Co-Ni-Mn Sulfide Mixed-Phase Composite Electrode Recovered from Spent LIB Black Mass for High-Performance Supercapacitors

  • Onar O
  • Yasa S
  • Aydin O
  • et al.
0Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

This study reports an integrated hydrometallurgical and hydrothermal route that converts NMC-type black mass from spent Li-ion batteries into a mixed cobalt-nickel-manganese sulfide (CNMS) and demonstrates its application as a high-performance positive electrode for asymmetric supercapacitor (ASC). Black mass is leached in 3 M H 2 SO 4 with 10% v/v H 2 O 2 (S/L = 1:50) at room temperature. The dissolved Co, Ni and Mn are co-precipitated as a mixed hydroxide (CNMOH) by pH adjustment and subsequently sulfidized to produce CNMS via thioacetamide-assisted ion exchange in a hydrothermal reactor (180 °C, 12 h). Electrochemical characterization in a three-electrode cell yields an areal capacitance of 1262 mF.cm −2 (CV, 5 mV.s −1 ) and 1103 mF.cm −2 (GCD, 5 mA.cm −2 ). An ASC (CNMS//graphite, 6 M KOH) delivers an areal capacitance of 88.3 mF.cm −2 (5 mV.s −1 ), respectively. This ASC device shows the energy and power density values of 11.06 μWh.cm −2 and 367 μW.cm −2 and retains 80.6% capacitance after 5000 cycles. The combined recovery-to-device approach highlights the feasibility of upcycling the battery black mass into ternary transition metal sulfide. This work provides a practical pathway to couple critical materials recovery with advanced electrochemical energy storage.

Cite

CITATION STYLE

APA

Onar, O., Yasa, S., Aydin, O., Birol, B., & Gencten, M. (2026). Co-Ni-Mn Sulfide Mixed-Phase Composite Electrode Recovered from Spent LIB Black Mass for High-Performance Supercapacitors. ECS Journal of Solid State Science and Technology, 15(5), 051001. https://doi.org/10.1149/2162-8777/ae672f

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free