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铝卟啉与地球上储量最丰富的金属引发的水的单电子引发双电子氧化反应

One Electron-Initiated Two-Electron Oxidation of Water by Aluminum Porphyrins with Earth's Most Abundant Metal.

作者信息

Kuttassery Fazalurahman, Mathew Siby, Sagawa Shogo, Remello Sebastian Nybin, Thomas Arun, Yamamoto Daisuke, Onuki Satomi, Nabetani Yu, Tachibana Hiroshi, Inoue Haruo

机构信息

Department of Applied Chemistry, Center for Artificial Photosynthesis, Tokyo Metropolitan University, 1-1 Minami-ohsawa, Hachiohji, Tokyo, 192-0397, Japan.

出版信息

ChemSusChem. 2017 May 9;10(9):1909-1915. doi: 10.1002/cssc.201700322. Epub 2017 Apr 10.

Abstract

We report herein a new molecular catalyst for efficient water splitting, aluminum porphyrins (tetra-methylpyridiniumylporphyrinatealuminum: AlTMPyP), containing earth's most abundant metal as the central ion. One-electron oxidation of the aluminum porphyrin initiates the two-electron oxidation of water to form hydrogen peroxide as the primary reaction product with the lowest known overpotential (97 mV). The aluminum-peroxo complex was detected by a cold-spray ionization mass-spectrometry in high-resolution MS (HRMS) mode and the structure of the intermediate species was further confirmed using laser Raman spectroscopy, indicating the hydroperoxy complex of AlTMPyP to be the key intermediate in the reaction. The two-electron oxidation of water to form hydrogen peroxide was essentially quantitative, with a Faradaic efficiency of 99 %. The catalytic reaction was found to be highly efficient, with a turnover frequency up to ∼2×10  s . A reaction mechanism is proposed involving oxygen-oxygen bond formation by the attack of a hydroxide ion on the oxyl-radical-like axial ligand oxygen atom in the one-electron-oxidized form of AlTMPyP(O ) , followed by a second electron transfer to the electrode.

摘要

我们在此报告一种用于高效水分解的新型分子催化剂——铝卟啉(四甲基吡啶基卟啉铝:AlTMPyP),其中心离子为地球上含量最丰富的金属。铝卟啉的单电子氧化引发水的双电子氧化,以形成过氧化氢作为主要反应产物,且过电位为已知最低(97 mV)。通过冷喷雾电离质谱在高分辨率质谱(HRMS)模式下检测到铝过氧配合物,并使用激光拉曼光谱进一步确认了中间物种的结构,表明AlTMPyP的氢过氧配合物是该反应中的关键中间体。水双电子氧化形成过氧化氢的过程基本定量,法拉第效率为99%。发现该催化反应效率极高,周转频率高达约2×10 s 。提出了一种反应机理,即氢氧根离子攻击单电子氧化形式的AlTMPyP(O )中类似氧自由基的轴向配体氧原子,形成氧 - 氧键,随后发生第二次电子转移至电极。

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