Core–Shell NiFe-LDH@NiFe-Bi Nanoarray: In Situ Electrochemical Surface Derivation Preparation toward Efficient Water Oxidation Electrocatalysis in near-Neutral Media
Source abstract
Abstract
The corrosion issue with acidic and alkaline water electrolyzers can be avoided by developing water oxidation catalysts performing efficiently under benign conditions. In this Letter, we report that a NiFe-borate layer can be generated on a NiFe-layered double hydroxide nanosheet array hydrothermally grown on carbon cloth via an in situ electrochemical surface derivation process in potassium borate (K–B i ) solution. The resulting 3D NiFe-LDH@NiFe-B i nanoarray (NiFe-LDH@NiFe-B i /CC) demonstrates high activity for water oxidation, demanding overpotentials of 444 and 363 mV to achieve 10 mA cm –2 in 0.1 and 0.5 M K–B i (pH: 9.2), respectively, rivaling the performances of most reported non-noble-metal catalysts in near-neutral media. Notably, this electrode also shows strong electrochemical durability with a high turnover frequency of 0.54 mol O 2 s –1 at overpotential of 600 mV. All these features promise its use as an efficient earth-abundant catalyst material for water oxidation under eco-friendly conditions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, Shandong, China
Chengdu Institute of Geology and Mineral Resources, Chengdu 610064, China
Chemistry Department, King Abdulaziz University, Jeddah 21589, Saudi Arabia
Chemical Synthesis and Pollution Control, Key Laboratory of Sichuan Province, School of Chemistry and Chemical Engineering, China West Normal University, Nanchong 637002, Sichuan, China
Funding
National Natural Science Foundation of China · Sichuan Province
References (30)
Show source-provided references
1. 10.1021/ar00051a00710.1021/ar00051a007 ↗
2. 10.1021/ar200301310.1021/ar2003013 ↗
3. 10.1021/acsami.6b1482710.1021/acsami.6b14827 ↗
4. 10.1126/science.118537210.1126/science.1185372 ↗
5. 10.1002/adma.20150269610.1002/adma.201502696 ↗
6. 10.1021/jz201650710.1021/jz2016507 ↗
7. 10.1126/science.117977310.1126/science.1179773 ↗
8. 10.1016/0360-3199(83)90162-310.1016/0360-3199(83)90162-3 ↗
9. Symes M. D. · 2012 · 59210.1039/BK9781849734073-00592 ↗
10. 10.1126/science.aaf503910.1126/science.aaf5039 ↗
11. 10.1038/nature1645510.1038/nature16455 ↗
12. 10.1073/pnas.100185910710.1073/pnas.1001859107 ↗
13. 10.1021/ja312643210.1021/ja3126432 ↗
14. 10.1021/ja503372r10.1021/ja503372r ↗
15. 10.1002/anie.20161077610.1002/anie.201610776 ↗
16. 10.1002/cssc.20170011310.1002/cssc.201700113 ↗
17. 10.1021/ja405351s10.1021/ja405351s ↗
18. 10.1039/C7TA00740J10.1039/C7TA00740J ↗
19. 10.1039/C6CC09893B10.1039/C6CC09893B ↗
20. 10.1021/acs.inorgchem.6b0317110.1021/acs.inorgchem.6b03171 ↗
21. 10.1039/C7TA00982H10.1039/C7TA00982H ↗
22. 10.1021/ja402771510.1021/ja4027715 ↗
23. 10.1039/C4NR03371J10.1039/C4NR03371J ↗
24. 10.1021/jp408153b10.1021/jp408153b ↗
25. 10.1016/S0926-860X(02)00390-310.1016/S0926-860X(02)00390-3 ↗
26. 10.1016/j.jcat.2005.01.02010.1016/j.jcat.2005.01.020 ↗
27. 10.1021/acssuschemeng.6b0239110.1021/acssuschemeng.6b02391 ↗
28. 10.1002/anie.20150340710.1002/anie.201503407 ↗
29. 10.1002/anie.20140384210.1002/anie.201403842 ↗
30. 10.1039/C2EE23862D10.1039/C2EE23862D ↗