Enhanced Superhydrophobic Performance of BN-MoS2 Heterostructure Prepared via a Rapid, One-Pot Supercritical Fluid Processing.

Fabrication of highly crystalline BN-MoS2 heterostructure with >95% yield was demonstrated using one-pot supercritical fluid processing within 30 min. The existence of 20-50 layers of BN-MoS2 in the prepared heterostructure was confirmed by AFM analysis. The HR-TEM imaging and mapping analysis revealed the well-melded BN and MoS2 nanosheets in the heterostructure. The drastic reduction in XRD line intensities corresponding to the (002) plane and broadening of the peaks for the BN system over MoS2 indicated the effective exfoliation and lateral size reduction in BN nanosheets during SCF processing. Also, the exfoliated MoS2 nanosheets are preferentially exposed rather than BN nanosheets; consequently, the MoS2 nanosheets sturdily covered BN nanosheets in the heterostructure. The exfoliated BN and MoS2 nanosheets with nanoscale roughness make the surface highly hydrophobic in nature. As a result, the BN-MoS2 heterostructure showed superior superhydrophobic performance with high water contact angle of 165.9°, which is much higher than the value reported in the literature.

Design of P-Doped Mesoporous Carbon Nitrides as High-Performance Anode Materials for Li-Ion Battery.

Herein, we demonstrate a simple and unique strategy for the preparation of P-doped into the substructure of mesoporous carbon nitride materials (P-MCN-1) with ordered porous structures as a high-energy and high-power Li-ion battery (LIB) anode. The P-MCN-1 as an anode in LIB delivers a high reversible discharge capacity of 963 mAh g-1 even after 1000 cycles at a current density of 1 A g-1, which is much higher than that of other counterparts comprising s-triazine (C3H3N3, g-C3N4), pristine MCN-1, and B-containing MCN-1 (B-MCN-1) subunits or carbon allotropes like CNT and graphene (rGO) materials. The P-MCN-1 electrode also exhibits exceptional rate capability even at high current densities of 5, 10, and 20 A g-1 delivering 685, 539, and 274 mAh g-1, respectively, after 2500 cycles. The high electrical conductivity and Li-ion diffusivity (D), estimated from electrochemical impedance spectra (EIS), very well support the extraordinary electrochemical performance of the P-MCN-1. Higher formation energy, lower bandgap value, and high Li-ion adsorption ability predicted by first principle calculations of P-MCN-1 are in good agreement with experimentally observed high lithium storage, stable cycle life, high power capability, and minimal irreversible capacity (IRC) loss. To the best of our knowledge, it is an entirely new material with the combination of ordered mesostructures with P codoping in carbon nitride substructure which offers superior performance for LIB, and hence we believe that this work will create new momentum for the design and development of clean energy storage devices.