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Highly Efficient and Stable Iridium Oxygen Evolution Reaction Electrocatalysts Based on Porous Nickel Nanotube Template Enabling Tandem Devices with Solar-to-Hydrogen Conversion Efficiency Exceeding 10

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Journal Adv Sci (Weinh)
Date 2022 Jan 24
PMID 35068083
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Abstract

Ir is one of the most efficient oxygen evolution reaction (OER) catalysts; however, it is also one of the rarest and most expensive elements. Therefore, it is highly desirable to develop Ir catalysts with nanostructures that reduce Ir consumption by maximizing the surface-to-volume ratio without limiting the mass transport of reactants and products of reactions. Ir OER catalysts on a template that consisted of porous nanotubes (PNTs) based on Ni are fabricated. The Ir/Ni PNTs offer multiple benefits, including high catalytic performance (potential of 1.500 V vs. reversible hydrogen electrode (RHE) at an operating current density of 10 mA cm and Tafel slope of 44.34 mV decade ), minimal use of Ir (mass activity of 3273 A g at 1.53 V vs RHE), and facile mass transport through the NT-sidewall pores (stable operation for more than 10 h). The Ir/Ni PNTs are also applied to a tandem device, consisting of a Cu(In,Ga)Se -based photocathode and halide perovskite photovoltaic cell, for unassisted water splitting. A solar-to-hydrogen conversion efficiency that exceeded 10% is also demonstrated, which is nearly 1% point greater than when a planar Ir film is used as the anode instead of Ir/Ni PNTs.

Citing Articles

Organometal Halide Perovskite-Based Photoelectrochemical Module Systems for Scalable Unassisted Solar Water Splitting.

Choi H, Seo S, Yoon C, Ahn J, Kim C, Jung Y Adv Sci (Weinh). 2023; 10(33):e2303106.

PMID: 37752753 PMC: 10667810. DOI: 10.1002/advs.202303106.


Highly Efficient and Stable Iridium Oxygen Evolution Reaction Electrocatalysts Based on Porous Nickel Nanotube Template Enabling Tandem Devices with Solar-to-Hydrogen Conversion Efficiency Exceeding 10.

Nam Y, Kim D, Chu J, Park N, Kim T, Kim K Adv Sci (Weinh). 2022; 9(9):e2104938.

PMID: 35068083 PMC: 8948658. DOI: 10.1002/advs.202104938.

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