3 research outputs found
Stacked Porous Iron-Doped Nickel Cobalt Phosphide Nanoparticle: An Efficient and Stable Water Splitting Electrocatalyst
Exploration of proficient electrocatalyst
from earth-abundant nonprecious
metals in lieu of noble metal-based catalysts to obtain clean hydrogen
energy through large-scale electrochemical water splitting is still
an ongoing challenge. Herein, iron-doped nickel cobalt phosphide nanoplate
arrays grown on a carbon cloth (NiCoFe<sub><i>x</i></sub>P/CC) are fabricated using a simple hydrothermal route, followed
by phosphorization. The electrochemical analysis demonstrates that
the NiCoFe<sub><i>x</i></sub>P/CC electrode possesses high
electrocatalytic activity for water splitting in alkaline medium.
Benefits from the synergistic effect between the metal centers, two-dimensional
porous nanoplates, and unique three-dimensional electrode configuration
of NiCoFe<sub><i>x</i></sub>P/CC provide small overpotentials
of 39 at 10 mA cm<sup>–2</sup> and 275 mV at 50 mA cm<sup>–2</sup> to drive the hydrogen evolution reaction and oxygen evolution reaction,
respectively. Furthermore, the assembled two-electrode (NiCoFe<sub><i>x</i></sub>P/CC∥NiCoFe<sub><i>x</i></sub>P/CC) alkaline water electrolyzer can achieve 10 mA cm<sup>–2</sup> current density at 1.51 V. Remarkably, it can maintain
stable electrolysis over 150 h. The excellent activity and stability
of this catalyst is proved to be a economical substitute of commercial
noble metal-based catalysts in technologies relevant to renewable
energy
Amorphous Phosphorus-Incorporated Cobalt Molybdenum Sulfide on Carbon Cloth: An Efficient and Stable Electrocatalyst for Enhanced Overall Water Splitting over Entire pH Values
The
development of economical, proficient, and highly stable catalysts
to substitute the expensive noble metal electrodes for electrocatalytic
water-splitting applications is exceedingly desirable. In this context,
the most fascinating and challenging approach is the rational design
of a nanocomposite encompassing multiple components with unique functionalities.
Herein, we describe the fabrication of a strongly catalytic and superb
durable phosphorus-incorporated cobalt molybdenum sulfide electrocatalyst
grown on carbon cloth (P-CoMoS/CC). The hybrid material exhibited
excellent activity for hydrogen and oxygen evolution reactions over
a wide range of pH (1–14) with extremely high stability (∼90%
retention of the initial current density) after 24 h of electrolysis.
Importantly, when P-CoMoS/CC was used as both cathode and anode for
overall water splitting, a very low cell voltage of 1.54 V is required
to attain the 10 mA cm<sup>–2</sup> current density, and the
hybrid material exhibited a long-term stability (89.8% activity retention
after 100 h). The outstanding overall water-splitting performance
compared to an electrolyzer consisting of the noble-metal-based catalysts
Pt/C and RuO<sub>2</sub> makes P-CoMoS one of the most efficient earth-abundant
water-splitting catalysts. Phosphorus incorporation was proved to
be a vital aspect for the improved charge-transfer properties and
catalytic durability of the P-CoMoS/CC catalyst
Enhanced Supercapacitive Performance of Chemically Grown Cobalt–Nickel Hydroxides on Three-Dimensional Graphene Foam Electrodes
Chemical growth of mixed cobalt–nickel hydroxides (Co<sub><i>x</i></sub>Ni<sub>1–<i>x</i></sub>(OH)<sub>2</sub>), decorated on graphene foam (GF) with desirable three-dimensional (3D) interconnected porous structure as electrode and its potential energy storage application is discussed. The nanostructured Co<sub><i>x</i></sub>Ni<sub>1–<i>x</i></sub>(OH)<sub>2</sub> films with different Ni:Co (<i>x</i>) compositions on GF are prepared by using the chemical bath deposition (CBD) method. The structural studies (X-ray diffraction and X-ray photoelectron spectroscopy) of electrodes confirm crystalline nature of Co<sub><i>x</i></sub>Ni<sub>1–<i>x</i></sub>(OH)<sub>2</sub>/GF and crystal structure consists of NiÂ(OH)<sub>2</sub> and CoÂ(OH)<sub>2</sub>. The morphological properties reveal that nanorods of CoÂ(OH)<sub>2</sub> reduce in size with increases in nickel content and are converted into NiÂ(OH)<sub>2</sub> nanoparticles. The electrochemical performance reveals that the Co<sub>0.66</sub>Ni<sub>0.33</sub>(OH)<sub>2</sub>/GF electrode has maximum specific capacitance of ∼1847 F g<sup>–1</sup> in 1 M KOH within a potential window 0 to 0.5 V vs Ag/AgCl at a discharge current density of 5 A g<sup>–1</sup>. The superior pseudoelectrochemical properties of cobalt and nickel are combined and synergistically reinforced with high surface area offered by a conducting, porous 3D graphene framework, which stimulates effective utilization of redox characteristics and communally improves electrochemical performance with charge transport and storage