Macroporous perovskite nanocrystal composites for ultrasensitive copper ion detection.

Accumulation of heavy metal ions, including copper ions (Cu2+), presents a serious threat to human health and to the environment. A substantial amount of research has focused on detecting such species in aqueous solutions. However, progress towards ultrasensitive and easy-to-use sensors for non-aqueous solutions is still limited. Here, we focus on the detection of copper species in hexane, realising ultra-sensitive detection through a fluorescence-based approach. To achieve this, a novel macroporous composite material has been developed featuring luminescent CsPbBr3 nanocrystals (NCs) chemically adhered to a polymerized high internal phase emulsion (polyHIPE) substrate through surface thiol groups. Due to this thiol functionality, sub-monolayer NC formation is realised, which also renders outstanding stability of the composite in the ambient environment. Copper detection is achieved through a direct solution based immersion of the CsPbBr3-(SH)polyHIPE composite, which results in concentration-dependent quenching of the NC photoluminescence. This newly developed sensor has a limit of detection (LOD) for copper as low as 1 × 10-16 M, and a wide operating window spanning 10-2 to 10-16 M. Moreover, the composite exhibits excellent selectivity among different transition metals.

Moisture-Assisted near-UV Emission Enhancement of Lead-Free Cs4CuIn2Cl12 Double Perovskite Nanocrystals.

Lead-based halide perovskite nanocrystals (NCs) are recognized as emerging emissive materials with superior photoluminescence (PL) properties. However, the toxicity of lead and the swift chemical decomposition under atmospheric moisture severely hinder their commercialization process. Herein, we report the first colloidal synthesis of lead-free Cs4CuIn2Cl12 layered double perovskite NCs via a facile moisture-assisted hot-injection method stemming from relatively nontoxic precursors. Although moisture is typically detrimental to NC synthesis, we demonstrate that the presence of water molecules in Cs4CuIn2Cl12 synthesis enhances the PL quantum yield (mainly in the near-UV range), induces a morphological transformation from 3D nanocubes to 2D nanoplatelets, and converts the dark transitions to radiative transitions for the observed self-trapped exciton relaxation. This work paves the way for further studies on the moisture-assisted synthesis of novel lead-free halide perovskite NCs for a wide range of applications.

Predicting Novel 2D MB2 (M = Ti, Hf, V, Nb, Ta) Monolayers with Ultrafast Dirac Transport Channel and Electron-Orbital Controlled Negative Poisson's Ratio.

Three-dimensional diborides MB2, featured in stacking the M layer above the middle of the honeycomb boron layer, have been extensively studied. However, little information on the two-dimensional counterparts of MB2 is available. Here, by means of evolutionary algorithm and first-principles calculations, we extensively studied the monolayer MB2 crystal with M elements ranging from group IIA to IVA covering 34 candidates. Our computations screened out eight stable monolayers MB2 (M = Be, Mg, Fe, Ti, Hf, V, Nb, Ta), and they exhibit Dirac-like band structures. Dramatically, among them, groups IVB-VB transition-metal diboride MB2 (M = Ti, Hf, V, Nb, Ta) are predicted to be a new class of auxetic materials. They harbor in-plane negative Poisson's ratio (NPR) arising mainly from the orbital hybridization between M d and Boron p orbitals, which is distinct from previously reported auxetic materials. The unusual NPR and the Dirac transport channel of these materials are applicable to nanoelectronics and nanomechanics.

Single tungsten atom supported on N-doped graphyne as a high-performance electrocatalyst for nitrogen fixation under ambient conditions.

Electrochemical reduction of dinitrogen molecules (N2) to value-added ammonia by using renewable electricity under mild conditions is regarded as a sustainable and promising strategy for N2 fixation. However, the lack of efficient, robust and inexpensive electrocatalysts for such electrochemical reduction has prevented its wide application. Herein, we report a novel single-atom catalyst, i.e., a single tungsten (W) atom anchored on N-doped graphyne (W@N-doped graphyne) as a highly efficient and low-cost electrocatalyst for the N2 reduction reaction. The inert N[triple bond, length as m-dash]N triple bond can be sufficiently activated when an N2 molecule is adsorbed on the W atom. A single atom of W coordinated with one N atom (doping into an sp-hybridized carbon atom) exhibits the highest catalytic performance with ultra-low onset potential of 0.29 V for N2 reduction reactions. The 'distal mechanism' is identified as the most favourable catalytic pathway. Moreover, the improved electrical conductivity of W@N-doped graphyne compared to that of pristine graphyne can ensure better electron transfer efficiency during the reduction processes. Our study provides a novel electrocatalyst with excellent catalytic performance for electrochemical reduction of N2 to NH3 under ambient conditions.

Computational exploration of two-dimensional silicon diarsenide and germanium arsenide for photovoltaic applications.

The properties of bulk compounds required to be suitable for photovoltaic applications, such as excellent visible light absorption, favorable exciton formation, and charge separation are equally essential for two-dimensional (2D) materials. Here, we systematically study 2D group IV-V compounds such as SiAs2 and GeAs2 with regard to their structural, electronic and optical properties using density functional theory (DFT), hybrid functional and Bethe-Salpeter equation (BSE) approaches. We find that the exfoliation of single-layer SiAs2 and GeAs2 is highly feasible and in principle could be carried out experimentally by mechanical cleavage due to the dynamic stability of the compounds, which is inferred by analyzing their vibrational normal mode. SiAs2 and GeAs2 monolayers possess a bandgap of 1.91 and 1.64 eV, respectively, which is excellent for sunlight harvesting, while the exciton binding energy is found to be 0.25 and 0.14 eV, respectively. Furthermore, band-gap tuning is also possible by application of tensile strain. Our results highlight a new family of 2D materials with great potential for solar cell applications.

Versatile two-dimensional silicon diphosphide (SiP2) for photocatalytic water splitting.

The development of two-dimensional (2D) photocatalysts with excellent visible light absorption and favorable band alignment is critical for highly-efficient water splitting. Here we systematically study the structural, electronic and optical properties of an experimentally unexplored 2D Silicon Diphosphide (SiP2) based on density functional theory (DFT). We found that the single-layer SiP2 is highly feasible to obtain experimentally by mechanical cleavage and it is dynamically stable by analyzing its vibrational normal mode. Two dimensional SiP2 possesses a direct band gap of 2.25 eV, which is much smaller than those of more widely studied photocatalysts including titania (3.2 eV) and graphitic carbon nitride (2.7 eV), thus displaying excellent ability for sunlight harvesting. Most interestingly, the positions of the conduction band minimum (CBM) and valence band maximum (VBM) in 2D SiP2 fit perfectly the water oxidation and reduction potentials, making it a potential new 2D material that is suitable as a nanoscale photocatalyst for photo-electrochemical water splitting.