ArticleAngewandte Chemie (International ed. in English)2026
Day-Long Persistent Luminescence in Intrinsically Integrated Donor-Acceptor Carbon Dots Enabled by Defect-Mediated Charge Trapping.
Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Long-persistent luminescence (LPL) materials capable of storing and releasing optical energy over extended timescales are highly desirable for next-generation photonic technologies, yet structurally stable integrated donor-acceptor (D-A) systems capable of day-scale, color-tunable LPL remain elusive. Here, we report intrinsically integrated D-A carbon dots exhibiting continuously tunable LPL from deep blue to yellow-green, featuring day-scale persistence of up to 36 h and a naked-eye visible afterglow exceeding 4 h. Structurally, nitrogen-doped carbon-core donor domains are covalently coupled with arylboronic acid derived acceptor moieties through B─N linkages, forming an integrated D-A framework enriched with intrinsic defect-related trap states. Upon photoexcitation, intraparticle charge transfer (CT) generates long-lived charge-separated states, some of which are stabilized by intrinsic traps. Subsequent thermally activated detrapping releases the stored carriers and drives charge recombination, ultimately giving rise to day-scale LPL. Furthermore, modulation of the acceptor electronic structure regulates the energy of the emissive CT state, enabling rationally tunable multicolor LPL. Benefiting from its day-scale persistence and continuously tunable multicolor emission, this system enables potential applications in high-resolution displays, dynamic anti-counterfeiting, and intelligent information encryption. More importantly, this work establishes an intrinsically integrated D-A-trap design principle for ultralong LPL and a rational acceptor-engineering strategy for multicolor persistent luminescence.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.