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Near-infrared (NIR) synaptic devices integrate NIR optical sensitivity and synaptic plasticity, emulating the basic biomimetic function of the human visual system and showing great potential in NIR artificial vision systems. However, the lack of semiconductor materials with appropriate band gaps for NIR photodetection and effective strategies for fabricating devices with synaptic behaviors limit the further development of NIR synaptic devices. Here, a two-terminal NIR synaptic device consisting of the In

Two-dimensional (2D) bismuth oxychalcogenide (Bi

Solar-blind photodetectors have widespread applications due to the unique merit of a "black background" on the earth. However, most solar-blind photodetectors reported previously exhibited quite low rejection ratios (R200nm/R280nm 103 and R220nm/R290nm > 104), a low dark current (102 fA), and a large detectivity (3.9 × 1010 Jones). It is noteworthy that the rejection ratio (R220nm/R290nm) here is superior to most of those previously reported based on traditional semiconductors. This large-scale, clean, and uniform multilayer h-BN film will contribute to the progress of next-generation optoelectronic devices.

Multilayer InSe is a promising material for high-performance optoelectronic applications because of its small direct band gap and good light absorption. However, as a photoconductive photodetector, multilayer InSe photodetectors endure large dark current and high driving power. In this work, we study the electrical properties of InGaSe alloys and demonstrate the high-performance devices based on multilayer InSe-In

Although single ultra-high-performance indicators have been achieved based on two-dimensional (2D) semiconductors, the comprehensive performances of the photodetectors of them are not so desirable. The response speed and responsivity are two key figures of merit for photodetectors, while these two parameters are always mutually suppressive and can not be synchronously satisfied. Here, we proposed a feasible strategy that can simultaneously improve the responsivity and response speed of In

Modifications to the surface of polymeric membranes to integrate supplemental properties like surface charge or catalytic activity are the cornerstone of the membrane process advancement to effectuate improvements in functionality and selectivity. Herein, a new approach is demonstrated to construct nanofiltration membranes with a metal-organic coordinated selective layer. Polyethylenimine (PEI) was integrated with phosphite linkages to form a characteristic aminophosphonate ester polymer based on the Kabachnik-Fields reaction, and a thin polymer layer was deposited on an ultrafiltration (UF) membrane to form the aminophosphonate networks surface-modified membranes. The aminophosphonate polymer interlayer facilitated the immobilization of metal cation moieties through the strong coordinative chemical bonding with the amino groups and phosphite moieties. Typically, the incorporated Fe3+ strengthened the membranes' electropositivity leading to excellent heavy metal ion removal (>98%) and efficient organic dye separation (>99.8%). Meanwhile, the strategy also enabled the embedment of a photocatalytic layer comprising nanoneedle-like α-FeOOH that endowed the membrane with high photo-Fenton activity for organic dye mineralization. Subsequently, the α-FeOOH-embedded membrane afforded the photocatalytic self-cleaning potentiality for organic fouling mitigation. This contribution underscores the prospect of advancing the integration of metal-specific functionalities and the membrane process for advanced membrane technologies in water treatment.

Multilayer InSe has emerged as a promising candidate for applications in novel electronic and optoelectronic devices due to its direct bandgap, high electron mobility, and excellent photoresponse with a broad response range. Here, we report synthesis of superlattice InSe nanosheets by simple thermal annealing for the first time. The mobility is increased to 299.1 cm

The electronic and optoelectronic properties of 2D alloy Ga

Here, we report electronic and optoelectronic performance of multilayer In

We developed a simple and facile approach to covalently immobilize Ag nanoparticles (NPs) onto polyamide surfaces of thin film composite membranes through layer-by-layer interfacial polymerization (LBL-IP) for biofouling mitigation. Stable and uniform bovine serum albumin (BSA) capped Ag NPs with an average diameter of around 20 nm were synthesized using BSA as a template under the assistance of sonication, and Ag NPs incorporated thin film composite (TFC) polyamide membrane was then fabricated by LBL-IP on a nanoporous polysulfone (PSf) substrate upon sequential coating with m-phenylenediamine (MPD) aqueous solution, trimesoyl chloride (TMC)-hexane solution, and finally BSA-capped Ag NPs aqueous solution. The influence of Ag NPs incorporation was investigated on the surface physicochemical properties, water permeability, and salt rejection of TFC polyamide membrane. Our findings show that Ag NPs functionalized membrane exhibited excellent antibacterial properties without sacrificing their permeability and rejection, and Ag NPs incorporation affected very little surface roughness and charge of polyamide layer. Moreover, the incorporated Ag NPs presented a low release rate and excellent stability on polyamide surface in cross-flow conditions. Given the simplicity and versatility of this approach, our study provides a practicable avenue for direct incorporation of various surface-tailored nanomaterials on the polyamide surface to develop high-performance TFC membranes with fouling-resistant properties on a large scale.

Microbial attachment and biofilm formation on filtration membrane can greatly compromise its flux and separation efficiency. Here, a simple and facile approach has been developed to in situ generate silver nanoparticles (Ag NPs) on the thin film composite forward osmosis (TFC FO) membrane for sustainable antibiofouling performances. Mussel-inspired dopamine chemistry was applied to grow polydopamine coating on both surfaces of FO membranes, followed by the generation of Ag NPs upon a simple dip coating in silver nitrate aqueous solution. Furthermore, the Ag NPs deposited membranes had a long-term silver release profile with rechargability for multiple times upon their depletion, and exhibited strong sustainable bactericidal efficacy against Gram-negative bacteria and Gram-positive bacteria. The Ag NPs had a controllable effect on the membrane performances including the water flux and reverse salt flux in the FO test mode. Our practicable antibacterial strategy may apply to other types of filtration membranes with diverse material surfaces and may pave a new way to achieve the sustainable membrane antibiofouling performance on a large scale.