Superconductivity of strongly correlated electrons on the honeycomb lattice

A microscopic theory of the electronic spectrum and of superconductivity within the t-J model on the honeycomb lattice is developed. We derive the equations for the normal and anomalous Green functions in terms of the Hubbard operators by applying the projection technique. Superconducting pairing of d + id′-type mediated by the antiferromagnetic exchange is found. The superconducting Tc as a function of hole doping exhibits a two-peak structure related to the van Hove singularities of the density of states for the two-band t-J model. At half-filling and for large enough values of the exchange coupling, gapless superconductivity may occur. For small doping the coexistence of antiferromagnetic order and superconductivity is suggested. It is shown that the s-wave pairing is prohibited, since it violates the constraint of no-double-occupancy.


Introduction
Graphene, the two-dimensional carbon honeycomb lattice, has been recently extensively studied due its peculiar electronic properties caused by the low energy cone-type electronic spectrum at the Dirac points K and K in the Brillouin zone (BZ) (for a review see [1]). The effects of electronic interactions play a minor role close to halffilling at low density of electronic states at the Dirac points, but for large doping interactions appear to be important. Studies of graphene beyond the simple model of noninteracting electrons by taking into account the Coulomb interaction reveal a rich phase diagram with phase transitions to the antiferromagnetic (AF) state, spin-density wave (SDW), charge-density wave (CDW), and unconventional superconductivity (SC) (for a review see [2]).
The superconducting order parameters in the twodimensional honeycomb lattice described by the hexagonal symmetry group D 6h have a complex character. A general symmetry analysis of available irreducible representations (IR) and superconducting order parameters is given in reference [3]. In the case of the singlet pairing, the extended s-wave s x 2 +y 2 order parameter (E 1g IR), d x 2 −y 2 and d xy order parameters (E 2g IR) preserving the time-reversal symmetry and its time-reversal symmetry breaking complex combination d x 2 −y 2 ± id xy (d ± id ) are commonly discussed. The triplet pairing with the a e-mail: plakida@theor.jinr.ru p x + ip y (p + ip ) order parameter (E 1u IR) is also often discussed in the literature. This symmetry consideration is very important in discussing SC in graphene. But it can also be applied in studies of other electronic systems with the two-dimensional honeycomb lattice, such as the transition metal dichalcogenides [4].
Several models of the Bardeen-Cooper-Schrieffer-type (BCS) were discussed. In reference [5] a model with the on-site and the nearest-neighbor (nn) electron interactions of the BCS-type was considered. Assuming bondindependent anomalous correlation functions on the nn lattice sites, the s-wave pairing with k-independent gap induced by the on-site interaction and the extended s-wave pairing induced by the nn interaction were found. At the Dirac points close to half filling the latter can be described as p + ip phase. At large value of coupling constants a gapless SC emerges at half-filling.
The superconducting phase transition caused by the Coulomb interaction was studied within the Hubbard model [6] on the honeycomb lattice in a wide range of the on-site Coulomb repulsion U/t from weak to strong coupling (in graphene U/t = 4-5 and t ∼ 2.8 eV [1]). The renormalization group (RG) approach was used in [7] to study phase transitions in the extended Hubbard model with the on-site interaction U , the nn repulsion V , and the spin-exchange interaction J. Close to half-filling, the SDW or CDW orders occur for large U and V , while for a large doping f -wave triplet-pairing and d + idwave singlet-pairing emerge. In reference [8], the extended Hubbard model for graphene with the nn repulsion V and on-site interaction U was considered. Using the variational cluster approximation and the cellular dynamical meanfield theory the SC of different symmetries was studied. Depending on the values of V and U , the triplet p-wave symmetry and the chiral combination p + ip were found, while the singlet SC (extended s-or d-wave) was not clearly detected.
Superconductivity on the honeycomb lattice is commonly studied also within the phenomenological t-J model, where the exchange interaction (J ∼ t) is considered as a fitting parameter. In reference [9] SC was studied in a graphite layer within the resonating valence bonds (RVB) approach [10] for the t-J model. Both the extended s-wave and d-wave pairing with the order parameter determined by bond-dependent anomalous correlation functions were considered. The superconducting T c for the d-wave pairing appears to be much larger than for the extended s-wave pairing and has a high value with a maximum at doping δ = 0.25. A similar model was considered in reference [11] for the d + id -pairing with the bond-dependent anomalous correlation functions. The spectrum of electronic excitations in the superconducting state is determined by two gaps g ± = |∆(±k)| with spin up in one valley and spin down in the other valley with zeros at K and K points of the BZ, respectively. The excitations are gapless at half filling for any value of the coupling constant. The t-J model with the on-site interaction of intermediate strength U/t = 2.4 was considered in reference [12] using the variational Monte Carlo study. The superconducting ground state with the d + id pairing for doping 0 < δ < 0.4 was found. It was estimated that the superconducting T c can reach room temperatures at an optimal doping around δ = 0.15. The extended t-J model with the nn and the next-nearest-neighbor (nnn) exchange interaction J 1 and J 2 , respectively, was considered in reference [13]. In the heavily doped case (around 3/8 and 5/8 filling), a chiral d + id symmetry was obtained. The competition between antiferromagnetism and SC in the vicinity of half filling was considered by applying the functional RG.
The quantum phase diagrams of both the Hubbard model and the t-J model on the honeycomb lattice at 1/4 doping were studied in reference [14]. At this doping, in the nn tight-binding model the nested Fermi surface emerges which is unstable in the presence of a weak interaction. Using a combination of exact diagonalization, density matrix renormalization group, the variational Monte Carlo method, and quantum field theories, it was shown that in a wide range of the Hubbard repulsion, 1 < U/t < 40, or the exchange interaction, 0.1 < J/t < 0.8, the quantum ground state is either a chiral SDW state or a spin-charge-Chern liquid, but not a d + id superconductor. For the t-J model at larger J/t > 0.8 a first-order phase transition to the d + id superconductor occurs.
A detailed study of the t-J model on the honeycomb lattice was presented in reference [15]. Using the Grassmann tensor product state approach, exact diagonalization and density-matrix renormalization methods, the ground-state energy, the staggered magnetization in the AF phase, and the SC order parameter as a function of doping δ have been calculated. The occurrence of the time-reversal symmetry breaking d + id -wave SC up to δ = 0.4 was found. Moreover, a coexisting of the SC and AF order was observed for low doping, 0 < δ < 0.1, where the triplet pairing is induced (see also [16]). In reference [3], SC on the honeycomb lattice close to the Mott state at half filling was studied within the t-J model using the renormalized mean-field theory and in the Hubbard model by quantum Monte Carlo calculations. It was shown that the chiral d + id -wave state is the most favorable state for a wide range of the on-site repulsion U . At the same time, a mixed chirality d-wave state, such as a state with d + id -wave symmetry in one valley but d − idwave symmetry in the other valley, is not possible in the t-J model without reducing the translational symmetry. No energetically favorable d-wave solution with an overall zero chirality was found within the t-J model.
The van Hove singularity (VHS) scenario of SC being developed for cuprates (see, e.g., [17]) was discussed in several publications. In reference [18] the extended VHS in doped graphene was found using the angle-resolved photoemission spectroscopy. Considering the conventional fluctuation exchange approximation [19] with the weak Hubbard interaction U/t 4, the competition between magnetic instability and SC was analyzed. It was found that SC plays a dominant role when the Fermi level is placed close enough to the extended VHS, where the transition temperature T c can be quite high. In reference [20] it was shown that, due to the strong anisotropy of the electron scattering at the VHS, attractive coupling channels appear from the originally repulsive interaction that results in the superconducting pairing with T c ∼ 10 K. In reference [21] studies of the Hubbard model on the honeycomb lattice with nn and nnn interactions show the appearance of the extended VHS, where the density of states diverges in a power law. Using the random-phaseapproximation and determinant quantum Monte Carlo approaches a possible triplet p + ip SC with relatively high T c was found at low filling. The interplay between SC and SDW order in graphene close to the VHS was considered in reference [22]. The instabilities to both the chiral d + id SC and the uniaxial SDW were found in a model with four different interactions between fermions near saddle points. The SC is strongest at the VHS, but slightly away from it SDW appears first. To investigate the possibility of coexistence of SC and SDW, the Landau-Ginzburg functional was derived. It was shown that SDW does not coexist with SC, because both phases are separated by first-order transitions. The dynamic cluster approximation was used in reference [23] to study SC in the Hubbard model with U/t = 2-6. A transition from the d + id -wave singlet pairing, which dominates close to the VHS filling, to the p-wave triplet pairing at larger coupling was found.
In several studies the renormalized mean field theory for the t-J model was employed. To take into account strong correlations of electrons in the singly occupied band, the hopping parameter t and exchange interaction J were renormalized by the statistical weighting factors g t = 2δ/(1 + δ) and g J = 4/(1 + δ) 2 , as in the RVB theory for cuprates [24]. We point out that this renormalization is rather crude, e.g., for δ = 0 it results in the zero bandwidth ∼δt though at low doping spinpolaron quasiparticles appear with a finite bandwidth of the order J (see, e.g., [25]). Moreover, in the undoped case the four times stronger exchange interaction 4J results while the Heisenberg model with the original exchange interaction J should be found. The slave-boson approximation also strongly violates the statistics of the projected electrons in the original t-J model [26]. To take into account the restriction of no-double-occupancy in the t-J model, a technique for the projected electron operators, the Hubbard operators [27], should be used.
In the present paper we develop a microscopic theory of SC of strongly correlated electrons on the honeycomb lattice employing the Hubbard operator technique. This technique was used in our previous paper for the calculation of the electronic spectrum, the spin-excitation spectrum, and of thermodynamic quantities within the t-J model [28]. Using the projection operator technique [29] developed for the thermodynamic Green functions (GFs) [30,31] in reference [32], we derive equations for the normal and anomalous (pair) GFs. In the generalized mean-field approximation (GMFA) a self-consistent system of equations for the singlet order parameters is obtained and the superconducting T c as a function of doping δ is calculated. It is shown that the condition of the no-double-occupancy of quantum states in the t-J model is violated for the s-wave pairing, while the d + id pairing obeys this restriction.
The paper is organized as follows. In Section 2 the t-J model for the honeycomb lattice is formulated. Equations for the GFs are derived in Section 3. Gap equations and the calculation of T c are given in Section 4. The conclusion is presented in Section 5.

The t-J model
The Hubbard model [6] is commonly used in studies of correlated electronic systems. In the limit of strong correlations the model is reduced to the one-subband t-J model [26]. In the lattice site representation the model reads: are projected creation and annihilation electron operators on the site i with spin σ/2 (σ = ±1,σ = −σ), and the number operator n i = σã + i,σã i,σ . Here i, j denote the nearest neighbors for electron hopping with energy t and for spins S i with AF exchange interaction J.
It is convenient to employ the Hubbard operator (HO) technique [27] where the projected electron operators are written as: The HOs X nm i = |i, n i, m| describe transitions between three possible states at a lattice site i: |i, n = |i, 0 and |i, σ for an empty site and for a singly occupied site by an electron with spin σ/2, respectively.
The electron number operator and the spin operators are defined as The commutation relations for the HOs read: The upper sign refers to Fermi-type operators such as X 0σ i , while the lower sign refers to Bose-type operators such as n i (2) or the spin operators (3). The completeness relation for the HOs, X 00 i + σ X σσ i = 1, rigorously preserves the constraint of no-double-occupancy of the quantum state |i, n on any lattice site i.
In terms of HOs the t-J model (1) takes the form: We consider the t-J model on the honeycomb lattice which is bipartite with two triangular sublattices A and B. Each of the N sites on the A sublattice is connected to three nn sites α = 1, 2, 3 belonging to the B sublattice by vectors δ α , and N sites on B are connected to A by vectors −δ α : The basis vectors are where a 0 is the nn distance; hereafter we put a 0 = 1. The reciprocal lattice vectors are In the twosublattice representation it is convenient to split the site indices into the unit cell and sublattice indices, i → iA, iB.
The chemical potential µ depends on the average electron occupation number where N is the number of unit cells and ... denotes the statistical average with the Hamiltonian (5).

Green functions 3.1 Equations for the Green functions
To consider SC within the model (5), we introduce the anticommutator retarded matrix GF [30,31] where {X, Y } = XY + Y X, X(t) = e iHt Xe −iHt ( = 1), and θ(x) is the Heaviside function. Here we use Nambu notation and introduce the vector Hubbard operatorsX iσ andX † jσ with 4 components: The Fourier representation in (k, ω)-space is defined by The 4 × 4 matrix GF (8) can be written as where the components of the normal GF read aŝ and the components of the anomalous GF are given bŷ To calculate the GF (8), we use the equation of motion method. Differentiating the GF with respect to time t we obtain where Here,τ 0 is the 4 × 4 unit matrix and in the paramagnetic state, Q = X 00 iβ + X σσ iβ = 1 − n/2 . For a system of strongly correlated electrons as in the t-J model it is convenient to choose the mean-field contribution in the equations of motion (14) as the zerothorder quasiparticle (QP) energy. We calculate it in the GMFA using the projection operator method [32]. In this approach we write the operator [X iσ , H] in (14) as a sum of the linear part, proportional to the single-particle operatorX iσ , and the irreducible partẐ The orthogonality condition {Ẑ iσ ,X † jσ } = 0 determines the linear part, the zeroth-order QP energy: whereÊ ij and∆ ijσ are the normal and anomalous components of the matrix. The corresponding zeroth-order GF in (14) in the Fourier representation (10) is given by It is possible to calculate the self-energy operator given by the many-particle GF Ẑ (ir) iσ |X † jσ ω in (14) and to derive the Dyson equation for the GF (8), as has been done in our previous publications (see [33,34]). In the present paper we consider the theory in GMFA within the zerothorder approximation for the GF (17).
The components of the energy matrix (16) are determined by the commutators: Performing commutations and introducing the Fourier representation, X 0σ iA = (1/ √ N ) k e ikri X 0σ kA , we obtain: where γ(k) = α exp(ik − → δ α ) and |γ(k)| 2 = 1 + 4 cos( √ 3k x /2)[cos( √ 3k x /2) + cos(3k y /2)]. The renormalized chemical potential µ and hopping parameter t were calculated in reference [28] and are given by the relations: Here the nn correlation functions for electrons and spins are: The anomalous energy matrix for the gaps reads: Note that both gap functions ∆ σ and ∆ ABσ (k) are determined by the nn correlation functions X 0σ jB X 0σ iA , since we have no pairing on one lattice site contrary to reference [5].
Using equations (21) and (26) we obtain the energy matrix: We point out that the matrix (30) is similar to the matrix in the superconducting state in MFA for graphene obtained in references [5] and [11] but with the renormalized chemical potential µ and hopping parameter t. The GF in equation (17) is defined by the inverse matrix . Its calculation results in the GF: where A T σ (k, ω) is the transposed matrix of the cofactors of the matrix ωτ 0 − E σ (k) .
The diagonal and off-diagonal normal G αβ (k, ω) and anomalous F αβσ (k, ω) GFs components in the matrix (11) read: The coefficients A nm are given by the equations: The determinant D(k, ω) of the matrix, gives the equation for the spectrum in the superconducting state D(k, ω) = 0 which can be written in a general case (with notations ∆ σ± ≡ |∆ ABσ (±k)|) as: The solution of this equation for the extended s-pairing (see Eq. (54)) gives the spectrum of excitations: which coincides with the spectrum for graphene in MFA found in reference [5]. Note that for the gap ∆ σ = 0 the spectrum is gapless at µ = 0 at six corners of the BZ at K, K points: Ω s (k) = t |γ(k)| 1 + ∆ 2 ABσ / t 2 , as was pointed out in [5].
The spectrum for the d-pairing (see Eq. (55)) resulting from equation (41) with ∆ σ = 0 has a more complicated structure with two gaps ∆ σ± : A similar spectrum was found for the d-wave symmetry in reference [11]. Since the d-wave gap (55) is zero at three corners of the BZ at K points and has a maximum value at another three corners of the BZ at K points, the spectrum (43) is gapless at µ = 0 at K points and has a maximum value at K points (see also Refs. [2,13]).

Normal state Green function
The determinant for the normal state GFs (32) and (33) reads Here the electronic spectrum is given by the matrix (30) in the normal state (cf. Ref. [28]): The spectrum has the Dirac cone-type behavior at K and K points at the corners of the BZ as in graphene. The cones touch the Fermi surface (FS) at µ = 0 for half filling at the electron occupation number n = 2/3 in the t-J model. The detailed doping dependence of the FS was considered in reference [28]. For the normal state GFs (32) and (33) with the coefficients A 11 (36) and A 21 (37) we obtain: . (47) The density of electronic states (DOS) at the Fermi energy µ in the normal state is determined by the GF (46) and, for the dispersion ε ± (k) (45), is given by the equation: The DOS at the Fermi energy N ( µ) and the chemical potential µ for −3 ≤ µ/t ≤ 1.5 at zero temperature are plotted in Figure 1 for doping 0 ≤ δ ≤ 1. The two peaks of the DOS correspond to the VHS in two bands. The DOS is nonsymmetric with respect to µ = 0 in comparison with the DOS of graphene due to the renormalization of the hopping parameter in (48), where we use t = t Q = t (1 + δ)/2 neglecting the electron and spin contributions in equation (24). We note that there are misprints in reference [28], equations (26) and (29) for the GFs, in comparison with equations (46) and (47), where we have opposite signs. But the expressions for the correlation functions n Aσ (k) = X σ0 kA X 0σ kA and X σ0 kB X 0σ kA in reference [28] are correct.

Anomalous Green functions
To calculate the superconducting T c we use the linearized approximation for the anomalous GFs (34) and (35). They are determined by the relations: The corresponding anomalous correlation function in the gap equations (27) and (28) determined by the GF (51) is given by 4 Gap equations and T c Let us consider solutions for the gaps of different symmetries. In particular, the extended s-wave gap (28) determined by the bond-independent anomalous correlation function (53) can be written as: The d + id -wave pairing is determined by the gap which has different phases on bonds (Refs. [9,11,15]): The numerical solution of the gap equations yields T c as a function of doping given below, where we use the renormalized hopping parameter t = t (1 + δ)/2 (see Sect. 3.2). Note that in our mean-field approach in two dimensions, T c is the temperature of Cooper-pair formation without superconducting long-range order (see, e.g., Refs. [2,5]). It should be pointed out that for the conventional Fermi-liquid we can have the s-wave pairing on a single site given by the anomalous correlation function a iσ a iσ . In terms of HOs this pairing can be described by the equation: which shows that the double occupancy of one lattice site is permitted but in the two Hubbard subbands. For the Hubbard model in the limit of strong correlations, i.e., for the t-J model, this pairing is prohibited due to the nodouble-occupancy restriction which in terms of HOs, as was proposed in reference [35], can be written as: As shown in Section 4.4, both the k-independent s-wave pairing with the gap (27) and the extended s-wave pairing with the gap (54) violate this condition and must be excluded from a rigorous point of view. For the d-pairing with the gap (55) the condition (57) is fulfilled. However, in several publications this constraint has not been rigorously taken into account, for example using the phenomenological t-J model (see Ref. [9] where the double-site occupancy is included in the Hilbert space), or introducing the statistical weighting factors g t = 2δ/(1 + δ) and g J = 4/(1 + δ) 2 in the t-J model (see Refs. [3,13]), as discussed in Section 1, or using the Gutzwiller projector P g = i (1 − g n i↑ n i↓ ) with g < 1 treated as variational parameter (see, e.g., Ref. [12]). To compare our results with these studies we have considered the k-independent s-wave pairing in Section 4.1 and the extended s-wave pairing in Section 4.2.

k-independent s-wave gap equation
For the k-independent s-wave gap (27) we have Assuming that t J we can solve the equation for ∆ σ considering the q-dependent part of the gap ∆ ABσ (q) in A σ 41 (ω, q) (52) as a small perturbation. We obtain the gap equation: We find a solution for T c only for hole doping δ ≤ 0.32 whenμ > 0. It has a high maximum value, T c ∼ 0.25t, due to the strong pairing interaction t J. Note that the coupling proportional to the hopping parameter t is due to the kinematical interaction induced by the commutation relations (4) for the HOs. The same type of pairing occurs in the t-J model on the square lattice (see Ref. [35]) which has been disregarded, since it violates the constraint of no-double-occupancy (57). As shown in Section 4.4, the s-wave pairing described by the k-independent gap ∆ σ (58) on the honeycomb lattice also violates the constraint (57), and in what follows we take the solution ∆ σ = 0.

Extended s-wave gap equation
Using equation (53) the gap equation (28) reads Taking into account that the second term vanishes for the bond-independent gap ∆ ABσ (k) = ∆ ABσ γ(k) because of γ(q)|γ(q)| 2 − γ * (q) γ 2 (q) = 0 , we obtain the gap equation The solution of this equation shows that T c (δ) linearly increases with doping and vanishes for large δ depending on J, e.g., T c (δ) = 0 at δ > 0.2 for J = t/2. The maximum value of T c rapidly increases with the interaction J, e.g., T max c = 0.035 t (0.082 t) for J = t/3 ( t/2). Though the extended s-wave pairing also violates the constraint of no-double-occupancy (57), we consider it to compare our results with calculations for the t-J model, where this restriction has not been rigorously taken into account.

d-wave gap equation
In the case of d-wave symmetry (d + id ) for the bonddependent gap (55) we have the same equation (60). The direct numerical calculation for this gap reveals that the second term in the integral gives no contribution. It is convenient to consider the equation for a particular value of α for the phase sensitive contribution: Cancelling out the terms ∆ 1σ exp[ikδ α ] we write this equation as Considering the vectors a βα ≡ δ β − δ α we can see that different values of β − α correspond to a set of three vectors, one is equal to zero, and the other two are the lattice vectors. The change of α rotates the whole set by 2π/3 due to the C 3 symmetry of the lattice so that the above equation does not depend on α. Therefore, all three equations for various α are the same. The equation for α = 0 reads:  This equation was solved numerically for various values of J/t. The results for T c as a function of the hole doping δ are depicted in Figures 2 and 3. T c (δ) has a two-peak structure with the maxima corresponding to the VHS in the DOS shown in Figure 1.
The transition temperature T c rapidly increases with the interaction J/t in equation (64), as was also found in reference [9]. For small J/t = 1/3 in Figure 2 we get a smooth increase of T c with δ and T c = 0 (or exponentially small) for δ < 0.05 similar to the d-wave pairing in the one-band t-J model on the square lattice (see Ref. [33]). In reference [15] for J/t = 1/3 the superconducting order at T = 0 was found for 0 < δ < 0.4, but in reference [9] T c is exponentially small for δ < 0.05 when J = 0.8 t. For J = 3 t/4 in Figure 3 the maximum of T c ≈ 0.15t is comparable with the maximum value of T c ≈ 0.1t in reference [3] for J/t = 0.8 and larger than T c ≈ 0.05t in reference [9] for J/t = 0.8. As was claimed in these publications, such values of T c with the hopping parameter t ≈ 2.5 eV in graphene would result in a room high-T c SC of electrons on the honeycomb lattice at optimal doping. The variational Monte Carlo calculation for the RVB theory in reference [12] shows that T c can be estimated as about twice of the room temperature. For small values of J < J c = 0.75 t there is no pairing at half-filling for µ = 0. For large values of J/t a sharp increase of T c with δ is found in Figure 3, and for J > J c T c is nonzero at µ = 0. In this region we can observe the gapless SC, as was also found in reference [5] for the s-wave pairing in graphene for the nn BCS coupling parameter g 1 > g c 1 . Taking into account the results of reference [28] for the t-J model on the honeycomb lattice, where AF long-range order at T = 0 was observed for δ 0.1, we argue that the AF and superconducting ground-state order may coexist in the range δ 0.1, in agreement with the numerical calculations in reference [15].
Let us compare the results for the extended s-wave pairing and d-wave pairing. As was found in Section 4.2, the maximum value of T max c ≈ 0.082 t for J = t/2 is nearly the same as in the case of d-wave pairing in Figure 2. It contradicts to the results of reference [9], where T c for the d-wave pairing is much larger than for the extended s-wave pairing. Note that in reference [9] the mean-field RVB theory was used, where the restriction of no-doubleoccupancy has not been taken into account. On the other hand, in references [3,13], where the renormalized meanfield approximation determined by the parameters g t and g J for the t-J model was employed, the maximum value of the order parameter (and T c ) for the extended s-wave pairing and the d-wave pairing are quite close. So we can say that accounting for strong correlations both in our approach and in the renormalized mean-field approximation results in close maximum values of T c for the extended s-wave and d-wave pairing. However, it should be stressed that the constraint (57) excludes the s-wave pairing. This conclusion is supported by the calculations for the t-J model in reference [15], where the projected character of the electron operators has been implemented and only d-wave pairing has been found.

Constraint for the s-wave pairing
Let us consider the restriction of no-double-occupancy (57) for the Hubbard operators: Using the GF F σ AA (k, ω) (49) this condition reads where the function A σ 31 (k, ω) is given by (50). This condition for the s-wave pairing determined by the gap function ∆ σ (27), where A σ 31 (ω = ε ± (k)) = ∓2∆ σ µ t |γ(k)|, results in the relation: The summation over k does not vanish for a positively defined integrand. Therefore, the s-wave pairing with the k-independent gap ∆ σ violates the kinematic restriction (66) and is ruled out. For the extended s-wave pairing with the gap (54) we have A σ 31 (ω = ε ± (k)) = 2∆ ABσ µ t |γ(k)| 2 , and the relation (66) reads: The summation over k does not vanish except for µ = 0 when ε + (k) = −ε − (k). For other doping the correlation function (68) is non-zero that violates the kinematic restriction (66), and the extended s-wave pairing cannot be realized. Finally, let us consider the d-wave pairing with the bond-dependent gap (55). In this case, for the function (50) we have where the relation γ * (k) exp(ikδ α ) − γ(k) exp(−ikδ α ) = 2i Im(γ * (k) exp(ikδ α )) was used. For the correlation function (66) we obtain: In the first term the summation over k does not depend on α due to the C 3 symmetry of γ(k) and ε ± (k). Therefore, the summation over α of the gap function ∆ α σ can be done independently that results in the vanishing of the first term: α ∆ α σ = ∆ 1σ α exp(i(2π/3)α) = 0. The second term also gives no contribution due to summation over k of the odd in k function Im[γ * (k) exp(ikδ α )] = i β sin[k(δ α − δ β )]. So, the d-wave pairing with the gap (55) does not violate the condition of no-doubleoccupancy (66). This conclusion was checked by the direct integration over k in equation (70).

Conclusion
In this paper a microscopic theory of superconductivity in electronic systems with strong correlations is presented within the t-J model on the honeycomb lattice.
The constraint of no-double-occupancy in the two-band t-J model is rigorously taken into account by employing the HO technique. The superconducting T c as a function of doping is calculated for the d + id gap function. It reveals a two-peak structure related to the two VHS in the two-band electronic spectrum. For large values of J > J c = 0.75t a gapless superconductivity is found at µ = 0. It is suggested that for small doping, δ 0.1, the AF long-range order found in [28] may coexist with the d + id superconductivity.
We have also calculated T c for the extended s-wave pairing to compare it with the results obtained for the t-J model, where the constraint has been neglected or considered approximately. In the latter case the results for the maximum value of T c are comparable. However, we have shown that the s-wave pairing violates the constraint and should be ruled out.
In graphene with the large hopping parameter t ≈ 2.5 eV the single-site Coulomb repulsion is not strong enough, U/t = 4-5 [1]. Therefore, the application of the t-J model to graphene is questionable. In our theory we have the renormalized hopping parametert (24) which is small in the region δ ≤ 0.4, where the nn correlation function C 1 ≤ −0.1 [28]. Therefore, we have U/t 1, and the application of the t-J model can be justified. Moreover, complicated structures like sulfur-graphite composites [9] may result in a larger value of U/t, and high-T c superconductivity can be achieved.
Open access funding provided by Max Planck Society. The financial support by the Heisenberg-Landau program of JINR is acknowledged. One of the authors (N.P.) thanks the Directorate of the MPIPKS for the hospitality extended to him during his stay at the Institute, where a part of the present work has been done.