This study examines the thermophysical properties of ethylene glycol-glycerol (60:40 v/v) hybrid nanofluids containing graphene nanoplatelets (GNPs) and silver nanoparticles (Ag) at concentrations of 0.1-0.5 vol.%. The nanofluids were synthesized using a two-step method with Tween-80 surfactant to enhance dispersion stability. High-resolution transmission electron microscopy (TEM) and Raman spectroscopy confirmed the morphology, lateral size, few-layer structure of GNPs, and the attachment of Ag nanoparticles. The addition of surfactant increased the zeta potential from 15.7 mV to 35.2 mV for the 0.1 vol.% GNPs/Ag formulation, indicating a marked improvement in colloidal stability. Thermal conductivity enhancement reached 102.85% at 0.1 vol.% with only a 19.84% viscosity increase. Higher nanoparticle loadings improved conductivity further but caused significant viscosity increases and reduced stability. Specific heat capacity decreased by up to 46.45%, potentially benefiting rapid thermal response applications but limiting heat storage capacity. Comparison with recent literature showed that the present formulation outperforms several similar Ag- and GNP-based nanofluids in thermal conductivity enhancement while maintaining manageable viscosity. This study is the first to report such high conductivity improvement in an EG-GLY-based hybrid nanofluid at ultra-low loading, achieved through optimized surfactant use, validated structural characterization, and benchmarking against literature. Low-concentration GNPs/Ag hybrid nanofluids, particularly at 0.1 vol.%, offer strong potential for thermal management applications where high heat transfer performance and acceptable pumping requirements are critical. However, stability limitations at higher concentrations and viscosity-conductivity trade-offs highlight the need for further optimization before large-scale deployment.
Dye-Sensitized Solar Cells (DSSCs) have attracted great attention due to environmentally friendly low-cost processing, excellent working ability in diffuse light, and potential to meet the power demands of future buildings due the true class of building integrated photovoltaics (BIPV). Nevertheless, DSSCs have relatively low photoconversion efficiency (PCE) due to multiple issues. Several strategies have been employed to enhance its PCE. For instance, bi-layered structure of photoelectrode i.e., mesoporous TiO2 transparent layer with top scattering layer was introduced which scatter light inside on large angles improves the harvesting ability of photoelectrode thus enhanced PCE. However, scattering layer is composed of aggregated small particles which offer sluggish electron transport due to multiple grain boundaries, consequently, unwanted recombination reaction which leads to poor PCE. This issue has been addressed for transparent layer immensely but ignored for scattering layer. Mostly for scattering layer in previous studies novel structures have been proposed to enhance scattering properties and dye adsorption only. Therefore, in this study for the first time presenting dual functional graphene/TiO2 scattering layer in which solvent exfoliated graphene is incorporated in TiO2 submicron spheres which enhanced electron transport properties, while submicron spheres scatter light effectively. Scattering and electron transport characteristics of DSSCs are thoroughly investigated with the function of graphene loading. Electrochemical impedance spectroscopy (EIS) has revealed that diffusion coefficient length and coefficient and conductivity attained maximum value at 0.01 wt%. while other important parameters such as electron lifetime and electron density in conduction band have been improved till 0.020 wt% graphene loading. However, results indicated that with 0.01 w% graphene 33% higher PCE was achieved than without scattering layer and 13% higher than scattering layer without graphene. The depraving in PCE at >0.01 wt% graphene despite of excellent electron transport improvement is attributed to the loss of diffuse reflectance and higher optical absorption by graphene.