Flexible Bifunctional Electrode for Alkaline Water Splitting with Long-Term Stability

被引:10
|
作者
Ganguly, Abhijit [1 ]
Mcglynn, Ruairi J. [1 ]
Boies, Adam [2 ]
Maguire, Paul [1 ]
Mariotti, Davide [1 ]
Chakrabarti, Supriya [1 ]
机构
[1] Ulster Univ, Sch Engn, Belfast BT15 1AP, North Ireland
[2] Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England
基金
英国工程与自然科学研究理事会;
关键词
bifunctional and flexible electrode; macroscopicallyassembled carbon nanotube (CNT) ribbons; nickel oxides (NiO)quantum dots (QDs); plasma-induced nonequilibrium electrochemistry(PiNE); hydrogen evolution reaction (HER); oxygenevolution reaction (OER); water electrolysis; overallwater splitting (OWS) in alkaline media; alkaline electrolyzercell; long-term OWS stability; HYDROGEN EVOLUTION; CARBON NANOTUBE; SOLAR-CELLS; NICKEL FOAM; ELECTROCATALYSTS; EFFICIENT; GRAPHENE; FILMS;
D O I
10.1021/acsami.3c12944
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Progress in electrochemical water-splitting devices as future renewable and clean energy systems requires the development of electrodes composed of efficient and earth-abundant bifunctional electrocatalysts. This study reveals a novel flexible and bifunctional electrode ( NiO@CNTR ) by hybridizing macroscopically assembled carbon nanotube ribbons ( CNTRs ) and atmospheric plasma-synthesized NiO quantum dots (QDs) with varied loadings to demonstrate bifunctional electrocatalytic activity for stable and efficient overall water-splitting (OWS) applications. Comparative studies on the effect of different electrolytes, e.g., acid and alkaline, reveal a strong preference for alkaline electrolytes for the developed NiO@CNTR electrode, suggesting its bifunctionality for both HER and OER activities. Our proposed NiO@CNTR electrode demonstrates significantly enhanced overall catalytic performance in a two-electrode alkaline electrolyzer cell configuration by assembling the same electrode materials as both the anode and the cathode, with a remarkable long-standing stability retaining similar to 100% of the initial current after a 100 h long OWS run, which is attributed to the "synergistic coupling" between NiO QD catalysts and the CNTR matrix. Interestingly, the developed electrode exhibits a cell potential (E-10) of only 1.81 V with significantly low NiO QD loading (83 mu g/cm(2)) compared to other catalyst loading values reported in the literature. This study demonstrates a potential class of carbon-based electrodes with single-metal-based bifunctional catalysts that opens up a cost-effective and large-scale pathway for further development of catalysts and their loading engineering suitable for alkaline-based OWS applications and green hydrogen generation.
引用
收藏
页码:12339 / 12352
页数:14
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