TY - JOUR
T1 - Co3S4/Co9S8 doped nitrogen-enriched carbon polyhedron structures as an efficient catalyst for hydrogen evolution reaction
AU - Ayyaluri, Ramakrishna Reddy
AU - Krishna, B. N.Vamsi
AU - Kumar, Mohit
AU - Ankinapalli, Obula Reddy
AU - Yu, Jae Su
N1 - Publisher Copyright:
© 2024 Hydrogen Energy Publications LLC
PY - 2024/6/12
Y1 - 2024/6/12
N2 - The development of stable non-noble and cost-effective metal sulfide-based electrocatalyst materials for hydrogen evolution reaction (HER) is still a great challenge. Herein, we report the rationally designed electrocatalysts containing Co3S4/Co9S8 co-doped nitrogen-enriched porous carbon polyhedrons (Co3S4/Co9S8/NC PHs). The Co3S4/Co9S8/NC PHs were achieved from Zeolitic imidazolate framework-67 PHs by adding sulfur powder and then placing them in an inert atmosphere at 375 °C for 2 h. The prepared electrocatalyst materials were analyzed using X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy techniques. The HER catalytic activity of the Co3S4/Co9S8/NC PHs exhibited the superior overpotential performance of 134 mV at a current density of 10 mA cm−2 with the Tafel slope of −119 mV dec−1. Additionally, the results from chronopotentiometry maintained a strong kinetic response as well as the long cycling stability of 100 h for the Co3S4/Co9S8/NC PHs electrocatalyst at a constant current density of −10 mA cm−2 with 8.4% decay rate. This study demonstrates a new strategy for hydrogen generation synthesizing non-noble catalyst materials with excellent HER activities.
AB - The development of stable non-noble and cost-effective metal sulfide-based electrocatalyst materials for hydrogen evolution reaction (HER) is still a great challenge. Herein, we report the rationally designed electrocatalysts containing Co3S4/Co9S8 co-doped nitrogen-enriched porous carbon polyhedrons (Co3S4/Co9S8/NC PHs). The Co3S4/Co9S8/NC PHs were achieved from Zeolitic imidazolate framework-67 PHs by adding sulfur powder and then placing them in an inert atmosphere at 375 °C for 2 h. The prepared electrocatalyst materials were analyzed using X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller analysis, and X-ray photoelectron spectroscopy techniques. The HER catalytic activity of the Co3S4/Co9S8/NC PHs exhibited the superior overpotential performance of 134 mV at a current density of 10 mA cm−2 with the Tafel slope of −119 mV dec−1. Additionally, the results from chronopotentiometry maintained a strong kinetic response as well as the long cycling stability of 100 h for the Co3S4/Co9S8/NC PHs electrocatalyst at a constant current density of −10 mA cm−2 with 8.4% decay rate. This study demonstrates a new strategy for hydrogen generation synthesizing non-noble catalyst materials with excellent HER activities.
KW - CoS/CoS doping
KW - Hydrogen evolution reaction
KW - Nitrogen-enriched carbon
KW - Water splitting
KW - Zeolitic imidazolate frameworks
UR - http://www.scopus.com/inward/record.url?scp=85193424000&partnerID=8YFLogxK
U2 - 10.1016/j.ijhydene.2024.05.204
DO - 10.1016/j.ijhydene.2024.05.204
M3 - Article
AN - SCOPUS:85193424000
SN - 0360-3199
VL - 70
SP - 686
EP - 695
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
ER -