Abstract:The advancement in electronic device miniaturization has led to an increase in thermal issues. The reliability of these devices depends on heat dissipation, leading to the development of thermal interface materials (TIMs). In this study, the influence of morphology and surface modification on the thermal characteristics of magnesium oxide (MgO) incorporated epoxy composites was investigated. A wet precipitation method was employed for the synthesis of spherical S-MgO. However, oblong hexagonal H-MgO was obtain… Show more
“…Therefore, to enhance the bonding strength between PDMS an the hydrophilic surface of the MgO structures was modified to a hydrophobic using APTES, which is a silane coupling agent. This modification prevented the ysis of MgO and suppressed the formation of pores at the interface between th and polymer matrices [28]. A thin layer was uniformly coated on the surface modified MgO structures without a significant collapse in the structure (Figur Figure 3c illustrates the FT-IR spectra of the unmodified MgO and APTES and m MgO structures.…”
Owing to the increasing demand for the miniaturization and integration of electronic devices, thermal interface materials (TIMs) are crucial components for removing heat and improving the lifetime and safety of electronic devices. Among these, thermal pads are reusable alternatives to thermal paste-type TIMs; however, conventional thermal pads comprise a homogeneous polymer with low thermal conductivity. Composite materials of thermally conducting fillers and polymer matrices are considered suitable alternatives to high-performance pad materials owing to their controllable thermal properties. However, they degrade the thermal performance of the filler materials at high loading ratios via aggregation. In this study, we propose novel nanocomposites using densely aligned MgO nanowire fillers and polydimethylsiloxane (PDMS) matrices. The developed nanocomposites ensured the enhanced thermal conducting properties, while maintaining mechanical flexibility. The three-step preparation process involves the (i) fabrication of the MgO structure using a freeze dryer; (ii) compression of the MgO structure; and (iii) the infiltration of PDMS in the structure. The resulting aligned composites exhibited a superior thermal conductivity (approximately 1.18 W m−1K−1) to that of pure PDMS and composites with the same filler ratios of randomly distributed MgO fillers. Additionally, the MgO/PDMS composites exhibited adequate electrical insulating properties, with a room-temperature resistivity of 7.92 × 1015 Ω∙cm.
“…Therefore, to enhance the bonding strength between PDMS an the hydrophilic surface of the MgO structures was modified to a hydrophobic using APTES, which is a silane coupling agent. This modification prevented the ysis of MgO and suppressed the formation of pores at the interface between th and polymer matrices [28]. A thin layer was uniformly coated on the surface modified MgO structures without a significant collapse in the structure (Figur Figure 3c illustrates the FT-IR spectra of the unmodified MgO and APTES and m MgO structures.…”
Owing to the increasing demand for the miniaturization and integration of electronic devices, thermal interface materials (TIMs) are crucial components for removing heat and improving the lifetime and safety of electronic devices. Among these, thermal pads are reusable alternatives to thermal paste-type TIMs; however, conventional thermal pads comprise a homogeneous polymer with low thermal conductivity. Composite materials of thermally conducting fillers and polymer matrices are considered suitable alternatives to high-performance pad materials owing to their controllable thermal properties. However, they degrade the thermal performance of the filler materials at high loading ratios via aggregation. In this study, we propose novel nanocomposites using densely aligned MgO nanowire fillers and polydimethylsiloxane (PDMS) matrices. The developed nanocomposites ensured the enhanced thermal conducting properties, while maintaining mechanical flexibility. The three-step preparation process involves the (i) fabrication of the MgO structure using a freeze dryer; (ii) compression of the MgO structure; and (iii) the infiltration of PDMS in the structure. The resulting aligned composites exhibited a superior thermal conductivity (approximately 1.18 W m−1K−1) to that of pure PDMS and composites with the same filler ratios of randomly distributed MgO fillers. Additionally, the MgO/PDMS composites exhibited adequate electrical insulating properties, with a room-temperature resistivity of 7.92 × 1015 Ω∙cm.
“…They have reported that the MgO filler content was ≈20 wt.% which was much lower than 90 wt.% of a commercial alumina TIM. [ 14 ] Hence, MgO and the other materials [carbon nano‐tube (CNT), BN etc.] are used together to obtain the high thermal conductivity.…”
Section: Resultsmentioning
confidence: 99%
“…Recently, the TIM studies have begun to utilize MgO as a thermal filler material, TIM which has a low ratio of MgO filler ratio (≈20 wt.%) has been reported continuously. [ 14 ] In order to obtain high thermal conductivities in heat dissipation materials, the ratio of thermal filler must be high, and the ratio of ceramic filler is ≈90 wt.% in commercial heat dissipation materials. The usage of MgO alone as a ceramic filler is difficult, since MgO does not mix well with polymers due to the rough surface of a MgO filler.…”
The surface treatment for a polymer‐ceramic composite is additionally performed in advanced material industries. To prepare the composite without a surface treatment, the simplest way to manufacture an advanced ceramic‐particle is devised. The method is the formation of a nanocrystalline composite layer through the simple liquid‐phase sintering. Using magnesia (MgO) which shows hydrophilicity, a nanocrystalline surface layer is realized by liquid‐phase sintering. The amorphous matrix of nanocrystalline composite layer makes MgO hydrophobic and ensures miscibility with polymers, and the nanocrystalline MgO ensures high thermal conductivity. In addition, the liquid phase removes the open pores and makes the surface morphology smooth MgO with smooth surface (MgO‐SM). Thermal interface materials (TIM) prepared with MgO‐SM and epoxy show a high thermal conductivity of ≈7.5 W m−1K−1, which is significantly higher than 4.5 W m−1K−1 of pure MgO TIM. Consequently, the formation process of a nanocrystalline surface layer utilizing simple liquid‐phase sintering is proposed as a fabrication method for a next‐generation ceramic‐filler. In addition, it is fundamentally identified that the thermal conductivity of MgO depends on the Mg deficiency, and therefore a poly‐crystal MgO‐SM (produced at a low temperature) has a higher thermal conductivity than a single‐crystal MgO (produced at a high temperature).
“…6d). 2,5,7,9,11,[35][36][37][38][39][40][41][42][43][44][45][46]48 The heat transfer pathway of foams largely depends on their composition. Herein, MgO/Mg(OH) 2 /C foams are composed of MgO, Mg(OH) 2 , and amorphous C; MgO/Co/C foams consist of Co 0 , MgO, and amorphous C. Heat is transferred via electrons in Co 0 and crystal lattice vibrations (phonons) in MgO, Mg(OH) 2 , amorphous C, and pure silica films.…”
Section: The Thermal Performance and Mechanism Of Mgo/co/c Foamsmentioning
Developing multifunctional materials with superior thermal conductivity and microwave absorption is an effective mean to address the increasingly serious electromagnetic (EM) compatibility and heat dissipation problems in modern electron devices....
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