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MWCNT Aided Cobalt Antimony Sulfide Electrocatalyst for Dye-Sensitized Solar Cells and Supercapacitors: Designing Integrated Photo-Powered Energy System

  • I. John Peter
  • , S. Vijaya
  • , S. Anandan
  • , Smagul Karazhanov
  • , P. Nithiananthi*
  • *Šī darba korespondējošais autors
  • Gandhigram Rural University
  • National Institute of Technology Tiruchirappalli
  • Institute for Energy Technology

Zinātniskās darbības rezultāts: Devums žurnālam › Zinātniskais raksts (žurnālā) › koleģiāli recenzēts

27 Atsauces (Scopus)

Kopsavilkums

The objective of this study is to demonstrate low-cost Pt-free Dye-Sensitized Solar Cells (DSSCs) and an electrode for supercapacitor. Cobalt Antimony Sulfide (CoSbS) and Multiwalled Carbon Nanotubes supported CoSbS (CoSbS/MWCNT) composites are synthesized by a simple hydrothermal technique and are used as an electrocatalyst for the reduction of tri-iodide to iodide ( I3-/I- ). The crystalline structure, morphology, and quantum states of the synthesized samples are analyzed. In a series of electrochemical studies, the CoSbS/MWCNT demonstrated superior electroconductivity and electrocatalytic activity over pristine CoSbS. Notably, the Power Conversion Efficiency (PCE) is reached 6.0% with the CoSbS/MWCNT counter electrode, outpacing the corresponding CoSbS (4.4%) and Co9S8 (1.8%). It is also an effective material for supercapacitors. Moreover, CoSbS/MWCNT has the maximum specific capacity of 382 C g-1 with 3 A g-1 with the acceptable capacitance retention of around 82% over 1000 charge-discharge cycles and excellent rate capability (1/4143 C g-1 at 3 A g-1). Through these findings, it can be discovered that CoSbS/MWCNT is not only a feasible substitute for the standard Pt counter electrode in DSSCs but also has the capacity to store energy. The excellent conversion and storage performance highlight the potential of CoSbS/MWCNT for a photo-powered energy system.

OriģinālvalodaAngļu
Raksta numurs056518
ŽurnālsJournal of the Electrochemical Society
Sējums169
Izdevuma numurs5
DOIs
Publikācijas statussPublicēts - 1 maijs 2022
Ārēji publicētsJā

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