对MnO2/Mn2+化学的离子定策略,没有"死Mn"和腐蚀
Xilong Li1, Kaiwen Qi1, Zili Qin1
1School of Chemistry and Material Science, University of Science and Technology of China, Hefei 230026, P. R. China.
ACS nano
|September 21, 2024
概括
这项研究引入了一种凝离子定策略,以防止-二氧化物 (Zn-MnO2) 水性电池中的"死"和质子腐蚀,显著改善周期稳定性.
科学领域:
- 电化学 电化学 电化学
- 材料科学 材料科学 材料科学
- 储能 储能 储能 储能 储能 储能
背景情况:
- -二氧化物 (Zn-MnO2) 水性电池提供高能量密度,但面临"死"和质子腐蚀等挑战.
- 这些问题源于阴极反应中间体 (Mn3+) 和随后的质子 (H+) 穿到阳极的扩散.
研究的目的:
- 制定一种策略,以减轻Zn-MnO2水性电池中的"死"形成和质子腐蚀.
- 提高这些储能系统的循环稳定性和实际应用性.
主要方法:
- 在阴极接口上采用了pH中性水凝离子定策略.
- 在现场使用自由基聚合来制造水凝,以中等的结合能量定Mn3+.
- 用水凝中的阳离子和水友群来限制质子转移.
主要成果:
- 水凝有效地限制了Mn3+的扩散,防止了"死"的形成.
- 对阳极的质子转移被显著抑制,减少了腐蚀.
- -MnO2电池表现出异常的周期性稳定性,在1 mA/cm2下维持8500个周期.
结论:
- 在阴极接口上固Mn3+对于提高MnO2/Mn2+反应的可逆性至关重要.
- 水凝离子定策略为推进实际Zn-MnO2水性电池提供了一个有希望的方法.
更多相关视频
06:53Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
1.9K
05:47Preparation of Polyoxometalate-based Photo-responsive Membranes for the Photo-activation of Manganese Oxide Catalysts
Published on: August 7, 2018
7.7K
相关概念视频
Corrosion
23.9K
The degradation of metals due to natural electrochemical processes is known as corrosion. Rust formation on iron, tarnishing of silver, and the blue-green patina that develops on copper are examples of corrosion. Corrosion involves the oxidation of metals. Sometimes it is protective, such as the oxidation of copper or aluminum, wherein a protective layer of metal oxide or its derivatives forms on the surface, protecting the underlying metal from further oxidation. In other cases, corrosion is...
23.9K
Metal-Ligand Bonds
20.6K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
20.6K
Formation of Complex Ions
23.5K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
23.5K
Radical Oxidation of Allylic and Benzylic Alcohols
1.9K
Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
1.9K
Coordination Compounds and Nomenclature
21.2K
In most main group element compounds, the valence electrons of the isolated atoms combine to form chemical bonds that satisfy the octet rule. For instance, the four valence electrons of carbon overlap with electrons from four hydrogen atoms to form CH4. The one valence electron leaves sodium and adds to the seven valence electrons of chlorine to form the ionic formula unit NaCl (Figure 1a). Transition metals do not normally bond in this fashion. They primarily form coordinate covalent bonds, a...
21.2K
Colors and Magnetism
11.6K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
11.6K
