Boron-Doped Boron Nitride Photocatalyst for Visible Light-Driven H2 Evolution and CO2 Photoreduction

Author(s):  
Ravi Shankar ◽  
Daphne Lubert-Perquel ◽  
Elan Mistry ◽  
Irena Nevjestić ◽  
Sandrine Heutz ◽  
...  

<p>Developing robust, multifunctional photocatalysts that can facilitate both hydrogen evolution <i>via</i> photoreforming of water and gas phase CO<sub>2</sub> photoreduction is highly desirable with the long-term vision of integrated photocatalytic setups. Here, we present a step-change in the family of boron oxynitride materials by introducing the first example of a B-doped boron oxynitride (B-BNO). This material resolves an on-going bottleneck associated with BN-based materials, i.e. the lack of photoactivity under visible light. Detailed EPR studies revealed distinct hyperfine interactions between the free oxygen radicals and 3 neighbouring boron nuclei. This confirmed isolated OB<sub>3 </sub>sites, which contribute to band gap narrowing, as the radical species and origin of paramagnetism in BNO materials. We show that B-BNO can facilitate both liquid phase H<sub>2 </sub>evolution and gas phase CO<sub>2</sub> photoreduction, using UV-Vis and deep visible irradiation (λ > 550 nm), without any co-catalysts. The evolution rates, quantum efficiencies, and selectivities observed for both reactions with B-BNO exceed those of its porous BNO counterpart, P25 TiO<sub>2</sub> and bulk g-C<sub>3</sub>N<sub>4</sub>.</p>

2020 ◽  
Author(s):  
Ravi Shankar ◽  
Daphne Lubert-Perquel ◽  
Elan Mistry ◽  
Irena Nevjestić ◽  
Sandrine Heutz ◽  
...  

<p>Developing robust, multifunctional photocatalysts that can facilitate both hydrogen evolution <i>via</i> photoreforming of water and gas phase CO<sub>2</sub> photoreduction is highly desirable with the long-term vision of integrated photocatalytic setups. Here, we present a step-change in the family of boron oxynitride materials by introducing the first example of a B-doped boron oxynitride (B-BNO). This material resolves an on-going bottleneck associated with BN-based materials, i.e. the lack of photoactivity under visible light. Detailed EPR studies revealed distinct hyperfine interactions between the free oxygen radicals and 3 neighbouring boron nuclei. This confirmed isolated OB<sub>3 </sub>sites, which contribute to band gap narrowing, as the radical species and origin of paramagnetism in BNO materials. We show that B-BNO can facilitate both liquid phase H<sub>2 </sub>evolution and gas phase CO<sub>2</sub> photoreduction, using UV-Vis and deep visible irradiation (λ > 550 nm), without any co-catalysts. The evolution rates, quantum efficiencies, and selectivities observed for both reactions with B-BNO exceed those of its porous BNO counterpart, P25 TiO<sub>2</sub> and bulk g-C<sub>3</sub>N<sub>4</sub>.</p>


2020 ◽  
Author(s):  
Ravi Shankar ◽  
Daphne Lubert-Perquel ◽  
Elan Mistry ◽  
Irena Nevjestić ◽  
Sandrine Heutz ◽  
...  

<p>Developing robust, multifunctional photocatalysts that can facilitate both hydrogen evolution via photoreforming of water and gas phase CO2 photoreduction is highly desirable with the long-term vision of integrated photocatalytic setups. Here, we present a new addition to the boron nitride (BN) photocatalyst material platform, boron-doped boron oxynitride (B-BNO), capable of fulfilling this goal. Detailed EPR studies revealed hyperfine interactions between free charges located on discrete OB3 sites, exhibiting an out-of-plane symmetry, and the nuclei of neighbouring boron atoms. This material resolves two long-standing bottlenecks associated to BN-based materials concomitantly: instability in water and lack of photo activity under visible light. We show that B-BNO maintains prolonged stability in water for at least three straight days and can facilitate both liquid phase H2 evolution and gas phase CO2 photoreduction, using UV-Vis and deep visible irradiation (λ > 550 nm), without any cocatalysts. The evolution rates, apparent quantum yields, and selectivities observed for both reactions with B-BNO exceed those of its porous BNO counterpart, P25 TiO2 and bulk g-C3N4. This work provides scope to expand the BN photocatalyst platform to a wider range of reactions.</p>


2017 ◽  
Vol 46 ◽  
pp. 416-425 ◽  
Author(s):  
Jiang Wu ◽  
Chaoen Li ◽  
Xiantuo Chen ◽  
Jing Zhang ◽  
Lili Zhao ◽  
...  

RSC Advances ◽  
2019 ◽  
Vol 9 (71) ◽  
pp. 41977-41983 ◽  
Author(s):  
Beibei Wang ◽  
Ping Li ◽  
Chunlei Du ◽  
Yan Wang ◽  
Daxin Gao ◽  
...  

An efficient visible-light driven three components photocatalyst for carbamazepine (CBZ) degradation has been assembled by co-loading reduction cocatalyst Pt and oxidation cocatalyst Co3O4 (MnOx) on BiVO4. An obvious synergetic effect is observed.


Nature Energy ◽  
2018 ◽  
Vol 3 (10) ◽  
pp. 862-869 ◽  
Author(s):  
Christian M. Wolff ◽  
Peter D. Frischmann ◽  
Marcus Schulze ◽  
Bernhard J. Bohn ◽  
Robin Wein ◽  
...  

2014 ◽  
Vol 30 (1) ◽  
pp. 135-140 ◽  
Author(s):  
DONG Li-Li ◽  
◽  
WANG Ying-Yong ◽  
TONG Xi-Li ◽  
JIN Guo-Qiang ◽  
...  

2015 ◽  
Vol 3 (16) ◽  
pp. 8353-8360 ◽  
Author(s):  
Hui Song ◽  
Liping Zhu ◽  
Yaguang Li ◽  
Zirui Lou ◽  
Mu Xiao ◽  
...  

ZnFe2O4/ZnO nanoheterostructures are synthesized by a facile template method. The hydrogen generation rate of ZnFe2O4/ZnO nanoheterostructures without co-catalysts is up to 2.15 mmol h−1 g−1 under visible light irradiation (λ > 420 nm), which is 45 times higher than the best yields ever reported for ZnFe2O4-based photocatalysts.


2020 ◽  
Vol 11 (28) ◽  
pp. 7324-7328
Author(s):  
Jully Patel ◽  
Xiaojiao Yuan ◽  
Stéphanie Mendes Marinho ◽  
Winfried Leibl ◽  
Hynd Remita ◽  
...  

Nanostructured conjugated polymers of diphenylbutadiyne (nano-PDPB) can perform photocatalytic water oxidation under visible light excitation. Charge recovery delayed in time was exemplified by the reduction of quinone acting as a hydrogen reservoir.


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