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A decrease of anisotropy field and an increase of GMI with increasing annealing temperature up to 540 8C were observed and ascribed to the increase of the magnetic permeability and the d

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Effect of annealing on the microstructure and magnetic properties

of Fe-based nanocomposite materials

Manh-Huong Phana,*, Hua-Xin Penga, Michael R Wisnoma, Seong-Cho Yub, Nguyen Chauc

a

Department of Aerospace Engineering, Bristol University, Queen’s Building, University Walk, Bristol BS8 1TR, UK

b

Department of Physics, Chungbuk National University, Cheongju 361-763, South Korea

c

Center for Materials Science, National University of Hanoi, 334 Nguyen Trai, Hanoi, Vietnam Received 4 October 2004; revised 8 January 2005; accepted 11 January 2005

Abstract

The influence of annealing on microstructure, magnetic properties including the giant magnetoimpedance (GMI) effect of a Fe-based nanocomposite has been investigated The nanocomposite structure composed of ultra-fine Fe(Si) grains embedded in an amorphous matrix was attained by annealing the Fe-based amorphous alloy prepared by rapid quenching method The GMI profiles were measured for samples annealed at different temperatures ranging from 350 to 650 8C in vacuum and for 30 min It is found that the mean grain size of the a-Fe(Si) crystallites in the order of 12 nm remains almost unchanged until the annealing temperature reached 540 8C A decrease of anisotropy field and an increase of GMI with increasing annealing temperature up to 540 8C were observed and ascribed to the increase of the magnetic permeability and the decrease of the coercivity, whereas the opposite tendency was found for the sample annealed above 600 8C which is likely due to the microstructural change caused by high-temperature annealing This indicates that variation in the magnetic characteristic of the amorphous phase upon annealing changed the intergrain exchange coupling This altered both the magnetic softness and the effective anisotropy and consequently modified the GMI features The study of the temperature dependence of the GMI effect provides further understanding of the magnetic exchange between these crystallized grains through the amorphous boundaries in Fe-based nanocrystalline materials

q2005 Elsevier Ltd All rights reserved

Keywords: B Anisotropy; Magnetoimpedance

1 Introduction

Recent advances in magnetic sensing applications,

especially in the high-density magnetic recording

technol-ogy, has benefited from the discovery of new magnetic

materials with amorphous structure [1–3] In contrast to

crystalline magnetic materials where the periodicity of

constituent atoms plays an essential part, in an amorphous

substance, atoms are distributed randomly, taking a

topologically disordered structure The absence of crystal

structure (i.e the presence of a short range order and the

absence of a long range order) leads to superior properties

(e.g mechanical, chemical, electrical, and magnetic proper-ties) observed in these materials

It is known that the absence of magnetocrystalline anisotropy and grain boundaries in an amorphous magnetic material results in excellent soft magnetic properties (e.g high magnetic permeability and saturation induction), high electrical resistivity leading to small eddy current losses, high hardness and stiffness etc Importantly, a variety of properties can be achieved by the applications of external parameters (e.g magnetic field, pressure, temperature, etc.) and/or by controlling the fabrication processes [1] The combined magnetic, electrical, mechanical and chemical properties are making an amorphous magnetic material the most promising candidate material for many engineering applications[3]

In view of the existing materials, the discovery of Finemet-type nanocomposite magnetic materials with a composition of Fe73.5Si13.5B9Cu1Nb3 provided some insights into the science and technology of soft magnetic

www.elsevier.com/locate/compositesa

1359-835X/$ - see front matter q 2005 Elsevier Ltd All rights reserved.

doi:10.1016/j.compositesa.2005.01.033

* Corresponding author Tel.: C44 783 823 2277; fax: C44 117 927

2771.

E-mail address: m.h.phan@bristol.ac.uk (M.-H Phan).

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materials[4–8] This kind of materials, routinely obtained

by an appropriate heat treatment of an amorphous precursor,

exhibits excellent magnetic properties due to its unique

microstructure, namely, ultrafine nanocrystalline a-Fe(Si)

grains embedded in an amorphous matrix [6] This is

directly depending on the magnetic exchange coupling

between the grains through the amorphous boundaries

[9,10] However, the underlying physical mechanism of the

magnetic exchange coupling in a nanocrystalline magnetic

material is not well understood

Fortunately, a number of recent studies on the giant

magnetoimpedance (GMI) effect in Fe-based amorphous

soft magnetic alloys subjected to heat treatment showed

some insights into the nature of the magnetic exchange

coupling between these grains through the amorphous

boundaries in Fe-based nanocrystalline materials [7,8,11–

13] Because of the fact that the two-phase Fe-based

nanocomposite material has two distinct Curie

tempera-tures, one for the nanocrystalline grains and the other

belonging to the amorphous phase, the roles of the two

magnetic phases in the intergrain magnetic coupling can be

taken apart in a sufficiently high temperature region

In this context, the study of the temperature dependence

of the magnetic properties and the GMI effect in such a

Fe-based nanocomposite material composed of a

nanocrystal-line phase in an amorphous matrix can be of significant

importance in gaining more rudimentary insights into the

nature of the magnetic coupling in the material This paper

reports the effect of annealing on the structural and magnetic

properties and the GMI effect in a Fe73.5Si15.5Nb3Cu1B7

amorphous alloy

2 Experiment

Fe73.5Si15.5Nb3Cu1B7ribbons with a width of 4 mm and

a thickness of 20 mm were prepared by rapid quenching

method The nanocomposite materials composed of a

nanocrystalline phase in an amorphous matrix were

obtained by annealing these as-quenched amorphous

ribbons at different temperatures ranging between 350 and

650 8C for 30 min in vacuum The structures of the

as-quenched amorphous ribbons and the annealed ones were

examined by X-ray diffraction (XRD) Differential scanning

calorimeter (DSC) measurements on as-cast and annealed

ribbons were conducted with increasing temperature at a

rate of 20 8C/min in Ar atmosphere Accordingly, the

crystallization processes can be monitored by DSC

Transmission electron microscopy (TEM) images of the

nanocrystallized ribbons have been obtained for samples

thinned by using a Philips C30 ion etching device The M–H

hysteresis loops were measured using a vibrating sample

magnetometer (VSM) Magneto-impedance (MI)

measure-ments were carried out along the ribbon axis with the

longitudinal applied magnetic field The samples with a

length of about 15 mm were used for all MI measurements

Details on a MI measurements system can be found elsewhere[14]

3 Results and discussion 3.1 Microstructural analyses

Fig 1 shows the XRD pattern of the Fe-based as-quenched amorphous ribbon It is clear that the pattern exhibited only one broad peak around 2qZ458, which is often known as a diffuse halo, indicating that the sample prepared is amorphous No indication of presence of crystallites was observed by TEM This reflects the absence

of crystal structure, i.e the absence of a long range order

To find out a proper annealing regime for as-quenched amorphous ribbon samples, we carried out DSC measure-ments Typical DSC curves for the as-cast and 540 8C-annealed ribbons are shown inFig 2 It is easy to see clearly fromFig 2that for the as-cast sample the curve has a typical behavior with the two mainly exothermic peaks; the first exothermic peak (first peak at w550 8C) is attributed to the primary crystallization of the nanocrystalline phase (e.g the a-Fe(Si) soft magnetic phase) while the second one is attributed either to the further crystallization of the remaining amorphous phase, or to phase transformation of existing metastable phases, such as Fe3B, following the primary crystallization In the case of the annealed sample, the crystallization peaks shifted to a higher temperature due

to a significant contribution of nucleation It was also found that the first peak disappeared for the sample annealed at

650 8C for 30 min, indicating a full crystallization state Based on the DSC results, as-cast amorphous alloys were annealed at different temperatures ranging between 350 and

650 8C for 30 min in vacuum to achieve the nanocrystalline materials with a-Fe(Si) phase

Furthermore, it is known that the crystallization fraction determines magnetostriction of the ribbon while the grain

Fig 1 The X-ray diffraction pattern of the Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 as-cast amorphous alloy.

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size determines the magnitude of the effective magnetic

anisotropy Both magnetostriction and effective magnetic

anisotropy play a decisive role in the soft magnetic

properties of nanocrystalline magnetic materials It is

therefore necessary to evaluate the crystallization fraction

of the sample after annealing Recently, Leu and Chin[15]

have first proposed the method that allows one to evaluate

the crystallization fraction (cf) from the DSC diagram,

which is expressed by:

cfZDHaKDHt

where DHaand DHt are the crystallization enthalpy of the

as-cast amorphous ribbon and the ribbon annealed for a time

t, respectively An example is also shown inFig 2, where

the crystallization fraction of the sample annealed at 540 8C

for 30 min, corresponding to the a-Fe(Si) phase at the first

peak, reaches a value of 82% We have found that the

amorphous sample became fully crystallized (cfZ100%)

when annealed above 650 8C It should, however, be noted

that the soft magnetic property may be degraded by

excessive crystallization Because, for annealing over

650 8C, the BCC crystallites will grow, and large crystallites

lead to the decoupling of magnetic exchange, and

consequently the good soft magnetic properties are lost

To further scrutinize this feature, the structure of the

amorphous samples after annealing was examined by XRD

and TEM [see Fig 3, for example] After the thermal

treatments the XRD peaks of a-Fe(Si) are seen to emerge

from the amorphous halos The relative intensity of the

various peaks indicates that there is no preferred orientation

in the crystallized phase Furthermore, the mean grain size

(t) of a-Fe(Si) was determined according to the Scherrer

expression[16]:

t Z 0:96l

where l is the X-ray wavelength (lZ1.54056 A˚ ), q is the diffraction angle, and B is the full width at half maximum (FWHM)

In Fig 4 we display the annealing-temperature depen-dence of the mean grain size of the bcc phase estimated from broadening its relation to the peak in the X-ray diffraction patterns using Eq (2) It should be noted that the growth of a-Fe(Si) is controlled by the slow diffusion of Nb and Cu which leads to a nanocrystalline structure As can be seen

Fig 2 DSC curves for Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 ribbons (as-cast and annealed

at 540 8C for 30 min).

Fig 3 X-ray diffraction pattern (in the upper panel) and TEM image (in the lower panel) for the Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 amorphous alloy annealed at

540 8C for 30 min.

Fig 4 The annealing temperature dependence of the mean grain size of the bcc phase estimated from the broadening of the relations in the X-ray diffraction patterns using Eq (2).

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clearly fromFig 4, the mean grain size is about 12 nm and it

remains almost constant until the annealing temperature

reaches 540 8C This indicates that the primary

crystal-lization (the first peak of the DSC curve inFig 2) is actually

the formation of nanocrystalline structure, where a-Fe(Si)

grains are embedded in an amorphous matrix [see the TEM

image inFig 3(b)] Annealing at higher temperatures not

only leads to grain growth of a-Fe(Si), but also additional

phases are formed from the amorphous matrix phase at TaZ

650 8C This second stage of crystallization corresponds to

the second peak in the DSC curve (Fig 2) and boride phases

(e.g Fe3B and Fe2B) are found

3.2 Magnetic characteristics

The crystallization kinetics of the ribbons can be

observed by measurements of thermomagnetic curve, as

shown inFig 5 It is clear to see from this figure that the

ribbon is amorphous at room temperature As the

temperature increases, the magnetization is abruptly

reduced marking the Curie temperature (TC) of the

amorphous phase With further increasing temperature, the

magnetization is small and constant over a large

tempera-ture interval up to a region where crystallization of a-Fe(Si)

leads to an increase of the magnetization The increase of

the magnetization at the crystallization onset (w500 8C

seen in the DSC curve ofFig 2) indicates the formation of

some crystalline magnetic phase(s) On returning from high

temperature, a large amount of a-Fe(Si) grains are

crystal-lized in the sample and this leads to a strong increase of the

magnetization below the TCof a-Fe(Si) [see the curve 2 in

Fig 5] This reflects that any variation in the magnetic

nature of the amorphous phase could change the intergrain

exchange coupling and consequently the magnetic softness

of the nanocomposite material

In order to further evaluate influences of annealing on the

magnetic properties, we measured hysteresis loops and the

annealing-temperature dependence of the coercivity (Hc) is

displayed inFig 6 It is clear that the coercivity decreased

with increasing annealing temperature (Ta) up to 540 8C and then increased at higher temperatures This can be interpreted as following: the gradual decrease of Hcat Ta

well below the onset crystallization temperature (i.e w500 8C, see Fig 2) is a result of structural relaxation, while the drop of Hc in the temperature range of the first crystallization stage (w540 8C) is likely due to the appearance of nanosized a-Fe(Si) grains where magneto-crystalline anisotropies are averaged out Annealing over

540 8C caused a rapid increase of Hc, indicating a large degradation of the soft magnetic properties This coincides well with microstructural change (i.e the abrupt increase of the mean grain size for annealing above 540 8C as seen in

Fig 4) In this case, the increase of nanoparticles size can considerably reduce the magnetic exchange coupling in the nanocrystalline material [9] Furthermore, it is found that the change of Hcwith annealing temperature is correlated well to the temperature dependence of the permeability, where the permeability resulting from the rotational magnetization increased with increasing annealing tem-perature up to 540 8C and then decreased at higher temperatures [13] It is known that the permeability is inversely proportional to the coercivity in the temperature range investigated

3.3 Magnetoimpedance analyses The magnetoimpedance ratio DZ/Z can be defined as

DZ=Zð%ÞZZðHÞ=ZðHmaxÞK1 where Hmax is the external magnetic field sufficient to saturate the impedance and equals to 150 Oe in the present study The GMI profiles of the amorphous samples annealed at different temperatures ranging between 350 and 650 8C were measured and used

to assess the anisotropy field

As reported in Ref [17], the contribution of the transverse permeability to GMI from magnetization rotation becomes dominant in the high frequency range (w10 MHz) and a simple single-domain model was proposed According

to this model, the width of measured GMI peak could reflect

Fig 5 Thermomagnetic curves of the Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 amorphous

alloy: (1) heating cycle and (2) cooling cycle.

Fig 6 The coercive force (H c ) as a function of annealing temperature for

Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 alloys annealed for 30 min.

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the distribution of anisotropy field As shown inFig 7, at a

fixed frequency of 10 MHz, the anisotropy field and GMI

change sensitively with annealing temperature This also

implies that the permeability in the transverse direction

changes sensitively with annealing temperature [13] The

changes in anisotropy field (Hk, as depicted inFig 7) and

the magnitude of GMI [DZ/Z(%)] are plotted as a function

of the annealing temperature inFig 8 It is clear that, with

increasing temperature up to 540 8C, a decrease of the

anisotropy field and an increase of GMI were observed, but

an opposite tendency was found when the annealing

temperature exceeded 600 8C This is respectively related

to the increase of magnetic softness and the microstructural

change of the sample as the annealing temperature is

increased, as discussed in Sections 3.1 and 3.2 These results

also coincided with the annealing-temperature dependence

of the magnetostriction saturation and the effective

anisotropy constant evaluated by separate magnetization

measurements[4–8]

Now let us discuss the interaction between the magnetic

properties and the GMI effect in the Fe-based amorphous

alloy upon annealing by considering a two-phase random

anisotropy model[9] Within the framework of this model,

the nanocrystalline grains in nanocrystalline alloys are

strongly coupled through magnetic exchange interactions, and the local magnetocrystalline anisotropies of grains are averaged out Meanwhile, the intergranular amorphous phase plays an indispensable role, because, only through

it, can the exchange coupling be conveyed Thus, any variation in the magnetic nature of the amorphous phase will consequently change the intergrain exchange coupling, then alter the magnetic softness and the effective anisotropy, and finally modify the GMI features Here, we assume that, for

an amorphous alloy (i.e as-cast state), the amorphous phase

is ferromagnetic and maintaining the exchange coupling As the amorphous sample was annealed at a temperature close

to the crystallization temperature of the soft magnetic phase

of a-Fe(Si), a combination of stress release and the magnetocrystalline anisotropy decrease in the amorphous phase further softens the ribbon magnetically, thus enhance the GMI effect In the present work, the optimal GMI profile was observed for the alloy annealed at 540 8C, as a result of the largest increase in magnetic softness (i.e the largest permeability and the smallest coercivty as seen in Fig 6) The annealing of amorphous ribbons drastically reduced the coercive force and increased the effective magnetic permeability, thus resulted in an increase in GMI effect When annealing temperatures were relatively high, e.g over

600 8C, and close to the crystallization temperature of the hard magnetic Fe-B phase (725 8C, see Fig 2), annealing may damage the soft magnetic phase of a-Fe(Si) and cause a ferromagnetic to paramagnetic transition, the material becomes incapacitated in conveying the intergrain magnetic exchange coupling, an overwhelming decrease in GMI was observed

4 Conclusions

A thorough study of the effect of annealing on structural and magnetic properties and the giant magnetoimpedance effect in the Fe73.5Si15.5Nb3Cu1B7 amorphous alloy has been made It is found that the mean grain size of the a-Fe(Si) crystallites in the order of 12 nm remains almost unchanged until the annealing temperature reached 540 8C The decrease of anisotropy field and the increase of GMI with increasing annealing temperature up to 540 8C were observed and ascribed to the increase of the magnetic permeability and the decrease of the coercivity, whereas the opposite tendency was found for the sample annealed above

600 8C which is likely due to the microstructural change caused by high-temperature annealing This indicates that variation in the magnetic characteristic of the amorphous phase upon annealing changed the intergrain exchange coupling This altered both the magnetic softness and the effective anisotropy and consequently modified the GMI features It is proposed that the temperature-dependent GMI profile is useful to further understand the magnetic exchange coupling between these grains through the amorphous boundaries in Fe-based nanocrystalline materials

Fig 7 GMI profile at fZ10 MHz in Fe 73.5 Si 15.5 Nb 3 Cu 1 B 7 as-cast and

annealed alloys.

Fig 8 Variation of the anisotropy field and magnitude of GMI with

annealing temperature.

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The authors wish to acknowledge the Scientific

cooperation between UK, Korea and Vietnam Research at

Chungbuk National University supported by the Korean

Science and Engineering Foundation through the Research

Center for Advance Magnetic Materials at Chungnam

National University Research at Center for Materials

Science was supported by the Vietnam National Program

for Fundamental Research Grant No 420110

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