98%
921
2 minutes
20
The specific detection of peroxydisulfate (SO, PDS) is significant and challenging due to the rapid development of PDS-related technologies and their widespread application in multiple fields. However, traditional analytical methods are mainly based on their strong oxidizing properties, making it difficult to simultaneously achieve specific identification and high sensitivity for PDS detection in complex water environments. Here, we purposely prepared amino-rich SiQDs (N-SiQDs) as an effective catalyst and introduced HO acts as a co-reactant for PDS activation and determination with strong intrinsic chemiluminescence (CL) emission. High yield of reactive active oxygen (mainly O˙ and ˙OH) were generated during CL process, which trigger electron-hole annihilation between the N-SiQDs˙ and N-SiQDs˙ accounted for extraordinary CL emission. On this basis, a new CL assay for PDS detection was fabricated with broad linear range of 5 × 10M-5 × 10 M and low detection limit (3.2 × 10 M). Due to the absence of SO˙ involvement during CL emission, the sensing platform is sensitive enough, satisfactory selectivity and does not respond to transition-metal ions and inorganic anions that have interferences in the PDS CL sensors reported before. This work not only deepens insight into the mechanisms of nanomaterials assisted PDS activation but also provides a new perspective on the modified metal-free QDs CL probe for chemical species detection.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.talanta.2024.126931 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China.
Reverse intersystem crossing (RISC) process is critical for thermally activated delayed fluorescence (TADF) materials to realize spin-flip of triplet excitons in organic light-emitting diodes (OLEDs), but the RISC processes of most TADF materials are not fast enough, undermining electroluminescence (EL) efficiency stability and operational lifetime. Herein, a symmetry breaking strategy to accelerate RISC processes is proposed. By designing asymmetric electron-withdrawing backbone consisting of benzonitrile and xanthone/thioxanthone groups, two new asymmetric TADF molecules, 4tCzCN-pXT and 4tCzCN-pTXT, with multiple 3,6-di-tert-butylcarbazole donors are successfully developed.
View Article and Find Full Text PDFSmall
September 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, P. R. China.
Perovskites have a large number of intrinsic defects and interface defects, which often lead to non-radiative recombination, and thus affect the efficiency of perovskite solar cells (PSCs). Introducing appropriate passivators between the perovskite layer and the transport layer for defect modification is crucial for improving the performance of PSCs. Herein, two positional isomers, 1-naphthylmethylammonium iodide (NMAI) and 2-naphthylmethylammonium iodide (NYAI) are designed.
View Article and Find Full Text PDFAdv Mater
September 2025
Key Laboratory of In-Fiber Integrated Optics of Ministry of Education, College of Physics and Optoelectronic Engineering, Harbin Engineering University, Harbin, 150001, China.
Recently, joint replacement surgery is facing significant challenges of patient dissatisfaction and the need for revision procedures. In-situ monitoring of stress stability at the site of artificial joint replacement during postoperative evaluation is important. Mechanoluminescence (ML), a novel "force to light" conversion technology, may be used to monitor such bio-stress within tissues.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Advanced Materials Engineering for Information & Electronics, Kyung Hee University, Gyeonggi-do 17104, Republic of Korea. Electronic address:
We present a supramolecular templating strategy for inducing chirality in hybrid perovskites via confined crystallization within chiral super spaces-nanoconfined, helically ordered cavities formed by the self-assembly of achiral bent-core molecules with chiral additives. Upon removal of the additives, the resulting porous films retain permanent chirality. Quasi-2D hybrid organic-inorganic perovskites crystallized within these templates exhibit distinct chiroptical activity, including mirror-image circular dichroism and circularly polarized light emitting (CPLE), with CPLE dissymmetry factors reaching up to 1.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Key Laboratory of Textile Fiber and Products, Wuhan Textile University, Ministry of Education, Wuhan, 430200, China.
0D hybrid manganese halides represent an emerging class of luminescent materials, yet their practical application has been hindered by the intrinsic trade-off between optical performance and mechanical flexibility. Here, a green synthesis of 0D (ECMP)MnBr crystal is reported, exhibiting unprecedented triple-mode emission (photoluminescence, X-ray scintillation, and mechanoluminescence) through rationally designed highly symmetric [MnBr] tetrahedra, achieving near-unity photoluminescence quantum yield (98.97%), record-low X-ray detection limit (15.
View Article and Find Full Text PDF