scholarly journals Proton-assisted electron transfer and hydrogen-atom diffusion in a model system for photocatalytic hydrogen production

2020 ◽  
Vol 1 (1) ◽  
Author(s):  
Yuanzheng Zhang ◽  
Yunrong Dai ◽  
Huihui Li ◽  
Lifeng Yin ◽  
Michael R. Hoffmann

Abstract Solar energy can be converted into chemical energy by photocatalytic water splitting to produce molecular hydrogen. Details of the photo-induced reaction mechanism occurring on the surface of a semiconductor are not fully understood, however. Herein, we employ a model photocatalytic system consisting of single atoms deposited on quantum dots that are anchored on to a primary photocatalyst to explore fundamental aspects of photolytic hydrogen generation. Single platinum atoms (Pt1) are anchored onto carbon nitride quantum dots (CNQDs), which are loaded onto graphitic carbon nitride nanosheets (CNS), forming a Pt1@CNQDs/CNS composite. Pt1@CNQDs/CNS provides a well-defined photocatalytic system in which the electron and proton transfer processes that lead to the formation of hydrogen gas can be investigated. Results suggest that hydrogen bonding between hydrophilic surface groups of the CNQDs and interfacial water molecules facilitates both proton-assisted electron transfer and sorption/desorption pathways. Surface bound hydrogen atoms appear to diffuse from CNQDs surface sites to the deposited Pt1 catalytic sites leading to higher hydrogen-atom fugacity surrounding each isolated Pt1 site. We identify a pathway that allows for hydrogen-atom recombination into molecular hydrogen and eventually to hydrogen bubble evolution.

2020 ◽  
Vol 525 ◽  
pp. 146596 ◽  
Author(s):  
Patrycja Parnicka ◽  
Alicja Mikolajczyk ◽  
Henry P. Pinto ◽  
Wojciech Lisowski ◽  
Tomasz Klimczuk ◽  
...  

2007 ◽  
Vol 1042 ◽  
Author(s):  
R. M. Valladares ◽  
Alexander Valladares ◽  
A. G. Calles ◽  
Ariel A. Valladares

AbstractNanoporous carbon has been considered an interesting and potentially useful material for storing hydrogen. Using nanoporous carbon periodic supercells with 216 atoms and 50 % porosity, constructed with a novel ab initio approach devised by us, the dangling bonds of the carbon atoms were first saturated with hydrogen, then relaxed and its total energy calculated with and without hydrogen. Next the same number of hydrogen atoms, in molecular form, was randomly placed within the pore of the pure carbon supercell, then the sample relaxed, and finally its total energy calculated, also with and without hydrogens. From these results the average energy per hydrogen atom is obtained for both cases. For the molecular hydrogen sample the binding energy found per hydrogen atom is 343.89 meV, which compares favourably with values reported in the literature, 300-400 meV/molecule.


2014 ◽  
Vol 540 ◽  
pp. 35-38
Author(s):  
Yu Su Song ◽  
Li Qing Zhou ◽  
Guang Zhe Chu

The hydrogen residued process of the High-strength steel surface during the phosphorization process was studied. By the hydrogen permeation experiment, that penetration speed of the hydrogen residued in the metal surface were measured. The result of shows:the more hydrogen gas generated in the process of phosphorization,the more hydrogen atom inside the metal. That means the hydrogen embrittlement criticality of the High-strength steel were more fearful。Dense phosphorizing film always block hydrogen atoms to penetrate into the metal,So that cuold to reduce the hydrogen embrittlement extend of the steel in phosphorization.


Author(s):  
Fengjiao Zhao ◽  
Feng Zhang ◽  
Dongxue Han ◽  
Kai Huang ◽  
Yang Yang ◽  
...  

77% enhanced light-driven H2 generation of CQDs with TiO2 nanoparticles by an efficient electron transfer to highly active redox band.


2021 ◽  
Vol 46 (1) ◽  
pp. 486-498
Author(s):  
Onur Cavdar ◽  
Anna Malankowska ◽  
Daniel Amgar ◽  
Paweł Mazierski ◽  
Justyna Łuczak ◽  
...  

2021 ◽  
Author(s):  
Alexander Schleusener ◽  
Mathias Micheel ◽  
Stefan Benndorf ◽  
Markus Rettenmayr ◽  
Wolfgang Weigand ◽  
...  

The combination of CdSe nanoparticles as photosensitizers and [FeFe]-hydrogenase mimics is known to result in efficient systems for light-driven hydrogen generation. Nevertheless, little is known about the details of the light-induced charge-transfer processes. Here we investigate the timescale of light-induced electron transfer between CdSe quantum dots and a simple [FeFe]-hydrogenase mimic adsorbed on the surface of the quantum dot under non-catalytic conditions. Our time-resolved spectroscopic investigation shows that hot electron transfer on a sub-ps timescale and band-edge electron transfer on a sub-10-ps timescale occurs. Fast recombination is observed in the absence of a sacrificial agent or protons, which under real catalytic conditions would quench remaining holes or could stabilize the charge separation. <br>


2021 ◽  
Author(s):  
Alexander Schleusener ◽  
Mathias Micheel ◽  
Stefan Benndorf ◽  
Markus Rettenmayr ◽  
Wolfgang Weigand ◽  
...  

The combination of CdSe nanoparticles as photosensitizers and [FeFe]-hydrogenase mimics is known to result in efficient systems for light-driven hydrogen generation. Nevertheless, little is known about the details of the light-induced charge-transfer processes. Here we investigate the timescale of light-induced electron transfer between CdSe quantum dots and a simple [FeFe]-hydrogenase mimic adsorbed on the surface of the quantum dot under non-catalytic conditions. Our time-resolved spectroscopic investigation shows that hot electron transfer on a sub-ps timescale and band-edge electron transfer on a sub-10-ps timescale occurs. Fast recombination is observed in the absence of a sacrificial agent or protons, which under real catalytic conditions would quench remaining holes or could stabilize the charge separation. <br>


1953 ◽  
Vol 6 (4) ◽  
pp. 409 ◽  
Author(s):  
SJ Leach ◽  
JH Baxendale ◽  
MG Evans

The rates of oxidation of N-methylacridan by 2,6-dichlorophenolindophenol have been measured between pH 2.74 and 6.91 at 20 to 22 �C in the presence of 8 to 22 per cent. ethanol. The reaction was of the second order and was found to proceed by ' two simultaneous mechanisms, both involving the conjugate acid of N-methylacridan. The oxidation of this cation by the indophenol anion proceeded at a rate which was 19 times greater than the oxidation by the uncharged indophenol molecule. It is shown that oxidation probably occurs by hydrogen atom transfer rather than electron transfer. A similar mechanism for the oxidation of dihydro-coenzyme I would account for its slow reactivity towards molecular oxygen and the biological necessity for mediating systems involving both hydrogen atoms and electrons.


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