Stabilizing a Ru single atom catalyst through electronic metal-support interaction with a NiCo2O4 support for overall water splitting and urea electrolysis

被引:1
|
作者
Gupta, Astha [1 ]
Ghosh, Swarup [2 ]
Bhalothia, Dinesh [3 ]
Thangarasu, Sadhasivam [4 ]
Ghosh, Biplab [5 ]
Urkude, Rajashri [5 ]
Chowdhury, Joydeep [2 ]
Pande, Surojit [1 ]
机构
[1] Birla Inst Technol & Sci, Dept Chem, Pilani 333031, Rajasthan, India
[2] Jadavpur Univ, Dept Phys, 188 Raja SC Mallick Rd, Kolkata 700032, India
[3] NTHU, Dept Engn & Syst Sci, Hsinchu, Taiwan
[4] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
[5] Bhabha Atom Res Ctr, Beamline Dev & Applicat Sect, Mumbai 400085, India
关键词
HYDROGEN EVOLUTION; ELECTROCATALYSTS; NANOSTRUCTURES;
D O I
10.1039/d4ta04284k
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
Single atom catalysts have manifested themselves as a new frontier in heterogeneous catalysis owing to their maximum atom utilization efficiency. However, their tendency to aggregate leads to poor stability, which limits their application. Herein, we overcome this challenge by stabilising a noble metal single atom catalyst through anchoring it on a metal oxide support, where a strong electronic metal-support interaction prevents their aggregation. Specifically, we have synthesized Ru single atoms anchored on the NiCo2O4 support by using an ultra-low amount of Ru. XAS and HAADF-STEM analysis confirm the presence of isolated Ru single atoms on the support. These isolated Ru atoms have a high density of unoccupied orbitals, which is favourable for electrocatalytic activity. The synthesized Ru single atom catalyst (Ru-SAC) on NiCo2O4 shows superior activity for overall water splitting with a cell potential of 1.57 V, showing excellent stability of 60 h. The synthesized Ru-SAC NiCo2O4 is also active in urea electrolysis and exhibits a cell potential of 1.41 V to generate a current density of 10 mA cm(-2). Density functional calculations reveal that supported single Ru atoms optimized the binding energies of the intermediate of both the HER and OER.
引用
收藏
页码:23819 / 23836
页数:18
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