Salzl S, Ertl M, Knör G
Johannes Kepler University Linz (JKU), Institute of Inorganic Chemistry, Altenbergerstr. 69, A-4040 Linz, Austria.
Phys Chem Chem Phys. 2017 Mar 22;19(12):8141-8147. doi: 10.1039/c6cp07725k.
The water-soluble zinc porphyrin complex Zn(TPPS) with TPPS = tetrakis-(4-sulfonatophenyl)porphyrin surprisingly was found to produce significant amounts of hydrogen from aqueous sulfite or amine solutions under visible-light exposure without requiring any other components such as electron relays or additional proton reduction catalysts. Although the production rates and total amounts of chemically stored fuel obtained under these conditions are still much too low to be relevant for practical applications, the background of this unprecedented observation was further studied in its own right. Since the central metal zinc is unlikely to be involved in proton-coupled electron transfer steps upon long-wavelength irradiation and the process does not seem to be much affected by variations of the electron donor added, the mechanism of photocatalytic H release is suggested to involve previously neglected redox features of the in situ generated hydroporphyrin ligand system in aqueous solution.
令人惊讶的是,水溶性锌卟啉配合物Zn(TPPS)(其中TPPS为四-(4-磺基苯基)卟啉)在可见光照射下,无需任何其他组分(如电子中继体或额外的质子还原催化剂),就能从亚硫酸盐或胺水溶液中产生大量氢气。尽管在这些条件下获得的化学储存燃料的产率和总量仍远低于实际应用所需,但这一前所未有的现象本身仍被进一步研究。由于中心金属锌在长波长照射下不太可能参与质子耦合电子转移步骤,且该过程似乎不受所添加电子供体变化的太大影响,因此光催化氢释放的机制被认为涉及水溶液中原位生成的氢卟啉配体系统先前被忽视的氧化还原特性。