Fundamental properties of transition-metals-adsorbed graphene
The revealing properties of transition metal (T)-doped graphene systems are investigated with the use of the first-principles method. The detailed calculations cover the bond length, position and height of adatoms, binding energy, atom-dominated band structure, adatom-induced free carrier density as well as energy gap, spin-density distributions, spatial charge distribution, and atom-, orbital- and spin-projected density-of-states (DOS). The magnetic configurations are clearly identified from the total magnetic moments, spin-split energy bands, spin-density distributions and spin-decomposed DOS. Moreover, the single- or multi-orbital hybridizations in T-C, T-T, and C-C bonds can be accurately deduced from the careful analyses of the above-mentioned physical quantities. They are responsible for the optimal geometric structure, the unusual electronic properties, as well as the diverse magnetic properties. All the doped systems are metals except for the low-concentration Ni-doped ones with semiconducting behavior. In contrast, ferromagnetism is exhibited in various Fe/Co-concentrations but only under high Ni-concentrations. Our theoretical predictions are compared with available experimental data, and potential applications are also discussed.
Keywords: Transition metal, graphene, first-principles, electronic, magnetic.
Quantum Topological Center, National Cheng Kung University, Tainan 701, Taiwan \alsoaffiliationHierachical Green-Energy Materials (Hi-GEM) Research Center, National Cheng Kung University, Tainan 70101, Taiwan
More than a decade has elapsed since 2004 when the discovery of few-layer graphene systems was reported. Ever since then, as a consequence of its remarkable properties, graphene has been considered as one of the promising materials that could greatly improve the performance of many products, e.g., capacitors 1, 2, Li-ion batteries 3, 4, gas sensors 5, 6, 7, 8, and spintronic devices 9, 10, 11. Finding ways to greatly diversify the fundamental properties of layered graphene is one of the main-stream topics in physical, chemical and material sciences so as to expand their potential applications. Available methods include modulation of the number of layers, stacking configuration, guest-atom adsorption/intercalation/substitution, and defects. Significant efforts for creating dramatic transformations of graphene’s fundamental properties have been extensively reported in the literature. So far, chemical modification is considered to be the most efficient technique. The adatom-doped graphene structures have been attracting a considerable amount of theoretical 12, 13, 14, 15, 16 and experimental 17, 18, 19 attention. The dopant-created chemical bonding will continue to play a critical role in determining the most stable configuration and thus other essential properties. More recently, the transition metal (T)-doped graphene structures have gained a great deal of attention 20, 21, 22, 23. These systems have been reported to exhibit magnetism and other interesting properties that are promising for spintronic devices and batteries 24, 25, 26. The aim of our present work is to investigate the transition metal-enriched fundamental properties of monolayer graphene.
It is worthy noting that the chemisorption of transition metal adatoms to carbon honeycomb lattice creates a fully modified system without damaging the distinctive one-atom-thick construction itself. Fe- 27, 24, 28, Co- 29, 30, 28, and Ni- 26, 31, 28 doped graphene materials have been successfully produced. In general, there exist two available methods for depositing transition metals onto graphene-based materials. These are the direct adsorption on graphene sheets 32, 33, 34, 35, 36, 37, 38 and substitution via vacancy defects 39, 40, 41, 42. The most stable adsorption sites of Fe/Co/Ni on graphene have been verified using scanning tunneling microscopy (STM) 43, 44, 45. Additionally, the magnetic moment of Co-absorbed graphene is delicately measured by STM spin-excitation spectroscopy 45. From a theoretical point of view, the previous studies are conducted on many adatom types of transition-metal-doped graphene systems 25, 26, 23, however, the close relations among the geometrical structure, electronic properties, magnetic configuration, and various adatom concentrations as well as their distributions have not been thoroughly analyzed from the numerical calculations. The multi-orbital hybridization between adatom and graphene, an important issue in understanding the electronic properties modifications, is only slightly mentioned in several studies. Most of them mostly focus on low adatom-concentrations 23, 46 and on investigation of the high-concentration (case 50% single-side doping) 22 in the absence of any detailed discussions. That is, the critical mechanisms and pictures for the distinct physical properties are so far lacking.
In this paper, a theoretical framework is further developed to systematically investigate the orbital hybridizations and spin distributions, which play critical roles in creating the diverse electronic properties and magnetic configurations of the structures under investigation. It should be noticed that the single- or multi-orbital chemical bondings can be revealed from the atom-dominated energy bands, the spatial charge distributions, and the atom- and orbital-projected DOS. Additionally, the magnetic configurations, namely non-magnetic, ferromagneti, and anti-ferromagnetic, are examined by using spin-split band structures, the magnetic moments, and the spin-decomposed DOS. For example, the electronic properties of oxygen doped monolayer and few-layered graphene structures (finite-gap semiconductors, zero-gap semiconductors, and semimetals) due to the critical chemical bondings in C-C, C-O, and O-O bonds are indentified by the O-, (C,O)-, and C-dominated bands, the spatial charge density before and after oxygen adsorptions, and the orbital-projected DOS 13. The anti-ferromagnetic configurations of zigzag graphene nanoribbons, being created by the carbon edge’s spins, are observed in the spin-degenerate band structure and DOS, and the opposite spin directions across the ribbon centers 47. This will serve as a first step toward a full understanding of the varied electronic and magnetic properties not only for adatom-doped graphene systems, but also could be further generalized for other one-dimensional (1D) and 2D materials such as silicene-, germanene-, tinene-, MoS-, and phosphorene-related layered systems. This work provides accurate results for the diversified properties due to the Fe-, Co-, and Ni-adsorptions with a wide range of adatom concentrations from fully (100%; double-side) to low adsorptions (3%; single-side) through first-principles calculations by employing the density functional theory (DFT) 48. Most important of all, concise chemical and physical pictures are proposed to account for the presented rich and unique phenomena.
The first-principles calculations on Fe, Co and Ni-adsorbed graphene systems include determining the binding energies, bond lengths, positions and heights of adatoms, atom-dependent band structures, adatom-induced free carrier densities, spatial charge distributions, spin configurations, magnetic moments, and atom-, orbital- and spin-projected DOSs. The meticulous analyses of the calculated results are very useful for fully understanding the cooperative/competitive relations between the honeycomb lattice, the critical orbital hybridizations in carbon-adatom bonds, and the spin configurations. Whether there exist distinct electronic properties (semiconductors or metals) and magnetic configurations (non-magnetism, ferromagnetism, and anti-ferromagnetism) is carefully explored.The above-mentioned results can be verified by experimental measurements, such as, STM 43, TEM 49, angle resolved photoemission spectroscopy (ARPES) 50, and scanning tunneling spectroscopy 51(STS). Our complete and reliable results should be very helpful in the design and development of potential device applications.
2 Theoretical model
We note here that our first-principles calculations were performed with the use of the density functional theory through the Vienna ab initio simulation software package (VASP) 52, 53.The projector augmented wave method was employed to evaluate the electron-ion interactions 54, whereas the electron-electron Coulomb interactions belong to the many-particle exchange and correlation energies under the Perdew-Burke-Ernzerhof generalized gradient approximation method 55. To carefully explore the chemical adsorption effects on the magnetic properties, the spin configurations are taken into account. The vacuum distance along the z-axis is set to be 15 in order to suppress the van der Waals interactions between two neighboring cells. A plane-wave basis set, with a maximum energy cutoff of 500 eV is available in the calculations of Bloch wave functions. All atomic coordinates are relaxed until the Hellmann-Feynman force on each atom is less than 0.01 eV/. The pristine first Brillouin zone is sampled in a Gamma scheme along the two-dimensional periodic direction by k-points for structure relaxations, and then by -points for further evaluations on electronic properties. Equivalent -point mesh are builded for other enlarged cells depending on their sizes. Furthermore, the van der Waals force, which utilizes the semiemprical DFT-D2 correction of Grimme 56 is very useful in understanding the significant atomic interactions between layers.
A fitting question which might be asked is how many kinds of electronic properties (finite-gap semiconductors, zero-gap semiconductors, semimetals and metals) and magnetic configurations (non-magnetism, ferromagnetism and anti-ferromagnetism) will be verified using the proposed theoretical framework. The answer lies in the way we deal with the delicate atom- and orbital-projected DOS, the atom-dominated energy bands and the spatial charge densities before and after the adatom adsorptions, which provide much information about the dominating chemical bondings. They could be used to identify the complex multi-orbital hybridizations in C-C, C-T and T-T chemical bonds, being one of the topics we focus on. Such bondings play a critical role in the fundamental properties, accounting for the rich and unique geometric structures and electronic properties of the Fe/Co/Ni-doped graphen systems. Moreover, the spin distributions are important for creating the diverse magnetic configurations. The spin-polarized calculations are utilized to confirm the Fe-, Co- and Ni-enriched magnetic configurations by the use of magnetic moments, spin-split energy bands, spin arrangements, and spin-projected DOS.
3 Geometric, electronic and magnetic properties
The various Fe/Co/Ni-adsorption structures, critical multi-orbital hybridizations, significant nonmagnetism/ferromagnetism, and metallic/semiconducting behaviors are worthy of systematic investigation. The typical adatoms, concentrations, and distributions will clearly illustrate diversified phenomena. The up-to-date experimental examinations and potential applications are also discussed in this section.
3.1 Optimal geometric structures
The fundamental properties of transition-metal-adsorbed graphene systems are fully explored under the various adatoms, concentrations and distributions. Based on the completely calculated results, transition metals are preferably adsorbed at the hollow-site compared to the top- and bridge-sites, which is consistent with previous theoretical predictions 25, 57, 26, 58. The adatom distribution of transition metals on a graphene surface could be examnied by experimental measurement, for which STM is an efficient tool. The hollow-site adsorption of Co and Ni adatoms on graphene has been successfully executed using STM 43, 44, 45. Specially, it is very hard for STM measurements to verify the single doping site of Fe on graphene at low concentrations due to its small difussion barrier 59. The main characteristics of optimal geometries, the C-C bond lengths, C-T bond lengths, and heights of the T adatoms relative to the graphene plane, are strongly dependent on the adatom configurations, as obviously indicated in Table 1. Clearly depicted by the side-view structure in Fig. 1, Fe/Co/Ni-doped graphene configurations do not generate significant buckling even at high concentrations. That is, the planar honeycomb lattice almost remains planar so that the bondings due to (2s,2p,2p) orbitals of carbon atoms hardly change after the strong chemisorption (discussed later pertaining to Fig. 6). The nearest C-C bond lengths of passivated C atoms are slightly increased in the specific ranges of 1.43-1.46 , reflecting the weak modifications in the bondings. Regarding the C-T bond lengths and adatom heights (measured from the graphene plane) at low concentrations (Fig. 1(f)), their magnitudes slightly vary within the range of 2.11-2.13 and 1.51-1.54 , respectively. At high concentration, the C-T bond lengths and adatom heights are increased to almost 3.0 at 100% T-concentrations, which we discuss later on.
The binding energy, which characterizes the lowered total ground state energy after the chemical adsorption of transition metal adatoms, is expressed as: , where , , and are the total energies, corresponding to the adatom-adsorbed graphene system, the graphene sheet and the isolated transition metal atoms, respectively. Also, is the number of adatoms per unit cell. In general, based on our calculated results, presented in Table 1, Fe-adsorbed graphene systems are more stable than the Co- and Ni-adsorbed cases at high-concentration, which is in agreement with previous results presented in 60, 22, 59. Specifially, for the highest concentrations (100% for the double-side adsorption), when the C-C bond length is increased from 1.4 Å to 1.7Å during the optimization procedure, and the height of adatom is significantly to lie in the range of 3.2 1.3 Å as shown in Fig. 2. This might be due to the van der Waals interactions between adatom layers and graphene plane 61. Based on the total ground state energy, the larger interlayer distance between an adatom and graphene shows greater stability, in which the corresponding C-C bond length and adatom height of 1.45Å and 3.0 Å is the most stable. These adatom heights could be verified using transmission electron microscopy (TEM), a useful tool for identifying the interlayer distances of few-layer graphene 49.
3.2 Electronic properties and magnetic configurations
The 2D band structures along the high-symmetry directions are helpful in examining the main features of the electronic properties. For pristine monolayer graphene in Fig. 3(a), there exists a pair of linear valence and conduction bands intersecting at the K/K point because of the hexagonal symmetry. The intersection is located at the Fermi level () and is usually referred to as a Dirac point. The sp orbitals of (2s,2p,2p) form very strong covalent -bonds between nearest-neighbor carbon atoms, while the 2p orbitals create perpendicular bondings, thereby leading to the low-lying a Dirac cone structure. The orbitals form the valence bands at the deeper-energy range of eV, in which the band edge states initiate from the point. On the other hand, the valence and conduction bands dominate the electronic structures when 2.5 eV. This is responsible for most of the essential properties. e.g., magnetic quantizations 62 and quantum Hall effects 63. Regarding the middle-energy electronic states, the saddle points are closely related at the points (the middle ones between two corners in the hexagonal first Brillouin zone, as shown in the inset of Fig. 3(a)). Such critical points in the energy-wave-vector space accumulate a lot of states. Therefore, they are expected to exhibit the unusual van Hove singularities for the DOS (shown in Fig. 7) and thus the special optical absorption structures 64, 65.
The low-lying Dirac-cone structure of graphene is dramatically modified after the Fe/Co/Ni-adsorptions. For low-concentration distributions (as presented in Figs. 3(b)-3(d)), Ni-doped graphene (shown in Fig. 3(d)) differs from the other two adatoms cases, whereby the former is a zero-gap semiconductor and the latter cases are semimetals. This can be observed from the position of the Dirac-cone structure compared with the Fermi level (marked by green ellipses). For Fe and Co-doping configurations with energy bands in Figs. 3(b) and 3(c), the Fermi level appears at the conduction Dirac cone, indicating the induced free electrons (n-type doping). In case of Ni-doping (3(d)), the Dirac point remains the same at as pristine case. The similarity among Fe, Co, and Ni bands is that their Dirac-cone structures formed by 2p orbitals of carbons are isotropic in the range of 0.5 eV and becomes anisotropic in the presence of band mixing with the adatom-dominated ones. Moreover, there exists spin-up and spin-down energy band splittings near the K and M points except for the case of Ni-doping. There exist the newly created flat s in the energy range of eV to 1 eV, mainly dominated by transition metal and carbon atoms, as shown by the blue circles contribution, in the valence and conduction bands, respectively. This indicates that adatoms make major contributions from low-lying valence electronic states.
The significant Fe/Co/Ni-adsorption modifications of the electronic structure can be achieved by tuning the concentration and distribution of adatoms, as clearly presented in Figs. 4(a)-4(h). There still exists a Dirac-cone structure for even fully absorded configurations, indicating that the bondings are not terminated due to the substantial adatom heights. It is well known that the Dirac cone of graphene is initiated from the K valley. However, it is worth noting that in some unit cells, e.g., corresponding to Figs. 1(a), 1(c) and 1(e), it will be transferred to the point as a consequence of the of zone-folding effect. The Dirac point, originally locates at the Fermi level, has a blue shift of 00.8 eV corressonding to the increasing of T-concentrations. In addition to the anisotropy for 0.5 eV around the Dirac point, the Dirac cone structure quicly becomes parabolic then partially flat bands. Specifically for the case of Fe doping at 5.6%. This illustrates the semiconducting case arising from the slightly separated Dirac cones. This unusual result id likely due to the partial frustration of the bonding extended in the honeycomb lattice, and we refer to Fig. 4(d). There exist important differences between the high and low adatom-concentrations. At high T-concentration (larger than 50%), the electronic dispersions are fully or partially dominated by the adatoms, indicating the T-T and T-C bonding, in a wide energy range -4 eV 2 eV. Under lower concentrations, the T-dominated bands become narrower. Based on a literature review, the Fe/Co-doped systems are classified as magnetic materials whereas the Ni-doped case is non-magnetic 25, 66, 26. After detailed and careful calculations, our results show that this is true only for low Ni-concentration. At high Ni-concentration, e.g. 100% as shown in Fig. 4(g), the system also has spin-up and spin-down energy splitting, indicating a ferromagnetic configuration. At lower concentrations, they possess zero magnetic moments, as shown in Table 1, resulting in the absence of spin split bands, as we can see in e.g, Fig. 4(h). More details related to the magnetic configurations will be discussed later in the spin density subsection (Figs. 5). On the other hand, the deeper strong band is hardly affected by the hollow-site chemisorption, only slightly modified at high T-concentrations (partially T-C co-dominated bands). Obviously, there exist a red shift of the band 0.10.8 eV away from , depending on adatom types and concentrations.
From an experimental point of view, the rich features of the band structure could be investigated with the use of ARPES. It is worth noting that ARPES has been employed as a powerful experimental tool to probe the electronic band structure of graphene-related systems, which is not possible in a transport measurement. It has been used to confirm the Dirac cone linear energy dispersion for graphene layers on SiC 67. Moreover, ARPES can be used to verify the effects due to doping. High-resolution ARPES observations on chemically doped graphene of Li 68, 69 and K 70, 71 atoms have confirmed high density of free electrons in the linear conduction band as evidenced by a red shift of 1.0 1.5 eV of the and bands. Similarly, the Dirac-cone shift of about 2.6 eV below the Fermi level is observed for graphene-capped Ni silicides 50. The feature-rich bands of transition metal doped graphene, including the red shift of the Dirac point, the degeneracy and anisotropy with different slopes of the Dirac-cone structure, and the adatom-dependent energy bands, can furthermore be examined with ARPES.
The configurations for the spin density distributions could provide additional information regarding their magnetic properties. All the Fe-doped graphene structures display ferromagnetic behavior, as it is clearly illustrated in Figs. 5(a) and 5(h). The spin-up magnetic moments almost dominate the spin-density arrangement, being closely related to the adatom-dominated spin-split energy bands near the Fermi level (Figs. 3(b) and 4(a)-4(d)) and the low-energy DOS of adatom orbitals (Figs. 7(a)-7(d)). This is in good agreement with the spatial spin densities accumulated around the adatoms (Figs. 5(a)-5(h)). Typical magnetic moments per Fe adatoms are about 2-3 (Bohr magneton). They are sensitive to adatom concentrations and distribution configurations (Table 1). In addition, similar ferromagnetic configurations with magnetic moment 1-2 per adatom are observed in Co-adsorption graphene (e.g., fully occupied case in Fig. 5(g)). On the other hand, Ni-doped graphene exhibits an average magnetic moment of 0.83 per adatom under full and half adsorption cases, whereas the non-magnetic behavior comes to exist at low Ni-concentrations. Obviously, the ferromagnetic moment rapidly decreases in the order of Fe Co Ni adatoms. This behavior also occurs for other Fe/Co/Ni related systems, such as Fe/Co/Ni clusters and monolayers on Au/Ir/Pt (111) 72, XPt (X= Fe,Co,Ni) 73, and Fe/Co/Ni nanowires encapsulated in SiC nanotube 74. In addition to the dependence on adatom type, the magnetic moment is almost proportional to the percentage of transition metal adatoms, which might be due to the interaction between adatoms. We note that the transition metal-created magnetic properties on graphene surfaces could be verified using spin-polarized STM 75, 76.
The charge density , presented in Figs. 6(a)-6(d), and the charge density difference in Figs. 6(e)-6(g)) can provide very useful information regarding the orbital hybridization as well as an understanding of the dramatic changes in the electronic properties. The latter is created by subtracting the charge density of graphene and transition metal atoms from that of the whole system. Apparently, the bonding, which is formed perpendicular and continuously extended on a graphene plane, could survive in all Fe/Co/Ni-adsorbed graphene-related systems, as clearly illustrated by the Dirac cone structure in low-lying energy bands, and for this we refer to Figs. 3 and 4. However, for all concentration ranges (from 100% to 3.1%), it is still somehow affected by the extra transition metal atoms as evidenced by the pink rectangles in Figs. 6(b)-6(d) and the pink arrows in Figs. 6(e)-6(g). This implies that the T-C bond between (4s,3d) orbitals of the adatom and the 2p orbital of carbon. On the other hand, the strong bondings, with very high charge density between two carbon atoms as seen in the red regions inside the black rectangles of Figs. 6(b) and 6(c) hardly depend on the Fe/Co/Ni adsorptions, corresponding to the slightly modification of at high adatom concentration (Figs. 6(e) and 6(f)) then vanishing at lower concentrations (e.g, 3.1% in Figs. 6(g)). This is responsible for the red shift of the carbon- bands at deeper energies of co-dominated (Fe/Co/Ni)-C bands in the middle energy. Specifically, the observable charge variation within the x-y plane is seen between two neighboring transition metal atoms at sufficiently high concentrations (100% in Fig. 6(e)), clearly indicating the multi-orbital hybridization of T-T bonds. In short, there exist T-T, T-C and C-C bonds, for which the former is observed under higher concentrations.
The main characteristics of the band structure are directly reflected in the atomic, orbital and spin-projected DOS, which is responsible for the orbital contributions and hybridization in chemical bonds. The form, number and energy of the special structures in the DOS, originating from the band-edge states (the critical points in energy-wave vector space), are very sensitive to chemical bonding and Fe/Co/Ni concentrations. A dip, marked by red circles in Fig. 7(a), prominent symmetric peaks, and shoulder structures come from the almost linear bands, the saddle point and the local extrema points, respectively. For pristine graphene, the and prominent symmetric peaks due to 2p-2p bondings between C atoms dominate the DOS within the range of 2.5 eV 77. Furthermore, the isotropic Dirac cone creates vanishing DOS at the Fermi level. Therefore, monolayer graphene is a zero gap semiconductor (Fig. 7(b)). In general, these two prominent peaks emerge into several more because of zone-folding effects. The 2p-dependent DOS of carbon atoms are drastically changed after adsorption. The orbital- and spin-projected DOSs show very complex van Hove singularities and thus identify the significant multi-orbital hybridizations in T-C, C-C and T-T bonds. All the Fe/Co/Ni-adsorbed graphene systems (Figs. 7(b)-7(g)) present a structure with a dip due to the Dirac cone at low-lying energies with an obvious blue shift from the Fermi momentum states, except the case of low-concentration Ni (Fig. 7(h)) with vanishing DOS at .
There exist a considerable number of unusual T-dominated van Hove singularities, mainly arising from the (4s,3d,3d,3d,3d,3d) orbitals of (Fe/Co/Ni) atoms as a result of the T-T bonds in a wide range of eV to . At higher concentrations, the Fe/Co/Ni-dominated DOS is created with broadened energy range, indicating the T-T bonds of (3d,3d,3d,3d,3d) orbitals. Particularly, there are two pairs of orbital hybridizations, (3d, 3d) and (3d, 3d) and multi-hybridizations between them with 3d orbital, in which 3d orbitals contribute to the presence of the prominent peaks. Except for low concentration Ni-doped system (Fig. 7(h)), the DOS with regard to the conduction -states is finite at , indicating high induced free carrier density. At low T-concentrations (Figs. 7(e), 7(f), and 7(h)), the distorted and peaks are gradually recovered with spin-up and spin-down splitting for the cases of Fe/Co-adsorbed graphene and without splitting for the ones of Ni adsorption. Part of the peaks of C atoms (pink curve) are co-dominated by the Fe/Co/Ni-created peaks at -3.0 eV E 2 eV, clearly illustrating significant hybridization of (4s,3d,3d,3d,3d,3d) orbitals of (Fe/Co/Ni) atoms and 2p orbitals of C atoms. Apparently, the co-dominated peaks between the 2p orbital of carbon and (3d, 3d) and (3d, 3d) orbitals of transition metals are illustrated by the yellow and cyan color arrows, respectively. Moreover, at very low concentration, such as 5.6% and 3.1%, the 2p4s hybridization in the C-T bonds (marked by green arrows) appear at the range of 0.2 1.2 eV. In addition, the orbital-projected DOS also agrees well with the predictions from band structure and spatial charge densities that the bonds between carbon atoms almost do not take part in the T-C bond (except at very high concentrations) and only show a slightly red shift from (marked by the deep blue arrows).
So far, STS measurement has been considered to be a powerful tool for examining special features in the DOS. The differential conductance (dI/dV) is approximately proportional to the DOS and directly reflects the shape, number and intensity of special structures in the DOS. Additionally, STS 51 and spin-polarized STS could be used to identify the unusual electronic and magnetic configurations, and has served to verify the finite DOS near of graphene flakes on graphite 78, the Fermi level red shift of Bi-doped graphene 79. The aforementioned characteristics could also be verified by STS measurements on special features of the DOS, including the dip structure below/near , the transition metal-induced extended peaks, and the preserved shoulder. Measurements with STS on the low and middle-energy peaks are expected to identify the configurations and concentrations of different transition-metals types adsorbed on graphene.
Hitherto, graphene-based devices are fast developed, owing to their vital potential. Fe/Co/Ni-doped graphene materials are well-known in the application of gas sensors to absorb harmful gas molecules such as CO, CO, SO and HS 80, 81, 82, 83, 84, 58. It also could be high performance electrocatalysts for oxygen reduction 85. Moreover, the performance of Li-ion batteries (LIBs) can be improved by inserting graphene into the anode to achieve morphological optimization and performance 86, 87, 88. Graphene can be added in the manufacture of batteries that are light, durable and suitable for high capacity energy storage, with greatly reduced charging time. It is expected that future studies on adatoms adsorbed graphene will achieve many interesting applications. As reported, transition metal (Fe/C/Ni) oxides have been grown on graphene at hollow sites based on the Kirkendall effect 89. Compared to most transition metals to date, this material shows excellent performance as an anode for LIB with strong reversible capacities and stability at a high current density. When transition metal atoms are adsorbed on graphene, the bonding in pristine graphene is modified due to complex hybridization of 2p orbitals of C atoms and the (4s,3d,3d,3d,3d,3d) orbitals of (Fe/Co/Ni) adatoms. This leads to the transformation from zero-gap semiconductor (pristine graphene) to semimetallic systems (doped-systems). The energy difference between the Fermi level and the Dirac point increases with higher adatom concentrations, indicating a larger number of free electrons in the conduction cone. This implies that the electronic conductivity of Fe/Co/Ni-doped graphene is somehow enhanced since the conductivity is proportional to the carrier concentration. Further systematic studies are needed to find out the most suitable absorbers on graphene in order to replace graphite in the anode material of LIBs.
4 Concluding remarks
We have demonstrated that the chemical and physical properties of transition metal-doped graphene systems are enriched by their configurations and the concentration of adatoms. Their geometrical, electronic and magnetic properties are closely related to the complicated hybridizations between 2p orbitals of the C atoms and the (4s,3d,3d,3d,3d,3d) orbitals of Fe/Co/Ni. The significant orbital hybridization, the strong bonding and the weak bonding greatly diversify the band structures. Transition metal adsorbed graphene might exhibit anisotropic and a split Dirac cone structure, as well as (T-T)- and (C,T)-dominated bands at low-lying energies. There exist significant differences between Fe/Co and Ni configurations. Most of our investigated systems display semimetallic behavior except the low-Ni concentration cases. Additionally, the spin distributions are found to be important for creating the diverse magnetic configurations. Specifically, for passivation of the same sublattice, ferromagnetic configurations are revealed for all the Fe/Co-doped systems but only for high Ni-concentration systems. Concerning the DOS, the extra orbital hybridizations are revealed in the DOS as several merged structures when -3 2 eV. A decrease in T-concentration results in more low-lying special structures arising from the and electronic states.
The theoretical framework proposed in this work will be useful for characterizing other emergent materials, since we have demonstrated its effectiveness for examining the rich and unique properties of low-dimensional structures. Further experimental examiation involving STM, ARPES, and STS, is desirable for the aforementioned main structures of the geometric and electronic properties of Fe/Co/Ni-adsorbed graphene systems. These materials are expected to play a role in potential applications in gas sensors and LIBs’ anode. The present work should serve as a first step towards further investigation into other necessary properties of transition metal-doped graphene for fabrication and potential device applications. In addition, it could pave the way for tight-binding model researchers in determining the important hopping integrals (atomic interactions).
This work was financially supported by the Hierarchical Green-Energy Materials (Hi- GEM) Research Center, from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) and the Ministry of Science and Technology (MOST 107-3017-F-00-003) in Taiwan.
|C-C (Å)||C-T (Å)||(Å)||(eV)||(eV)||()|
Side- and top-view geometric structures of Fe/Co/Ni-doped graphene for various concentrations and distributions: (a) T:C = 2:6 = 33.3%, (b) T:C = 2:8 = 25%, (c) T:C = 1:6 = 16.7%, (d) T:C = 1:8 = 12.5%, (e) T:C = 1:18 = 5.6%, and (f) T:C = 1:32 = 3.1%.
Total ground state energy () and the height between graphene and adatom layer of fully Fe/Ni-adsorptions with respect to various nearest C-C bond lengths.
Band structures in a supercell (32 C atoms per cell) for (a) monolayer graphene, and the (b) Fe-, (c) Co-, and (d) Ni-doped graphene with concentration T:C = 1:32 = 3.1%. The blue circles represent the contributions of adatoms. The red and black curves correspond to the spin-up and spin-down states, respectively.
Band structures of Fe-, Co- and Ni-doped graphene: (a) Fe:C = 6:6 = 100% (double-side), (b) Fe:C = 3:6 = 50% (single-side), (c) Fe:C = 1:8 = 12.5% (single-side), (d) Fe:C = 1:18 = 5.6% (single-side), (e) Co:C = 6:6 = 100% (double-side), (f) Co:C = 1:18 = 5.6% (single-side), (g) Ni:C = 6:6 = 100% (double-side), and (h) Ni:C = 1:18 = 5.6% concentrations. The blue circles correspond to the contributions of adatoms.
The spin-density distributions with top and side views under different concentrations and distributions: (a) Fe:C = 6:6 = 100%, (b) Fe:C = 2:6 = 33.3%, (c) Fe:C = 1:6 = 16.7%, (d) Fe:C = 1:8 = 12.5%, (e) Fe:C = 1:18 = 5.6%, (f) Fe:C = 1:32 = 3.1%, (g) Co:C = 6:6 = 100%, and (h) Ni:C = 6:6 = 100%. The red isosurfaces represent the charge density of spin-up configuration.
The spatial charge densities for: (a) pristine graphene, (b) Fe:C = 6:6 = 100%, (c) Fe:C = 1:8 = 12.5%, and (d) Fe:C = 1:32 = 3.1%. The corresponding charge density differences of Fe-doped graphene are, respectively, shown in (e)-(g).
Orbital-projected DOS of Fe-, Co- and Ni-doped graphene for concentrations and distributions: (a) pristine graphene, (b) Fe:C = 6:6 = 100%, (c) Fe:C= 3:6 = 50%, (d) Fe:C = 1:8 = 12.5%, (e) Fe:C = 1:32 = 3.1%, (f) Co:C = 1:32 = 3.1%, (g) Ni:C = 6:6 = 100%, and (h) Ni:C = 1:32 = 3.1%. The dim vertical red line illustrates the Fermi level.
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