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Kautsar et al. Energy Mater. 2025, 5, 500129  https://dx.doi.org/10.20517/energymater.2025.26  Page 3 of 14

               This study aims to investigate how variations in grain size and intergranular phase (IGP) influence σ , κ,
                                                                                                      xx
               and S  in the Nd-Fe-B permanent magnets. These magnets were fabricated from rapidly solidified
                    ANE
               Nd-Fe-B ribbon powders with an initial nano-sized grain structure [36,37] . During the different processing
               stages of hot-pressing, hot-deformation, and grain boundary diffusion process (GBDP), significant
               microstructural changes occur [38-41] , which will be systematically analyzed. The findings are expected to shed
               light on the relationship between microstructural evolution and transport properties in the Nd-Fe-B
               magnets, contributing to the design and optimization of permanent magnet materials for transverse
               thermoelectric applications.

               EXPERIMENTAL
               Nd-Fe-B magnets preparation
               The starting material used in this study was a commercial Nd-Fe-B crushed melt-spun ribbon powder,
               MQU-F, with the composition of Nd Fe Co Ga B  (at%), supplied by Magnequench Co. Ltd. The
                                                        6.6
                                                            0.6 5.6
                                                    73.6
                                                13.6
               MQU-F powder was first hot-pressed at 650 °C under 300 MPa to produce a hot-pressed (HP) compact.
               This HP compact was then hot-deformed at 750 °C with a 75% height reduction, resulting in an anisotropic
               hot-deformed (HD) magnet. To produce GBDP magnets, alloy ribbon flakes of Dy Nd Cu  (at%),
                                                                                               60
                                                                                           20
                                                                                                   20
               Nd Cu  (at%), and Pr Cu  (at%) were prepared using a single-roll melt-spinning machine, followed by
                  80
                                      20
                     20
                                  80
               mechanical crushing. These diffusion sources were chosen based on prior reports demonstrating their
               effectiveness in achieving high coercivity in the ultra-fine grained Nd-Fe-B magnets [39-41] . Due to the limited
               studies on the impact of GBDP on ANE performance, this factor was not considered in the selection
               process. The c-plane surfaces of the HD magnet (2 mm thick) were coated by diffusion sources in the form
               of ribbon flakes (~20 wt%) using a polymer adhesive. The magnets were then heat-treated at 650-750 °C for
               3 h under vacuum, followed by furnace cooling to ambient temperature, resulting in RE-Cu (RE = Dy-Nd,
               Nd, Pr) GBDP HD magnets.
               Characterization and measurements
               Microstructural analysis was conducted using Scanning Electron Microscopy (SEM, Carl ZEISS CrossBeam
               1540EsB) and Transmission Electron Microscopy (TEM, FEI Titan G2 80-200). Sample preparation for
               these analyses was carried out using a focused ion beam (FIB)-SEM device (FEI Helios G4). The magnets
               were sectioned into specific sample dimensions to suit each type of measurement, with the c-axis indicating
               the easy magnetization direction of the magnet (if applicable): 1.5 mm (c-axis) × 1.0 mm × 1.0 mm for
               magnetic  property  measurements,  2  mm  (c-axis)  ×  2  mm  ×  15  mm  for  σ   and  thermoelectric
                                                                                      xx
               measurements, 1.5 mm (c-axis) × 10 mm × 10 mm for thermal diffusivity (D) measurements, and 0.5 mm (c
                                                                               t
               -axis) × 1 mm × 5 mm for Hall measurements. Magnetic properties were evaluated by measuring the
               magnetization curves of the samples using a 7 T superconducting quantum interference device vibrating
               sample magnetometer (SQUID-VSM, Quantum Design MPMS3). A demagnetization correction factor for a
               prism-shaped magnet, as described in ref. , was applied to the measured hysteresis loop to account for the
                                                  [42]
               open-loop measurement. This resulted in a correction factor of 0.25 for the sample used in magnetic
               property measurements and 0.47 for the samples used in lock-in thermography (LIT) measurements. Grain
               alignment was assessed using X-ray diffraction (XRD, Rigaku MiniFlex600, Cr Kα source) by analyzing the
               surface normal to the pressing direction for all bulk samples. The values of σ  and the Seebeck coefficient
                                                                                 xx
               (S ) were simultaneously determined using Seebeck Coefficient/Electric Resistance Measurement System
                 xx
               (ZEM-3, ADVANCE RIKO, Inc.). To quantify S , we measured the anomalous Ettingshausen effect
                                                           ANE
               (AEE), Onsager reciprocal of ANE, using the LIT method [27,43-48] . The LIT technique, based on infrared
               thermometry, enables high-resolution observation of temporal response and spatial distribution induced by
               an external periodic input, with exceptional sensitivity (< 0.1 mK) and spatial resolution (~20 µm) . In the
                                                                                                  [23]
               LIT measurements, the thermal images were captured using an infrared camera while applying a
               square-wave modulated AC charge current with amplitude J  = 1.0 A, frequency f = 1.0-10.0 Hz, and zero
                                                                   c
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