Fractional shot noise of an SU(N) Kondo system

• Damian Krychowski and
• Stanisław Lipiński

Beilstein J. Nanotechnol. 2026, 17, 515–540, doi:10.3762/bjnano.17.34

Probing internal continua and atomic ultrafast charge transfer within size-controlled nanoparticles by post-collision interaction in core-hole clock spectroscopy

• Johannes Lütgert,
• Erika Giangrisostomi,
• Nomi L. A. N. Sorgenfrei and
• Alexander Föhlisch

Beilstein J. Nanotechnol. 2026, 17, 505–514, doi:10.3762/bjnano.17.33

• in the DOS inflicted by an increased quantum confinement for the smallest shell QDs. In core–shell QDs, however, electron transfer can in principle occur either within the ZnS shell or toward the CdSe core, giving rise to two competing charge transfer channels with presumably different charge

• expected to be faster than electron transfer within the shell. This implies that the charge delocalization is faster within those layers of the ZnS shell that are closest to the CdSe core. Limited by the escape depth of the emitted electrons, the CHC approach is highly surface-sensitive. In the thinner QDs

Upcycling agroindustrial waste into graphene oxide supports for gold nanoparticles: toward sustainable nanomaterials

• Juan Marcos Castro-Tapia,
• Selene Acosta,
• Hiram Joazet Ojeda-Galván,
• Elsie Evelyn Araujo-Palomo,
• Edgar Giovanni Villabona-Leal and
• Mildred Quintana

Beilstein J. Nanotechnol. 2026, 17, 489–504, doi:10.3762/bjnano.17.32

• organic pollutants, including nitroaromatic compounds and dye molecules, under mild reaction conditions [57][58][59]. The synergistic interaction between AuNPs and GO enhances electron transfer, enabling lower noble-metal loading while maintaining high catalytic performance. Furthermore, AuNPs@GO

Defects and defect-mediated engineering of two-dimensional materials: challenges and open questions

• Arkady V. Krasheninnikov,
• Matthias Batzill,
• Anouar-Akacha Delenda,
• Marija Drndić,
• Chris Ewels,
• Katharina J. Franke,
• Mahdi Ghorbani-Asl,
• Alexander Holleitner,
• Ado Jorio,
• Ute Kaiser,
• Daria Kieczka,
• Hannu-Pekka Komsa,
• Jani Kotakoski,
• Manuel Längle,
• David Lamprecht,
• Yun Liu,
• Steven G. Louie,
• Janina Maultzsch,
• Thomas Michely,
• Katherine Milton,
• Anna Niggas,
• Hanako Okuno,
• Joshua A. Robinson,
• Marika Schleberger,
• Bruno Schuler,
• Alexander Shluger,
• Kazu Suenaga,
• Kristian S. Thygesen,
• Richard A. Wilhelm,
• E. Harriet Åhlgren and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2026, 17, 454–488, doi:10.3762/bjnano.17.31

• from triplet to singlet during dissociation [62]. Although O2 incorporation into the WS2 surface involves electron transfer from the substrate, the reaction may proceed via non-adiabatic pathways, as previously discussed for O2 adsorption on metal surfaces [66][67]. This underscores the limitations of

• has been found on S vacancies in a monolayer of MoS2 on Au(111) [146]. However, in this case, the metallic Au substrate provided not only the electron bath for screening the magnetic moment, but also enabled the electron transfer to the vacancy due to the favorable alignment of the work functions [147

Biomimetic nanoparticles in cancer photodynamic therapy: a review of targeted delivery systems and therapeutic outcomes

• Valentina I. Gorbacheva,
• Alexey S. Grabovoy,
• Polina S. Marukhina,
• Anastasiia O. Syrocheva and
• Ekaterina P. Kolesova

Beilstein J. Nanotechnol. 2026, 17, 396–422, doi:10.3762/bjnano.17.27

• nanostructured materials, significantly expanding the range of agents available for PDT applications [18]. The photochemical pathway for ROS generation involves non-radiative relaxation of the excited PS, typically occurring through two primary mechanisms [19]. Type-I reactions involve electron transfer

Gold nanoparticle-decorated reduced graphene oxide as a highly effective catalyst for the selective α,β-dehydrogenation of N-alkyl-4-piperidones

• Brenda Flore Kenyim,
• Mihir Tzalis,
• Marilyn Kaul,
• Robert Oestreich,
• Aysenur Limon,
• Chancellin Pecheu Nkepdep and
• Christoph Janiak

Beilstein J. Nanotechnol. 2026, 17, 218–238, doi:10.3762/bjnano.17.15

• AC therefore also stems from the synergistic interfacial C–O–Au arrangements, which act as bifunctional active sites for both, electron transfer and oxygen activation. The oxygenated functional groups of rGO (–OH, C=O, –CO) (Supporting Information File 1, Figure S6) anchor and electronically couple

• catalysts synthesized via the reduction–precipitation method and stabilized with SiW9 polyoxometallate show the highest efficiency in the oxidative dehydrogenation (ODH) of N-methyl-4-piperidone. The superior activity of these catalysts arises from electron transfer from rGO to Au via C–O–Au interfacial

Optical bio/chemical sensors for vitamin B₁₂ analysis in food and pharmaceuticals: state of the art, challenges, and future outlooks

• Seyed Mohammad Taghi Gharibzahedi and
• Zeynep Altintas

Beilstein J. Nanotechnol. 2025, 16, 2207–2244, doi:10.3762/bjnano.16.153

Rapid synthesis of highly monodisperse AgSbS₂ nanocrystals: unveiling multifaceted activities in cancer therapy, antibacterial strategies, and antioxidant defense

• Funda Ulusu,
• Adem Sarilmaz,
• Yakup Ulusu,
• Faruk Ozel and
• Mahmut Kus

Beilstein J. Nanotechnol. 2025, 16, 2105–2115, doi:10.3762/bjnano.16.145

• ratio and enhanced surface reactivity [30]. These features, combined with the tunable surface chemistry of nanoparticles, allow for efficient interactions with free radicals and facilitate electron transfer reactions, resulting in robust antioxidant activity [49]. This activity involves scavenging free

• effective exposure of surface facets to the reaction medium. Green-synthesized nanoparticles in various studies have consistently shown elevated FRAP responses compared to their bulk counterparts, due to improved electron transfer kinetics at the nano–bio interface [51][52]. When considered alongside DPPH

• scavenging data, the FRAP outcome supports a dual-mechanism antioxidant model (both radical quenching and electron transfer). This suggests that the surface chemistry of AgSbS2 NCs effectively mediates both redox and radical-based pathways, making them promising candidates for applications requiring moderate

Ambient pressure XPS at MAX IV

• Mattia Scardamaglia,
• Ulrike Küst,
• Alexander Klyushin,
• Rosemary Jones,
• Jan Knudsen,
• Robert Temperton,
• Andrey Shavorskiy and
• Esko Kokkonen

Beilstein J. Nanotechnol. 2025, 16, 1677–1694, doi:10.3762/bjnano.16.118

• intercalate beneath graphene at around 220 °C, initiating a slower, undercover oxidation of copper to Cu2O. This process is a galvanic reaction facilitated by graphene’s high conductivity, enabling electron transfer from copper to oxygen atoms. However, the graphene/Cu2O hybrid structure slows further

Laser processing in liquids: insights into nanocolloid generation and thin film integration for energy, photonic, and sensing applications

• Akshana Parameswaran Sreekala,
• Pooja Raveendran Nair,
• Jithin Kundalam Kadavath,
• Bindu Krishnan,
• David Avellaneda Avellaneda,
• M. R. Anantharaman and
• Sadasivan Shaji

Beilstein J. Nanotechnol. 2025, 16, 1428–1498, doi:10.3762/bjnano.16.104

Soft materials nanoarchitectonics: liquid crystals, polymers, gels, biomaterials, and others

• Katsuhiko Ariga

Beilstein J. Nanotechnol. 2025, 16, 1025–1067, doi:10.3762/bjnano.16.77

• aforementioned example. It is also anticipated that soft materials nanoarchitectonics using polymers will be applied in other fields, including the control of the functions of polymer semiconductors. The process of chemical doping of molecular semiconductors is based on electron transfer reactions between the

• semiconductors and the dopant molecules. The redox potential of the dopant is a critical factor in regulating the Fermi level of the semiconductor. The research group led by Ishii and Yamashita utilizes proton coupling electron transfer reactions, which are extensively employed in biochemical processes [278

• ]. They make effective use of intercalation into the nanospaces formed in thin polymer films (Figure 17). Molecular redox reactions that are precisely controlled at room temperature are employed in biochemical processes, including proton coupling electron transfer reactions. For instance, two-electron

A calix[4]arene-based supramolecular nanoassembly targeting cancer cells and triggering the release of nitric oxide with green light

• Cristina Parisi,
• Loredana Ferreri,
• Tassia J. Martins,
• Francesca Laneri,
• Samantha Sollima,
• Antonina Azzolina,
• Antonella Cusimano,
• Nicola D’Antona,
• Grazia M. L. Consoli and
• Salvatore Sortino

Beilstein J. Nanotechnol. 2025, 16, 1003–1013, doi:10.3762/bjnano.16.75

• activatable with blue light, and encouraging the NO release with the more biocompatible green light probably by an intra-cage photoinduced electron transfer. Keywords: calixarenes; cell targeting; fluorescence; light; nitric oxide; Introduction Calix[n]arenes are a family of polyphenolic macrocycles

• electron transfer. Either reductive or oxidative pathways usually lead to NO loss and the concomitant formation of an anlinyl radical intermediate, which evolves to the stable photoproduct 2b after H transfer. In our case, such a process involves mainly the lowest singlet state of ABF. This hypothesis is

Synthesis of biowaste-derived carbon-dot-mediated silver nanoparticles and the evaluation of electrochemical properties for supercapacitor electrodes

• Navya Kumari Tenkayala,
• Chandan Kumar Maity,
• Md Moniruzzaman and
• Subramani Devaraju

Beilstein J. Nanotechnol. 2025, 16, 933–943, doi:10.3762/bjnano.16.71

• reduction of Ag+ to Ag(0) via oxygen-containing functionalities on their surfaces. The electrostatic attraction between the oxygen-containing functionalities on the surface of CDs binds with the positively charged Ag+ ions, which were then reduced by electron transfer from PG-CDs to the Ag+ ions [27]. The

Insights into the electronic and atomic structures of cerium oxide-based ultrathin films and nanostructures using high-brilliance light sources

• Paola Luches and
• Federico Boscherini

Beilstein J. Nanotechnol. 2025, 16, 860–871, doi:10.3762/bjnano.16.65

• was possible to identify different types of interactions between Pt NPs and cerium oxide surfaces including electron transfer from Pt NPs to CeO2 and transport of oxygen atoms from ceria to Pt NPs, the latter occurring only when the ceria support surface is nanostructured [26]. In addition, thanks to

• FEL was also exploited to investigate the electron transfer process in a composite plasmonic/semiconductor system, based on silver NPs embedded in a CeO2 film [63]. Pump–probe XANES measurements were performed at the Ce N4,5 edge upon photoexcitation of plasmonic resonances in the metal NPs by visible

Synchrotron X-ray photoelectron spectroscopy study of sodium adsorption on vertically arranged MoS₂ layers coated with pyrolytic carbon

• Alexander V. Okotrub,
• Anastasiya D. Fedorenko,
• Anna A. Makarova,
• Veronica S. Sulyaeva,
• Yuliya V. Fedoseeva and
• Lyubov G. Bulusheva

Beilstein J. Nanotechnol. 2025, 16, 847–859, doi:10.3762/bjnano.16.64

• fast intercalation reaction kinetics. Flower-like MoS2–carbon hybrids have demonstrated superior alkali metal storage capability and high rate performance due to the fast Na+ diffusion in radially orientated ultrathin MoS2 and graphene layers; the latter component ensured high electron transfer and

Colloidal few layered graphene–tannic acid preserves the biocompatibility of periodontal ligament cells

• Teissir Ben Ammar,
• Naji Kharouf,
• Dominique Vautier,
• Housseinou Ba,
• Nivedita Sudheer,
• Philippe Lavalle and
• Vincent Ball

Beilstein J. Nanotechnol. 2025, 16, 664–677, doi:10.3762/bjnano.16.51

• include superoxide radicals, hydroxyl radicals, and hydrogen peroxide, are natural byproducts of the oxidative metabolism. Mammalian cells maintain balanced ROS levels for homeostasis and cellular proliferation. However, excess ROS creates an electron imbalance that triggers continuous electron transfer

• multiple sources including metal impurities (such as Fe, Ni, or Cu) present in the graphene structure, as well as from the intrinsic electronic properties of graphene itself. Indeed, graphene’s sp2 hybridization and delocalized π electrons can participate in electron transfer reactions, potentially leading

• capabilities through multiple mechanisms, namely, electron transfer, where hydroxy groups donate electrons to neutralize free radicals, and hydrogen atom transfer, where hydrogen atoms from hydroxy groups are donated to stabilize ROS [17][34]. This retained antioxidant activity could play a crucial role in

Functionalized gold nanoflowers on carbon screen-printed electrodes: an electrochemical platform for biosensing hemagglutinin protein of influenza A H1N1 virus

• Carlos Enrique Torres-Méndez,
• Sharmilee Nandi,
• Klara Martinovic,
• Patrizia Kühne,
• Yifan Liu,
• Sam Taylor,
• Maria Lysandrou,
• Maria Ines Berrojo Romeyro Mascarenhas,
• Viktoria Langwallner,
• Javier Enrique Sebastián Alonso,
• Ivana Jovanovic,
• Maike Lüftner,
• Georgia-Vasiliki Gkountana,
• David Bern,
• Abdul-Raouf Atif,
• Ehsan Manouchehri Doulabi,
• Gemma Mestres and
• Masood Kamali-Moghaddam

Beilstein J. Nanotechnol. 2025, 16, 540–550, doi:10.3762/bjnano.16.42

• , which implies that electron transfer at the electrode surface was enhanced, increasing the redox reversibility for the [Fe(CN)6]3−/4− pair. CSPEs are reported to possess a rough surface at the nanoscale [34]. The electrodeposition technique employed takes advantage of this to control the nucleation

• increased. This effect is known as tunneling charge transfer enhancement and significantly improved the sensitivity of the biosensor. It can be attributed to electron transfer through bonds due to the small length (0.59 nm) and the delocalized π-electron system of the 4-ATP linker molecule. Interestingly

• the concentration range from 10 to 10 000 pg/mL. The experimental EIS data suggest that the electron transfer on the electrode was enhanced by a factor of 100 due to the increase in surface area and to a tunneling charge transfer effect. This improvement is attributed to the synergistic effect of the

Quantification of lead through rod-shaped silver-doped zinc oxide nanoparticles using an electrochemical approach

• Ravinder Lamba,
• Gaurav Bhanjana,
• Neeraj Dilbaghi,
• Vivek Gupta and
• Sandeep Kumar

Beilstein J. Nanotechnol. 2025, 16, 422–434, doi:10.3762/bjnano.16.33

• electrode can provide additional details about the electrochemical process. It can help to understand the kinetics of electron transfer reactions, analyte diffusion, and electrode surface contact mechanisms. A modified Ag@ZnO NRs electrode with greater impedance is more stable and durable. This provides

• of lead chemical sensors. The significant rise in peak height is indicative of a faster electron-transfer event because it causes a sharper, more defined peak. Furthermore, the absence of a cathodic current in the reverse cycle indicates the irreversibility of the electrochemical response that was

Emerging strategies in the sustainable removal of antibiotics using semiconductor-based photocatalysts

• Yunus Ahmed,
• Keya Rani Dutta,
• Parul Akhtar,
• Md. Arif Hossen,
• Md. Jahangir Alam,
• Obaid A. Alharbi,
• Hamad AlMohamadi and
• Abdul Wahab Mohammad

Beilstein J. Nanotechnol. 2025, 16, 264–285, doi:10.3762/bjnano.16.21

• heterojunctions are classified based on their charge transfer mechanism and the presence or absence of mediators. The direct Z-scheme relies on the direct electron transfer between photocatalysts; eliminating the electron mediator simplifies the design and enhances stability but may suffer from higher charge

• light exposure, the rates of TC degradation by pure ZnO, g-C3N4, and defective ZnO/g-C3N4 composite were found to be 35.20%, 71.48%, and 93.47%, respectively. Because of the existence of N defects, the constructed nanocomposite promotes the electron transfer efficiently with lower recombination rates

• molar ratios of AgX. With the inclusion of AgX, there was a significant enhancement in the removal rate of antibiotics. This was achieved by augmenting the positive potential and accelerating electron transfer rates. The most recent research on using tungsten oxide as photocatalyst to remove antibiotics

Characterization of ZnO nanoparticles synthesized using probiotic Lactiplantibacillus plantarum GP258

• Prashantkumar Siddappa Chakra,
• Aishwarya Banakar,
• Shriram Narayan Puranik,
• Vishwas Kaveeshwar,
• C. R. Ravikumar and
• Devaraja Gayathri

Beilstein J. Nanotechnol. 2025, 16, 78–89, doi:10.3762/bjnano.16.8

• frequency (ω), Y, and n. The obtained results suggest robust electron transfer and enhanced electrocatalytic efficiency in dextrose oxidation [19][20][21] (Figure 5). Antibacterial activity of ZnO NPs The biogenic ZnO NPs presented a good dispersion and exhibited antibacterial activity against both Gram

• synthesized from different biological sources. In our study, cyclic voltammetry was used to assess the electrochemical properties of ZnO NPs, which exhibited reversible redox behavior and efficient electron transfer. A similar study by Matinise et al. [25] on ZnO NPs synthesized using Moringa oleifera also

• ) EDX spectroscopy for elemental composition. (e) Zeta potential measurement. (f) DLS results showing the size distribution of ZnO NPs. (a, b) Cyclic voltammetry response of the ZnO electrode in 0.1 M KCl solution at varying scan rates, showing redox behavior and electron transfer characteristics. (c

Facile synthesis of size-tunable L-carnosine-capped silver nanoparticles and their role in metal ion sensing and catalytic degradation of p-nitrophenol

• Akash Kumar,
• Ridhima Chadha,
• Abhishek Das,
• Nandita Maiti and
• Rayavarapu Raja Gopal

Beilstein J. Nanotechnol. 2024, 15, 1576–1592, doi:10.3762/bjnano.15.124

• nanoparticle surface, followed by the electron transfer from NaBH4 to the adsorbed P-NP molecules facilitated by the AgNPs. The obtained rate constants indicate that ʟ-carnosine-capped AgNPs are comparable to or more efficient than other noble metal nanoparticles (Table 2), underscoring their potential as cost

Electrochemical nanostructured CuBTC/FeBTC MOF composite sensor for enrofloxacin detection

• Thi Kim Ngan Nguyen,
• Tien Dat Doan,
• Huy Hieu Luu,
• Hoang Anh Nguyen,
• Thi Thu Ha Vu,
• Quang Hai Tran,
• Ha Tran Nguyen,
• Thanh Binh Dang,
• Thi Hai Yen Pham and
• Mai Ha Hoang

Beilstein J. Nanotechnol. 2024, 15, 1522–1535, doi:10.3762/bjnano.15.120

• capacity, and an acceptable efficacy of the electron transfer, Cu3(BTC)2 exhibited a good sensitivity to 2,4-dichlorophenol in the range from 0.04 to 1.00 μM with a limit of detection (LOD) of 9 nM in differential pulse voltammetry measurements. Moreover, the combination of metal oxides and MOFs showed better

• electrochemical detection ability than pristine MOFs. For example, Wang et al. developed a MOF/TiO2 composite to quantify chlorogenic acid in a range from 0.01 to 1.00 μM with a low LOD of 7 nM [30]. Utilizing carbon-based materials can provide not only enhanced electron transfer but also catalytic functions for

Nanoarchitectonics with cetrimonium bromide on metal nanoparticles for linker-free detection of toxic metal ions and catalytic degradation of 4-nitrophenol

• Akash Kumar and
• Raja Gopal Rayavarapu

Beilstein J. Nanotechnol. 2024, 15, 1312–1332, doi:10.3762/bjnano.15.106

Enhanced catalytic reduction through in situ synthesized gold nanoparticles embedded in glucosamine/alginate nanocomposites

• Chi-Hien Dang,
• Le-Kim-Thuy Nguyen,
• Minh-Trong Tran,
• Van-Dung Le,
• Nguyen Minh Ty,
• T. Ngoc Han Pham,
• Hieu Vu-Quang,
• Tran Thi Kim Chi,
• Tran Thi Huong Giang,
• Nguyen Thi Thanh Tu and
• Thanh-Danh Nguyen

Beilstein J. Nanotechnol. 2024, 15, 1227–1237, doi:10.3762/bjnano.15.99

• mechanism involves the transfer of electrons from BH4− (the electron donor) to the dye (the electron acceptor) facilitated by the surface of the metal nanoparticles [42][43]. Prior to electron transfer, dye and BH4− are adsorbed onto the catalyst surface, as depicted in Figure 5. Consequently, the

Unveiling the potential of alginate-based nanomaterials in sensing technology and smart delivery applications

• Shakhzodjon Uzokboev,
• Khojimukhammad Akhmadbekov,
• Ra’no Nuritdinova,
• Salah M. Tawfik and
• Yong-Ill Lee

Beilstein J. Nanotechnol. 2024, 15, 1077–1104, doi:10.3762/bjnano.15.88

• charge on the polymer. It is critical in enabling quick electron transfer between an enzyme and an electrode surface, triggering the enzyme’s catalytic function for rapid biosensing [100]. Environmental sensing applications One key advantage of using nanosensors in environmental sensing is their ability