Photoelectrochemical hydrogen generation employing a Cu2O-based photocathode with improved stability and activity by using NixPy as the cocatalyst

2018 ◽  
Vol 20 (22) ◽  
pp. 15300-15306 ◽  
Author(s):  
Manjeet Chhetri ◽  
C. N. R. Rao

With the tactical integration of band edge energetics concepts in semiconducting films to reduce charge recombination and photocorrosion, an improvement in the photocurrent can be achieved by introducing CuO and NixPy into Cu2O films.

2021 ◽  
pp. 2001056
Author(s):  
Sebastian Wilken ◽  
Dorothea Scheunemann ◽  
Staffan Dahlström ◽  
Mathias Nyman ◽  
Jürgen Parisi ◽  
...  

MRS Advances ◽  
2016 ◽  
Vol 1 (46) ◽  
pp. 3121-3126
Author(s):  
Sunith Varghese ◽  
Charuksha Walgama ◽  
Mark Wilkins ◽  
Sadagopan Krishnan ◽  
Kaan Kalkan

ABSTRACTThe present work investigates sol-gel synthesized vanadium oxyhydrate (V2O5·H2O) nanowires decorated with Au nanoparticles as potential photolytic H2 generators. As determined by UV photoelectron and optical spectroscopies, the conduction band edge of V2O5·H2O lies 0.6 eV below standard H+ reduction potential, implying no H2 can be generated. On the contrary, as measured by gas chromatography, our nanoconjugates yield reproducible light-to-hydrogen conversion efficiency of 5.3%, for the first hour of photolysis under 470 nm excitation. To explain the observed hydrogen reduction, we have hypothesized the vanadia electron energy levels are raised by some negative surface charge. With the objective of validating this hypothesis, we have performed cyclic current-voltage measurements. The derived conduction and valence band edge energies are not only consistent with the optical band gaps, but also validate the hypothesized energy increase by 1.6 eV, respectively. The negative surface charge is also corroborated by the ζ-potential. Based on the measured pH of 2.4, we attribute the negative surface charge to Lewis acid nature of the nanowires, establishing dative bonding with OH−. The present work establishes the importance of surface charge in photoelectrochemical reactions, where it can be instrumental and enabling in photolytic fuel production.


2011 ◽  
Vol 115 (33) ◽  
pp. 16418-16424 ◽  
Author(s):  
Changneng Zhang ◽  
Shuanghong Chen ◽  
Li’e Mo ◽  
Yang Huang ◽  
Huajun Tian ◽  
...  

2013 ◽  
Vol 135 (5) ◽  
pp. 1806-1815 ◽  
Author(s):  
Andrew C. Stuart ◽  
John R. Tumbleston ◽  
Huaxing Zhou ◽  
Wentao Li ◽  
Shubin Liu ◽  
...  

2012 ◽  
Vol 1387 ◽  
Author(s):  
Katsushi Fujii ◽  
Kayo Koike ◽  
Mika Atsumi ◽  
Takashi Itoh ◽  
Takenari Goto ◽  
...  

ABSTRACTPhotoelectrochemical properties of nitride semiconductors are paid attention due to their possibilities of water splitting by visible light absorption. However, the photocurrent density of InxGa1-xN, which absorbs visible light, is usually lower than that of GaN, which has larger band-gap and absorbing only UV light. The reasons of this are thought to be the band-edge position at the semiconductor-electrolyte interface and the crystal quality. The conduction band-edge decreases with increasing of indium composition and across the hydrogen generation energy at around the indium composition of 0.2. This means that the hydrogen generation ability decreases with increasing of indium composition. Low crystal quality is obtained because the lower growth temperature of InxGa1-xN than that of GaN to achieve the indium incorporation. In order to improve the photocurrent density, band-edge energy control and quantum tunneling effect are tried using the structure of thin GaN layer on InxGa1-xN here. The effect for the photocurrent densities is also discussed.


Nanomaterials ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 244 ◽  
Author(s):  
Guangzhao Wang ◽  
Feng Zhou ◽  
Binfang Yuan ◽  
Shuyuan Xiao ◽  
Anlong Kuang ◽  
...  

By means of a hybrid density functional, we comprehensively investigate the energetic, electronic, optical properties, and band edge alignments of two-dimensional (2D) CdS/g-C 3 N 4 heterostructures by considering the effect of biaxial strain and pH value, so as to improve the photocatalytic activity. The results reveal that a CdS monolayer weakly contacts with g-C 3 N 4 , forming a type II van der Waals (vdW) heterostructure. The narrow bandgap makes CdS/g-C 3 N 4 suitable for absorbing visible light and the induced built-in electric field between the interface promotes the effective separation of photogenerated carriers. Through applying the biaxial strain, the interface adhesion energy, bandgap, and band edge positions, in contrast with water, redox levels of CdS/g-C 3 N 4 can be obviously adjusted. Especially, the pH of electrolyte also significantly influences the photocatalytic performance of CdS/g-C 3 N 4 . When pH is smaller than 6.5, the band edge alignments of CdS/g-C 3 N 4 are thermodynamically beneficial for oxygen and hydrogen generation. Our findings offer a theoretical basis to develop g-C 3 N 4 -based water-splitting photocatalysts.


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