A systematic synthetic method involving the anion exchange
process
was designed and developed to fabricate the superior functioning three-dimensional
(3-D) urchin-architectured copper cobalt oxide (CuCo2O4; CCO) and copper cobalt sulfide (CuCo2S4; CCS) electrode materials from copper–cobalt carbonate double
hydroxide [(CuCo)2(CO3)(OH)2; CCH].
The effective tuning of chemical, crystalline, and morphological properties
was achieved during the derivatization process of CCH, based on the
anion exchange effect and phase transformation without altering the
3-D spatial assembly. Benefiting from morphological and structural
advantages, CCO and CCS exhibited superior electrochemical activity
with capacity values of 1508 and 2502 C g–1 at 10
A g–1 to CCH (1182 C g–1 at 10
A g–1). The thermal treatment of CCH has generated
a highly porous nature in nanospikes of 3-D urchin CCO structures,
which purveys betterment in electrochemical phenomena than pristine
smooth-surfaced CCH. Meanwhile, the sulfurization reaction induced
the anion effect to a greater extent in the CCS morphology, resulting
in hierarchical 3-D urchins formed by 1-D nanospikes constituting
coaxially swirled 2-D nanosheets with high exposure of active sites,
specific surface areas, and 3-D electron/ion transportation channels.
The asymmetric supercapacitor was constructed with a superior CCS
electrode as a cathode and an activated carbon electrode as an anode,
showing a high specific capacity of 287.35 C g–1 at 7 A g–1 and durability for 5000 cycles with
94.2% retention at a high current density of 30 A g–1. The ultrahigh energy and power density of 135.3 W h kg–1 (10 A g–1) and 44.35 kW kg–1 (30 A g–1) were harvested during the PC device
performance. Our finding proposes an idea about the importance of
anions and phase transformation as a versatile tool for engineering
high-functioning electrode materials and their endeavor toward overwhelming
the major demerit of SCs by aggrandizing the energy density value
and rate performance.