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Bifunctional Water Splitting Catalysts: Large Current Density

Fuel cell technology is one of the most emerging fields with ecofriendly and everlasting energy source way of producing energy for the urgent requirements. Further it needs to be improved to make it cheap and more environmental friendly.

Among all fuel cells, the hydrogen (H2) and oxygen (O2) fuel cell is the one with zero carbon emission, more ecofriendly, high potential and the byproduct is just only the water. However, supplying the fuels in the purest form (at least the H2) is very essential to ensure higher life cycles and less decay in cell efficiency. Nowadays, commercially available large scale H2 production is mainly dependent on steam reforming of fossil fuels which can also generates CO2 along with H2 and the source that is going to be depleted, and this byproduct is not environmental friendly. Therefore, an emerging alternate technology is needed; in this case the electrolysis of water has given a greater attention than the steam reforming. 

Recently many scientific findings on “electrolysis of water with solid catalysts” were reported, but developing an efficient bifunctional water electrolysis catalysts applied at large current density is the most desirable one.

Adsorption of oxygen and hydrogen on solid surface can induce water electrolysis and reactivity of catalysts is a main key factor for the design of new catalysts for electrochemical water splitting.

Hydrogen (H2) is one of the sustainable energy and the most prospective substitute for traditional fossil fuels owing to its high efficient, environmental friendly and pollution-free properties, good sustainability with a high energy density (146 kJ· g−1 ) [1].

Up-to-date, many efficient catalysts has been developed to reduce the overpotential, particularly in the bifunctional catalysts with high activity and durability at large current density (≥500 mA cm−2) are in demand to further reduce the cost and to improve the practicality.

Platinum- and iridium-based catalysts have performed high activity for HER and OER reactions, but it is very difficult to apply for the commercial application basically because of their rareness and high price.

However, Ru is the cheapest among the entire platinum group metals with 1/3 price of Pt and Ru-based catalysts have excellent activity for water electrolysis under basic condition.
Figure 1. Synthesis procedure of CoOx−RuO2/NF and the process of water splitting [2].

Water electrolysis is one of the most efficient process which can produce high-purity H2. It also can produce conveniently with zero carbon emission, hence becoming one of the most prospective H2 production technology [3].

Prof. Shibin Yin and his team have reported on amorphous CoOx decorated crystalline RuO2 nanosheet catalyst self-supported on nickel foam (CoOx−RuO2/NF) with high performance for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) is prepared successfully by hydrothermal method and annealing. This catalyst with facile preparation and high performance is meaningful for large scale H2 production [2].

Our SNB team have mainly emphasize this new research article to enrich our viewer’s knowledge about the area of intense research on the bifunctional catalysts of water splitting produced with a large current density. Furthermore, their main research findings explains the following aspects viz., (i) A nanosheet self-supported on NF as a bifunctional catalyst is synthesized successfully via hydrothermal method and annealing, which is composed of crystalline RuO2 and amorphous CoOx. (ii) Benefiting from the effective amorphous CoOx decoration to crystalline RuO2 and self-supporting nanosheet structure, the CoOx−RuO2/NF shows superb catalytic activity for both OER and HER with the Tafel slope (69.6 and 42.1 mV dec−1) and overpotential (420 and 215 mV) at ±1500 mA cm−2. (iii) demonstrates good durability (48 h) for OER, HER, and OWS at ±1500 mA cm−2. Hence, this work proposes a strategy for preparing bifunctional water electrolysis catalysts with high performance, especially at large current density.

 References

1. S. Y. Bae, et al., Nanoscale Horiz. 2020, 5, 43−56.

2. T. Yu, et al., ACS Sustainable Chem. Eng. 2020, 8, 17520−17526.

3. X. Zou, et al., Chem. Soc. Rev. 2015, 44, 5148−5180.

--- Dr. A. S. Ganeshraja

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