Collision induced charge separation in ground-state water splitting dynamics. Issue 17 (24th April 2018)

• Record Type: Journal Article
• Authors: Yamamoto, Kentaro; Takatsuka, Kazuo
• Is Part Of: Physical chemistry chemical physics. Volume 20:Issue 17(2018)
• Page Start: 12229
• Page End: 12240
• Publication Date: 2018-04-24
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp00520f
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : The pathway of one-way electron–hole transfer induced by proton reciprocating motions, thereby realizing the collision induced ground-state charge separation. Abstract : In one type of photocatalytic dynamics of water splitting formally summarized as2H2 O + 4 hν + MH → 2H2 O + M*H → 4H + + 4e − + O2 + MH the catalytic center M mainly composed of Mn oxides (clusters) along with supporting molecules like proteins is directly photoexcited and discharges electrons and protons. The mechanism can be comprehended in terms of the coupled proton electron-wavepacket transfer (CPEWT). In another type proposed in the literature, M is not directly photoexcited, and instead, lights are absorbed somewhere other than M, thereby creating complicated sequential steps (a ladder) of oxidation–reduction potential, thus sucking electrons successively from one molecular site to the next, and the final place providing electrons and protons is the catalytic center M. During charge separation dynamics, M is assumed to remain in the electronic ground state, and this type can be schematically summarized asM − H + + Ω + → M + H + + Ω + e − where Ω indicates a cation species (a hole carrier) at the site of photon absorption. It is widely believed that the latter mechanism is responsible for water splitting in plants and cynobacteria, and M in photosystem II (PSII) is known to include Mn4 CaO5 . However, difficult questions about this mechanism of ground-state charge separation in the latter reaction arise as to whether it is quantum mechanically possible and what is it, if indeed possible? Besides, the time-constant for this reaction reported in the literature is so long, actually far longer than the time-scale for energy dissipation for inter- and intra-molecular vibrational energy redistribution, that the quantum mechanical coherence of the reaction should not be able to be maintained. More seriously, we wonder how protons and electrons can be isolated in the ground state, if any, and how they can be transferred unidirectionally (with no return)? We address these fundamental questions affirmatively by proposing a general chemical principle; collision induced charge separation dynamics in the ground state.