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Chemiluminescence resonance energy transfer (CRET) efficiency can be enhanced by confining CRET donors and acceptors within nanoscale spaces. However, this enhanced efficiency is often affected by uncertainties stemming from the random distribution of CRET donors and acceptors in such confined environments. In this study, a novel confined nanospace was created through the surfactant modification of carbon dots (CDs) exhibiting aggregation-induced emission (AIE) characteristics. Hydrophobic CRET donors could be effectively confined within this nanospace. The distance between the CRET donors and acceptors could be controlled by anchoring the AIE-CDs as the CRET acceptors, resulting in significantly improved CRET efficiency. Furthermore, this AIE-CDs-based CRET system was successfully applied to the detection of hydrogen peroxide (H 2 O 2 ) in rainwater, showcasing its potential for practical applications., (© 2024 John Wiley & Sons Ltd.)

High-efficiency chemiluminescence (CL) resonance energy transfer (CRET) can be obtained by shortening the donor-acceptor distance and/or improving the luminescence efficiency of CRET acceptors. However, careful design and stringent experimental conditions are usually required for the ordered assembly of CRET acceptors on support materials to avoid aggregation-caused quenching problems. In this work, an aggregation-induced emission (AIE)-active fluorophore was disorderly adsorbed on the surface of layered double hydroxides (LDHs), which could exhibit high-efficiency luminescence. On the other hand, the positively charged LDHs can further adsorb peroxynitrite (ONOO - ) on the surface of LDHs. Therefore, the LDH-supported AIE fluorophore could dramatically amplify weak CL signals from ONOO - donors as a result of ultra-high CRET efficiency by coupling the shorter donor-acceptor distance with efficient CRET acceptors. The proposed CL system has been successfully applied for the detection of NaNO 2 in the concentration range from 1.0 to 100 μM with a detection limit as low as 0.5 μM. Satisfactory recoveries (98-106%) and good accuracy were achieved for sausage samples. Our success will open new avenues for the convenient design of high-efficiency CRET systems.

Finding an efficient photosensitizer is crucial in ensuring a therapeutic effect of photodynamic treatment. Currently, screening of photosensitizers during photodynamic therapy is achieved by evaluating the total yield of singlet oxygen ( 1 O 2 ), rather than monitoring the formation dynamics of 1 O 2 . 1 O 2 -based chemiluminescence (CL) is a suitable method to directly monitor the generated amount of 1 O 2 . Herein, the tetraphenylethene-sodium dodecyl sulfonate surfactant with aggregation-induced emission characteristics can remarkably amplify the intrinsic CL emission from 1 O 2 by integrating its micellar microenvironment with a CL energy acceptor effect in a cage-like structure. We present a new luminescence platform for the rapid screening of photosensitizers by monitoring the formation dynamics of 1 O 2 during photodynamic therapy. This study will not only be critical in optimizing the irradiation time during photodynamic therapy but also open a new door to the discovery of efficient photosensitizers.

It is essential to probe the coordination number (CN) because it is a crucial factor to ensure the catalytic capability of single‐atom catalysts (SACs). Currently, synchrotron X‐ray absorption spectroscopy (XAS) is widely used to measure the CN. However, the scarcity of synchrotron X‐ray source and complicated data analysis restrict its wide applications in determining the CN of SACs. In this contribution, we have developed a d‐band center‐regulated acetone cataluminescence (CTL) probe for a rapid screening of the CN of Pt‐SACs. It is disclosed that the CN‐triggered CTL is attributed to the fact that the increased CN could induce the downward shift of d‐band center position, which assists the acetone adsorption and promotes the subsequent catalytic reaction. In addition, the universality of the proposed acetone‐CTL probe is verified by determining the CN of Fe‐SACs. This work has opened a new avenue for exploring an alternative to synchrotron XAS for the determination of CN of SACs and even conventional metal catalysts through d‐band center‐regulated CTL. [ABSTRACT FROM AUTHOR]

Organic solid‐state luminescence materials have shown great promise in many forefront areas of modern chemistry. However, the well‐developed organic luminescent solids usually provoke a mass of synthetic steps. To better utilize their performances, the development of simple strategies for host materials is a goal of general concern. Herein, a series of highly efficient solid‐state luminescence materials are attained with aid of one‐step acidification of commercially available molecules. The mechanism demonstrates that the luminous efficiency of the solid‐state molecules is efficiently improved due to the synergy from the emergence of cation–π interaction and the formation of excimer. The cation–π interaction replaces π–π packing, leading to the formation of dimers with higher rigidity in solid state accompanied by red‐shifted emissions. Therefore, this one‐step acidification design concept will light the great passion of scientists for the fabrication of cation−π‐triggered analogous organic solid‐state luminescence materials with different colors by changing the substituents on benzene moieties. [ABSTRACT FROM AUTHOR]

Luminescent films have received great interest for chemo-/bio-sensing applications due to their distinct advantages over solution-based probes, such as good stability and portability, tunable shape and size, non-invasion, real-time detection, extensive suitability in gas/vapor sensing, and recycling. On the other hand, they can achieve selective and sensitive detection of chemical/biological species using special luminophores with a recognition moiety or the assembly of common luminophores and functional materials. Nowadays, the extensively used assembly techniques include drop-casting/spin-coating, Langmuir–Blodgett (LB), self-assembled monolayers (SAMs), layer-by-layer (LBL), and electrospinning. Therefore, this review summarizes the recent advances in luminescent films with these assembly techniques and their applications in chemo-/bio-sensing. We mainly focused on the discussion of the relationship between the sensing properties of the films and their architecture. Furthermore, we discussed some critical challenges existing in this field and possible solutions that have been or are being developed to overcome these challenges. [ABSTRACT FROM AUTHOR]

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