Rapid self-reconstruction of nickel in amorphous nickel borate nanosheets for efficient oxygen evolution in alkaline seawater splitting

被引:0
|
作者
Sakthivel, Thangavel [1 ]
Rajendran, Abiyazhini [2 ]
机构
[1] Kumoh Natl Inst Technol, Dept Chem Engn, Gumi Si, Gyeongsangbuk D, South Korea
[2] Bharathiar Univ, Dept Phys, Coimbatore, Tamil Nadu, India
关键词
Seawater splitting; Oxygen evolution reaction; Hydrogen evolution reaction; Redox couple; Active site; ELECTROCATALYSTS; METAL;
D O I
10.1016/j.flatc.2024.100804
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Enhancing the transformation of true (Ni2+ to Ni3+) active site in amorphous nickel borate (NiB) is the paramount importance in alkaline water/ seawater splitting. In this study, we strengthen the oxygen evolution reaction (OER) performance of amorphous NiB nanosheets by adding Fe. The incorporated Fe enriches conductivity which facilitating formation of real active site in the NiFeB. This unique nanosheet structure of NiFeB features more active sites and large open surface area that permit the better electrolyte diffusion. The optimized electrocatalyst demonstrates impressive OER activity with an ultra-low overpotential of 180 mV (50 mA cm- 2), a small Tafel slope (63 mV dec- 1) also exhibits exceptional durability over 24 h in alkaline water. Similarly, in alkaline seawater, the catalyst displays a low over potential of 185 mV to reach 50 mA cm- 2, a small Tafel slope 46 mV dec- 1 and excellent durability over 24 h. For the hydrogen evolution reaction in alkaline water, the amorphous NiFe0.5B nanosheet shows low overpotential as 290 mV at 10 mA cm- 2, a small Tafel slope 195 mV dec- 1. In overall alkaline seawater splitting, the catalyst delivers 50 mA cm- 2 at the lowest cell voltage of 1.63 V with exceptional stability. This work provides valuable insights into the cost-effective design of amorphous transition metal borate OER catalyst for seawater splitting.
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页数:8
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