Charge Detection Research Articles

Physical properties of InxSey and CuInSe2 thin films with potential application in radiation detectors

A study of InxSey and CuInSe2 thin films processed by the thermal co-evaporation technique by evaluating its physical properties is carried out. Both InxSey as well as CuInSe2 thin films were synthesized by multi-source thermal co-evaporation technique, using Knudsen-type effusion cells. The optical, structural, electrical, and morphological properties of each film were analyzed in order to determine the feasibility at the formation of a p-CuInSe2/n-InxSey heterojunction. InxSey films exhibited bandgap values in the range of 2.4–2.7 eV which was determined by UV–vis spectroscopic analysis. Vibrational modes associated to In2Se3 as well as Se are presented in the InxSey films according to Raman studies. The irregular morphology of the grains on the InxSey surface, with an average size of 380 nm are related to both In2Se3 and Se materials according to Raman spectroscopy and Scanning Electron Microscopy analysis. The InxSey thin films showed resistivity vales around 10–3 Ω·cm. The Hackee´s figure of Merit (FOMH) analysis supported the physical assumption that InxSey thin films are feasible to be used as window layer in a photovoltaic device because of the high values of FOMH obtained for samples processed at 300 °C. On the other hand, an influence on the morphology of the CuInSe2 films was observed when the films were synthetized at different substrate temperature. Uniform CuInSe2 films with agglomerated cauliflower-like grains with an average size of 1.8 μm were observed by SEM. The presence of binary phases within the CuInSe2 compound were detected through Raman and x-ray characterization. Average crystallite size of 61 nm and microstrain around 2.5 × 10–3 were estimated for the CuInSe2 films through x-ray analysis. According to the physical properties analyzed the InxSey/CuInSe2 semiconductor bilayer can be a suitable candidate for application in photovoltaic devices as well as charged particle detector.

Protein complex heterogeneity and topology revealed by electron capture charge reduction and surface induced dissociation.

We illustrate the utility of native mass spectrometry (nMS) combined with a fast, tunable gas-phase charge reduction, electron capture charge reduction (ECCR), for the characterization of protein complex topology and glycoprotein heterogeneity. ECCR efficiently reduces the charge states of tetradecameric GroEL, illustrating Orbitrap m/z measurements to greater than 100,000 m/z. For pentameric C-reactive protein and tetradecameric GroEL, our novel device combining ECCR with surface induced dissociation (SID) reduces the charge states and yields more topologically informative fragmentation. This is the first demonstration that ECCR yields more native-like SID fragmentation. ECCR also significantly improved mass and glycan heterogeneity measurements of heavily glycosylated SARS-CoV-2 spike protein trimer and thyroglobulin dimer. Protein glycosylation is important for structural and functional properties and plays essential roles in many biological processes. The immense heterogeneity in glycosylation sites and glycan structure poses significant analytical challenges that hinder a mechanistic understanding of the biological role of glycosylation. Without ECCR, average mass determination of glycoprotein complexes is available only through charge detection mass spectrometry or mass photometry. With narrow m/z selection windows followed by ECCR, multiple glycoform m/z values are apparent, providing quick global glycoform profiling and providing a future path for glycan localization on individual intact glycoforms.

Compaction, Relaxation, and Linearization of Megadalton-Sized DNA Plasmids: DNA Structures Probed by CD-MS.

High purity plasmid DNA is a raw material for recombinant protein production as well as an active ingredient in DNA vaccines. There are four primary plasmid structures that can be observed in a typical plasmid formulation: supercoiled, relaxed (circular), linearized, and condensed. Determining what structures are present in a sample is important, as the structure can affect activity; the supercoiled structure has the highest activity, and >90% supercoiled is desired for industry standards. Recently, charge detection mass spectrometry (CD-MS) was used to distinguish two of the structures, supercoiled and condensed, by measuring the charge deposited on the ions by positive mode electrospray. Here, CD-MS is used to probe the structures of DNA plasmids during compaction with polycations, and through enzymatic treatment to relax and linearize plasmids. We find that all four structural types for plasmid DNA have unique charging profiles that can be distinguished using CD-MS. The extent of mechanical shearing of the DNA plasmids during electrospray is strongly influenced by the structural type.

Interstellar Neutral Hydrogen in the Heliosphere: New Horizons Observations in the Context of Models

Interstellar neutral (ISN) hydrogen is the most abundant species in the outer heliosheath and the very local interstellar medium (VLISM). Charge-exchange collisions in the outer heliosheath result in filtration, reducing the ISN hydrogen density inside the heliosphere. Additionally, these atoms are intensively ionized close to the Sun, resulting in a substantial reduction of their density within a few astronomical units from the Sun. The products of this ionization—pickup ions (PUIs)—are detected by charged particle detectors. The Solar Wind Around Pluto instrument on New Horizons provides, for the first time, PUI observations from the distant heliosphere. We analyze the observations collected between 22 and 52 au from the Sun to find the ISN hydrogen density profile and compare the results with predictions from global heliosphere models. We conclude that the density profile derived from the observations is inconsistent with steady-state model predictions. This discrepancy is not explained by time variations close to the Sun and thus may be related to the temporal evolution of the outer boundaries or VLISM conditions. Furthermore, we show that the cold and hot models of ISN hydrogen distribution are not a good approximation closer to the termination shock. Therefore, we recommend a new fiduciary point based on the available New Horizons observations at 40 au from the Sun, at ecliptic direction (285.°62, 1.°94), where the ISN hydrogen density is 0.11 cm−3. The continued operation of New Horizons should give better insight into the source of the discussed discrepancy.

High-Throughput Fluorometric Assay For Quantifying Polysorbate In Biopharmaceutical Products Using Micelle Activated Fluorescence Probe N-Phenyl-1-Naphthylamine.

Polysorbates are among the most used surfactants in biopharmaceutical products containing proteins. Our work aims to develop a high-throughput fluorometric assay to further diversify the analytical toolbox for quantification of PSs. The assay leverages the micelle activated fluorescence signal from N-Phenyl-1-Naphthylamine (NPN). The development and optimization of assay parameters were guided by the pre-defined analytical target profile. Furthermore, NMR was used to probe the interaction between protein, PS80 and NPN in the measurement system and understand protein interference. All assay parameters including excitation and emission wavelengths, standard curve, NPN concentration, and incubation time have been optimized and adapted to a microplate format, making it compatible with automated solutions that will be pursued in the near future to drive consistency and efficiency in our workflows. The specificity, accuracy, and precision of the assay have been demonstrated through a case study. Furthermore, NMR results provided additional insight into the change of the interaction dynamics between PS80 and NPN as the protein concentration increases. The results indicate minimal interaction between the protein and PS80 at lower concentration. However, when the concentration exceeds 75mg/mL, there is a significant interaction between the protein and PS-80 micelle and monomer. A high-throughput fluorometric assay has been developed for quantification of polysorbates in biopharmaceutical samples including in-process samples, drug substance and drug product. The assay reported herein could serve as a powerful analytical tool for polysorbate quantification and control, complementing the widely used liquid chromatography with charged aerosol detection method.

Submicrometer Particle Impact Dynamics and Chemistry.

Experimental studies of the collision phenomena of submicrometer particles is a developing field. This review examines the range of phenomena that can be observed with new experimental approaches. The primary focus is on single-particle impact studies enabled by charge detection mass spectrometry (CDMS) implemented using the Aerosol Impact Spectrometer (AIS) at the University of California, San Diego. The AIS combines electrospray ionization, aerodynamic lens techniques, CDMS, and an electrostatic linear accelerator to study the dynamics of particle impact over a wide range of incident velocities. The AIS has been used for single-particle impact experiments on positively charged particles of diverse composition, including polystyrene latex spheres, tin particles, and ice grains, over a wide range of impact velocities. Detection schemes based on induced charge measurements and time-of-flight mass spectrometry have enabled measurements of the impact inelasticity through the determination of the coefficient of restitution, measurements of the angular distributions of scattered submicrometer particles, and the chemical composition and dissociation of solute molecules in hypervelocity ice grain impacts.

Characterization of Mass, Diameter, Density, and Surface Properties of Colloidal Nanoparticles Enabled by Charge Detection Mass Spectrometry.

A variety of scattering-based, microscopy-based, and mobility-based methods are frequently used to probe the size distributions of colloidal nanoparticles with transmission electron microscopy (TEM) often considered to be the "gold standard". Charge detection mass spectrometry (CDMS) is an alternative method for nanoparticle characterization that can rapidly measure the mass and charge of individual nanoparticle ions with high accuracy. Two low polydispersity, ∼100 nm diameter nanoparticle size standards with different compositions (polymethyl methacrylate/polystyrene copolymer and 100% polystyrene) were characterized using both TEM and CDMS to explore the merits and complementary aspects of both methods. Mass and diameter distributions are rapidly obtained from CDMS measurements of thousands of individual ions of known spherical shape, requiring less time than TEM sample preparation and image analysis. TEM image-to-image variations resulted in a ∼1-2 nm range in the determined mean diameters whereas the CDMS mass precision of ∼1% in these experiments leads to a diameter uncertainty of just 0.3 nm. For the 100% polystyrene nanoparticles with known density, the CDMS and TEM particle diameter distributions were in excellent agreement. For the copolymer nanoparticles with unknown density, the diameter from TEM measurements combined with the mass from CDMS measurements enabled an accurate measurement of nanoparticle density. Differing extents of charging for the two nanoparticle standards measured by CDMS show that charging is sensitive to nanoparticle surface properties. A mixture of the two samples was separated based on their different extents of charging despite having overlapping mass distributions centered at 341.5 and 331.0 MDa.

Comparative Observations of the Outer Belt Electron Fluxes and Precipitated Relativistic Electrons

AbstractRelativistic electron precipitation (REP) refers to the release of high‐energy electrons initially trapped in the outer radiation belt, which then precipitate into Earth's upper atmosphere, contributing significantly to the rapid depletion of radiation belt electron flux. This study presents a statistical analysis of REP observations collected by the Calorimetric Electron Telescope (CALET) experiment aboard the International Space Station from 2015 to the present day. Specifically, the analysis utilizes count rates acquired from the two top scintillators constituting the top charge detector, each sensitive to electrons with energies above 1.5 and 3.4 MeV, respectively. Analysis of CALET data reveals a previously unreported semi‐annual variation in the occurrence of REP events. REP periodicities resemble those observed for trapped electron fluxes in the outer belt. Furthermore, their amplitude follows the overall trend of solar wind high‐speed streams and the solar activity.

Characterization of ribostamycin and its impurities using a nano-quantity analyte detector: Systematic comparison of performance among three different aerosol detectors

Characterization of aminoglycoside antibiotics like ribostamycin is important due to the complex composition and common toxic impurities. Aerosol detectors are often employed for determination of these non-absorbent analytes. In this work, a robust and cost-effective method was developed for simultaneous detection of ribostamycin and its related substances using high-performance liquid chromatography (HPLC) with a relative new aerosol detector named nano-quantity analyte detector (NQAD). With the introduction of less toxic but more compatible ion-pairs pentafluoropropionic acid (PFPA) and trifluoroacetic acid (TFA) in the eluent, an optimized separation effect was achieved. Compared with the other two aerosol detectors namely ELSD (evaporative light scattering detector) and CAD (charged aerosol detector), method verification and quantitative detection results revealed that NQAD had higher sensitivity than ELSD with a 0.8 μg/mL limit of detection, as well as wider linear range (from 2 μg/mL to 1000 μg/mL) than both CAD (from 2 μg/mL to 200 μg/mL) and ELSD (from 8 μg/mL to 200 μg/mL) detector. The performance of NQAD helped to realize detection of ribostamycin and its impurities with significant concentration differences in a single run. With a cation suppressor to eliminate the ion-suppression caused by the ion-pairs in the eluent, the structure of nine impurities in ribostamycin sample was characterized by liquid chromatography-mass spectrum (LC-MS). Both external standard and area normalization calculation were investigated, and NQAD obtained more accurate results due to its full-range linear response-to-concentration relationship, providing an alternative for routine quality control of multi analyte systems.

Electrostatic charging of material webs in production machines and how to eliminate it

The elimination of electrostatic charges, especially on material webs is critical to preventing ignition hazards and personal injury hazards in industry. The use of discharge bars (called “ionizers”) is an important method for eliminating electrostatic charges.The possibility of electrostatic discharge in a production machine is real. The metrological detection of charges on material webs is also discussed and the special phenomenon of a super brush discharge is described. A useful arrangement for active ionizers is described and justified.

Higher-order structure and proteoforms of co-occurring C4b-binding protein assemblies in human serum

The complement is a conserved cascade that plays a central role in the innate immune system. To maintain a delicate equilibrium preventing excessive complement activation, complement inhibitors are essential. One of the major fluid-phase complement inhibitors is C4b-binding protein (C4BP). Human C4BP is a macromolecular glycoprotein composed of two distinct subunits, C4BPα and C4BPβ. These associate with vitamin K-dependent protein S (ProS) forming an ensemble of co-occurring higher-order structures. Here, we characterize these C4BP assemblies. We resolve and quantify isoforms of purified human serum C4BP using distinct single-particle detection techniques: charge detection mass spectrometry, and mass photometry accompanied by high-speed atomic force microscopy. Combining cross-linking mass spectrometry, glycoproteomics, and structural modeling, we report comprehensive glycoproteoform profiles and full-length structural models of the endogenous C4BP assemblies, expanding knowledge of this key complement inhibitor’s structure and composition. Finally, we reveal that an increased C4BPα to C4BPβ ratio coincides with elevated C-reactive protein levels in patient plasma samples. This observation highlights C4BP isoform variation and affirms a distinct role of co-occurring C4BP assemblies upon acute phase inflammation.

Investigation of triaxial cables and microdetectors in small field dosimetry

Background. Small field dosimetry presents unique challenges with source occlusion, lateral charged particle equilibrium and detector size. As detector volume decreases, signal strength declines while noise increases, deteriorating the signal-to-noise ratio (SNR). This issue may be compounded by triaxial cables connecting detectors to electrometers. However, effects of cables, critical for precision dosimetry, are often overlooked. There is a need to evaluate triaxial cable and detector impacts on SNR in small fields. The purpose of this study is to evaluate the influence of triaxial cables and microdetectors on signal-to-noise ratios in small-field dosimetry. This study also aims to establish the importance of cable quality assurance for measurement accuracy. Methods. Six 9.1 m length triaxial cables from different manufacturers were tested with six microdetectors (microDiamond, PinPoint, EDGE, Plastic scintillator, microSilicon, SRS-Diode). A 6 MV photon beam (TrueBeam) was used, with a water phantom at 5 cm depth with 0.5 × 0.5 cm2 to 10 × 10 cm2 fields at 600 MU min−1. Readings were acquired using cable-detector permutations with a dedicated electrometer (except the scintillator which has its own). Cables had differing connector types, conductor materials, insulation, and diameters. Detectors had various sensitive volumes, materials, typical signals, and bias voltages. Results. Normalized field output correction factors (FOFs) relative differences of 13.4% and 4.6% between the highest and lowest values across triaxial cables for 0.5 × 0.5 cm2 and 1 × 1 cm2 fields, respectively. The maximum difference in FOF between any cable-detector combinations was 0.2% for the smallest field size. No consistent FOF trend was observed across all detectors when increasing cable diameter. Additionally, the non-normalized FOF differences of 0.9% and 0.3% were observed between cables for 0.5 × 0.5 cm2 and 1 × 1 cm2 fields, respectively. Conclusions. Regular triaxial cable quality assurance is critical for precision small field dosimetry. A national protocol is needed to standardize cable evaluations/calibrations, particularly for small signals (<pC) from modern detectors. This could enhance measurement accuracy and treatment delivery with advanced small-field radiotherapy techniques that promise improved patient outcomes. Further studies should expand detector and cable models tested across institutions to establish robust quality control guidelines.

The Charged Particle Detection System of the SRD Module onboard the China Space Station

The radiation field environment outside the Earth varies greatly with space location and the cycle of solar activity, and the radiation environment near the space station’s orbit is much more complex than that on the Earth’s surface. Various high-energy cosmic ray particles and secondary particles produced by them and the bulkhead of the space station greatly impact the health of astronauts and the working conditions of instruments. Each aircraft is always equipped with some dedicated radiation monitoring instruments to assess the exposure risk for astronauts, and to analyze the causes of instrument failures. The Space Radiation Detector Module (SRDM) is working in the China Space Station (CSS) to measure the radiation environment inside, including two parts: the Charged Particle Detection System (CPDS) and the Neutron Detection System (NDS). The CPDS, which is the main content of this paper, contains a detector unit, that consists of three silicon detectors a BGO calorimeter, and the corresponding readout electronics unit of the detector unit. Ground test results show that the detection system can detect various charged particles from hydrogen to nitrogen ions with an energy resolution of less than 15%. The actual measurement results for a period in orbit show that the main types of charged particles in the cabin are protons and α particles, with measured energies ranging from 0.8 to 265.2 MeV for protons and from 1.0 to 61.6 MeV/A for α particles(where A is the mass number), and linear energy density (LET) range mainly from 1.0 to 612.4 keV/μm. The radiation environment data measured in CSS can provide an important reference value for the exposure risk, life science experiments, and the status of instruments on board.

Not All Arms of IgM Are Equal: Following Hinge-Directed Cleavage by Online Native SEC-Orbitrap-Based CDMS.

Immunoglobulins M (IgM) are key natural antibodies produced initially in humoral immune response. Due to their large molecular weights and extensive glycosylation loads, IgMs represent a challenging target for conventional mass analysis. Charge detection mass spectrometry (CDMS) may provide a unique approach to tackle heterogeneous IgM assemblies, although this technique can be quite laborious and technically challenging. Here, we describe the use of online size exclusion chromatography (SEC) to automate buffer exchange and sample introduction, and demonstrate its adaptability with Orbitrap-based CDMS. We discuss optimal experimental parameters for online SEC-CDMS experiments, including ion activation, choice of column, and resolution. Using this approach, CDMS histograms containing hundreds of individual ion signals can be obtained in as little as 5 min from single injections of <1 μg of sample. To demonstrate the unique utility of online SEC-CDMS, we performed real-time kinetic monitoring of pentameric IgM digestion by the protease IgMBRAZOR, which cleaves specifically in the hinge region of IgM. Several digestion intermediates corresponding to processive losses of F(ab')2 subunits could be mass-resolved and identified by SEC-CDMS. Interestingly, we find that for the J-chain linked IgM pentamer, cleavage of one of the F(ab')2 subunits is much slower than the other four F(ab')2 subunits, which we attribute to the symmetry-breaking interactions of the J-chain within the pentameric IgM structure. The online SEC-CDMS methodologies described here open new avenues into the higher throughput automated analysis of heterogeneous, high-mass protein assemblies by CDMS.

Point mutation in a virus-like capsid drives symmetry reduction to form tetrahedral cages

Protein capsids are a widespread form of compartmentalization in nature. Icosahedral symmetry is ubiquitous in capsids derived from spherical viruses, as this geometry maximizes the internal volume that can be enclosed within. Despite the strong preference for icosahedral symmetry, we show that simple point mutations in a virus-like capsid can drive the assembly of unique symmetry-reduced structures. Starting with the encapsulin from Myxococcus xanthus, a 180-mer bacterial capsid that adopts the well-studied viral HK97 fold, we use mass photometry and native charge detection mass spectrometry to identify a triple histidine point mutant that forms smaller dimorphic assemblies. Using cryoelectron microscopy, we determine the structures of a precedented 60-mer icosahedral assembly and an unexpected 36-mer tetrahedron that features significant geometric rearrangements around a new interaction surface between capsid protomers. We subsequently find that the tetrahedral assembly can be generated by triple-point mutation to various amino acids and that even a single histidine point mutation is sufficient to form tetrahedra. These findings represent a unique example of tetrahedral geometry when surveying all characterized encapsulins, HK97-like capsids, or indeed any virus-derived capsids reported in the Protein Data Bank, revealing the surprising plasticity of capsid self-assembly that can be accessed through minimal changes in the protein sequence.

The phospholipid chromatographic fingerprint: An analytical cutting-edge strategy in the distinguished characterization of olive oil

In this study, two basics are addressed to achieve the characterization of edible vegetable oils from a universal perspective. Firstly, the use of a very specific chemical fraction scarcely studied, such as the phospholipids, is proposed to tackle vegetable oil characterization. For this, a new analytical method for phospholipid fraction is developed, which is based on reverse phase liquid chromatography coupled to universal detector such as charged aerosol detector (LC-CAD). In addition, a additional method using LC-(Q-Orbitrap)MS has been developed for the chemical identification of the compounds present in the phospholipid fraction. Secondly, it is proved that the instrument-agnostizing methodology is suitable to obtain a unique and time-consistent chromatographic fingerprint for each vegetable oil, which is independent of the instrument used. This could lead for the setting up of universal databases and the development of a single global multivariate model enabling edible vegetable oils discrimination by any laboratory at any time. This ultimately leads to resource and time reduction, generating lower analysis costs. The main results have been to be able to unequivocally characterise the different edible vegetable oils under study using data mining/machine learning methods such as partial least squares-discriminant analysis, support vector machine and classification a regression trees. In addition, more than 60 chemical compounds have been characterised in samples of olive oil of different categories and other edible vegetable oils respectively. This resulted in the proposal of tentative chemical markers which could be used to identify a particular edible vegetable oil.

Compact Monoenergetic Proton Generator in MeV Region Using NANOGAN

For simple applications, such as the calibration of a charged particle detector, a multi-MeV proton generator may be preferable to cyclotrons or electrostatic accelerators such as Van de Graaff. Thus, a compact proton generating system, consisting of 10Ghz ECR ion source NANOGAN and a deuteron target, was developed at the Research Center for Nuclear Physics at Osaka University. A 3He2+ beam was generated by the NANOGAN with the acceleration voltage of 20∼45 kV in an experiment that utilized the fusion reaction 3He + deuteron (d) → proton(p) + 4He. The monochromatic protons with energies of 14.67 MeV were successfully obtained at the atmosphere side of the target in the experimental setup, when a novel target base with a thin metal foil and Polyimide film window are used.

Robust orbital-angular-momentum-based underwater acoustic communication with dynamic modal decomposition method.

Recently, acoustic communication employing orbital angular momentum (OAM) opens another avenue for efficient data transmission in aquatic environments. Current topological charge (TC) detection of OAM beams relies on the orthogonality among different-order OAM beams. However, such strategy requires measurements of the complete azimuthal acoustic pressure, which inevitably reduces the efficiency and increases the bit error rate (BER). To address these challenges, this study proposes a modified dynamic modal decomposition (DMD) method by partially sampling the acoustic field for precise TC detection. Numerical simulations confirm the accuracy of this approach in extracting single or multiple TCs magnitudes within a partially sampled acoustic field. We theoretically compare the performance of the modified DMD approach with conventional orthogonal decoding method. Simulation results indicate that our modified DMD scheme exhibits lower BER under the same noise interference and is more robust to the array misalignment. This research introduces an efficient demodulation solution for acoustic OAM communication, offering potential benefits for simplifying receiver array design and enhancing long-distance underwater data transmission.

Effective Strategies for EV Battery Monitoring and Maintenance

Abstract: The growing popularity of Electric Vehicles (EVs) has led to an increased demand for sophisticated battery management systems that guarantee safety and efficiency. In order to track and control the operation of electric vehicle batteries in real time, this project presents a novel pairing of an Internet of Things gadget with an Android application. This integrated solution gives customers greater safety and extends battery life by delivering critical insights and notifications regarding battery health, percentage, temperature, and essential events including full charge, low battery, overheating, and fire detection. The technology prioritizes user safety and battery longevity while optimizing the EV experience through user-friendly interfaces and timely notifications.

Charge Detection Mass Spectrometry for Megadalton Polymer Characterization and Measurement of Electrospray-Generated Charged Droplet Dynamics with a New "Direct Visualization of the Rayleigh Limit" Approach to Aid in m/z Calibration.

A charge detector has been constructed and mounted inside the vacuum housing of a commercial mass spectrometer (Micromass-Waters Quattro I, Waters Corp., Manchester, UK). The in-house built single-pass charge detector is composed of a designed, complete electronics system that includes a low-noise charge amplifier. Communication to the data acquisition system was enabled, and analog and digital filters were devised, followed by their tuning and programming. Data treatment scripts for data analysis and plotting were automated, and the assembled system was calibrated and tested. The instrument has an acquisition speed of ∼200 detection events/s, and it permits detection down to ∼510 charges (= three times RMS noise) for a single measured particle. The charge detector was employed to determine the oligomer distribution of a megadalton polymer, polyethylene glycol (PEG). The PEG size distribution exhibits a maximum at ∼ m/z 5910 with the oligomeric population mass distribution peaking near 4.45 MDa. In studies of methanol droplet dynamics, "charge vs time-of-flight" plots enabled clear visualization of the zone near the Rayleigh limit to droplet charging. The highest population of methanol droplets near the Rayleigh limit carried 5000-7000 charges. This corresponds to droplet weights of 10-20 GDa, with the high-end tail extending above 70 GDa. This visualization of the most highly charged droplets (that bear numbers of charges near those defined by the Rayleigh equation) was exploited as a calibration aid for our charge detector, which lacks a means of precisely defining ion energy. A maximum m/z error of -12.3% was calculated for the method, i.e., less than the potential error in assigning the true level of charging of the most highly charged droplets relative to the Rayleigh limit. With these limitations in mind, the introduced method will provide a new means for aiding the calibration of m/z values in charge detectors.