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The high-intactness and ultraclean fabrication of suspended 2D materials has always been a challenge due to their atomically thin nature. Here, we present a universal polymer-free transfer approach for fabricating suspended 2D materials by using volatile micro-molecule cyclododecane as the transfer medium, thus ensuring the ultraclean and intact surface of suspended 2D materials. For the fabricated monolayer suspended graphene, the intactness reaches 99% for size below 10 µm and suspended size reaches 36 µm. Owing to the advantages of ultra-cleanness and large size, the thermal conductivity reaches 4914 W m − 1 K − 1 at 338 K. Moreover, this strategy can also realize efficient batch transfer of suspended graphene and is applicable for fabricating other 2D suspended materials such as MoS2. Our research not only establishes foundation for potential applications and investigations of intrinsic properties of large-area suspended 2D materials, but also accelerates the wide applications of suspended graphene grid in ultrahigh-resolution TEM characterization. Here, the authors report a polymer-free transfer method to fabricate suspended 2D materials with high intactness and thermal conductivity, facilitating the application of graphene grids for high-resolution electron microscopy. [ABSTRACT FROM AUTHOR]

Thermal interface materials (TIMs) are the key to solving heat dissipation problems in high-power electrical equipment. TIMs with high thermal conductivity and low thermal contact resistance (TCR) will enhance interfacial heat transfer. In this work, a phase-change mediated graphene composite hydrogel with low TCR and high thermal conductivity is designed. In addition, by introducing the hydrogel cross-linked network into the phase change material, the phase change material leakage problem is effectively solved. The thermal conductivity of the phase change hydrogel is enhanced by 324% from 0.3 W m − 1 K − 1 to 1.23 W m − 1 K − 1 at a filling rate of 7 wt% of graphene. The effects of temperature and pressure on phase change composite hydrogels are investigated. When the temperature is increased from 50 °C to 80 °C, TCR decreases rapidly from 90 K ∙ c m 2 / W to 0.2–0.5 K ∙ c m 2 / W , which is attributed to the improved interfacial wettability mediated by the phase change. When the pressure is increased from 10 Psi to 50 Psi with 80 °C, TCR decrease from 20 K ∙ c m 2 / W to 0.5 K ∙ c m 2 / W , improving interfacial contact and enhancing interfacial heat transfer. Combining a hydrogel with a cross-linked structure with the phase change material resulted in an excellent encapsulation of the phase change material. The thermal management performance of the phase change hydrogel is evaluated using infrared thermography and shows good thermal response behavior as the temperature rose to 68.7 °C after 120 s of heating. The strategy of combining phase change materials with hydrogels will provide new ideas for the design of TIMs. [Display omitted] [ABSTRACT FROM AUTHOR]

Vertically oriented graphene (VG), owing to its sharp edges, non-stacking morphology, and high surface-to-volume ratio structure, is promising as a consummate material for the application of photoelectric detection. However, owing to high defect and fast photocarrier recombination, VG-absorption-based detectors inherently suffer from poor responsivity, severely limiting their viability for light detection. Herein, we report a high-performance photodetector based on a VG/indium tin oxide (ITO) composite structure, where the VG layer serves as the light absorption layer while ITO works as the carrier conduction channel, thus achieving the broadband and high response nature of a photodetector. Under the illumination of infrared light, photoinduced carriers generated in VG could transfer to the floating ITO layer, which makes them separate and diffuse to electrodes quickly, finally realizing large photocurrent detectivity. This kind of composite structure photodetector possesses a room temperature photoresponsivity as high as ~0.7 A/W at a wavelength of 980 nm, and it still maintains an acceptable performance at temperatures as low as 87 K. In addition, a response time of 5.8 s is observed, ~10 s faster than VG photodetectors. Owing to the unique three-dimensional morphology structure of the as-prepared VG, the photoresponsivity of the VG/ITO composite photodetector also presented selectivity of incidence angles. These findings demonstrate that our novel composite structure VG device is attractive and promising in highly sensitive, fast, and broadband photodetection technology. [ABSTRACT FROM AUTHOR]

With the booming development of electronic devices usually used in a dynamic working environment, there is an urgent need for thermal interface materials with low thermal contact resistance, high thermal conductivity, excellent elasticity, and self-healing properties. A novel thermal interface material is obtained by incorporating graphene into a polyacrylate-based double cross-linked hydrogel. The introduction of graphene into the hydrogel can improve the thermal conductivity of the thermal interface material and enhance the tensile properties of the hydrogel. The composite thermally conductive hydrogel has self-healing properties, precisely meeting the thermal interface material's dynamic working environment. Besides, the effects of pressure and temperature on the thermal contact resistance are investigated. When the pressure increases from 10 Psi to 50 Psi at 35 °C, the thermal contact resistance is reduced to 0.069 K ∙ cm 2/ W. Under certain pressure, the effect of temperature on the thermal contact resistance is minor. Overall, the thermal contact resistance remains low (0.5–0.9 K ∙ cm 2/ W). The composite hydrogel is demonstrated excellent thermal management performance under the combined effect of high thermal conductivity and low thermal contact resistance by steady-state thermal analysis simulations and infrared thermography. Highly elastic, self-healing, low thermal resistance composites will present ideas for further construction of new thermal interface materials. [ABSTRACT FROM AUTHOR]

Reducing thermal contact resistance (TCR) is an important way to enhance heat dissipation of electronic devices. Elastomer is easy to deform, increase the contact area and reduce the TCR, but its wetting condition is not satisfying. In this work, a novel elastomeric thermal interface materials (TIMs) polyethylene glycol/unsaturated polyester resin/graphene (PEG/UPR/G) was designed and prepared. With the increase of temperature, PEG near surface of PEG/UPR/G was released due to phase transformation, and a thin molten layer would be attached to the surface. By this way, the micro bumps on the solid surface were all soaked by the thin layer of molten PEG, which greatly reduced the TCR. In addition, the effect of temperature and pressure on TCR of elastomeric PEG/UPR/G were studied. When the pressure increases from 10 Psi to 50 Psi (65 °C), TCR decreases from 11–14 K ∙ cm 2/ W to 2–4 K ∙ cm 2/ W. The TCR will be further reduced to 0.7–0.9 K ∙ cm 2/ W (75 °C) due to the phase transition of PEG. Moreover, the heat dissipation effect of PEG/UPR/G was evaluated by infrared thermal imager. These results demonstrate that the total thermal resistance is the decisive factor for the final steady-state temperature and the time of unsteady heat transfer. [ABSTRACT FROM AUTHOR]