Strain and pH facilitated artificial photosynthesis in monolayer MoS2 nanosheets

2017 ◽  
Vol 5 (42) ◽  
pp. 22265-22276 ◽  
Author(s):  
Dimple Dimple ◽  
Nityasagar Jena ◽  
Ashima Rawat ◽  
Abir De Sarkar

Strain and pH induced optimization of artificial photosynthetic activity in single layer MoS2.

2021 ◽  
Vol 130 (5) ◽  
pp. 055301
Author(s):  
Zhenzhen Li ◽  
Mehmet Baskurt ◽  
Hasan Sahin ◽  
Shiwu Gao ◽  
Jun Kang

ACS Nano ◽  
2014 ◽  
Vol 8 (7) ◽  
pp. 6922-6933 ◽  
Author(s):  
Wenyan Yin ◽  
Liang Yan ◽  
Jie Yu ◽  
Gan Tian ◽  
Liangjun Zhou ◽  
...  

2021 ◽  
Author(s):  
Debajeet BORA

<p><a>Here, we describe the exfoliation of 2D Hematene single layer from a Hematite nanoparticle-based nanoarchitectures obtained by a water-mediated synthesis route with the ultrasonication method in a brief period which is 5 min. The Hematene obtained shows the fine structure of honeycomb lattice resembling the Hematite hexagonal crystallographic pattern. Here, we found that the ultrasonicated Hematite film with Hematene flakes shows enhanced current density than the pristine Hematite film which can be extended further to increase the efficiency of well-performing or champion photoanode for the artificial photosynthesis application. Besides this, a new photocurrent transient spike is obtained, which we ascribed as the generation of the sub-surface state by Hematene flakes. Followed by this, we have also deciphered a qualitative predictive mechanism for the fast exfoliation of Hematene in which surface energies and hydroxylation of crystal facets are proposed to be the factor responsible for the quick exfoliation process. </a></p>


2018 ◽  
Vol 6 (18) ◽  
pp. 8693-8704 ◽  
Author(s):  
Ashima Rawat ◽  
Nityasagar Jena ◽  
Dimple Dimple ◽  
Abir De Sarkar

Artificial photosynthesis in group VI B transition metal dichalcogenide monolayers.


2020 ◽  
Vol 8 (8) ◽  
pp. 1692-1698 ◽  
Author(s):  
Man-Jyun Wu ◽  
Wei-Lung Tseng

Surface functionalization of MoS2 nanosheets with FRET-based flares was conducted for ratiometric sensing and imaging of TK1 mRNA in HeLa and MCF-7 cells.


2015 ◽  
Vol 5 (3) ◽  
pp. 20150014 ◽  
Author(s):  
R. L. Purchase ◽  
H. J. M. de Groot

This contribution discusses why we should consider developing artificial photosynthesis with the tandem approach followed by the Dutch BioSolar Cells consortium, a current operational paradigm for a global artificial photosynthesis project. We weigh the advantages and disadvantages of a tandem converter against other approaches, including biomass. Owing to the low density of solar energy per unit area, artificial photosynthetic systems must operate at high efficiency to minimize the land (or sea) area required. In particular, tandem converters are a much better option than biomass for densely populated countries and use two photons per electron extracted from water as the raw material into chemical conversion to hydrogen, or carbon-based fuel when CO 2 is also used. For the average total light sum of 40 mol m −2 d −1 for The Netherlands, the upper limits are many tons of hydrogen or carbon-based fuel per hectare per year. A principal challenge is to forge materials for quantitative conversion of photons to chemical products within the physical limitation of an internal potential of ca 2.9 V. When going from electric charge in the tandem to hydrogen and back to electricity, only the energy equivalent to 1.23 V can be stored in the fuel and regained. A critical step is then to learn from nature how to use the remaining difference of ca 1.7 V effectively by triple use of one overpotential for preventing recombination, kinetic stabilization of catalytic intermediates and finally generating targeted heat for the release of oxygen. Probably the only way to achieve this is by using bioinspired responsive matrices that have quantum–classical pathways for a coherent conversion of photons to fuels, similar to what has been achieved by natural selection in evolution. In appendix A for the expert, we derive a propagator that describes how catalytic reactions can proceed coherently by a convergence of time scales of quantum electron dynamics and classical nuclear dynamics. We propose that synergy gains by such processes form a basis for further progress towards high efficiency and yield for a global project on artificial photosynthesis. Finally, we look at artificial photosynthesis research in The Netherlands and use this as an example of how an interdisciplinary approach is beneficial to artificial photosynthesis research. We conclude with some of the potential societal consequences of a large-scale roll out of artificial photosynthesis.


2021 ◽  
Author(s):  
Debajeet BORA

<p><a>Here, we describe the exfoliation of 2D Hematene single layer from a Hematite nanoparticle-based nanoarchitectures obtained by a water-mediated synthesis route with the ultrasonication method in a brief period which is 5 min. The Hematene obtained shows the fine structure of honeycomb lattice resembling the Hematite hexagonal crystallographic pattern. Here, we found that the ultrasonicated Hematite film with Hematene flakes shows enhanced current density than the pristine Hematite film which can be extended further to increase the efficiency of well-performing or champion photoanode for the artificial photosynthesis application. Besides this, a new photocurrent transient spike is obtained, which we ascribed as the generation of the sub-surface state by Hematene flakes. Followed by this, we have also deciphered a qualitative predictive mechanism for the fast exfoliation of Hematene in which surface energies and hydroxylation of crystal facets are proposed to be the factor responsible for the quick exfoliation process. </a></p>


Author(s):  
Mark D. Symes ◽  
Richard J. Cogdell ◽  
Leroy Cronin

Artificial photosynthesis aims at capturing solar energy and using it to produce storable fuels. However, while there is reason to be optimistic that such approaches can deliver higher energy conversion efficiencies than natural photosynthetic systems, many serious challenges remain to be addressed. Perhaps chief among these is the issue of device stability. Almost all approaches to artificial photosynthesis employ easily oxidized organic molecules as light harvesters or in catalytic centres, frequently in solution with highly oxidizing species. The ‘elephant in the room’ in this regard is that oxidation of these organic moieties is likely to occur at least as rapidly as oxidation of water, meaning that current device performance is severely curtailed. Herein, we discuss one possible solution to this problem: using self-assembling organic–polyoxometalate hybrid structures to produce compartments inside which the individual component reactions of photosynthesis can occur without such a high incidence of deleterious side reactions.


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