Thermal Conductivity Enhancement Research Articles

Influence of graphene nanoplatelets on the thermal conductivity of heat transfer oils based on the developed hotwire method

The thermal conductivity measurements of graphene nanoplatelets (GNP) loaded mineral oil suspensions are obtained using an unconventional custom-made Transient Hot-Wire setup using tungsten. The presence of a few layers of graphene in the prepared GNP using a single-step ultrasonication of graphite microparticles without the use of a surfactant is verified by AFM, TEM, Raman Spectroscopy, XRD, and XPS techniques. We measured the thermal conductivity and the specific heat capacity ( Cp ) of GNP-loaded mineral oil suspensions. The experimental result shows a maximum of 45.5% increment in the thermal conductivity of the mineral oil with 1 mg ml−1 (11.481 ×10−4 weight fraction) loading of GNP at 30 °C. Despite thermal conductivity enhancements, the results indicate that the Cp is not compromised, since a low concentration of nanoplatelets was used. The experimental results agree with the Maxwell-Garnett effective medium approach (MGEMA) model for the thermal conductivity of nanofluids which we found to be suitable for lower loading of nanoparticles. We propose GNP incorporated mineral oil suspensions are effective when it comes to heat transfer fluids even with the lower volume and mass fractions.

Influence of reinforcement with multimodal distribution on thermophysical properties and fracture behavior in Al-Si/SiC composites infiltrated under super-gravity field

Super-gravity field assisted infiltration is reported as an effective method to obtain the nearly fully-dense Al-Si/SiC composites at relatively lower temperature, which inhibit the interfacial reaction and result in the enhancement of thermal conductivity (TC) and bending strength (BS). Currently, SiC reinforcement with multimodal distribution was designed to further enhance the TC and BS with lower coefficient of thermal expansion (CTE) of Al-Si/SiC composites. For the composites with monomodal SiC distribution, enlarging the size of SiC results in an enhancement of TC with the sacrifice of BS. Interestingly, for the composites with multimodal SiC distribution, the TC can be stabilized within an extended range (175-187W/m·K at 373K) with reduced CTE and higher BS. When the large to small size ratio was 1:2, the optimal comprehensive properties (CTE: 8.66×10-6K-1 ranged from 323 to 373K, TC: 179.2W/m·K at 373K, BS: 309 ± 9MPa) can be obtained. Hasselman-Johnson, Turner, and Kerner models are established to better understand the thermophysical properties, while the fracture behavior is discussed based on the track of crack propagation.

Enhancing Thermal Conductivity of Phase Change Materials Using Nanomaterials and its Effectiveness in Cooling Solar Cells

The latent heat storage system is considered the most promising technology in thermal energy storage (TES) because of its many advantages. This technique uses phase change material (PCM) as a TES medium. However, the low thermal conductivity (TC) of PCM is the major drawback of the system. Previous studies have shown that the addition of nanomaterials to PCM generally increases its TC. On the other hand, researchers tend to study the possibility of using enhanced PCM to cool solar cells. In fact, raising the solar cell’s operating temperature negatively impacts its efficiency. This problem is considered one of the biggest problems in solar energy systems, and researchers are still working to solve it. This paper focused on the possibility of enhancing the TC of paraffin by adding different shapes of silver nanomaterials to it (silver nanoparticles, silver nanowires and nanohybrid with silver nanoparticles and silver nanowires). Nanomaterials were added at volume fractions of 0.5% and 1%. Then, the study examined the ability to use this improved material to reduce the temperature of solar cells. We used the “Solidworks” program to create a 3D system, and then we used the “Ansys Fluent” software to simulate five cases; PV without PCM, PV with PCM, PV with PCM enhanced by nanoparticles, PV with PCM enhanced by nanowires, PV with PCM enhanced by nanohybrid (a mixture of nanoparticles and nanowires). The results show that using PCM enhanced by nanowire at a volume fraction of 0.5% gave the best results in decreasing the temperature of PV. The average temperature of PV declined by 14.9[Formula: see text]. In addition, the efficiency of PV rose by about 7.6%. Followed by using PCM enhanced by nanoparticles at a volume fraction of 1%. The average temperature of PV declined by 12.9[Formula: see text]. Moreover, the efficiency of PV rose by about 6.6%.

Experimental and numerical study on thermal management performance of PCM-based heat sinks with various configurations fabricated by additive manufacturing

Due to the low thermal conductivity of PCM, the enhancement of thermal performance becomes a crucial issue for the application of PCM-based heat sinks in electronic device cooling. To address this, efficient and integrative PCM-based heat sinks using fin and structured porous material (SPM) are designed and fabricated by additive manufacturing (AM). This work aims to investigate thermal performance of PCM-based heat sinks and the role of fin and SPM used as thermal conductivity enhancers (TCEs). The enhanced heat transfer mechanisms in PCM-based heat sinks using different types of TCEs are determined, and parametric analysis is conducted considering various volume fractions of TCEs (10 %, 15 %, and 20 %). Moreover, the effects of heating power levels and convective heat transfer coefficients on thermal behavior of PCM-based heat sink are analyzed. The results indicate that incorporating SPM in heat sink enhances thermal performance more effectively than using fins for an equivalent TCE fraction. Both heating power and convective heat transfer coefficient have a significant on thermal performance. This research demonstrates the potential of the novel heat sink with SPM in cooling electronic devices and provides the experimental and numerical database for the optimal design and future application of PCM-based heat sink.

Effect of nanosized carbon nanotubes, Titanium Nitride and cubic Boron Nitride powders on mechanical and thermal properties of SLA 3D printed resin composites

AbstractThis study explores the development of nanocomposites by incorporating multi‐walled carbon nanotubes (MWCNT), titanium nitride (TiN), and cubic boron nitride (c‐BN) nano powders into photo‐polymer epoxy resins for use in Stereolithography (SLA) additive manufacturing. Mechanical and thermal properties were systematically investigated to assess their performance. Initially, MWCNT, TiN, and c‐BN nano powders were homogeneously mixed with the resin to ensure uniformity. The resulting mixtures were then processed using SLA technology to evaluate production quality and material performance. The study revealed significant improvements in mechanical and thermal properties compared to pure resin, aligning with previous research outcomes. Specifically, the incorporation of MWCNT led to a notable enhancement in thermal conductivity, showing an increase of 24.21% as the thermal conductivity coefficient increased from 0.19 to 2.36 W/m·k. On the other hand, c‐BN significantly boosted mechanical strength, resulting in a substantial 20.45% increase as the shore D hardness went from 88.53 to 106.64. These findings highlight the promising potential of nanocomposites across various industries including electronics, aerospace, automotive, construction, medical devices, and manufacturing.Highlights Developed nanocomposites with MWCNT, TiN, and c‐BN in SLA resin. c‐BN increased hardness by 20.45%, proving its effectiveness in composites. MWCNT enhanced thermal conductivity by 24.21%, boosting material performance. Pioneering use of TiN and c‐BN in SLA, addressing gaps in existing research. Applications span electronics, aerospace, automotive and medical devices.

Enhanced magnon thermal transport in yttrium-doped spin ladder compounds Sr14−xYxCu24O41

Magnons are quasiparticles of spin waves, carrying both thermal energy and spin information. Controlling magnon transport processes is critical for developing innovative magnonic devices used in data processing and thermal management applications in microelectronics. The spin ladder compound Sr14Cu24O41 with large magnon thermal conductivity offers a valuable platform for investigating magnon transport. However, there are limited studies on enhancing its magnon thermal conductivity. Herein, we report the modification of magnon thermal transport through partial substitution of strontium with yttrium (Y) in both polycrystalline and single crystalline Sr14−xYxCu24O41. At room temperature, the lightly Y-doped polycrystalline sample exhibits 430% enhancement in thermal conductivity compared to the undoped sample. This large enhancement can be attributed to reduced magnon-hole scattering, as confirmed by the Seebeck coefficient measurement. Further increasing the doping level results in negligible change and eventually suppression of magnon thermal transport due to increased magnon-defect and magnon-hole scattering. By minimizing defect and boundary scattering, the single crystal sample with x = 2 demonstrates a further enhanced room-temperature magnon thermal conductivity of 19Wm−1K−1, which is more than ten times larger than that of the undoped polycrystalline material. This study reveals the interplay between magnon-hole scattering and magnon-defect scattering in modifying magnon thermal transport, providing valuable insights into the control of magnon transport properties in magnetic materials.

Enhanced Thermal Conductivity of EP Composites by Introducing BN-Al2O3 Hybrid

Enhanced Thermal Conductivity of EP Composites by Introducing BN-Al2O3 Hybrid

Thermal Energy Storage in Concrete by Encapsulation of a Nano-Additivated Phase Change Material in Lightweight Aggregates.

This work discusses the applicability of lightweight aggregate-encapsulated n-octadecane with 1.0 wt.% of Cu nanoparticles, for enhanced thermal comfort in buildings by providing thermal energy storage functionality to no-fines concrete. A straightforward two-step procedure (impregnation and occlusion) for the encapsulation of the nano-additivated phase change material in lightweight aggregates is presented. Encapsulation efficiencies of 30-40% are achieved. Phase change behavior is consistent across cycles. Cu nanoparticles provide nucleation points for phase change and increase the rate of progression of phase change fronts due to the enhancement in the effective thermal conductivity of n-octadecane. The effective thermal conductivity of the composites remains like that of regular lightweight aggregates and can still fulfil thermal insulation requirements. The thermal response of no-fines concrete blocks prepared with these new aggregates is also studied. Under artificial sunlight, with a standard 1000 W·m-2 irradiance and AM1.5G filter, concrete samples with the epoxy-coated aggregate-encapsulated n-octadecane-based dispersion of Cu nanoparticles (with a phase change material content below 8% of the total concrete mass) can effectively maintain a significant 5 °C difference between irradiated and non-irradiated sides of the block for ca. 30 min.

0D/2D Co-Doping Network Enhancing Thermal Conductivity of Radiative Cooling Film for Electronic Device Thermal Management.

The radiative cooling has great potential for electronic device cooling without requiring any energy consumption. However, a low thermal conductivity of most radiative cooling materials limits their application. Herein, a multishape codoping strategy was proposed to achieve collaborative enhancement of thermal conductivity and radiative properties. The hBN-coated hollow SiO2 particles were prepared based on electrostatic self-assembly technology, which were then mixed with hBN platelets and doped into a poly(vinylidene fluoride-co-hexafluoropropylene) substrate. Discrete dipole approximation theory was employed to reveal the mechanism and optimize the particle size. The results showed that the multishape codoping method can significantly improve the radiative performance, with 94.9% reflectivity and 91.2% emissivity. In addition, this zero-dimensional and two-dimensional composite doping structure facilitated the formation of a thermal conduction network, which enhanced the thermal conductivity of the film up to 1.32 W m-1 K-1. The high thermal conductivity radiative cooling film can decrease the heater temperature from 58.8 to 31.3 °C, with a further reduction of temperature by 7.2 °C compared to the radiative cooling substrates with low thermal conductivity. The net cooling power of the film can reach 102.5 W m-2 under direct sunlight. This work provides a novel strategy for high-efficiency electronic device cooling.

Physical Adsorption of Polyacrylic Acid on Boron Nitride Nanotube Surface and Enhanced Thermal Conductivity of Poly(vinyl alcohol) Composites.

To fully tap into the potential of boron nitride nanotubes (BNNTs), addressing their inherent insolubility was imperative. In this study, a water-soluble polymer, poly(acrylic acid) (PAA), was employed as a surface-active reagent, using an accessible and scalable approach. The physical properties and structure of PAA-BNNT were meticulously confirmed through valuable characterization techniques, encompassing X-ray diffraction, scanning electron microscopy, Fourier-transform infrared, X-ray photoelectron spectroscopy, and thermogravimetric analysis. PAA-BNNT exhibited remarkable dispersion in water and demonstrated compatibility with the poly(vinyl alcohol) (PVA) matrix. When incorporating 30 wt % of PAA-BNNT (about 24.75 wt % net BNNT) into the PVA matrix, the thermal conductivity surged by over 21.7 times compared to pure PVA due to the uniform dispersion of high-concentration PAA-BNNT in the polymer matrix.

Molecular insights into thermal conductivity enhancement and interfacial heat transfer of molten salt/porous ceramic skeleton composite phase change materials

Molten salt has been considered as one of the most promising candidate materials for thermal energy storage (TES) systems owing to its remarkable energy density and consistent thermal performance. These properties render it particularly advantageous for the applications in concentrated solar power (CSP) and industrial process heat utilization. Nonetheless, their practical applications still face nonnegligible challenges such as the low thermal conductivity and risk of leakage. Packing molten salts into porous skeletons could be an effective way for addressing these issues. In the present work, the heat transfer characteristics of a composite phase change material (CPCM) consisting of binary chloride salt and a porous ceramic skeleton, are investigated at the microscale level using molecular dynamics (MD) simulations. Simulation results indicate that the integration of a porous SiC skeleton can substantially enhance the thermal conductivity of binary molten salt NaCl/KCl. At the temperature of 1000 K, a notable enhancement of 625.74 % in thermal conductivity has been observed. Moreover, the underlying mechanism of heat conduction enhancement has been revealed from the microscopic perspective. The results demonstrate that auxiliary thermal conductivity paths and interfacial heat transfer play primary roles in determining the thermal conductivity of CPCMs. The method of surface charge modification can effectively improve the interfacial heat transfer and the reason can be attributed to the additional thermal conductivity paths and the large number of particles involved in the interfacial heat transfer. The results gained in this work may provide insights into the heat transfer mechanism of composite molten salt/porous skeleton as well as practical guidance for designing CPCM for thermal storage applications.

Tensile strain induced enhancement of lattice thermal conductivity and its origin in two-dimensional SnC

Tensile strain induced enhancement of lattice thermal conductivity and its origin in two-dimensional SnC

Reversible two-way tuning of thermal conductivity in an end-linked star-shaped thermoset

Polymeric thermal switches that can reversibly tune and significantly enhance their thermal conductivities are desirable for diverse applications in electronics, aerospace, automotives, and medicine; however, they are rarely achieved. Here, we report a polymer-based thermal switch consisting of an end-linked star-shaped thermoset with two independent thermal conductivity tuning mechanisms—strain and temperature modulation—that rapidly, reversibly, and cyclically modulate thermal conductivity. The end-linked star-shaped thermoset exhibits a strain-modulated thermal conductivity enhancement up to 11.5 at a fixed temperature of 60 °C (increasing from 0.15 to 2.1 W m−1 K−1). Additionally, it demonstrates a temperature-modulated thermal conductivity tuning ratio up to 2.3 at a fixed stretch of 2.5 (increasing from 0.17 to 0.39 W m−1 K−1). When combined, these two effects collectively enable the end-linked star-shaped thermoset to achieve a thermal conductivity tuning ratio up to 14.2. Moreover, the end-linked star-shaped thermoset demonstrates reversible tuning for over 1000 cycles. The reversible two-way tuning of thermal conductivity is attributed to the synergy of aligned amorphous chains, oriented crystalline domains, and increased crystallinity by elastically deforming the end-linked star-shaped thermoset.

Metal ion-crosslinked thermoconductive sugar-functionalized graphene fluoride-based cellulose papers with enhanced mechanical properties and electrical insulation

Thermally conductive papers with electrical insulation and mechanical robustness are essential for efficient thermal management in modern electronics. In this study, we introduced a metal ion-assisted interfacial crosslinking strategy to strengthen sugar-functionalized graphene fluoride (SGF) and cellulose nanofibers (CNF) by hydrogen bonding and metal ion crosslinking that leads to simultaneous enhancements in thermal conductivity and mechanical properties. The facile sugar-assisted ball-milling exfoliation method was developed to achieve the exfoliation of graphite fluoride and hydroxyl group functionalization on the surface of graphene fluoride. Thanks to the good dispersibility of the SGF sheets in water, the flexible SGF/CNF composite papers with hydrogen bonding were prepared via vacuum-assisted filtration. We introduced hydrogen bonding and metal ion crosslinking into SGF/CNF papers to obtain densely packed composite papers. Ca2+ or Al3+ ion-crosslinked SGF/ CNF papers exhibited superior thermal and mechanical properties owing to hydrogen bonding and metal ion crosslinking. SGF/CNF-Ca2+ and SGF/CNF-Al3+ papers at 50 wt% of SGF yield in-plane thermal conductivities of 72.93 and 75.02 W m–1 K–1, and tensile strengths of 121.5 and 135.7 MPa, respectively. A thermal percolation value was observed at 12.6 vol% of SGF filler content. In addition, the SGF/CNF papers exhibited electrical insulation properties. These remarkable characteristics of the metal ion-crosslinked SGF/CNF papers are attributed to the densely packed structures caused by the strong interfacial interactions from hydrogen bonding as well as metal ion crosslinking that could promote phonon transport. High-performance metal ion-crosslinked SGF/CNF papers with these fascinating advantages offer great potential for the thermal management of flexible electronics.

MHD nonlinear thermally radiative Ag − TiO 2/H 2 O hybrid nanofluid flow over a stretching cylinder with Newtonian heating and activation energy

Hybrid nanofluids are significant in biomedical, industrial, transportation, as well as several engineering applications due to their high thermal conductivity and mass transfer enhancement nature in contrast to regular fluids and nanofluids. Taking this into consideration, the present problem explores the flow of hybrid nanofluid (Ag − TiO 2/H 2 O) over a stretching cylinder subject to Newtonian heat and mass conditions. The novel aspect of the current work is to analyze the heat and mass transfer characteristics of MHD hybrid nanofluid flow on Darcy-Forchheimer porous medium in addition to activation energy, nonlinear thermal radiation, heat generation/absorption, viscous and Joulian dissipation. Further, Silver (Ag) and Titanium oxide (TiO 2) are the constituent nanoparticles of the water-based hybrid nanofluid owing to their stable chemical features and extensive industrial manufacturing. By introducing suitable similarity transformations, the governing partial differential equations (PDEs) of the developed model are reduced to ordinary differential equations (ODEs), and then the numerical solution is procured with shooting technique by using MATLAB solver bvp4c. The influence of the pertinent parameters is depicted graphically and described elaborately. The analysis indicates that velocity exhibits a declining trend against the permeability and Forchheimer parameters, while the temperature profiles show opposite behavior. The radiation and conjugate heat parameters (R, γ 1) upgrade the heat transfer rate, while the curvature and conjugate mass parameters (α c , γ 2) amplify the mass transfer rate. The maximum heat transfer rate of Ag − TiO 2/H 2 O hybrid nanofluid is 2.3344 attained for γ 1 = 0.6. The investigation demonstrates larger heat and mass transfer rates for Ag − TiO 2/H 2 O hybrid nanofluid than Ag − H 2 O nanofluid. The outcomes of the present investigation have practical applications in conjugate heat transfer over fins, development of vaccines, effluent treatment plants, solar cells, heat exchangers, and many more. An excellent agreement is achieved on comparing our numerical results with the published results in the literature.

Thermal conductivity of different materials nanofluids Nanofluids of MXenes, metal organic frameworks, and other Nanostructured materials in heat transfer applications: Review

Nanoparticles display great potential in heat transfer applications due to their impressive thermophysical properties and unique properties, which enhances the performance of a system. This review delves into the thermophysical characteristics of various nanoparticles, including MXenes, MOFs, CNTs, and graphene, and understand the importance of nanoparticles in heat transfer. MXenes are a relatively new nanoparticle that shows a lot of potential in heat transfer applications; yet, when compared to MOFs, the results demonstrated weren't nearly as impressive because of their larger area and pore size. Conversely, the superior heat transfer performance of CNTs and graphene led to their widespread use in various applications. Thermal conductivity enhancements of 30.6, 64, and 64% for MXene, graphene, and MWCNT were observed when nanoparticles were dispersed in water, indicating better heat transfer for CNT and graphene nanoparticles. Nonetheless, even though some displayed better results than others, each nanoparticle is unique and affects the system distinctively. Additionally, in this review, nanoparticles were investigated computationally, and the results were similar to experimental findings, offering further insight into which nanofluids most effectively influence heat transfer. Overall, nanoparticles enhance system efficiency, making nanofluids reliable for diverse processes despite ongoing challenges. However, nanoparticles in many systems are still being discovered and face many challenges. Therefore, future research should try to focus on studying the effects of nanoparticles in new and large-scale applications and seek solutions to the challenges faced by certain nanoparticles to improve these systems.

Anisotropic Thermal Conductivity Enhancement of the Aligned Metal-Organic Framework under Water Vapor Adsorption.

Metal-organic frameworks (MOFs) exhibit high adsorption and catalytic activities for various gas species. Because gas adsorption can cause a temperature increase in the MOF, which decreases the capacity and adsorption rate, a strict evaluation of its effect on the thermal conductivity of MOFs is essential. In this study, the thermal conductivity measurement of the MOF under water vapor adsorption was performed using an oriented film of copper tetrakis(4-carboxyphenyl)porphyrin (Cu-TCPP) MOF. A recently developed bidirectional 3ω method enabled the anisotropic thermal conductivity measurement of layered Cu-TCPP while maintaining its ordered structure. The water adsorption was found to increase the thermal conductivity in both in-plane and cross-plane directions with different trends and magnitudes, owing to the structural anisotropy. Molecular dynamics simulations suggest that additional vibrational modes provided by the adsorbed water molecules were the reason for the thermal conductivity enhancement.

Enhanced thermal conductivity of reduced graphene oxide reinforced polymer films through a novel GO reduction mechanism

AbstractGraphene's remarkable thermal conductance characteristics makes it a very promising thermal interface material for polymeric composites. In this study, we propose an innovative approach aimed at augmenting the thermal conductivity of flexible composite films, employing reduced graphene oxide (rGO) and polyvinyl alcohol (PVA) as the constituent materials. The fabrication process involves the utilization of solution casting coupled with a low‐temperature chemical reduction method for graphene oxide (GO). Given that the high thermal conductivity of polymer nanocomposites typically correlates with increased crystallinity and reduced defects, our primary objective is to investigate the impact of reduction of GO in order to associate enhance crystallinity within the graphene oxide‐polymer system, with the overall increased thermal conductivity of the resulting GO/PVA films. The diethylene glycol‐GO/PVA films thus, generated through this methodology exhibit an exceptional thermal conductivity of approximately 5.1 W/mK, achieved with a mere 10 wt.% filler loading. This surpasses the thermal conductivity observed in films comprised solely of GO/PVA. The notable enhancement in thermal conductivity can be attributed to several factors, including improved crystallinity and reduced defects of GO with effective polymeric bridging facilitated by the rGO with PVA. Collectively, these advancements contribute to the overall thermal performance of the material, presenting a promising methodology for future developments in the field of thermal conductivity materials.Highlights Reduction of GO through a streamlined and facile methodology. Orchestrated a controlled reduction process at lower temperatures and simultaneously enhancing the crystallinity and decreasing the defects of GO. Fabricated reduced GO/PVA polymer films exhibited an exceptional thermal conductivity of approximately 5.1 W/mK with just a 10 wt.% filler loading.

Interweaved filler network in epoxy resin with reduced interface thermal resistance via in-situ high-temperature “welding” for significantly improved thermal conductivity

For heterogeneous integration in harsh environments, polymeric materials are required to integrate excellent insulating property with significant thermal conductivity. Traditional discrete fillers used in polymeric matrix to create thermal pathways introduce numerous contact interfaces, leading to limited thermal conductivity enhancement efficiency (TCE) and unstable dielectric properties. Here, a distinctive strategy, involving the preparation of an interweaved thermally conductive filler with inherent heat channels through self-templated electrospinning and in-situ high-temperature “interface welding”, is proposed to reduce the interface thermal resistance (ITR). The growth of grains at high temperature facilitates the process of “interface welding”, while self-templated electrospinning establishes intrinsic thermal conduction pathways. Consequently, the epoxy resin fortified with this interweaved filler exhibits an exceptionally TCE of 162.15 % and enhanced in-plane thermal conductivity of 3.75 W m−1 K−1 at ultra-low filler ratio of 7.10 vol%. The combination of high electrical insulation of filler and low filler content results in excellent electrical insulating property (>1017 Ω cm) and stable dielectric properties over a frequency range of 103-106 Hz, enabling the successful implementation of heterogeneous integration in challenging environments. This work has the potential to offer a groundbreaking approach for achieving interconnected functional networks within polymer-based composites.

Synthesis and thermophysical property characterization of aqueous graphene quantum dot dispersions for air-conditioning applications

Air-conditioning systems are on track to demand most of the electricity consumed by buildings around the world. The authors propose that dispersing quantum dots into the chilled water loops of air-conditioners represents a path towards improving the efficiency of air-conditioners. As such, the thermophysical properties of carbon-based quantum dot ‘nanofluids’ (e.g., nanoparticles dispersed in liquids) are presented in this study for sub-ambient temperatures (5–15°C)—an under-explored temperature range which requires understanding for air-conditioning applications. This study also explores dispersion stability and materials compatibility—another under-explored area in the literature which is required for commercial uptake. In this study, carbon quantum dots were synthesized via the hydrothermal route and characterized with UV–Vis, FT-IR, Raman spectroscopy, and TEM. Next, the thermophysical properties of specific heat capacity, thermal conductivity, and viscosity of the nanofluids were experimentally measured between 5 and 15°C (not previously reported for aqueous quantum dots). The highest thermal conductivity enhancement was ∼11% (compared to DI water) for 0.3 wt.% at ∼11 °C. Finally, the stability of the fluid was monitored over time and after exposing the fluids to common materials used in air-conditioning systems (e.g., copper, brass, and stainless steel). Unchanged UV–Vis spectra and the lack of sedimentation indicate that the developed dispersions are indeed suitable for chilled water air-conditioning applications.