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Electronic modulation and proton transfer by iron and borate co-doping for synergistically triggering the oxygen evolution reaction on a hollow NiO bipyramidal prism
Designing an Earth-abundant and inexpensive electrocatalyst to drive the oxygen evolution reaction (OER) for high-purity hydrogen production is of great importance. Herein, the cation (iron) and anion (borate) co-doping strategy was proposed to effectively trigger the OER performance on a low-cost N...
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Published in: | Nanoscale 2021-09, Vol.13 (33), p.14156-14165 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Designing an Earth-abundant and inexpensive electrocatalyst to drive the oxygen evolution reaction (OER) for high-purity hydrogen production is of great importance. Herein, the cation (iron) and anion (borate) co-doping strategy was proposed to effectively trigger the OER performance on a low-cost NiO material. The optimal hollow Fe/B
i
-NiO bipyramidal prism shows superior OER performance, and displays a low overpotential (261 mV) at 10 mA cm
−2
, accompanied by a low Tafel slope (46 mV dec
−1
), excellent intrinsic activity and robust stability. The overall alkaline water splitting using Fe/B
i
-NiO/NF as an anode affords low cell voltages of 1.50 and 1.63 V at 10 and 100 mA cm
−2
, and operates steadily at a high current density of 100 mA cm
−2
for 55 h without decay. The excellent electrocatalytic activity could be ascribed to the hollow structure to shorten the mass transfer pathway, the electronic modulation by Fe doping, the increased accessible electroactive sites created by oxygen vacancies through borate doping, and the formation of BO
3
3−
-OH
−
to accelerate the deprotonation of OH
ads
.
The porous hollow Fe/Bi-NiO prism shows excellent OER performance due to the borate doping for accelerating the reaction as M-OH
ads
→ M-O
ads
+ H, abundant oxygen vacancies and the electronic modulation by Fe doping. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d1nr03500b |