TY - JOUR
T1 - Heterointerface-engineered 2D/2D layered heterojunction with electronic coupling for energy storage
AU - Savariraj, Antonysamy Dennyson
AU - Marotrao, Kale Amol
AU - Sivakumar, Periyasamy
AU - Manikandan, Ramu
AU - Gangadhar, Lekshmi
AU - Kim, Byung Chul
AU - Jung, Hyun
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/2/1
Y1 - 2025/2/1
N2 - Co(OH)2 layers were grown on nickel foam by an instantaneous nucleation mechanism regulated by cathodic electrodeposition. Treating Co(OH)2 layers as the template, Ni(OH)2 layers were cladded onto to form Co(OH)2/Ni(OH)2 heterojunction. The resultant self-supported binder-free architectures with abundant active sites and reduced aggregation facilitate faradaic redox reactions and shorten electron transport distance. The heterointerface-engineered Co(OH)2/Ni(OH)2 architecture with interfacial electronic coupling as electrodes highlighted its merits by delivering an areal capacity of 1965 mC cm−2 at 1 mA cm−2, a high specific capacity of 444 C g−1, and a specific capacitance of 889 F g−1 at 1 A g−1. Moreover, the electrode demonstrated its chemical stability and structural endurance, with an 89.5 % retention of specific capacity at the 5000 th cycle. Additionally, the hybrid device assembled with Co(OH)2/Ni(OH)2//activated carbon composition delivered a specific capacity of 181 C g−1 at 1 A g−1, a maximum specific energy of 53.1 Wh kg−1 at 1 A g−1, and an appreciable specific power of 16.56 kW kg−1 at 20 A g−1. The proposed strategy takes advantage of yielding replicated two-dimensional sheets (2D) with interfacial electronic coupling, ample active sites, and high synergy between the two layers, which help in designing high-energy electrochemical storage devices.
AB - Co(OH)2 layers were grown on nickel foam by an instantaneous nucleation mechanism regulated by cathodic electrodeposition. Treating Co(OH)2 layers as the template, Ni(OH)2 layers were cladded onto to form Co(OH)2/Ni(OH)2 heterojunction. The resultant self-supported binder-free architectures with abundant active sites and reduced aggregation facilitate faradaic redox reactions and shorten electron transport distance. The heterointerface-engineered Co(OH)2/Ni(OH)2 architecture with interfacial electronic coupling as electrodes highlighted its merits by delivering an areal capacity of 1965 mC cm−2 at 1 mA cm−2, a high specific capacity of 444 C g−1, and a specific capacitance of 889 F g−1 at 1 A g−1. Moreover, the electrode demonstrated its chemical stability and structural endurance, with an 89.5 % retention of specific capacity at the 5000 th cycle. Additionally, the hybrid device assembled with Co(OH)2/Ni(OH)2//activated carbon composition delivered a specific capacity of 181 C g−1 at 1 A g−1, a maximum specific energy of 53.1 Wh kg−1 at 1 A g−1, and an appreciable specific power of 16.56 kW kg−1 at 20 A g−1. The proposed strategy takes advantage of yielding replicated two-dimensional sheets (2D) with interfacial electronic coupling, ample active sites, and high synergy between the two layers, which help in designing high-energy electrochemical storage devices.
KW - Binder-free architectures
KW - Cathodic electrodeposition
KW - Heterojunction
KW - Interfacial electronic coupling
KW - Nucleation mechanism
UR - https://www.scopus.com/pages/publications/85215209298
U2 - 10.1016/j.cej.2025.159702
DO - 10.1016/j.cej.2025.159702
M3 - Article
AN - SCOPUS:85215209298
SN - 1385-8947
VL - 505
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 159702
ER -