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Transition metal selenides (TMS) have excellent research prospects and significant attention in supercapacitors (SCs) owing to their high electrical conductivity, superior electrochemical activity and excellent structural stability. However, the commercial utilization of TMS remains challenge due to their elaborate synthesis. Present study designed a hierarchical cobalt selenide (CoSe2) nanowire array on Ni-foam to serve as a positive electrode for asymmetric SCs (ASCs). The nanowires-like morphology of CoSe2 was highly advantageous for SCs, as it offered enhanced electrical conductivity, plenty of surface sites, and short ion diffusion. The as-obtained, CoSe2 nanowire electrode demonstrated outstanding electrochemical features, with an areal capacity of 1.08 mAh cm−2 at 3 mA cm−2, high-rate performance (69.5 % at 50 mA cm−2), as well as outstanding stability after 10,000 cycles. The iron titanium nitride@nitrogen-doped graphene (Fe-TiN@NG) was prepared as a negative electrode to construct the ASCs cell. The obtained ASCs cell illustrated an energy density of 91.8 W h kg−1 at a power density of 281.4 W kg−1 and capacity retention of 94.6% over 10,000 cycles. The overall results provide a more efficient strategy to develop redox-ambitious active materials with a high capacity for advanced energy-storage systems.

Glutamic aciduria Type II is an uncommon inborn error of metabolism. It has a rare late-onset variant that can present in adulthood with recurrent lethargy, vomiting, metabolic acidosis, and myopathy. This is a case of a 27-year-old previously healthy gentleman who presented with complains of daily vomiting and generalized body aches that started 3 days after initiation of strenuous exercise and poor oral intake. Initially found to have high anion gap metabolic acidosis, elevated creatinine kinase levels and hypoglycaemia that improved with intravenous fluids. He later deteriorated and he was transferred to the intensive care unit for intubation and monitoring of his mental status. Labs were evident of hyperammonaemia not responding to lactulose. Further management with continuous venovenous hemodialysis (CVVHD) for ammonia clearance was required. This presentation raised the suspicion for metabolic disease and work up done was suggestive of Type II glutaric aciduria. After a long stay of 28 days in the hospital the patient recovered his mental status and was discharged home on carnitine and riboflavin. The diagnosis was confirmed with further genetic testing. He was later found to have concurrent celiac disease that was confirmed by duodenal biopsy.

In this study, a low-cost granular activated carbon doped with Fe2O3 nanoparticles (Fe–GAC) was prepared via a modified sol-gel technique and utilized for the elimination of lead (Pb(II)) and chromium (Cr(T)) ions from synthetic and actual brackish water. The effect of adsorption parameters on the removal of Pb(II) and Cr(T) ions from the water was evaluated in batch adsorption tests. The characterization results validated the distribution of well-defined Fe2O3 nanoparticles onto the GAC surface. GAC loaded with 5 wt.% of Fe2O3 (Fe–GAC 5) exhibited a maximum surface area of 848.2 m2 g−1. The equilibrium data of Cr(T) adsorption were in close agreement with the Langmuir and Sips models with R2 values of 0.95 and 0.96, respectively. However, the R2 values of the equilibrium data for Pb(II) adsorption were greater than 0.91 for all four models, i.e., Langmuir, and Sips, Freundlich and Redlich-Peterson. The maximum Langmuir adsorption capacities of Pb(II) and Cr(T) by Fe–GAC 5 at pH 5.6 and room temperature were 11.9 and 22.1 mg g−1, respectively. Pseudo-second order (R2Pb(II) = 0.99, R2Cr(T) = 0.99) and Elovich kinetic models (R2Pb(II) = 1, R2Cr(T) = 1) were found the most suitable for describing the adsorption kinetics data of Pb(II) and Cr(T) using Fe–GAC 5. The adsorption/desorption studies illustrated that the Fe–GAC is reusable and can be regenerated using 1.0 M HCl. Moreover, the Fe–GAC 5 was found effective to reduce heavy metals loading in actual brackish water to the allowed international standards of drinking water. Accordingly, the Fe–GAC could be a promising material for large-scale applications for the elimination of heavy metals from water.

Capacitive deionization (CDI) shows promising potential for water desalination due to its high performance, energy efficiency, and environmental friendliness. Because of their excellent conductivit...

Microbial fuel cell (MFC) is a promising technology for simultaneous wastewater treatment and energy harvesting. The properties of the anode material play a critical role in the performance of the MFC. In this study, graphene oxide was prepared by a modified hummer's method. A thin layer of graphene oxide was incorporated on the carbon brush using an electrophoretic technique. The deoxygenated graphene oxide formed on the surface of the carbon brush (RGO-CB) was investigated as a bio-anode in MFC operated with real wastewater. The performance of the MFC using the RGO-CB was compared with that using plain carbon brush anode (PCB). Results showed that electrophoretic deposition of graphene oxide on the surface of carbon brush significantly enhanced the performance of the MFC, where the power density increased more than 10 times (from 33 mWm−2 to 381 mWm−2). Although the COD removal was nearly similar for the two MFCs, i.e., with PCB and RGO-CB; the columbic efficiency significantly increased in the case of RGO-CB anode. The improved performance in the case of the modified electrode was related to the role of the graphene in improving the electron transfer from the microorganism to the anode surface, as confirmed from the electrochemical impedance spectroscopy measurements.

In this work, Cu2O nanoparticles were successfully prepared onto the surface of two-dimensional graphitic carbon nitride (g-C3N4) by using a simple solution chemistry approach. An environment-friendly reducing agent, glucose, was used for the synthesis of Cu2O NPs onto the surface of g-C3N4 without using any surfactant or additives. The surface composition, crystalline structure, morphology, as well as other properties have been investigated using XPS, XRD, SEM, FTIR, FESEM, EDS, etc. The electrochemical measurements of the prepared materials demonstrated that Cu2O exhibited a weak oxidation activity towards urea, while g-C3N4 has no activity towards urea oxidation. The Cu2O supported on the surface of g-C3N4 (Cu2O-g-C3N4) demonstrated a significant activity towards urea oxidation that reached two times that of the unsupported one. The significant increase in the performance was related to the synergetic effect between the Cu2O and g-C3N4 support. The prepared composite materials demonstrated high stability towards urea oxidation as confirmed from the stable current discharge for around 3 h without any noticeable degradation performance.

A g-C3N4/VC composite material comprising of graphitic carbon nitride (g-C3N4) and Vulcan carbon (VC) with different ratios, i.e., 2:1, 1:1, and 1:2 were prepared through hydrothermal method without using any additives. These composite materials were further utilized as a support for Ni(OH)2 nanoparticles. These materials formed new type of Ni/(g-C3N4/VC) composite materials. The SEM images show the sheet-like structure of the graphitic carbon nitride. Although Ni nanoparticles' electrochemical activity over the surface for graphitic carbon nitride was slightly more compared to Ni supported on the Vulcan carbon, the Ni supported on the different composite supports demonstrated an outstanding activity compared with that over the single supports. Among the different composite ratios of the graphitic carbon nitride to the Vulcan carbon, the one with high Vulcan carbon, i.e., 2:1, exhibited the best performance that is nine-times the current density in comparison to that of Ni over Vulcan carbon at 0.5 V using 2 M urea in 1 M potassium hydroxide. The stability for the prepared Ni over the composite support was high, where the degradation in the current density for more than 2 hours was negligible.

In this work, standalone cobalt dendrites are prepared then doped with graphene flakes by a simple electroplating technique. Microstructural examination using SEM with EDX, as well as Raman spectroscopy measurements, verified the successful formation of graphene. The prepared material exhibit a favorably high electrochemical methanol oxidation activity with an onset oxidation potential of 0.07 V vs. Ag/AgCl, which is significantly lower than that of the Ni (0.35 V vs. Ag/AgCl). The doping process causes a decrease in the ohmic resistance of the material from 3.2 Ohm cm−2 to 2 Ohm cm−2, which consequently resulted in a significant increase in the current density from 35 mA cm−2 to 62 mA cm−2 using 1 M methanol at 0.5 V vs. Ag/AgCl. After two hours of current discharge at 0.5 V vs. Ag/AgCl, the catalyst doped with graphene showed a current density of 62 mA cm−2. This is an eight-times higher than that obtained in the case of the Ni nano-powder. An electrode prepared by depositing the catalyst on the surface of a highly conductive porous Ni foam was successfully used as the anode of a passive air cathode direct methanol fuel cell, demonstrating an open circuit voltage of 0.75 V using 0.25 M methanol in 1 M KOH.

A simple electrodeposition technique has been used to synthesize Co nanoparticles with a 3D leaf-like morphology at room temperature. The prepared Co material has a layered sheet structure of a few nanometers thickness. The surface area of the Co leaf-like structure is three times higher than that of the Co nanoparticles. The prepared nanoparticles exhibit high activity towards ethanol oxidation in alkaline media with an onset potential of 0 V vs Ag/AgCl, which is one of the lowest reported potentials for a non-precious catalyst. The current density is observed to increase with increasing ethanol concentration from 0.1 M to 2 M, after which it plateaus. Mixing the Co catalyst with Vulcan carbon (20 wt%) resulted in a 50% increase in current discharge at different ethanol concentrations due to the improvement in mass and charge transfer rates as confirmed by EIS measurements. Also, Co deposited in situ on the surface of nickel foam (NF) exhibited a high activity towards ethanol oxidation as a standalone electrode that is 10 times that of bare NF.

Particulate matter (PM) specimens from a traffic site were sampled on Teflon filters using a low volume sampler. The sampling campaign ran over a one-year period with sampling frequency of twice a week for both PM2.5 and PM10. X-ray diffraction (XRD) methods, which are not commonly used in PM analysis, have been utilized successfully to identify crystalline phases present, including secondary pollutants. XRD data confirmed results obtained by X-ray fluorescence, positive matrix factorization modeling, and scanning electron microscopy. PM2.5 consisted mainly of secondary sulfates, like Mascagnite [(NH4)2SO4], Koktaite [(NH4)2Ca(SO4)2·H2O], and Gypsum [CaSO4·2H2O]. For PM10, it was found that the major phases are mostly originating from natural sources, such as dust storms and sea salts, in addition to secondary compounds, such as sodium nitrate. The main phases identified were Calcite, Quartz, Gypsum, Halite, and Palygorskite.

We report a density functional theory study of ZnO cluster doped with Eu and Mg along with native point defects using the generalized gradient approximation including the Hubbard parameter. The Zn atomic positions are found to be energetically more favorable doping sites than O. The Eu has a lower formation energy than Zn and O vacancies, helps in lowering the formation energy of point defects and induces spin polarization. Mg is less favorable dopant energetically and is not inducing any magnetism in the cluster. Presence of Eu and point defects along with Mg can help in sustaining spin polarization, implying that transition metal and rare earth dopant is a favorable combination to invoke desirable properties in ZnO based materials. Eu–Eu doping pair prefers ferromagnetic orientation and a spin flip is induced by Eu in the Eu–Mg configuration. Further, Eu doping increases the value of static refractive index and optical absorption in the UV region compared to the undoped ZnO cluster.

Due to the rapid increase in their efficiencies, third generation photovoltaics rose to prominence in recent years, and became serious competitors to conventional silicon based and thin film solar cells. This work investigates various techniques to grow and/or deposit copper oxide (CuO) on a copper substrate for utilization as a counter electrode in dye sensitized solar cell (DSSC) applications. Copper has many attractive thermal, electrical and mechanical properties and is widely used in solar thermal applications, but its use is limited in solar photovoltaic cells. The experimental results reported herein have proven the success of growing an intrinsic copper oxide layer on a pure copper substrate. Among the methods, the chemical ageing process followed by heat treatment has resulted in a homogenous and adherent oxide layer that attenuated the electronic conductivity and chemical reactivity of pure, bare copper electrodes. These electrodes are incorporated into solar cells that are constructed and tested against a platinum reference cell. The cells showed comparable short circuit current to their platinum counterparts, with efficiencies of 0.2% compared with 0.5% for platinum under the same conditions. The copper counter electrode with the CuO deposition exhibited good promise, especially when comparing figures of merit (power generated/price) as a cheap and effective alternative to platinum in third generation solar cell applications.

The quest for high performance supercapacitors from the energy-power point of view is commonly addressed from the constituting electrode materials and/or the electrolyte. Carbon-based double-layer capacitors are known for their high power density, whereas pseudocapacitors which use transition metal oxides/nitrides/sulfides or conductive polymers are known for their high energy density. In this work we show that one can modulate the energy storage capability of supercapacitors by mixing at preset ratios two types of carbon materials having two different energy storage capabilities. The time-domain and frequency-domain electrochemical characterization of five symmetric devices, in which electrodes made of carbon nanofibers (CNF) are mixed with cobalt-modified CNF (Co-CNF) at different mass proportions, show that as the Co-CNF content is increased, the effective capacitance, and hence the restored energy, is increased without affecting the power performance of the device. This opens up new opportunities for the modular design of supercapacitor electrodes using a small set of electric double-layer capacitive materials.

Direct urea fuel cell (DUFC) is an attractive and inexpensive method for the simultaneous wastewater treatment (urine and urea-contaminated water) and electricity generation. Many efforts have been made to increase the catalytic activity of Ni-based DUFC anodic catalyst toward urea oxidation, which is considered to be the best non-precious catalyst in alkaline media so far. Alloying Ni with other metals and/or non-metals, and increasing its surface area demonstrated a power of up to 26.9 mW cm−2 at room temperature, which is comparable to that obtained in direct alcoholic fuel cells using high loading of precious catalyst. However, this is still viewed as low-performance. This review presents a comprehensive picture of the mechanism of urea oxidation on Ni-based catalysts, the poisoning effect of catalysts and its possible remedies, as well as the different approaches in preparing highly active catalysts. We also analyze the performance and associated issues of DUFC using newly applied strategies to increase its open-circuit voltage and power output via alternative oxidants and re-designed chemical conditions in the cell.

Eriochrome Black T (EBT) and chromium (Cr) are considered to be potential pollutants due to their toxicity and severe impact on the environment. In the current study, hydrotalcite-derived Mg-Ca-Al-LDO mixed metal oxide composite was prepared using a conventional co-precipitation method and explored in terms of the removal of Cr and EBT dye from aqueous solution in a batch mode adsorption process. The prepared Mg-Ca-Al-LDH, Mg-Ca-Al-LDO and spent Mg-Ca-Al-LDO adsorbents were characterized to propose the adsorption mechanism. Different adsorption parameters were examined, such as adsorbent dosage, initial concentration, pH, reaction temperature and contact time. The EBT adsorption kinetic results matched strongly with the pseudo-second-order model for both Cr (R2 = 0.991) and EBT (R2 = 0.999). The Langmuir isotherm model exhibited a maximum adsorption capacity of 65.5 mg/g and 150.3 mg/g for Cr and EBT, respectively. The structure and morphology results obtained after Cr and EBT dye adsorption reveal that the adsorption mechanism is associated with electrostatic interactions and surface complexation of Cr and EBT dye with Mg-Ca-Al-LDO surface functional groups. Moreover, more than 84% of the initial adsorption capacity of EBT and Cr can be achieved on the Mg-Ca-Al-LDO surface after five adsorption/desorption cycles. Finally, the Mg-Ca-Al-LDO mixed metal oxide composite can be potentially used as a cost-effective adsorbent for wastewater treatment processes.

International audience; Severe acute respiratory syndrome SARS-CoV-2 virus led to notable challenges amongst researchers in view of development of new and fast detecting techniques. In this regard, surface-enhanced Raman spectroscopy (SERS) technique, providing a fingerprint characteristic for each material, would be an interesting approach. The current study encompasses the fabrication of a SERS sensor to study the SARS-CoV-2 S1 (RBD) spike protein of the SARS-CoV-2 virus family. The SERS sensor consists of a silicon nanowires (SiNWs) substrate decorated with plasmonic silver nanoparticles (AgNPs). Both SiNWs fabrication and AgNPs decoration were achieved by a relatively simple wet chemical processing method. The study deliberately projects the factors that influence the growth of silicon nanowires, uniform decoration of AgNPs onto the SiNWs matrix along with detection of Rhodamine-6G (R6G) to optimize the best conditions for enhanced sensing of the spike protein. Increasing the time period of etching process resulted in enhanced SiNWs’ length from 0.55 to 7.34 µm. Furthermore, the variation of the immersion time in the decoration process of AgNPs onto SiNWs ensued the optimum time period for the enhancement in the sensitivity of detection. Tremendous increase in sensitivity of R6G detection was perceived on SiNWs etched for 2 min (length=0.90 µm), followed by 30s of immersion time for their optimal decoration by AgNPs. These SiNWs/AgNPs SERS-based sensors were able to detect the spike protein at a concentration down to 9.3 × 10−12 M. Strong and dominant peaks at 1280, 1404, 1495, 1541 and 1609 cm−1 were spotted at a fraction of a minute. Moreover, direct, ultra-fast, facile, and affordable optoelectronic SiNWs/AgNPs sensors tuned to function as a biosensor for detecting the spike protein even at a trace level (pico molar concentration). The current findings hold great promise for the utilization of SERS as an innovative approach in the diagnosis domain of infections at very early stages.

Capacitive deionization (CDI) is one of the emerging desalination technologies that attracted much attention in the last years as a low-cost, energy-efficient, and environmentally-friendly alternative to other desalination technologies, such as multi-stage flash desalination (MSF) and multiple effect distillation (MED). The implementation of faradaic electrode materials is a promising method for enhancing CDI systems' performance by achieving higher salt removal characteristics, lower energy consumption, and better ion selectivity. Therefore, a novel CDI technology named Faradaic CDI (FCDI) that implements faradaic electrode materials arose as a high-performance CDI cell design. In this work, the application of FCDI cells in desalination and wastewater treatment systems is reviewed. First, the progress done on using various FCDI systems for saline water desalination is summarized and discussed. Next, the application of FCDI in wastewater treatment applications and selective ion removal is presented. A thorough comparison between FCDI and conventional carbon-based CDI is carried out in terms of working principle, electrode material's cost, salt removal performance, energy consumption, advantages, and disadvantages. Finally, future research consideration regarding FCDI technology is included to drive this technology closer towards practical application.

Generating true random bits of high quality at high data rates is usually viewed as a challenging task. To do so, physical sources of entropy with wide bandwidth are required which are able to provide truly random bits and not pseudorandom bits, as it is the case with deterministic algorithms and chaotic systems. In this work we demonstrate a reliable high-speed true random bit generator (TRBG) device based on the unpredictable electrical current time series of atmospheric pressure air microplasma (APAMP). After binarization of the sampled current time series, no further post-processing was needed in order for the bitstreams to pass all 15 tests of the NIST SP 800-22 statistical test suite. Several configurations of the system have been successfully tested at different sampling rates up to 100 MS/s, and with different inter-electrode distances giving visible/non-visible optical emissions. The cost-effectiveness, simplicity and ease of implementation of the proposed APAMP system compared to others makes it a very promising solution for portable TRBGs.

The harmful effect of carbon pollution leads to depletion of the ozone layer, which is one of the main challenges confronting the world. Although progress is made in developing different carbon dioxide (CO2) capturing methods, these methods are still expensive and face several technical challenges. Fuel cells (FCs) are efficient energy converting devices that produce energy via an electrochemical process. Recently varying kinds of fuel cells are considered as an effective method for CO2 capturing and/or conversion. Among the different types of fuel cells, solid oxide fuel cells (SOFCs), molten carbonate fuel cells (MCFCs), and microbial fuel cells (MFCs) demonstrated promising results in this regard. High-temperature fuel cells such as SOFCs and MCFCs are effectively used for CO2 capturing through their electrolyte and have shown promising results in combination with power plants or industrial effluents. An algae-based microbial fuel cell is an electrochemical device used to capture and convert carbon dioxide through the photosynthesis process using algae strains to organic matters and simultaneously power generation. This review present a brief background about carbon capture and storage techniques and the technological advancement related to carbon dioxide captured by different fuel cells, including molten carbonate fuel cells, solid oxide fuel cells, and algae-based fuel cells.

Microbial fuel cell (MFC) is an emerging method for extracting energy from wastewater. The power generated from such systems is low due to the sluggish electron transfer from the inside of the biocatalyst to the anode surface. One strategy for enhancing the electron transfer rate is anode modification. In this study, iron nanostructure was synthesized on a carbon cloth (CC) via a simple electroplating technique, and later investigated as a bio-anode in an MFC operated with real wastewater. The performance of an MFC with a nano-layer of iron was compared to that using bare CC. The results demonstrated that the open-circuit voltage increased from 600 mV in the case of bare CC to 800 mV in the case of the iron modified CC, showing a 33% increase in OCV. This increase in OCV can be credited to the decrease in the anode potential from 0.16 V vs. Ag/AgCl in the case of bare CC, to &minus, 0.01 V vs. Ag/AgCl in the case of the modified CC. The power output in the case of the modified electrode was 80 mW/m2&mdash, two times that of the MFC using the bare CC. Furthermore, the steady-state current in the case of the iron modified carbon cloth was two times that of the bare CC electrode. The improved performance was correlated to the enhanced electron transfer between the microorganisms and the iron-plated surface, along with the increase of the anode surface- as confirmed from the electrochemical impedance spectroscopy and the surface morphology, respectively.

Remote areas and poor communities are occasionally deprived of access to freshwater. It is, therefore, critical to providing a cheap and efficient desalination system that encourages the development of those communities and benefiting society at large. Solar stills are an affordable, direct method of water desalination, but its productivity is the critical challenge hindering its application. To ease this, research has focused on the role of nanofluids to improve heat transfer. Other works have focused on improving the design in consort with utilizing the nanofluids. This review reports and discusses the substantial role of nanofluids to enhance the productivity and energy utilization efficiency of the solar stills. Specifically, the mechanism of energy transfer between the nanoparticles and the base fluid. This includes both plasmonic and thermal effects. It is evident that nanofluid utilization in small fraction enhanced the thermal conductivity compared to base fluid alone. Alumina was found to be the most suitable nanoparticle used as nanofluid inside the solar stills due to its availability and lower cost. Still, other competitors such as carbon nanostructures need to be investigated as it provides higher enhancement of thermal conductivity. Also, several aspects of energy utilization enhancement have been discussed, including innovative application techniques. The challenges of such integrated systems are addressed as well.

Exploration of novel strategies for fabricating SERS substrates attracted enormous research potential as achieving high sensitivity, reproducibility along with cost effectiveness is really challenging. Herein, we have fabricated hierarchical silver nanoprism/graphene oxide/silicon nanowire (Ag/GO/SiNWs) arrays as surface-enhanced Raman scattering (SERS) sensors for the effective detection of atrazine. Homogenous and vertically aligned SiNWs have been successfully synthesized using silver assisted chemical etching. Further, Ag/GO/SiNWs arrays were assembled by subsequent spin-coating of GO followed by drop-casting deposition of Ag nanoprisms. Micro-structural properties of as-fabricated nano-arrays have been well examined by scanning electron and atomic force microscopic techniques. Nanowire bunches have been decorated by GO layers; which further facilitates homogenous deposition of Ag nanoprisms. Using rhodamin 6G as probe molecule, high SERS activity and excellent reproducibility of as-fabricated substrates have been demonstrated. High efficiency of 3.2 × 108 and was obtained for the fabricated sensors; attributed to the synergetic charge transfer between GO and Ag nanoprisms on high surface area Si nanowires. Charge transfer mechanism that leading to enhanced surface plasmon resonance effect of the as-fabricated array was established as well. Further, these low cost Ag/GO/SiNWs sensors exhibited ultrasensitive detection of pollutants such as methylene blue and atrazine residues down to picomolar levels; these can serve as potential chemical sensors for rapid monitoring of environmental pollutants in trace levels.

We report the synthesis of aryldiazonium tetrachloroaurate(III) salts [X-4-C6H4N≡N]AuCl4 (X = F, Cl, Br, I, CN, NO2) and their mild reduction to covalently functionalized nanoparticles. The synthesis of the salts was carried out by the oxidation of anilines, dissolved in HCl, using sodium nitrite followed by the exchange of the counter anion with [AuCl4]- in water. In another procedure, the anilines were protonated with H[AuCl4] in acetonitrile followed by one-electron oxidation using nitrosonium salt [NO]X (X = BF4−, PF6−). Raman and ATR-FTIR spectroscopy displayed the diazonium νN≡N and Raman showed the tetrachloroaurate νAu-Cl stretching frequencies. X-ray crystal structure of [NO2-4-C6H4N≡N]AuCl4 salt showed N≡N bond distance typical of a triple bond. Gold-aryl nanoparticles were constructed by the mild chemical reduction of the diazonium gold(III) salts using 9-borabicyclo[3.3.1]nonane (9-BBN). Nanoparticles hydrodynamic diameter, elemental composition, dynamics information, and stability data were determined. Transmission electron microscopy (TEM) measurements showed limited aggregation due to the small suppressing organic shell. However, dynamic light scattering (DLS) measurements showed considerable aggregation in acetonitrile. X-ray photoelectron spectrometry (XPS) showed the gold core in zero oxidation state and manifested the gold-organic shell connectivity. The –N=N-aryl interfacial formation on the gold surface can be ruled out since the N1s peak assigned to the diazonium moiety showed no sign in the XPS nitrogen area in addition to its absence in the ATR-FTIR spectra. Raman spectroscopy measurements showed a peak assigned to gold-carbon bonding supported by density functional calculations (DFT) on Au20-C6H4-CN model.

There is a tremendous interest in the fabrication of novel hemocompatible nanoparticles for applications in theranostics. In this context, bovine serum albumin (BSA) conjugates with the water-soluble and super robust gold-aryl nanoparticles truncated with carboxylic functionals were synthesized. The gold-aryl nanoparticles were fabricated by the mild reduction of the diazonium gold(III) salt [HOOC-4-C6H4N≡N]AuCl4. The gold core size and the presence of BSA sheath encapsulating Au−COOH nanoparticles were concluded from transmission electron microscopy (TEM). Clear spectral changes supported by quantitative X-ray photoelectron spectrometry (XPS) surface analysis are visible: the C1s/Au4d intensity ratio increased sharply and the gold features were very well attenuated after BSA attachment, which brings more nitrogen essentially due to NH-C = O peptide links. The conjugation of BSA with Au−COOH nanoparticles resulted in the isoelectric point (pI) change from 4.7 to a range of 4.1-5.0. The robustness of the bioconjugates can be concluded based on the high ζ-potential values and the resistance to drastic pH conditions. The high encapsulation efficiency percentage (EE%) calculated using Bradford protein assay was in a range of 90.0–94.6% under physiological pH values. Taken together, overall studies imply the presence of interaction between the Au−COOH nanoparticles and BSA. In this study we investigated the interaction of gold nanoparticles and their BSA conjugates with human red blood cells (RBCs), which might cause cell deformity and hemolysis. To elaborate on the uniqueness of the bioconjugates, they showed negligible hemolysis or morphology deformation to cells membrane visualized using light and phase contrast microscopes. Quantitative measurements of hemoglobin leached out of the cell membrane using UV–vis showed negligible hemolysis. The high physiological stability of the conjugates fosters their applications in intravenous drug delivery supported by the long blood circulation half-life.