Dear Vishal,

The quantitative determination of the relative contributions from experimental data can be quite evolved, especially when various extrinsic mechanisms are at play. Take, for instance, the minimal model of massive Dirac electrons in 2D [https://journals.aps.org/rmp/abstract/10.1103/RevModPhys.82.1539]. Assuming "white-noise" scalar disorder to simplify the analysis, one can show that AH and XX (=longitudinal) conductivities behave as:

• AH ~ XX0 ~ const. (intrinsic and side jump mechanism contributions);
• AH ~ XX1 ~ E t (skew scattering), where E is the Fermi energy and t the transport time

       (but see below for recent theoretical developments)

The skew scattering contribution dominates in the high conductivity regime, where t is large. Conventional semi-classical contributions to the AH conductivity result from individual scattering events, and hence their magnitude is proportional to a certain effective relaxation time, which is largest in cleaner samples.

For example, when impurity scattering dominates, and there's only a single type of impurities present, the relaxation time generally scales as n-1, where n is the impurity density, and thus AH ~ XX ~ n-1. Side jump (as well as weak-localization corrections; see below) kick in at the next leading order in the impurity density expansion of the response functions, i.e., n0-order. Thus, similarly to the Berry phase (intrinsic) contribution, they are independent of the impurity density. 

There is some confusion in the literature about how these scalings are to be determined experimentally. Many works suggest that the scaling (i.e., skew scattering versus not skew scattering) can be determined by varying the charge carrier density and/or temperature, and assessing the exponent p in AH ~ XXp. This procedure works provided that the AH and XX conductivities share similar (Fermi) energy dependences, which unfortunately is not always true. In fact, already in the minimal model aforementioned, the energy dependence of the response functions critically depend on the type of disorder considered [say, scalar versus magnetic, weak (Gaussian) versus strong (resonant), etc.]. A more rigorous set of relations would be, say at low temperature and assuming just one type of disorder limiting both XX and AH

AH ~ F(\epsilon, ...) *  XX0  (intrinsic, side jump mechanism, diffractive skew scattering (see below));

AH ~ G(\epsilon, ...) * XX1  (skew scattering),

where \epsilon is the Fermi energy and "..." stands for disorder energy scales and parameters of the model (spin-orbit strength, cutoff energy, etc.). Note that in dirty samples, various effects compete that generate AH conductivity of the order of the quantum of conductance (Berry phase, side jump, etc.). In such cases, the exponent can be arbitrary, and its theoretical determination requires ab initio calculations. So, in general, the “scaling-as-mobility” assumptions made to be considered very carefully.

An unbiased (model-independent) approach to determine the dominant mechanism would be to prepare samples with different disorder strengths. However, this requires the capability to modify the chemical/structural disorder, while keeping the carrier density under control (see e.g., http://iopscience.iop.org/article/10.1209). Moreover, a battery of transport measurements would be required to consistently check the transport regime, spin-orbit coupling, etc.

Two brief notes:

1. there are several mechanisms that can give rise to extrinsic contributions that mimic the conventional semi-classical (skew scattering) contribution, one example is asymmetric spin precession [https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.119.136804] other is phonon skew scattering [https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.115.076602], studied in the context of spin Hall effect, but similar physics occurs in the AHE.

2. electron localization physics can also affect the scaling; https://journals.aps.org/prb/abstract/10.1103/PhysRevB.87.094405;

3. weak-localization corrections encode diffractive skew scattering contribution (from coherent multi-impurity scattering), which can dominate under certain conditions (particularly, for weak Gaussian-type disorder); see https://journals.aps.org/prb/abstract/10.1103/PhysRevB.94.134202 and references therein for these recent developments.

Finally, concerning the magnetic field, H. A safe procedure seems to be to extrapolate the AH resistance vs H curves from high field back to H = 0, exploring the relation:

Ryx = r0H + rAH M(H),

where r0 and rAH are, respectively, the ordinary and anomalous terms.

(This assumes that the AH contribution is proportional to the magnetization M, see https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.93.016602)

To improve the estimation, one can take the average at positive and negative fields [Ryx(H) +Ryx(-H)]/2 to eliminate magneto-resistance and thermo-electric effects.

Hope this helps!

A.

https://journals.aps.org/rmp/abstract/10.1103/RevModPhys.82.1539

https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.115.076602

https://journals.aps.org/prb/abstract/10.1103/PhysRevB.94.134202

https://journals.aps.org/prb/abstract/10.1103/PhysRevB.87.094405

https://journals.aps.org/prl/abstract/10.1103/PhysRevLett.93.016602

http://iopscience.iop.org/article/10.1209/0295-5075/114/57004/meta;jsessionid=E772F0E3F17B43440FCF147A1ADF2C62.c2.iopscience.cld.iop.org

Very nicely elaborated answer given by Aires....

The AH resistivity (conductivity) always considered in zero field situation that can get by extrapolation of the high field region R-H curve. And off course the averaging remove the effects mentioned by Aires.

Since, the resistivity at high field contain magneto-resistance contribution so do not think to consider the resitivity at any field, therefore, the longitudinal conductivity calculate by the zero field resistivity measurement and use it to evaluate the intrisic and extrinsic contributions. These effect are  explained in the article (http://www.sciencedirect.com/science/article/pii/S0304885317303967?via%3Dihub). Look into this and reference their in.

Hope this help.

Thank You Prof. Aires and Sajid for your comments.

The anomalous Hall component is extracted by extrapolation of the high field R-H curve. Let us consider that change in the longitudinal resistivity is negligible as compared to change in Hall resistivity with change in magnetic field. There are two approaches that can be considered to characterize the component's S-shape curve after the extrapolation. One is the saturated AHE component at high fields or the residual component at 0 field. The first one has been used in the following paper that I came across.

" Universal scaling of the anomalous Hall effect in Fe3O4 epitaxial thin films" by A. Fernández-Pacheco et al., in Phys. Rev. B 77, 100403, 2008

Both the approaches make sense and it seems the relationships between longitudinal resistivity and anomalous Hall resistivity as discussed by Prof. Aires hold good for resistivity at 0 field as well as for resistivity at above saturation fields. Please let me know your views. Thank You.