mei
DOI: 10.1039/D1QO01219C
You might also like
What industries use (1R,3S)-1,3-Cyclopentanediol (CAS: 16326-97-9)?
(1R,3S)-1,3-Cyclopentanediol finds applications in various industries. In the ph...
What precautions should be taken when handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine (CAS: 637-31-0)?
When handling N'-[4-(Dimethylamino)phenyl]-N,N-dimethyl-1,4-benzenediamine, it i...
Are there alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine (CAS: 1352318-16-1) in synthesis?
There are several alternatives to 5-(2,4-Difluorophenyl)-2-methoxypyrimidine in ...
What regulatory guidelines apply to 1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6)?
1-(3-Methoxyphenoxy)propan-2-ol (CAS: 382141-68-6) must comply with the Globally...
Is Tetrodotoxin Citrate (CAS: 18660-81-6) safe?
Tetrodotoxin Citrate is extremely dangerous and should be handled with extreme c...
What are the main uses of 2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9)?
2-Methyl-2-propanyl [(1R,3S)-3-hydroxycyclopentyl]carbamate (CAS: 225641-84-9) i...
How should waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) be handled?
Waste containing 4-(2-Hydroxyhexafluoroisopropyl)Benzoic Acid (CAS: 16261-80-6) ...
How is 2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl}carbamate (CAS: 102507-19-7) typically synthesized?
2-Methyl-2-proanyl {(2S)-1-[(benzyloxy)amino]-3-hydroxy-3-methyl-1-oxo-2-butanyl...
What is Benzeneethanamine, α-ethyl-, hydrochloride (1:1) (CAS: 20735-15-3)?
Benzeneethanamine, α-ethyl-, hydrochloride (1:1) is an organic compound with the...
Are there alternatives to 3-{(E)-[4-(Dimethylamino)phenyl]diazenyl}benzoic acid (CAS: 20691-84-3) in synthesis?
In the synthesis of compounds similar to 3-{(E)-[4-(Dimethylamino)phenyl]diazeny...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.













![N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure N-[(5,6-Dichloro-1H-benzimidazol-2-yl)methyl]-9-(1-methyl-1H-pyrazol-4-yl)-2-(4-morpholinyl)-9H-purin-6-amine structure](https://static.chemtradehub.com/structs/238/2387704-62-1-25f4.webp)
