Journal of Materials Research and Technology (Nov 2023)

Redox-active pigeon excreta mediated metal oxides nanosheets for enhancing co-catalyst for photovoltaic performance in dye-sensitized solar cells

  • D. Karthigaimuthu,
  • B. Arjun Kumar,
  • T. Elangovan,
  • Gopal Ramalingam,
  • Sujith Kalluri,
  • Salah Addin Burhan Al Omari,
  • Sambasivam Sangaraju

Journal volume & issue
Vol. 27
pp. 4440 – 4451

Abstract

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Pigeon excreta (PE) contains a significant amount of organic components, which are harmful to the environment and humans. Hence, the proper disposal of PE deals with practical problems. Furthermore, using PE for other energy sources is an efficient innovation. In this study, an innovative technique was implemented for producing agglomeration free and distinct metal oxides using PE as a surfactant and capping agent. The different characterizations and their analysis explain the mechanism involved in forming distinct metal oxide nanosheets utilizing PE. The obtained samples were confirmed by the characteristic peaks of PE mediated metal oxides such as (NiO, Co3O4 and CuO) observed in X-ray diffraction (43.47°, 36.61° and 35.71°), and the UV-DRS band-gap narrowing (2.4, 2.13 and 2.02 eV). In the FTIR spectrum, it is clearly evident that there is a high amine group in the PE which plays a key role in reducing the agglomeration in the metal oxides. The morphology of PE mediated NiO, Co3O4 and CuO revealed nanoflakes and nanosheets like structures identified from FE-SEM analysis. The photovoltaic performance of the PE mediated metal oxides showed improved photocurrent conversion efficiencies of 1.2–1.6 times more than pure metal oxides. Among all, the CuO-PE had the most significant photovoltaic performance, with a photoconversion efficiency of 3.22 %. The reduction of I3− to 3I− along the counter electrode/electrolyte interaction is facilitated by the PE mediated transition metal oxides, as shown by the photocurrent response, Tafel plot and electrical impedance spectroscopy results, which were discussed in detail.

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