Cu Nano-Roses Self-Assembly from Allium cepa, L., Pyrolysis by Green Synthesis of C Nanostructures

: Carbon nanostructures are achieved by bio-waste Allium cepa , L., (onion vulgaris) peels through pyrolysis at 900 ◦ C. They contain dispersed elements derived by their bio-precursors, like Mg, Ca, S, Na, K, and Cu. Here, we report the self-assembly of new Cu ﬂower-shaped nanostructures organized as nano-roses. Remarkably, the nano-roses show rolled-up petals of Cu 0 with a high chemical stability in air, exhibiting an intrinsic pure Cu crystalline phase. This suggests the exceptional potentiality to synthesize Cu 0 nanostructures with novel physical / chemical properties. The size, morphology, and chemical composition were obtained by a combination of high-resolution scanning electron microscopy, spectroscopy, L.S., F.D.P., G.D.V., C.Q., S.S., G.H.


Introduction
With the fast development of nanotechnology in the last decades, the realm of nanostructures has unveiled all its beauty, giving unimaginable quantum systems, spanning all fields of physics, chemistry, and biology.
The close conjugation between the atomic and nanoscopic scale of materials and their physical properties, mainly derived from the 3D, 2D, 1D, or 0D quantum size confinement [12][13][14], directly takes us into the mechanics applied to nanoscience and its complexity [15,16].
found only on the samples pyrolyzed at the highest temperature (900 • C) and not on those obtained at 500 and 700 • C (not further described here).
The aim of the present manuscript is to report the discovery of a new Cu nanostructure coined here as Cu nano-rose, due to the particular characteristic exhibited by its layers, which are spirally rolled-up like the petals of a rose.
High-resolution scanning electron microscopy (HR-SEM), energy dispersive X-ray spectroscopy (EDS), energy dispersive X-ray diffraction (ED-XRD) and Raman spectroscopy were used to exploit the morphology, chemical, and structural properties of this new arrangement of copper.

Sample Preparation
Carbon nanostructures were produced from the peels of Allium cepa, L., [41], originating from the south of India [40]. The synthesis process is considered as green for two reasons: the first related to bio-waste recycling and the second to the absence of chemical reagents. The peels were manually separated from the waste, carefully cleaned with distilled water, dried in air, and then heated in the oven at a temperature of 80 • C. Subsequently, they were crushed, reduced to powder, and selected with the use of a sieve to a size of a few tens of microns. The micrometric powder was thus pyrolyzed inside a quartz crucible at the temperature of 900 • C in an inert nitrogen atmosphere [40]. The presence of metals in fresh red onion, for safety reasons, is usually determined by means of ICPM (inductively coupled plasma mass) spectrometry [39]. We did not check directly the starting materials for our experiments. Data from the literature, however, reveal the systematic presence of several elements, including copper [39], within Allium cepa, L., [41] from the same provenance and type as the samples that we used for our pyrolysis.

SEM Measurements
SEM measurements on C nanostructures were carried out by using two Zeiss systems: (1) FEG-SEM, LEO 1530 (Oberkochen-Germany), equipped with an in-lens secondary electrons detector (SE), a Centaurus back scattered electron (BSE) detector, and an EDS X-ACT (detector of 10 mm 2 ) Oxford with an AZTEC software microanalysis system at ENEA-Casaccia, S. Maria di Galeria Rome, Italy; and (2) a Gemini 300 FE-SEM (field emission SEM), equipped with two detectors for secondary electrons, a BSE detector with five sectors, and an EDS Bruker system (detector of 60 mm 2 ) at LIME, Science Department, University of Roma Tre. For all experiments, we used the C powder provided by the Centre for Nano-materials & Displays, B. M. S. College of Engineering, India, lying on freshly deposited Au films on Si slabs.

Energy Dispersive XRD Measurements
ED-XRD measurements were performed in room conditions in reflection mode θi = θr using the white Bremsstrahlung X-ray radiation ranging up to 50 KeV produced by a W-anode X-ray tube on a customized ED spectrometer (at CNR-ISM Rome, Italy) [42]. The detection is achieved by a cooled Ge solid state detector (SSD), probing both the incoming photons and their energy. In ED mode, there is an intrinsic reduced q-resolution of the exchanged momentum, due to the contribution of the SSD energy resolution, resulting in enlarging of the diffraction peaks, but, on the other hand, an enormous increase of the dynamic signal-to-noise ratio, with respect to the θ-2θ Bragg-Brentano geometry of conventional XRD apparatus.

Raman Spectroscopy
Raman spectra were collected with a Renishaw In-Via spectrometer, equipped with a 457-nm laser beam in standard confocal mode (at CNR-ISM Rome, Italy). The best experimental setup was obtained by combining a 2400 lines/mm grid with 100× optical magnification. The accumulation Raman spectra was 50 with a single spectrum acquisition time of 168 s. The energy resolution was 1 cm −1 . The same experimental conditions were used for all samples. Surface damage induced by the laser was not observed, thus allowing for accurate measurements to be performed.
It is worth noting that the SEM, ED-XRD, EDS, and Raman spectroscopy measurements were accurately repeated for reproducibility. In particular, SEM/EDS data were collected on four (see SI) samples from four different pyrolysis experiments at 900 • C and we systematically observed the presence of Cu nano-roses; moreover, the ED-XRD measurements and Raman spectroscopy were iterated after a long period of time (months) to carefully observe the stability in air of elemental Cu against its oxidation.

Results and Discussion
The morphologies and structures of the pyrolyzed carbon powders were determined using HRfield emission scanning electron microscopy equipped with selected area electron energy dispersive X-ray spectroscopy.
The SEM images at 53.54 × 66.33 µm 2 and that of the overlapped false color table from EDS total yield spectra, taken with the Zeiss system FEG-SEM, LEO 1530 operating at an accelerating high voltage (HV) of 20.0 KV, are reported in Figure 1a,b.
At this magnification, the C powders display the coexistence of structures at various scales, from large flakes a few µm across to small spheres of some nanometres.
They are inconsistently arranged, even if somehow, they keep the memory of their original shape attributed to the bio-waste, [40], Allium cepa, L., [41] (onion vulgaris) peels from which they derive. On the other hand, Figure 1b evidences the different chemical composition, Na, O, Ca, Cl, K, Si, Al, and Mg, in addition to the predominant carbon, in close agreement with what reported in [40] and to the fact that the red onion vulgaris already contains these elements as precursors and, probably, in a conjugate form.
The false color EDS images of C (red), Ca (light blue), K (green), O (dark blue), Mg (magenta), and S (yellow) and their corresponding Kα 1 and Kα 2 shells are shown in Figure 1c-h, whereas Figure 1i shows the intensity of the Lα 1 , Lα 2 and Kα 1 , Kα 2 emission lines as a function of increasing energy for these elements. We can easily note, from the inset, that the presence of chemical species different from carbon can mainly be assigned to impurities, including the Cu Lα 1 , Lα 2 emission lines that are clearly visible at around (0.93-0.95) KeV of energy, as well as the others Kα 1 , Kα 2, and Kα 3 less intense around (8.0-8.9) KeV, proving C to be over 80%. The Si peak originated from the substrate.
A typical HR-SEM image, (58.56 × 77.91) µm 2 , from C nanopowders supported on the gold substrate at magnifications of 3.54 K× and an electron acceleration HV of 2.0 KV, collected by using the Zeiss FE-SEM, is shown in Figure 2a. At first sight, we observe very defined and large C flakes (from 5 to 50 µm in length) randomly oriented and occupying most of the image area. Smaller structures scattered over the entire surface of these C flakes are clearly visible. Among these, three vaguely spherical objects (indicated with blue arrows) can be seen, the largest (red arrow) having a diameter of~7 µm and the other smaller two of approximately 0.5 µm (yellow arrows). These particles were studied in a detailed morphological and chemical analysis, described hereafter.  Figure 2b with the diameter B = 2.63 µm indicates one of the composite structures that in a mathematical similarity forms the entire larger sphere of diameter A = 7.54 µm marked with a dashed light-blue circle. The yellow dashed circle with a diameter C = 0.92 µm emphasizes a single small rounded structure that builds-up the entire larger object in the dashed red circle.
Although in our bi-dimensional SEM images (consider for example the dotted light-blue area), we collapsed the three-dimensional reality of the rounded nano-roses on two-dimensional projections, we could extract some geometrical relations of the similarity among the spheres. One should also bear in mind that the circles drawn in Figure 2b must be considered as an average. In particular, with the dotted light-blue circle we tried to enclose the maximum possible nanostructures. against its oxidation.

Results and Discussion
The morphologies and structures of the pyrolyzed carbon powders were determined using HRfield emission scanning electron microscopy equipped with selected area electron energy dispersive x-ray spectroscopy.
The SEM images at 53.54 × 66.33 μm 2 and that of the overlapped false color table from EDS total yield spectra, taken with Despite these simplifications, a close inspection of Figure 2 suggests some interesting points to consider: If we calculate the ratios between the diameters of the various circles, i.e., A:B and B:C, we get the same value of 2.86, which allows A:C to be expressed as about n times C, where n is an integer and is equal to 9. This means that the pseudo-fractal feature that is apparent at first visual inspection of the SEM images can be confirmed as a numerical relationship based on this simple geometric observation. diameter of ~7 μm and the other smaller two of approximately 0.5 μm (yellow arrows). These 185 particles were studied in a detailed morphological and chemical analysis, described hereafter.   By increasing the magnification, as shown in Figure 2c, we can observe the petals of the individual nano-rose better, indicated, as a guide for the eyes, by the dashed pink circle. Each single petal (Figure 2d) has, on average, a lateral dimension of about 172 nm (pink arrow), with few larger or smaller petals.
Furthermore, it seems that the individual nano-rose (see those within the yellow and red circles in Figure 2b) uniformly covers a hypothetical sphere, the largest, as a spherical shell of a smaller inner diameter. We can imagine that the two structures of a smaller diameter indicated in Figure 2a by yellow arrows are also composed, in the same way, by nano-roses, considering that they are shown to be jagged in their external lines, having a similar gleaning profile. This is an additional intriguing aspect since it would suggest that these pseudo-fractal structures present on the external surface of the sphere also occur inside its volume, assuming a 3D fractal similitude, where the single nano-rose may be considered as the building block.
To identify the chemical composition of the nano-roses, we performed EDS microanalysis using the Bruker system. Figure 3a shows the SEM image that outlines the area where the EDS data were collected (3.8 K×, HV = 15 KV). Figure 3b-f display, respectively, the X-ray fluorescence maps for C, Ca, Mg, O, and Cu collected on the same area as in Figure 3a.
formation of this new kind of Cu agglomeration, addressing both the physical and chemical aspects 243 involved. This is a crucial point to clarify considering that both our results and those of [43] 244 demonstrate that it is possible to obtain Cu 0 crystalline structures that are stable in air.

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To validate this result, the ED-XRD spectrum was collected on the carbon nanostructures as a 258 function of the quantum momentum scattering parameter. In Figure 4, we can easily observe the Interestingly, we may observe from these elemental maps that the nano-roses are constituted of Cu, as shown in Figure 3f, and in particular by comparison of Figure 3e,f that are mainly composed of metallic Cu 0 .
This represents a very intriguing point, since to date, no structures similar to our nano-roses have been described, considering both the morphology of the crystallites and their composition. Typically, the nanostructures of copper reported in the literature, which were mainly obtained from a liquid phase by the immersion of pure copper sheets, have been found to be systematically composed of oxidized copper, CuO [17][18][19][20][21][22][23][24][25], showing nanostructures in the form of flowers but completely dissimilar from those reported in this paper [25]. The only exception is the Cu nanoflowers, constituted of metallic Cu 0 according to X-ray diffraction and X-ray spectroscopy measurements [43], obtained by a wet chemical process using Cu[(acac) 2 ], acac = acetylacetonate as the reagent, oleyl amine both as the solvent and reducing agent, and cetyltrimethylammonium bromide as the capping agent.
We extrapolated that the main driving force used to obtain the Cu nano-roses from red onion peels is the high temperature applied during the annealing process performed in the inert nitrogen atmosphere. This produced both the expulsion of copper from its original organic molecules and the prevention of the oxidation onset to finally give rise to these particular Cu nanostructures. One cannot, however, exclude that the presence of elemental carbon may catalyze the Cu 0 nano-rose formation. In this respect, experiments are in progress to elucidate the actual mechanism of the formation of this new kind of Cu agglomeration, addressing both the physical and chemical aspects involved. This is a crucial point to clarify considering that both our results and those of [43] demonstrate that it is possible to obtain Cu 0 crystalline structures that are stable in air.
In the past, Ag structures have been obtained from the reaction of silver nitrate and ascorbic acid in an acidic aqueous solution of polynaphthalene [44]. Such structures are composed of metallic Ag 0 nanoparticles of about 10 nm in diameter linearly ordered inside a filamentous polymer sheath with a mesometric morphological structure in the flower form of about 10 microns in diameter, having meso-petals of a lanceolate shape. This constitutes an example where the Ag nanoparticles are kept chemically inert by a polymeric protective sheath that surrounds them. On the contrary, in the case of our copper nano-roses, as also reported in [43], the structures are self-protected against any oxidation or sulfurization, coming from air or from the precursors of the pyrolyzed carbon nanostructures.
To validate this result, the ED-XRD spectrum was collected on the carbon nanostructures as a function of the quantum momentum scattering parameter. In Figure 4, we can easily observe the presence of four peaks, two of which are assigned to the (002) and (101) reflections of the graphitic form of carbon indexed according to ICCD card number 00-001-0640 and corresponding to interplanar spacings with d = 3.380 Å and d = 2.020 Å, respectively; the other two are attributed to the (111) and (200) diffraction peaks of metallic copper [ICCD card number 00-001-1241] and are due to the interplanar spacings with d = 2.080 Å and d = 1.810 Å, respectively [21,24,25,43].
Finally, Figure 5 displays the Raman spectrum from the C nanostructures. Two main peaks labelled D and G, located at 1386 and 1587 cm −1 , are related to the E 2g in the plane vibrational mode of the hexagon atoms in the honeycomb C graphitic arrangement and to the defects peak [46][47][48].
The G-mode peak is found at 1587 cm −1 . Such a value, slightly blue-shifted with respect to highly crystalline graphite (G-mode at about 1580 cm −1 ) [46][47][48], can be attributed to the nanometric-sized C-particles. This agrees with [46][47][48], where a frequency shift of about 15 cm −1 towards higher wavenumbers was found in some samples with extremely small graphite crystal sizes [46]. Several Raman spectra were collected on different portions/grains of the C nanostructures in order to obtain appreciable reproducibility. Notably, the presence of the main Raman features from CuO (295 cm −1 ) [26] and CuS (473 cm −1 ) [27][28][29][30] was never detected.
The red rectangle in Figure 5 delimits a region between 250 and 820 cm −1 , enlarged in the inset, which shows a flat area without features, where typically the structures of Cu oxides and sulphides are found [26][27][28][29][30]. This observation is in perfect agreement with all the described data, confirming that the copper nano-roses exposed to air have the composition of metallic Cu 0 and thus are self-protected against oxidation from the external atmosphere.

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Finally, Figure 5 displays the Raman spectrum from the C nanostructures. Two main peaks labelled D and G, located at 1386 and 1587 cm −1 , are related to the E2g in the plane vibrational mode 276 of the hexagon atoms in the honeycomb C graphitic arrangement and to the defects peak [46][47][48].

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The G-mode peak is found at 1587 cm −1 . Such a value, slightly blue-shifted with respect to highly  Figure 5. Raman spectrum from C nanostructures. In the inset, the region evidenced by the red rectangle is highlighted.
One hypothesis that could explain this important result lies in the possibility of interpreting the petals of the nano-roses as consisting of stacked layers of Cu [111] planes, such as [43], graphitic-like arranged, and thus resistant to possible oxidation.

Conclusions
Green carbon nanostructures produced by the bio-pyrolysis of Allium cepa, L., [41] from India [39,40] were studied through a combination of SEM/EDS, ED-XRD, and Raman spectroscopy, showing the self-assembly formation of metallic copper nanostructures. SEM images displayed for the first time the presence of rolled-up structures, called nano-roses for their evident shape, distributed in a fractal-like pseudo-morphism. The single nano-rose unit of 0.92 µm in diameter revealed rolled petals of nanometric size, with a lateral dimension of about 172 nm. The single nano-roses are arranged in ordered groups, occupying ideal circular structures of about 2.63 µm. These structures further unite to form a larger circle of 7.54 µm in diameter, exhibiting a quite uniform distribution, although this description represents a geometric simplification. The global ensemble of observed nano-roses indeed consists of spherical three-dimensional objects. EDS microanalysis showed that the nano-roses are constituted by metallic Cu 0 , as confirmed by ED-XRD and Raman spectroscopy measurements. The data excluded the presence of copper oxides and/or copper sulphides.
Remarkably, in this work, the Cu nano-roses showed a morphology with an evidently increased surface/bulk ratio. This observation suggests, as also mentioned in [32] for protein-inorganic hybrid Cu 2+ phosphate nanoflowers, the possibility of novel featured applications for these Cu nano-roses. These include (1) efficient electrodes in catalytic processes for fuel cells or (2) sensors for revealing the oxidation of fruits in the agri-food sector, thanks to their metallic unoxidized ground state. Indeed, in the particular conditions of a pH environment, the Cu 0 nano-roses can be oxidized, revealing the ripeness of the fruits, i.e., the enzymatic polyphenols to quinones' oxidation process.