Zinc vanadate (Zn2V2O7) nanoparticles (NPs) are successfully synthesized through a solution combustion method, employing Menthaspicata leaves extract as a reducing agent (ZVP) and urea as a chemical fuel (ZVU). Subsequently, the resulting NPs undergo calcination at 600 °C for a duration of 3 h. The pure orthorhombic crystal structure with Cmce space group Bragg reflections are observed in ZVP NPs. However, along with pure orthorhombic phase, few planes corresponding to V2O5 are observed. Green extract helps to retain the single orthorhombic phase. Irregular shaped and bigger sized NPs are observed in ZVU whereas in ZVP, few hexagonal and irregular sized NPs gets decorated on the bigger sized NPs. Better crystalline structure and shape are observed in ZVP compared to ZVU. Transmission electron microscopy analysis matches well with the XRD results. The selected area electron diffraction pattern of ZVP confirms the formation of purity of the sample. The direct energy band gap estimated from the Wood and Tauc’s plot was found to be 3 and 3.04 eV for ZVU and ZVP NPs respectively. The photoluminescence experiment was carried out at 290 and 310 nm excitation wavelengths. As excitation wavelength changes, tuning of emission color is observed from blue to red region. This tuning of color is observed in CIE plot. The CCT value clearly indicates that the samples excited under 290 nm can be utilized for cool LEDs whereas, the sample excited under 310 nm can be utilized for warm LEDs. Thus, the synthesized Zinc vanadate NPs might be the promising candidates for warm/cool display technologies as a nanophosphor based on the excitation wavelength. The electrochemical studies and the capacitance process was evaluated in a 1.0 M Na2SO4 solution utilizing a specific three-electrode setup. The calculated specific capacitance values exhibited variability within the range of 56.8 to 89.7 F/g at scan rates ranging from 10 to 100 mV.