TY - JOUR
T1 - Intercalation of Nb2O5nano-flowers into the walls of few-layer black phosphorus creating a heterostructure of FL-BP@Nb2O5with the potential for environmental application
AU - Bhembe, Yoliswa Anittah
AU - Lukhele, Lungile Patricia
AU - Sinha Ray, Suprakas
AU - Dlamini, Langelihle Nsikayezwe
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2020.
PY - 2020/6/14
Y1 - 2020/6/14
N2 - Herein we report the successful exfoliation of few-layer BP (FL-BP) from bulk BPviaultrasonication inN-methylpyrrolidone (NMP). FL-BP exhibited an orthorhombic phase structure similar to that of bulk BP with weak electrostatic out-of-plane interactions and strong ionic in-plane bonds. The weakened out-of-plane bonds allowed the intercalation of Nb2O5nano-flowers that were hydrothermally synthesized, forming an intimate contact with the exfoliated BP. The successful formation of the heterointerface was confirmed by the co-existence of crystal phases of both compounds as per the XRD results. The formation of the new intrinsic Nb-P bond was confirmed by the presence of Raman shoulders of both compounds, further substantiated by the XPS analysis. The heterointerface enhanced Nb2O5light-harvesting capacity as per the UV-vis measurements. The FL-BP's properties of higher carrier effective mass and density were successfully incorporated in the composite, implying an increased flow of electrons in the composite's lattice structure. This was displayed by the great suppression of the fast recombination rate of charge carriers in the composites. The 3% BP@Nb2O5composite exhibited excellent optoelectrical properties, compared to the other composites, as suggested by the microstrain calculations, PL, and the EIS data. Mott-Schottky plots verified the p-n type heterojunction formed in the composites, and further verified the increased electron density/concentration in the composites, with respect to Nb2O5. Noteworthy, the incorporation of FL-BP in the lattice of Nb2O5increased the surface area and the pore size and volume, which is a character beneficial for photocatalysis as it presents active sites and diffusion pathways.
AB - Herein we report the successful exfoliation of few-layer BP (FL-BP) from bulk BPviaultrasonication inN-methylpyrrolidone (NMP). FL-BP exhibited an orthorhombic phase structure similar to that of bulk BP with weak electrostatic out-of-plane interactions and strong ionic in-plane bonds. The weakened out-of-plane bonds allowed the intercalation of Nb2O5nano-flowers that were hydrothermally synthesized, forming an intimate contact with the exfoliated BP. The successful formation of the heterointerface was confirmed by the co-existence of crystal phases of both compounds as per the XRD results. The formation of the new intrinsic Nb-P bond was confirmed by the presence of Raman shoulders of both compounds, further substantiated by the XPS analysis. The heterointerface enhanced Nb2O5light-harvesting capacity as per the UV-vis measurements. The FL-BP's properties of higher carrier effective mass and density were successfully incorporated in the composite, implying an increased flow of electrons in the composite's lattice structure. This was displayed by the great suppression of the fast recombination rate of charge carriers in the composites. The 3% BP@Nb2O5composite exhibited excellent optoelectrical properties, compared to the other composites, as suggested by the microstrain calculations, PL, and the EIS data. Mott-Schottky plots verified the p-n type heterojunction formed in the composites, and further verified the increased electron density/concentration in the composites, with respect to Nb2O5. Noteworthy, the incorporation of FL-BP in the lattice of Nb2O5increased the surface area and the pore size and volume, which is a character beneficial for photocatalysis as it presents active sites and diffusion pathways.
UR - http://www.scopus.com/inward/record.url?scp=85086286372&partnerID=8YFLogxK
U2 - 10.1039/d0dt01073a
DO - 10.1039/d0dt01073a
M3 - Article
C2 - 32436924
AN - SCOPUS:85086286372
SN - 1477-9226
VL - 49
SP - 7474
EP - 7487
JO - Dalton Transactions
JF - Dalton Transactions
IS - 22
ER -