scholarly journals Boron Carbon Oxynitride as a Novel Metal-Free Photocatalyst

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Liang Cheng Chien ◽  
Chen Wei Chiang ◽  
Chou Chio Lao ◽  
Yung-I Lin ◽  
Hao-Wu Lin ◽  
...  

AbstractBoron-based nanomaterials are emerging as non-toxic, earth-abundant (photo)electrocatalyst materials in solar energy conversion for the production of solar hydrogen fuel and environmental remediation. Boron carbon oxynitride (BCNO) is a quaternary semiconductor with electronic, optical, and physicochemical properties that can be tuned by varying the composition of boron, nitrogen, carbon, and oxygen. However, the relationship between BCNO's structure and -photocatalytic activity relationship has yet to be explored. We performed an in-depth spectroscopic analysis to elucidate the effect of using two different nitrogen precursors and the effect of annealing temperatures in the preparation of BCNO. BCNO nanodisks (D = 6.7 ± 1.1 nm) with turbostratic boron nitride diffraction patterns were prepared using guanidine hydrochloride as the nitrogen source precursor upon thermal annealing at 800°C. The X-ray photoelectron spectroscopy (XPS) surface elemental analysis of the BCNO nanodisks revealed the B, C, N, and O compositions to be 40.6%, 7.95%, 37.7%, and 13.8%, respectively. According to the solid-state 11B NMR analyses, the guanidine hydrochloride-derived BCNO nanodisks showed the formation of various tricoordinate BNx(OH)3−x species, which also served as one of the photocatalytic active sites. The XRD and in-depth spectroscopic analyses corroborated the preparation of BCNO-doped hexagonal boron nitride nanodisks. In contrast, the BCNO annealed at 600 °C using melamine as the nitrogen precursor consisted of layered nanosheets composed of B, C, N, and O atoms covalently bonded in a honeycomb lattice as evidence by the XRD, XPS, and solid-state NMR analysis (11B and 13C) analyses. The XPS surface elemental composition of the melamine-derived BCNO layered structures consisted of a high carbon composition (75.1%) with a relatively low boron (5.24%) and nitrogen (7.27%) composition, which indicated the formation of BCNO-doped graphene oxides layered sheet structures. This series of melamine-derived BCNO-doped graphene oxide layered structures were found to exhibit the highest photocatalytic activity, exceeding the photocatalytic activity of graphitic carbon nitride. In this layered structure, the formation of the tetracoordinate BNx(OH)3−x(CO) species and the rich graphitic domains were proposed to play an important role in the photocatalytic activity of the BCNO-doped graphene oxides layered structures. The optical band gap energies were measured to be 5.7 eV and 4.2 eV for BCNO-doped hexagonal boron nitride nanodisks and BCNO-doped graphene oxides layered structures, respectively. Finally, BCNO exhibited an ultralong photoluminescence with an average decay lifetime of 1.58, 2.10, 5.18, and 8.14 µs for BGH01, BGH03, BMH01, BMH03, respectively. This study provides a novel metal-free photocatalytic system and provides the first structural analysis regarding the origin of BCNO-based photocatalyst. Graphical Abstract

Nanoscale ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 4391-4397 ◽  
Author(s):  
Ivan Esteve-Adell ◽  
Jinbao He ◽  
Fernando Ramiro ◽  
Pedro Atienzar ◽  
Ana Primo ◽  
...  

A procedure for the one-step preparation of films of few-layer N-doped graphene on top of nanometric hexagonal boron nitride sheets based on the pyrolysis at 900 °C under an inert atmosphere is reported.


2015 ◽  
Vol 17 (2) ◽  
pp. 888-895 ◽  
Author(s):  
Sen Lin ◽  
Xinxin Ye ◽  
Jing Huang

Si-doped hexagonal boron nitride nanosheets and nanotubes have been investigated by first-principle methods.


2017 ◽  
Vol 110 (2) ◽  
pp. 023503 ◽  
Author(s):  
K. Ahmed ◽  
R. Dahal ◽  
A. Weltz ◽  
James J.-Q. Lu ◽  
Y. Danon ◽  
...  

2019 ◽  
Author(s):  
Rick W. Dorn ◽  
Matthew J. Ryan ◽  
Tae-Hoon Kim ◽  
Tian Wei Goh ◽  
Patrick M. Heintz ◽  
...  

Hexagonal boron nitride nanosheets (h-BNNS), the isoelectric analog to graphene, have received much attention over the past decade due to their high thermal oxidative resistance, high bandgap, catalytic activity and low cost. The molecular functional groups that terminate boron and nitrogen zigzag and/or armchair edges directly affect their chemical, physical and electronic properties. However, an understanding of the exact molecular edge termination present in h-BNNS is lacking. Here, high-resolution magic-angle spinning (MAS) solid-state NMR (SSNMR) spectroscopy and plane-wave density-functional theory (DFT) calculations are used to determine the exact molecular edge termination in exfoliated h-BNNS. 1H→11B cross-polarization MAS (CPMAS) SSNMR spectra of h-BNNS revealed multiple hydroxyl/oxygen coordinate boron edge sites that were not detectable in direct excitation experiments. A dynamic nuclear polarization (DNP)-enhanced 1H→15N CPMAS spectrum of h-BNNS displayed four distinct 15N resonances while a 2D 1H{14N} dipolar-HMQC spectrum revealed three distinct 14N environments. Plane-wave DFT calculations were used to construct model edge structures and predict the corresponding 11B, 14N and 15N SSNMR spectra. Comparison of the experimental and predicted SSNMR spectra confirms that zigzag and armchair edges with both amine and boron hydroxide/oxide termination are present. The detailed characterization of h-BNNS molecular edge termination will provide usefulness for many material science applications and the techniques outlined here should be applicable to comprehensively understand the molecular edge terminations in other 2D materials.


2020 ◽  
Vol 44 (37) ◽  
pp. 15919-15927
Author(s):  
Lignesh Durai ◽  
Pinki Yadav ◽  
Harita Pant ◽  
Vadali V. S. S. Srikanth ◽  
Sushmee Badhulika

Label-free, ultra-selective sensing of β-carotene using hBN nanosheets.


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