Interface Catalysts of Ni 3 Fe 1 Layered Double Hydroxide and Titanium Carbide for High-Performance Water Oxidation in Alkaline and Natural Conditions

The electrocatalytic oxygen evolution reaction (OER) is important for many renewable energy technologies. Developing cost-effective electrocatalysts with high performance remains a great challenge. Here, we successfully demonstrate our novel interface catalyst comprised of Ni Fe -based layered doubl...

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Veröffentlicht in:The journal of physical chemistry letters 2023-06, Vol.14 (24), p.5692-5700
Hauptverfasser: Song, Fuzhan, Debow, Shaun, Zhang, Tong, Qian, Yuqin, Huang-Fu, Zhi-Chao, Munns, Kaylee, Schmidt, Sydney, Fisher, Haley, Brown, Jesse B, Su, Yanqing, Zander, Zachary, DeLacy, Brendan G, Mirotznik, Mark S, Opila, Robert L, Rao, Yi
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container_end_page 5700
container_issue 24
container_start_page 5692
container_title The journal of physical chemistry letters
container_volume 14
creator Song, Fuzhan
Debow, Shaun
Zhang, Tong
Qian, Yuqin
Huang-Fu, Zhi-Chao
Munns, Kaylee
Schmidt, Sydney
Fisher, Haley
Brown, Jesse B
Su, Yanqing
Zander, Zachary
DeLacy, Brendan G
Mirotznik, Mark S
Opila, Robert L
Rao, Yi
description The electrocatalytic oxygen evolution reaction (OER) is important for many renewable energy technologies. Developing cost-effective electrocatalysts with high performance remains a great challenge. Here, we successfully demonstrate our novel interface catalyst comprised of Ni Fe -based layered double hydroxides (Ni Fe -LDH) vertically immobilized on a two-dimensional MXene (Ti C T ) surface. The Ni Fe -LDH/Ti C T yielded an anodic OER current of 100 mA cm at 0.28 V versus reversible hydrogen electrode (RHE), nearly 74 times lower than that of the pristine Ni Fe -LDH. Furthermore, the Ni Fe -LDH/Ti C T catalyst requires an overpotential of only 0.31 V versus RHE to deliver an industrial-level current density as high as 1000 mA cm . Such excellent OER activity was attributed to the synergistic interface effect between Ni Fe -LDH and Ti C T . Density functional theory (DFT) results further reveal that the Ti C T support can efficiently accelerate the electron extraction from Ni Fe -LDH and tailor the electronic structure of catalytic sites, resulting in enhanced OER performance.
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Developing cost-effective electrocatalysts with high performance remains a great challenge. Here, we successfully demonstrate our novel interface catalyst comprised of Ni Fe -based layered double hydroxides (Ni Fe -LDH) vertically immobilized on a two-dimensional MXene (Ti C T ) surface. The Ni Fe -LDH/Ti C T yielded an anodic OER current of 100 mA cm at 0.28 V versus reversible hydrogen electrode (RHE), nearly 74 times lower than that of the pristine Ni Fe -LDH. Furthermore, the Ni Fe -LDH/Ti C T catalyst requires an overpotential of only 0.31 V versus RHE to deliver an industrial-level current density as high as 1000 mA cm . Such excellent OER activity was attributed to the synergistic interface effect between Ni Fe -LDH and Ti C T . 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title Interface Catalysts of Ni 3 Fe 1 Layered Double Hydroxide and Titanium Carbide for High-Performance Water Oxidation in Alkaline and Natural Conditions
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