Charge transfer and intrinsic electronic properties of rGO-WO 3 nanostructures for efficient photoelectrochemical and photocatalytic applications

2018 ◽  
Vol 74 ◽  
pp. 136-146 ◽  
Author(s):  
S. Prabhu ◽  
S. Manikumar ◽  
L. Cindrella ◽  
O.J. Kwon
2015 ◽  
Vol 17 (3) ◽  
pp. 2199-2209 ◽  
Author(s):  
Sigismund Teunis Alexander George Melissen ◽  
Frédéric Labat ◽  
Philippe Sautet ◽  
Tangui Le Bahers

Applying DFT (HSE + spin orbit coupling) computed properties to five perovskites in the PbX3CH3NH3(X = I, Br, Cl) family of photovoltaic materials reveals that they can exhibit several interfacial charge transfer mechanisms.


2022 ◽  
Author(s):  
Hui Jiang ◽  
Jun Ye ◽  
Peng Hu ◽  
Shengli Zhu ◽  
Yanqin Liang ◽  
...  

Co-crystallization is an efficient way of molecular crystal engineering to tune the electronic properties of organic semiconductors. In this work, we synthesized anthracene-4,8-bis(dicyanomethylene)4,8-dihydrobenzo[1,2-b:4,5-b’]-dithiophene (DTTCNQ) single crystals as a template to...


2020 ◽  
Vol 7 (12) ◽  
pp. 200723
Author(s):  
Hai Duong Pham ◽  
Wu-Pei Su ◽  
Thi Dieu Hien Nguyen ◽  
Ngoc Thanh Thuy Tran ◽  
Ming-Fa Lin

The essential properties of monolayer silicene greatly enriched by boron substitutions are thoroughly explored through first-principles calculations. Delicate analyses are conducted on the highly non-uniform Moire superlattices, atom-dominated band structures, charge density distributions and atom- and orbital-decomposed van Hove singularities. The hybridized 2 p z –3 p z and [2s, 2 p x , 2 p y ]–[3s, 3 p x , 3 p y ] bondings, with orthogonal relations, are obtained from the developed theoretical framework. The red-shifted Fermi level and the modified Dirac cones/ π bands/ σ bands are clearly identified under various concentrations and configurations of boron-guest atoms. Our results demonstrate that the charge transfer leads to the non-uniform chemical environment that creates diverse electronic properties.


2019 ◽  
Vol 15 ◽  
pp. 2113-2132
Author(s):  
Ellen Swan ◽  
Kirsten Platts ◽  
Anton Blencowe

The unusual electronic properties and unique reactivity of fulvenes have interested researchers for over a century. The propensity to form dipolar structures at relatively low temperatures and to participate as various components in cycloaddition reactions, often highly selectively, makes them ideal for the synthesis of complex polycyclic carbon scaffolds. As a result, fulvene cycloaddition chemistry has been employed extensively for the synthesis of natural products. More recently, fulvene cycloaddition chemistry has also found application to other areas including materials chemistry and dynamic combinatorial chemistry. This highlight article discusses the unusual properties of fulvenes and their varied cycloaddition chemistry, focussing on applications in organic and natural synthesis, dynamic combinatorial chemistry and materials chemistry, including dynamers, hydrogels and charge transfer complexes. Tables providing comprehensive directories of fulvene cycloaddition chemistry are provided, including fulvene intramolecular and intermolecular cycloadditions complete with reactant partners and their resulting cyclic adducts, which provide a useful reference source for synthetic chemists working with fulvenes and complex polycyclic scaffolds.


2017 ◽  
Vol 3 (3) ◽  
pp. 1600521 ◽  
Author(s):  
Katelyn P. Goetz ◽  
Jun'ya Tsutsumi ◽  
Sujitra Pookpanratana ◽  
Jihua Chen ◽  
Nathan S. Corbin ◽  
...  

2013 ◽  
Vol 87 (15) ◽  
Author(s):  
A. C. Jacko ◽  
H. Feldner ◽  
E. Rose ◽  
F. Lissner ◽  
M. Dressel ◽  
...  

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