Exploring the Formation of CoO/ZnO Heterostructure to Enhance Electrocatalytic Oxygen Evolution Reaction
Source abstract
Abstract
Abstract Revealing the electrocatalytic microstructure is the basis for finding more efficient and stable electrode materials for clean energy conversion devices. However, there is still a lack of direct understanding of the phase transition process of the sample during heating, which makes the synthesis conditions of the catalyst often rely on experienced guidance. Herein, ZIF‐8@α‐Co(OH)2 core‐shell structure and uniformly coated α‐Co(OH)2 nanosheets on the surface of ZIF‐8 are synthesized. The effect of temperature on microstructure evolution is studied by in situ heating technique with high‐resolution transmission electron microscopy. Based on understanding the relationship between temperature, microstructure, and OER properties, a simple annealing synthesis strategy is designed effectively. During the annealing process, ZnO@CoO heterogeneous structure is formed at 400 °C, and the material reached a stable hydroxyl oxide structure after electrochemical cycle voltammetry in an alkaline solution. The OER performance test shows that the commercial IrO2 catalyst has comparable catalytic performance.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Information Materials and Intelligent Sensing Laboratory of Anhui Province Institutes of Physical Science and Information Technology Anhui University Hefei 230601 China
The First Affiliated Hospital of Anhui Medical University Hefei Anhui 230022 China
National Synchrotron Radiation Lab University of Science and Technology of China Hefei Anhui 230029 China
Funding
National Natural Science Foundation of China
References (33)
Show source-provided references
1. 10.1021/jacs.6b0849110.1021/jacs.6b08491 ↗
2. 10.1039/C8EE00611C10.1039/C8EE00611C ↗
3. Li X. R. · Adv. Funct. Mater. · 2018 · 28 · 7
4. 10.1038/s41467-019-12886-z10.1038/s41467-019-12886-z ↗
5. Zhao S. · Nat. Energy · 2016 · 1
6. 10.1039/C7TA01693J10.1039/C7TA01693J ↗
7. 10.1016/j.scib.2017.03.02710.1016/j.scib.2017.03.027 ↗
8. 10.1002/adma.20180512710.1002/adma.201805127 ↗
9. 10.1016/j.matlet.2018.11.12510.1016/j.matlet.2018.11.125 ↗
10. 10.1002/adfm.20120278610.1002/adfm.201202786 ↗
11. 10.1021/acsami.6b0276810.1021/acsami.6b02768 ↗
12. 10.1002/advs.20210034710.1002/advs.202100347 ↗
13. 10.1002/adma.20210516310.1002/adma.202105163 ↗
14. 10.1002/anie.20220935010.1002/anie.202209350 ↗
15. 10.1016/j.jcis.2022.07.03410.1016/j.jcis.2022.07.034 ↗
16. 10.1021/ja203184k10.1021/ja203184k ↗
17. 10.1039/c0cc05002d10.1039/c0cc05002d ↗
18. 10.1016/j.matlet.2012.05.07710.1016/j.matlet.2012.05.077 ↗
19. 10.1016/j.apsusc.2009.10.03210.1016/j.apsusc.2009.10.032 ↗
20. 10.1016/j.ceramint.2017.12.13610.1016/j.ceramint.2017.12.136 ↗
21. Mulik B. B. · Appl. Surf. Sci. · 2021 · 538
22. Suguna A. · J. Mater. Sci. · 2021 · 33 · 8868
23. 10.1021/ja511539a10.1021/ja511539a ↗
24. 10.1021/acsomega.7b0169310.1021/acsomega.7b01693 ↗
25. 10.1038/srep2366710.1038/srep23667 ↗
26. 10.1007/s11051-015-3312-y10.1007/s11051-015-3312-y ↗
27. 10.1002/smll.20220062210.1002/smll.202200622 ↗
28. Nie M. · Mater. Lett. · 2020 · 271
29. 10.1021/acsnano.1c0618910.1021/acsnano.1c06189 ↗
30. 10.1039/D1TA03036A10.1039/D1TA03036A ↗
31. 10.1038/am.2015.14310.1038/am.2015.143 ↗
32. Kowalik I. A. · J Phys Conf Ser · 2016 · 712
33. 10.1016/j.jascer.2013.03.00610.1016/j.jascer.2013.03.006 ↗