Interlayer sliding modulation of spin Hall and spin Nernst effects in two-dimensional altermagnets

Siyuan Liu , Ling Bai , Xiangju Wang , Libor Šmejkal , Jairo Sinova , Yuriy Mokrousov , Gui-Bin Liu , Wanxiang Feng

Front. Phys. ›› 2026, Vol. 21 ›› Issue (11) : 115203

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Front. Phys. ›› 2026, Vol. 21 ›› Issue (11) :115203 DOI: 10.15302/frontphys.2026.115203
RESEARCH ARTICLE
Interlayer sliding modulation of spin Hall and spin Nernst effects in two-dimensional altermagnets
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Abstract

Altermagnets constitute a recently identified magnetic phase that combines the absence of macroscopic magnetization, characteristic of antiferromagnets, with the spin splitting typically associated with ferromagnets. This hybrid nature enables stray-field-free spin transport and ultrafast spin dynamics, offering new opportunities for dissipationless spintronics and spin-caloritronics. Here, we perform a comprehensive symmetry analysis and advanced first-principles calculations to investigate the intrinsic spin Hall and spin Nernst effects in two-dimensional altermagnets, using bilayer MnPSe3 as a representative example. In the nonrelativistic limit, interlayer sliding induces a d-wave-like spin splitting and generates time-reversal-odd, intraband-dominated spin Hall and spin Nernst responses. Changing the sliding direction alters the associated symmetry operations, thereby modifying the spin splitting of the Fermi surface and enabling tunable control of spin-transport properties. This modulation originates from symmetry-driven variations in the relative contributions of opposite spins. Our findings identify interlayer sliding as an effective route to tuning spin transport in altermagnets, establishing a versatile two-dimensional platform for exploring the interplay between altermagnetism and spin transport, and paving the way for future advances in altermagnetic spintronics and spin-caloritronics.

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Keywords

altermagnet / spin Hall effect / spin Nernst effect / two-dimensional system

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Siyuan Liu, Ling Bai, Xiangju Wang, Libor Šmejkal, Jairo Sinova, Yuriy Mokrousov, Gui-Bin Liu, Wanxiang Feng. Interlayer sliding modulation of spin Hall and spin Nernst effects in two-dimensional altermagnets. Front. Phys., 2026, 21(11): 115203 DOI:10.15302/frontphys.2026.115203

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1 Introduction

Spintronics aims to exploit the interplay between spin and charge degrees of freedom to manipulate both equilibrium and nonequilibrium phenomena in materials and devices. Among its core objectives, the generation, detection, and control of transverse spin currents are of central importance [1]. A transverse spin current induced by a longitudinal electric field is known as the spin Hall effect (SHE) [2], which serves as a fundamental mechanism for creating and detecting spin currents. Analogously, a longitudinal temperature gradient can also drive a transverse spin current, giving rise to the spin Nernst effect (SNE). In both cases, the transverse spin response originates from two distinct mechanisms: extrinsic contributions — such as side-jump and skew-scattering processes — which strongly depend on carrier–impurity interactions [3, 4]; and intrinsic contributions, which arise purely from the electronic structure of a perfect crystal and are closely tied to band topology [5, 6].

From the perspective of time-reversal symmetry (T), the intrinsic SHE can be decomposed into T-even and T-odd components [7]. The T-even contribution originates from spin Berry curvature induced by spin-orbit-coupling (SOC) [5, 6] and has been extensively explored in both magnetic [79] and nonmagnetic systems [1014]. By contrast, the T-odd contribution depends sensitively on the detailed electronic band structure and does not rely on the strength of SOC. This provides a promising mechanism for generating and tuning spin currents in materials composed of light elements, where SOC is intrinsically weak. Despite these advantages, studies on the T-odd SHE remain limited. It is further believed to vanish in conventional collinear compensated magnetic systems due to the absence of essential spin splitting, which has imposed significant constraints on both fundamental understanding and practical development of spintronic functionalities.

Recently, a newly identified class of magnets — termed altermagnets (AMs) [15, 16] — has attracted considerable attention due to their promising potential in spintronic applications [17]. In AMs, magnetic sublattices with opposite spin orientations are connected by rotational or mirror symmetries, in contrast to conventional collinear antiferromagnets, where they are related through inversion or translational symmetries. These symmetry operations enforce alternating spin splittings across the electronic band structure, giving rise to a wide array of unconventional physical phenomena [1834]. Among these, the emergence of an intrinsic T-odd SHE is particularly notable, as it resolves the longstanding belief that such an effect is forbidden in collinear compensated magnetic systems [35], thereby expanding the pool of viable material platforms for spintronics. For instance, in altermagnetic RuO2, the corresponding transverse spin conductivity exceeds by a factor of three the record values reported in nonmagnetic materials and exhibits strong sensitivity to spin orientation. Despite these promising attributes, progress in exploiting AMs for generating and modulating T-odd SHE has been limited, particularly in two-dimensional (2D) systems. Moreover, it is essential to identify control mechanisms beyond spin reorientation to meet the demands of high-performance and device-compatible functionalities.

In this work, through comprehensive symmetry analysis and advanced first-principles calculations, we systematically investigate how interlayer sliding modulates the intrinsic SHE and SNE in 2D bilayer altermagnets, using MnPSe3 as a representative example. In the nonrelativistic limit, interlayer sliding induces a d-wave–like spin splitting in momentum space, whose pattern depends sensitively on the sliding direction and its associated symmetry operations. By varying the sliding direction, MnPSe3 exhibits pronounced orientation-dependent spin splitting. Based on spin and magnetic group analyses, we further determine the symmetry constraints on the spin Hall conductivity (SHC) and spin Nernst conductivity (SNC) tensors in both nonrelativistic and relativistic cases. Our calculations reveal that the T-odd intraband contribution dominates the SHE and SNE. More importantly, both the sign and magnitude of the SHC and SNC can be efficiently tuned by adjusting the sliding direction, and this sliding-induced modulation remains robust with or without SOC. These findings not only establish interlayer sliding as an effective route for controlling spin-transport properties but also highlight bilayer MnPSe3 as a compelling 2D platform for exploring the interplay between altermagnetism and spin transport, paving the way for advances in altermagnetic spintronics and spin-caloritronics.

2 Theory and computational details

Under an applied electric field E along the j direction, the linear response of a spin current flowing in the i direction and polarized along the s direction (i,j,s{x,y,z}) is given by

JiE,s=σijsEj,

where σijs denotes the SHC. According to its behavior under T, the SHC can be decomposed into two parts as [7]

σijs=σijs,odd+σijs,even,

with

σijs,odd=2ΓVn,m,kfmkfnkεnkεmkRe(n|Jk,is|mm|Jk,j|n)(εnkεmk)2+(Γ)2,

σijs,even=Vn,m,k(fmkfnk)Im(n|Jk,is|mm|Jk,j|n)(εnkεmk)2+(Γ)2.

Here, V is the volume and fnk=[e(εnkεF)/(kBT)+1]1 is the Fermi–Dirac distribution with Fermi energy εF. The current kernels are defined as Jk,is=12e(S^svk,i+vk,iS^s) and Jk,j=evk,j, where e is the elementary charge, S^s is the spin operator polarized along direction s, and vk,i/j is the velocity operator along direction i/j. The summand of σijs,odd(even) with respect to the band indices is denoted as Dijs,odd(even)(k). Furthermore, σijs,odd can be decomposed into an intraband contribution σijs,odd-intra (m=n) and an interband contribution σijs,odd-inter (mn).

In Eqs. (3) and (4), Γ=1/τ is an artificial spectral broadening parameter, where the relaxation time τ can be estimated using the semiclassical relation [36, 37]

τ=μm/e.

Here, μ and m denote the carrier mobility and the effective mass, respectively. Within the framework of deformation potential theory, μ can be evaluated, allowing τ to be expressed as [38, 39]

τ=3C2DkBTmdE12,

where C2D is the in-plane elastic modulus, kB is the Boltzmann constant, and T is the temperature. The quantity md=mxmy is the average effective mass, with mx and my denoting the effective masses along the x and y directions, respectively. The deformation potential constant E1 is defined as E1=dEedgedu, where Eedge is the energy of the conduction- or valence-band edge and u represents the applied uniaxial strain.

Similarly, a temperature gradient T can play the role analogous to that of an applied electric field E, driving transverse spin current through the sample. This thermal response, known as the SNE, can be expressed as

JiT,s=αijsTj,

where αijs denotes the SNC. According to the generalized Landauer–Büttiker formalism [4042], the SNC is related to the SHC through

αijs=(εεF)(fε)σijs(ε)dε.

Under an applied electric field E along the j direction (jx,y,z), the linear response of a charge current flowing in the same direction is given by

JjE=σjjEj,

where σjj denotes the longitudinal charge conductivity. Within the semiclassical Boltzmann transport formalism [43], σjj can be written as [4345]

σjj=e2+(fε)Σjj(ε)dε.

Here, the Σjj(ε) is the transport distribution function, defined as

Σjj(ε)=τVn,kvk,j2δ(εεnk),

where the constant relaxation-time approximation is adopted and δ(εεnk) represents the Dirac delta function.

The electronic structures were calculated using the Vienna ab initio simulation package (VASP) [46, 47], within the framework of density functional theory (DFT). The generalized gradient approximation (GGA) with the Perdew−Burke−Ernzerhof (PBE) parameterization [48] was employed to describe electron−electron exchange-correlation effects, while the projected augmented-wave (PAW) method [49] was used to account for electron−ion interactions. An energy cutoff of 500 eV was used for the plane-wave basis, along with a uniform k-mesh of 9 × 9 × 1 for 2D system. The self-consistent field calculations were considered converged when the total energy change was below 1 × 106 eV and the residual forces on atoms were less than 1 × 102 eV/Å. To properly describe the localization of Mn 3d orbitals, a Hubbard correction of Ueff = 5 eV was applied using the Dudarev scheme [50]. Long-range van der Waals interactions were included via the semiempirical DFT-D3 method [51]. A vacuum region of more than 15 Å was added along the out-of-plane direction to avoid spurious interactions between adjacent slabs. After obtaining converged ground-state charge densities, maximally localized Wannier functions were constructed using the Wannier90 package [52], incorporating the p orbitals of Se and the d orbitals of Mn atoms. The spin- and charge-transport properties were evaluated using an ab initio tight-binding Hamiltonian constructed from maximally localized Wannier functions. The transverse components were computed using our in-house developed codes, whereas the longitudinal components were obtained with the BoltzWann package [45]. To achieve well-converged transport results, we employed an ultradense k-mesh of at least 700×700×1.

3 Results and discussion

For collinear AMs, the nonrelativistic spin-split band structures can be systematically characterized within the framework of spin group theory. A spin point group S can be constructed from a crystallographic point group G through the relation [1317, 32]

S=[E||H]+[C2||GH],

where [Rs||Rl] denotes a combined symmetry operation consisting of Rs acting in spin space and Rl in real space. Here, E is the identity operation in spin space, C2 is a twofold rotation perpendicular to the collinear spin axis, and H is a halving subgroup of G. The term [E||H] preserves the spin orientation and operates within same-spin sublattices, whereas [C2||GH] relates sublattices with opposite spin orientations.

For the 2D case, the spatial operations appearing in [C2||GH] must exclude inversion P, mirror Mz, and the twofold rotation C2z (with the z axis perpendicular to the atomic plane), as these symmetries enforce spin degeneracy of the electronic bands, i.e., E(k,s)=E(k,s), where k and s denote momentum and spin indices, respectively [32]. The remaining admissible operations include the fourfold rotation C4z, in-plane twofold rotations C2α, and vertical mirrors Mα, where α specifies an arbitrary in-plane direction. When combined with the spin-space rotation C2, all three classes of operations can induce anisotropic spin splitting in the band structure [see Fig. 1]. For [C2||C2α] and [C2||Mα], varying the in-plane axis α — for example, rotating it to a new direction α — causes the corresponding band structure to evolve accordingly [see Figs. 1(a)–(d)]. This pronounced directional dependence enables effective tuning of nonrelativistic band structures by controlling the orientation of the underlying symmetries. In contrast, although the [C2||C4z] symmetry can also induce spin splitting, its directional character cannot be regulated in 2D systems, because multiple distinct spin-splitting patterns correspond to the same symmetry operation [see Figs. 1(e) and (f)]. Therefore, [C2||C4z] is unsuitable for symmetry-based tuning of nonrelativistic band structures in 2D AMs.

For 2D van der Waals layered materials, the orientation of symmetry operations can be readily and effectively controlled via interlayer sliding. Monolayer MnPSe3 exhibits an antiferromagnetic ground state with an in-plane easy axis and a Néel temperature of approximately 40 K [53]. As illustrated in Fig. 2, in the absence of SOC, stacking two MnPSe3 monolayers in a configuration that preserves the combined symmetry [C2||Mz] yields a bilayer type-IV collinear magnet [32] that exhibits robust magnetoelectric coupling [54]. The corresponding crystallographic point group is G=D3h, and the halving subgroup can be chosen as H=D3. The bilayer MnPSe3 thus retains the following spin point group symmetry operations: [E||E], [E||C3z±], [E||C2α] with α=[100],[010],[110], [C2||Mz], [C2||PC6z±], and [C2||Mα] with α=[210],[120],[11¯0]. Among these, the operation [C2||Mz] enforces spin degeneracy, as shown in the central part of Fig. 2. This bilayer type-IV magnet turns to reach its energy minimum when one monolayer is shifted relative to the other along any of six specific vectors, namely ±13a, ±13b, or ±13(a+b), where a=[100] and b=[010] [55]. Such interlayer sliding can be experimentally realized using in situ biasing Cs-corrected transmission electron microscopy (Cs-TEM) [56]. For any of these sliding directions, the spin-degenerate Fermi surface is lifted. This occurs because each sliding configuration preserves only a single vertical mirror symmetry, while all other symmetries except the identity operation are broken. Moreover, the resulting pattern of spin splitting depends sensitively on the sliding direction, which is confined to the corresponding preserved mirror plane (see the outer parts in Fig. 2). Since the intrinsic T-odd SHC and SNC are directly linked to the pattern of spin splitting [35], interlayer sliding provides an effective means of modulating these spin responses.

Prior to calculating the SHC and SNC, we analyze the symmetry constraints on their in-plane components, i.e., σxys and αxys, since the out-of-plane components are irrelevant in 2D systems. Because the SHC and SNC share identical symmetry constraints, we focus on the SHC here, and consider both the T-odd and T-even contributions for completeness. In the nonrelativistic limit, the symmetry constraints on the SHC can be determined using spin group theory. In this case, all collinear magnets possess an additional symmetry operation [C¯2||T] [15, 16], which imposes [C¯2||T]σxys,even=σxys,even, thereby forcing the T-even SHC to vanish regardless of whether sliding is present or not. In the absence of interlayer sliding, the T-odd SHC σxys,odd also vanishes due to the constraint imposed by the [C2||Mz] symmetry, that is, [C2||Mz]σxys,odd=σxys,odd. Under interlayer sliding along the ±13a, ±13b, or ±13(a+b) directions, however, only symmetry operations [C2||M[120]], [C2||M[210]], or [C2||M[11¯0]] remains, respectively. These operations impose no constraints on σxys,odd, and thus a finite T-odd SHC becomes allowed in the sliding configurations.

When SOC is taken into account, the magnetic point group must be used, as the spin and crystal degrees of freedom become coupled. For convenience, we define the Néel vector as N=S1S2, where S1 and S2 denote the antiparallel spin moments within a unit cell. When N is parallel to the [100] direction (x axis), the non-sliding magnetic structure belongs to the magnetic point group mm2.1 (No. 7.1.20). In this group, the mirror symmetry Mz imposes the constraint Mzσxyx(y)=σxyx(y), indicating σxyx(y)=0, while allowing a finite σxyz for both the T-odd and T-even components. For sliding along ±13a, the magnetic point group is reduced to m.1 (No. 4.1.9), where the vertical mirror M[120] enforces M[120]σxyy=σxyy, giving rise to σxyy=0, but permits finite σxyx and σxyz for both T-odd and T-even parts. In contrast, for sliding along ±13b or ±13(a+b), the magnetic point group further reduces to 1.1 (No. 1.1.1), where only the identity operation E remains. As a result, all in-plane SHC components become symmetry-allowed. The symmetry operations of the spin and magnetic point groups, together with their corresponding constraints on the SHC, are summarized in Tables 1 and 2, respectively.

For comparison, we also construct a bilayer MnPSe3 with intralayer ferromagnetic order and interlayer antiferromagnetic order (see Fig. A1). The symmetry operations of the spin and magnetic point groups, together with their constraints on the SHC and SNC, are summarized in Tables A1 and A2, respectively, and discussed in detail in Appendix A. The results demonstrate that the specific type of in-plane magnetic order strongly constrains the SHC and SNC, highlighting the pivotal role of magnetic symmetry in tailoring spin transport properties.

To quantitatively evaluate the SHC and SNC using Eqs. (3), (4), and (8), the temperature T and spectral broadening parameter Γ must be specified. Given that monolayer MnPSe3 has a Néel temperature exceeding 40 K and its bulk counterpart exhibits a Néel temperature of 68 K [57], we adopt a reasonable temperature of 50 K for the SHC and SNC calculations of bilayer MnPSe3. According to deformation potential theory, bilayer MnPSe3 possesses a high electron mobility of 418.6 cm2·V−1·s−1 in the valence band, which is considerably larger than the theoretical mobility of monolayer MoS2 (72.2 cm2·V−1·s−1) [58]. Based on Eq. (6), the corresponding relaxation time is estimated to be τ=238.0 fs, significantly longer than that of monolayer CrI3 (30–70 fs) [59] and NiI2 (22.7 fs) [36], indicating weak carrier scattering in bilayer MnPSe3. The associated spectral broadening is then determined to be Γ=2.8 meV.

The magnitude and sign of the nonrelativistic T-odd spin transport can be effectively modulated by interlayer sliding. Here, we take the spin Hall response with spin polarization along the x direction, σxyx,odd, as an illustrative example, as shown in the top row of Fig. 3, while the cases with spin polarization along the y and z directions (σxyy/z,odd) exhibit similar behavior. We analyze the interlayer sliding with the sequence of 13a13(a+b)13b13a13(a+b)13b, which proceeds counterclockwise in 60° intervals (see Fig. 2). For all sliding configurations, σxyx,odd is dominated by the intraband contribution, whereas the interband part is negligible. For the 13a sliding, as the Fermi level εF moves downward from the valence-band maximum, σxyx,odd-intra develops a deep valley of 12.3e/4π at 0.16eV and a peak of 11.6e/4π at 0.24eV. For the 13(a+b) sliding, σxyx,odd-intra exhibits similar behavior but with reduced magnitudes, with the extrema decreased to 6.3e/4π and 5.7e/4π, respectively. In contrast, for the 13b sliding, σxyx,odd-intra is exactly opposite in sign to that of the 13(a+b) case. This sign reversal arises because the two corresponding crystal structures are related by the symmetry operation [E||M[100]], which flips the sign of σxyx,odd-intra. Furthermore, for the 13a, 13b, and 13(a+b) slidings (i.e., the opposite displacements of 13a, 13b, and 13(a+b), respectively), σxyx,odd-intra retains the same magnitude but acquires the opposite sign compared with their positive-sliding counterparts. This behavior is enforced by the symmetry operation [C2||Mz], which connects each pair of opposite sliding configurations.

To elucidate the microscopic origin of the variation in nonrelativistic T-odd spin transport under different sliding configurations, we examine its momentum-space distribution by calculating Dxyx,odd-intra, as shown in the inset of the top row of Fig. 3. For the 13a sliding, Dxyx,odd-intra spreads almost uniformly along the Fermi surface, indicating that σxyx,odd-intra arises predominantly from Fermi-surface contributions. More specifically, the spin-up and spin-down Fermi surfaces contribute nearly equally. The distribution of Dxyx,odd-intra is symmetric with respect to both the kx and ky axes due to the symmetry constraints [C2||M[120]]Dxyx,odd-intra(kx,ky)=Dxyx,odd-intra(kx,ky) and [C2||T][C2||M[120]]Dxyx,odd-intra(kx,ky)=Dxyx,odd-intra(kx,ky). The same symmetry analysis applies to the 13a sliding, however, in this case the sign of Dxyx,odd-intra is reversed relative to the 13a configuration. This originates from the opposite spin polarizations of the Fermi surfaces produced by the two opposite sliding directions (also refer to Fig. 2), which are related by the symmetry operation [C2||Mz]. This symmetry imposes the constraint [C2||Mz]Dxyx,odd-intra(kx,ky)=Dxyx,odd-intra(kx,ky), thereby enforcing an overall sign reversal of σxyx,odd-intra. For the ±13(a+b) and ±13b slidings, the spin-up and spin-down Fermi surfaces remain symmetrically distributed with respect to the [C2||M[11¯0]] and [C2||M[210]] symmetry operations, respectively. However, the quantity Dxyx,odd-intra itself does not remain symmetric under these operations. As a result, the contributions from the two spin channels become unbalanced — and may even acquire opposite signs — which ultimately reduces the magnitude of σxyx,odd-intra.

Having clarified the sliding dependence of the SHC, we now turn to the SNC. As shown in the bottom row of Fig. 3, the SNC is likewise dominated by the T-odd intraband contribution, and its dependence on the sliding direction closely resembles that of the SHC, as both responses obey the same symmetry constraints. However, their energy-dependent behaviors differ markedly. At εF=0.16 eV, where the T-odd intraband SHC reaches an extremum, the corresponding SNC nearly vanishes. In contrast, at εF=0.18 eV, the SNC attains a maximum value of 9.9×109A/(Ke), coinciding with a region where the SHC exhibits a steep energy gradient. This correlation arises directly from the Mott relation,

αxyx=π23kB2Te(σxyx),

which dictates that the SNC is proportional to the first-order energy derivative of the SHC.

When SOC is included, the T-even components of the SHC and SNC become symmetry-allowed. However, as shown in Fig. 4, their magnitudes remain negligible, so both responses continue to be dominated by the T-odd intraband contribution. The overall sliding and energy dependences of the SHC and SNC are thus qualitatively preserved in the presence of SOC, although their magnitudes undergo quantitative modifications. For the 13a sliding, the first extremum of σxyx,odd-intra (located at εF=0.16 eV) is reduced to 6.0e/(4π), which corresponds to 1272.0S/(cme) when expressed in the conventional units of a three-dimensional system. Despite this decrease, the magnitude still exceeds those reported for non-collinear antiferromagnets Mn3X (X= Sn, Ge, Ga), which exhibit values around 219S/(cme) [60], as well as nonmagnetic Ni70Cu30 (1136S/(cme)) [61] and nonmagnetic ZrXY (X= Si, Ge; Y= S, Se, Te), which reach approximately 755S/(cme) [62]. Similarly, the extremum of αxyx,odd-intra (at εF=0.19 eV) decreases to 5.3×109A/(Ke) (corresponded to 5.2A/(Kme) in the unit of three-dimensional system). This value still surpasses those reported for nonmagnetic Ni70Cu30 (3.5A/(Kme)) [61] and nonmagnetic ZrSiS (1.5A/(Kme)) [62].

Figures 5(a) and 5(b) show the angular dependence of the T-odd intraband SHC and SNC with respect to the sliding direction. In the nonrelativistic limit, both quantities exhibit a clear 2π-periodic variation with the sliding angle β, defined as the angle between the sliding vector and 13a. The SHC and SNC reach their extrema for the ±13a slidings and vanish when the sliding occurs along the y axis. The results reveal a pronounced anisotropy in the sliding-induced SHC and SNC, demonstrating that both the magnitude and sign of the spin transport can be tuned continuously by adjusting the sliding direction. This control is intrinsic to the sliding degree of freedom and is independent of the applied electric field or temperature gradient, providing a new mechanism for tuning spin currents in 2D altermagnets. When SOC is included, the SHC and SNC retain the same 2π periodicity and phase positions. However, their magnitudes are reduced compared with the nonrelativistic case, indicating that SOC partially suppresses the spin-transport response while preserving the overall angular anisotropy.

Finally, we evaluate the longitudinal electronic conductivity σxx and the charge-to-spin conversion efficiency |CSE|, which quantify, respectively, the ability of an applied electric field to drive a longitudinal charge current and the efficiency with which that longitudinal charge current is converted into a transverse spin current. Specifically, the conversion efficiencies are defined as |CSE|SHE=|σxys/σxx|×100% and |CSE|SNE=|αxys/σxx|×100%. As shown in Figs. 6(a) and (b), the values of |σxx| are identical for the ±13a, ±13b, and ±13(a+b) sliding configurations. This equivalence arises because each pair of opposite sliding configurations is related by the symmetry operation [C2||Mz] in the absence of SOC (or by Mz when SOC is included), which preserves |σxx|. Moreover, the ±13b and ±13(a+b) slidings also yield identical |σxx|, as they are connected by the symmetry operation [E||M[100]] without SOC (or by M[100] with SOC), which likewise preserves |σxx|. Below the valence-band maximum, |σxx| increases monotonically with decreasing energy. For the ±13a slidings, a pronounced peak of approximately 3.9×104e2/h appears at εF=0.19 eV, whereas this peak shifts to εF=0.22 eV for the ±13b and ±13(a+b) slidings. Upon including SOC, the overall magnitude of |σxx| is slightly reduced, indicating that SOC weakly suppresses the longitudinal charge transport.

The energy-dependent |CSE| for different sliding configurations is shown in Figs. 6(c)−(f). In the absence of SOC, both |CSE|SHE and |CSE|SNE exhibit pronounced oscillations with multiple peaks below εF=0 eV, reflecting their strong sensitivity to hole doping. The maximum values reach approximately 12.5(/e)% for |CSE|SHE and 7.5×105(A/(SKe))% for |CSE|SNE. Upon inclusion of SOC, the overall magnitudes are moderately reduced, and the peak structures become slightly smoother. This suppression indicates that SOC partially diminishes the charge-to-spin conversion process. Since σxx is also reduced when SOC is included, the decrease in both |CSE|SHE and |CSE|SNE can be reasonably attributed to the concomitant reduction in the SHC and SNC. Despite this overall reduction, the energy dependence of |CSE| still faithfully reflects the intrinsic nature of the charge-to-spin conversion mediated by interlayer sliding.

4 Summary

In summary, by combining group-theory analysis and first-principles calculations, we have investigated the SHE and SNE in the 2D bilayer altermagnet MnPSe3. In the nonrelativistic limit, spin-group analysis reveals that interlayer sliding induces d-wave — like spin splittings, which give rise to nonvanishing spin Hall and spin Nernst responses. We shown that both the SHE and SNE are dominated by the T-odd intraband contribution. When the sliding direction changes, the associated symmetry operation is modified, leading to corresponding changes in the spin splitting of the Fermi surface and, consequently, to a tunable modulation of the spin-transport properties. This modulation originates from symmetry-induced variations in the opposite spin polarizations of the band structures generated by different directions of interlayer sliding. In addition, interlayer sliding can efficiently modulate the charge-to-spin conversion efficiency. When SOC is included, the proposed mechanism remains valid. Specifically, under the 13a sliding, the SHC and SNC reach large values of 6.0e/4π at εF=0.16 eV and 5.3×109A/(Ke) at εF=0.19 eV, respectively. Our findings establish interlayer sliding as an effective route to control the patterns of band spin-splitting as well as the spin Hall and Nernst transport in 2D layered altermagnets, paving the way for advancements in altermagnetic spintronics and spin-caloritronics.

5 Appendix A: Bilayer MnPSe3 with intralayer ferromagnetic order and interlayer antiferromagnetic order

Figure A1 shows the atomic and magnetic structures of non-sliding bilayer MnPSe3 with intralayer ferromagnetic order and interlayer antiferromagnetic order. In the absence of SOC, the T-even SHC has to vanish due to the additional symmetry operation [C¯2||T] arising from the collinear magnetic order. Without sliding, the crystallographic point group is G=D3h. Using its halving subgroup H=C3v, the spin point group is generated: [E||E], [E||C3z±], [E||Mα] with α=[120],[11¯0],[210], [C2||Mz], [C2||PC6z±], and [C2||C2α] with α=[100],[110],[010]. The T-odd SHC vanishes due to the constraint imposed by [C2||Mz]. With sliding along the ±13a direction, the spin point group changes to: [E||E] and [E||M[120]], where [E||M[120]]σxys,odd=σxys,odd, forcing the T-odd SHC to be zero. In contrast, with sliding along the ±13b (±13(a+b)) direction, the spin point group becomes [E||E] and [E||M[210]] ([E||E] and [E||M[11¯0]]), imposing no constraints on σxys,odd, and hence a finite T-odd SHC is expected.

When SOC is taken into account, the non-sliding configuration (Nxaxis) belongs to the magnetic point group mm2 (No. 7.3.22). In this group, the mirror symmetry Mz imposes the constraint Mzσxyx(y)=σxyx(y), and M[120]T imposes the constraint M[120]Tσxyz,odd=σxyz,odd. These two constraints force σxyx(y) and σxyz,odd to be zero, respectively, while a finite σxyz,even is allowed. When sliding is introduced along the ±13a direction, the magnetic point group is reduced to m (No. 4.3.11). Here, the symmetry operation M[120]T enforces M[120]Tσxyx(z),odd=σxyx(z),odd and M[120]Tσxyy,even=σxyy,even, giving rise to σxyx(z),odd=0 and σxyy,even=0, respectively, whereas finite values are permitted for the components σxyy,odd and σxyx(z),even. For slidings along the ±13b or ±13(a+b), the magnetic point group is further reduced to 1.1 (No. 1.1.1), where only the identity operation E remains. Consequently, all SHC components become symmetry-allowed. In summary, the symmetry operations of the spin and magnetic point groups, together with their constraints on the SHC, are collected in Tables A1 and A2, respectively.

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