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在锰化合物存在的情况下作为水氧化反应的催化剂候选物,从纳米颗粒到杂质:睁一只眼闭一只眼。

Candidate for Catalyst during Water-Oxidation Reaction in the Presence of Manganese Compounds, from Nanosized Particles to Impurities: Sleep with One Eye Open.

机构信息

Department of Chemistry, Center of Climate Change and Global Warming, and Research Center for Basic Sciences & Modern Technologies (RBST), Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan 45137-66731, Iran.

出版信息

Acc Chem Res. 2022 Aug 16;55(16):2260-2270. doi: 10.1021/acs.accounts.2c00277. Epub 2022 Jul 26.

Abstract

Water-oxidation reaction (WOR) catalysts are critical for energy conversion. WOR is a four-electron oxidation and sluggish reaction. WOR needs a high thermodynamic driving force; it is also a kinetically slow reaction. Different compounds have been used for WOR; among these compounds, Mn materials have proven to be interesting because Mn is low-cost and also nontoxic, at least compared to many transition metals. Naturally, it has also been used in the biological water-oxidizing complex (WOC). Indeed, WOR has occurred on a huge scale in natural photosynthesis.For a long time, efforts have been made to design and synthesize various ligands and generate Mn compounds toward WOR catalysts. However, the addition or removal of electrons inside Mn compounds during harsh WOR conditions can lead to the formation or the breakage of bonds and result in the conversion of a precatalyst to a catalyst.Here, our findings on the conversion of Mn compounds to catalysts during WOR are presented. Many Mn compounds have been claimed to be catalysts for WOR in the presence of various chemical oxidants or under electrophotochemical conditions. Currently, the advances in characterization techniques and different spectroscopic methods have enabled a better understanding of catalysts. Different conversions such as that of the Mn complex to Mn oxide and Mn salts to Mn oxide during WOR have been explained. Indeed, the morphology and size of the Mn oxide formed depend on several factors such as the origin compounds, pH, ligands, and conditions. Thus, different Mn compounds show different activities toward WOR. The biomimetic models with Mn-Ca clusters are also decomposed during WOR. On the other hand, stable Mn complexes such as Mn phthalocyanines, which are very stable in the absence of potential, are easily decomposed during WOR. It is noted that for many of these Mn compounds, two steps result in the formation of Mn oxide during WOR: (i) Mn(II) or (III) leaching into the electrolyte and (ii) deposition of the leached Mn ions into the solution.Considering these steps, it can be seen that challenges remain in the area of Mn compounds, given the fact that even in the catalytic cycle at low oxidation numbers no Mn(II) or (III) should be leached to the electrolyte.

摘要

水氧化反应(WOR)催化剂对于能量转换至关重要。WOR 是一个四电子氧化和缓慢反应。WOR 需要一个高的热力学驱动力;它也是一个动力学缓慢的反应。不同的化合物已被用于 WOR;在这些化合物中,锰材料已被证明是有趣的,因为锰的成本低,而且至少与许多过渡金属相比,毒性较低。自然地,它也被用于生物水氧化复合物(WOC)中。事实上,在自然光合作用中,WOR 已经大规模发生。长期以来,人们一直致力于设计和合成各种配体,并生成用于 WOR 催化剂的锰化合物。然而,在苛刻的 WOR 条件下,锰化合物内部电子的添加或去除会导致键的形成或断裂,并导致前催化剂转化为催化剂。在这里,我们介绍了在 WOR 过程中锰化合物转化为催化剂的发现。许多锰化合物在各种化学氧化剂或光电化学条件下被声称是 WOR 的催化剂。目前,表征技术和不同光谱方法的进步使人们对催化剂有了更好的理解。在 WOR 过程中,已经解释了不同的转化,例如锰配合物转化为锰氧化物和锰盐转化为锰氧化物。事实上,形成的锰氧化物的形态和尺寸取决于几个因素,如起始化合物、pH 值、配体和条件。因此,不同的锰化合物对 WOR 表现出不同的活性。在 WOR 过程中,具有 Mn-Ca 簇的仿生模型也会分解。另一方面,在没有电势的情况下非常稳定的稳定锰配合物,如锰酞菁,在 WOR 过程中很容易分解。值得注意的是,对于许多这些锰化合物,在 WOR 过程中形成锰氧化物需要两步:(i)Mn(II)或(III)浸出到电解质中,(ii)浸出的 Mn 离子在溶液中沉积。考虑到这些步骤,可以看出,由于即使在低氧化数的催化循环中也不应将 Mn(II)或(III)浸出到电解质中,因此锰化合物领域仍然存在挑战。

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