ABSTRACT

Rhodium oxides, including a misfit-layered structure with alternate stacking of a rock salt-type layer and a hexagonal RhO₂ layer, are expected to have good thermoelectric properties. Among them, the thermoelectric properties (electrical conductivity (σ), Seebeck coefficient (S), Figure of merit (ZT) and calculated thermal conductivity (κ) by S, σ, ZT, and absolute temperature (T)) of bismuth-based rhodium oxides ((Bi_1−x,Pb_x)₂Sr₂Rh₂O_y, x = 0 and 0.02, hereafter BSR and BPSR, respectively) were investigated. In comparison with Bi₂Sr₂Co₂O_y (BSC) at 700˚C, S and κ enhanced (increased S, 110 (BSR) and 105 μV K⁻¹ (BPSR) from 85 μV K⁻¹ (BSC) and decreased κ, 0.32 (BSR) and 0.50 W m⁻¹ K⁻¹ (BPSR) from 1.75 W m⁻¹ K⁻¹ (BSC)), whereas σ decreased (15 (BSR) and 31 S cm⁻¹ (BPSR) from 70 S cm⁻¹ (BSC)). BPSR reached the highest ZT value of 0.067 at 700˚C, compared to those of 0.056 (BSR) and 0.027 (BSC).

Keywords:

Electroceramics, Layered Rhodium Oxide, Misfit Layer Structure, Thermoelectric Material, Harman Method

1. Introduction

Thermoelectricity through the Seebeck effect is a technology for converting heat energy to electric power, thus it has a potential for recycling energy in the form of exhausted heat and is therefore expected to generate environmentally clean energy. Thermal-electric (TE) conversion efficiency is represented by a dimensionless figure of merit, ZT = S²σT/κ, where S, σ, κ, and T are the Seebeck coefficient, electrical conductivity, thermal conductivity, and absolute temperature, respectively [1] [2] . From these equations, large S and σ values and a low κ are necessary for high thermoelectric performance. After the discovery of NaCo₂O₄ in 1997 [3] , the two-dimensional structure with alternate stacking of Na (not fully-occupied) and CoO₂ layers attributes to the high ZT and thus, materials having CoO₂ as a common building block have been extensively investigated. Then, misfit layered oxides, such as Ca₃Co₄O_9+δ, Bi₂Ca₂Co₂O_y, and Bi₂Sr₂Co₂O_y have been recognized as potential thermoelectric materials [4] [5] [6] .

Regarding Bi₂Sr₂Co₂O_y (hereafter BSC), it is regarded as a candidate as a high-performance oxide thermoelectric material which can be used in high-temperature environments, ~1000 K [6] . BSC consists of an alternative stack of a rock salt-type Bi₂Sr₂O₄ layer and a hexagonal CoO₂ layer along c-axis with a misfit along b-axis. To improve the TE performance, extensive studies have been performed mainly by doping such as Pb and Na at a Bi-site, Ca at a Sr-site, and Ir at a Co-site [7] [8] [9] and by introducing a second phase [10] and a textured microstructure [11] [12] . In addition, different forms of BSC, a poly-crystal, single crystal, and thin film, were obtained by using various synthetic methods such as techniques of partial melting, pulsed laser deposition, floating-zone, and magnetic-field sputtering [13] [14] [15] .

Rh oxides with a RhO₂ layer are expected to have similar electronic states as Co oxides with a CoO₂ layer, and may be promising candidates for high-ZT materials as Co oxides. In fact, several Rh oxides with the RhO₂ layer, including Sr_1−xRh₂O₄, CuRh_1−xMg_xO₂ and so forth, exhibit high S by analogy to Co oxides [16] [17] [18] .

Bi₂Sr₂Rh₂O_y (BSR), total substitution of Rh for Co, was firstly prepared, and its σ and S values were reported [19] . Afterwards, magnetic properties of Bi-Ba-Rh-O system as well as σ and S were investigated [20] . However, as far as we know, κ and ZT of BSR have not been reported so far. By analogy with BSC, BSR is also expected to be a high-temperature, high-performance thermoelectric oxide. Then, herein we report thermoelectric properties (electrical conductivity (σ), Seebeck coefficient (S), thermal conductivity (κ), Figure of merit (ZT)) of BSR at 700˚C. In addition, the effect of Pb substitution for Bi in BSR, (Bi_1−x,Pb_x)₂Sr₂Rh₂O_y (x = 0.02, BPSR), on the thermoelectric properties was investigated.

2. Experimental

BSR and BPSR powders were synthesized using a conventional solid-state reaction with Bi₂O₃ (Kanto Kagaku, purity 99.9%), PbO (Kanto Kagaku, purity 99.5%), SrCO₃ (Kanto Kagaku, purity 96.0%), Co₃O₄ (Kanto Kagaku, purity 99.95%) and Rh₂O₃ (Kanto Kagaku, purity 99.9%) powders as starting materials. Stoichiometric amounts of the starting materials for BSR and BPSR were wet-ball milled in polyethylene bottles for 20 h using ZrO₂ balls as the milling medium. The mixture was dried and calcined in air at 700˚C for 12 h, followed by calcination in air at 800˚C for 24 h twice, to obtain calcined BSR or BPSR powders. The calcined powder was uniaxially pressed into a rectangular pellet (60 kN cm⁻²) with the dimensions ~ 5 × 1.3 × 20 mm, followed by sintering in air at 930˚C for 24 h. The crystal structures of the prepared samples were characterized by X-ray diffraction (XRD, PW-1700, Panalytical) after pulverizing the pellets. Quantitative analyses were performed by X-ray fluorescence (XRF) using a ZSXP PrimusII system (Rigaku). The valency of Rh ions was measured by X-ray photoelectron spectroscopy (XPS; Axis-Ultra, Shimadzu).

To measure σ and S, two or four Pt wires, respectively, were attached to the rectangular pellets using a Ag conductive paste. The temperature dependences of S (Digital Multi-meter, Model 7563, Yokogawa) with a temperature gradient of 5-15˚C and that of σ (Source/Monitor Unit, E5273A, Agilent Technologies) for the rectangular pellets were measured at 100 and 700˚C by conventional two-probe steady-state and four-probe methods, respectively. A modified Harman method was used to measure ZT at 700˚C, and then κ was calculated using the measured σ, S, and ZT values and the absolute temperature.

3. Results and Discussion

The XRD patterns of BSR and BPSR indicated that they included single phase of BSR indexed after previous report (Figure 1(a)) [19] . The degree of (00l) orientation of BSR was determined using the Lotgering’s factor (f) [21] . The f value was calculated to be 54%, indicating the moderate orientation (complete orientation when f = 100%, and complete random, non-orientation when f = 0%). In Figure 1(b), the XRD peak of BPSR shifted to a lower 2θ angle compared to BSR. This result is reasonable when one considers that the effective ionic radii of Bi³⁺ and Pb²⁺ (six-coordination) are 0.102 and 0.118 nm, respectively. The radius of Sr²⁺ (six-coordination) is 0.116 nm, being quite similar to that of Pb²⁺, and the previous reports on Pb substitution in Bi₂Sr₂Co₂O_y (BSC), concluding the Pb

substitution for a Bi site, not a Sr site [7] , so it is unlikely that Sr was replaced by Pb. Elemental analysis by XRF indicated that the molar ratio of Bi: Sr: Rh in BSR was 1.5:1.6:2.0, and that of Bi: Pb: Sr: Rh in BPSR was 1.6:0.017:1.6:2.0. This molar ratio was not consistent with the starting ratios used in the preparation of BSR and BPSR. The reason might be owing to the evaporation during repeated calcination and sintering processes.

XPS spectra were recorded to quantitatively determine the Rh⁴⁺/Rh³⁺ atomic ratios. Figure 2 shows the measured spectra for the Rh 3d orbital (Rh 3d_5/2 and Rh 3d_3/2; open circles) of BSR and BPSR. The component peaks determined by deconvolution using a Gaussian lineshape (broken line), and the baseline (gray solid line) and fitted peaks (black solid line) are also shown in the figure. The atomic ratios of Rh⁴⁺/Rh³⁺, which were determined by summing the areas of 3d_5/2 and 3d_3/2 for Rh⁴⁺ divided by those for Rh³⁺, were 1.0 and 1.1 for BSR and BPSR, respectively.

Figures 3(a)-(d) show σ, S, κ, and ZT for BSR and BPSR at 700˚C. σ and κ increased upon Pb substitution for Bi. This is reasonable to consider that the substitution of Pb²⁺ for Bi³⁺ causes the hole doping (i.e., carrier doping) as was observed in the BSC. In fact, the Rh⁴⁺/Rh³⁺ ratio was raised. S slightly decreased from BSR to BPSR. This behavior is not consistent with the previous report, demonstrating that S once increased up to x = 0.1 in (Bi_1−x,Pb_x)₂Sr₂Rh₂O_y and then decreased with further increasing x [19] . This discrepancy is still unknown, however, would be attributable to the increase in the Rh⁴⁺/Rh³⁺ ratio (increase in

the Rh⁴⁺ concentration) by Pb substitution. The increase in the Rh⁴⁺ concentration gives the smaller S value by Heike’s formula [14] [20] . The Pb substitution led to the enhancement of the ZT value up to 0.067.

Now, BSR is compared with BSC. In Figures 3(a)-(d), σ, S, κ, and ZT at 700˚C for BSC are also shown. Not shown here, but BSC was synthesized exactly the same way as BSR except for using Co₃O₄ in place of Rh₂O₃. The thermoelectric values of BSC were quite consistent with those reported previously [6] . σ of BSC was higher than that of BSR. This tendency is explained by the different sizes of the hexagonal block, CoO₂ and RhO₂, the RhO₂ block is larger than the CoO₂ block. σ of the Bi-based misfit oxides are predominantly determined by the relative size of the rock-salt block (Bi₂Sr₂O₄ in both BSC and BSR) to the conducting hexagonal block, and the smaller relative size gives the smaller σ [19] . Accordingly the Ioffe’s theory, higher σ of BSC leads to the lower S and higher κ. The ZT value of BSC at 700˚C was 0.027, which was lower than that of BSR, 0.056.

4. Conclusions

The thermoelectric performance of hole doped BPSR increased up to ZT = 0.067, compared to ZT = 0.056 of BSR at 700˚C, due to the fact that the increase in σ dominated the moderate decrease in S and increase in κ. The ZT values of BPSR and BSR were higher than that of BSC (ZT = 0.027). The ZT value for BPSR, which needs to be enhanced more than one order of magnitude to reach the minimum value considered to be required for practical use, which is greater than 1. We are currently seeking to achieve a higher ZT value by applying previously proposed methods to improve ZT of BSC.

This study has added one example, demonstrating that the RhO₂ can be a superior building block to CoO₂, responsible for the enhanced thermoelectricity. Using the RhO₂ block, we could design new Rh oxides, such as Sm-Sr-Rh-O, Bi-Ca-Rh-O and so on.

Acknowledgements

This work was supported by JKA and its promotion funds from KEIRIN RACE.

Cite this paper

Watanabe, T. and Irie, H. (2018) Thermoelectric Properties of Misfit Layered Bismuth-Based Rhodium Oxides, (Bi,Pb)₂Sr₂Rh₂O_y. Journal of Materials Science and Chemical Engineering, 6, 97-103. https://doi.org/10.4236/msce.2018.67011

References