We demonstrate a novel strategy enabling the use of a continuous-wave diode near-infrared (NIR) laser to disrupt block copolymer (BCP) micelles and trigger the release of their "payloads". By encapsulating NaYF(4):TmYb upconverting nanoparticles (UCNPs) inside micelles of poly(ethylene oxide)-block-poly(4,5-dimethoxy-2-nitrobenzyl methacrylate) and exposing the micellar solution to 980 nm light, photons in the UV region are emitted by the UCNPs, which in turn are absorbed by o-nitrobenzyl groups on the micelle core-forming block, activating the photocleavage reaction and leading to the dissociation of BCP micelles and release of co-loaded hydrophobic species. Our strategy of using UCNPs as an internal UV or visible light source upon NIR light excitation represents a general and efficient method to circumvent the need for UV or visible light excitation that is a common drawback for light-responsive polymeric systems developed for potential biomedical applications.

A novel mussel-inspired injectable hydrogel with self-healing and anti-biofouling capabilities is developed and it possesses great potential as a drug-delivery carrier. The hydrogel can heal autonomously from repeated structural damage and also effectively prevent non-specific cell attachment and biofilm formation.

Using a photosensitive hybrid hydrogel loaded with upconversion nanoparticles (UCNPs), we show that continuous-wave near-infrared (NIR) light (980 nm) can be used to induce the gel-sol transition and release large, inactive biomacromolecules (protein and enzyme) entrapped in the hydrogel into aqueous solution "on demand", where their bioactivity is recovered. This study is a new demonstration and development in harnessing the unique multiphoton effect of UCNPs for photosensitive materials of biomedical interest.

We report a facile method to synthesize Fe3O4@polydopamine (PDA)-Ag core-shell microspheres. Ag nanoparticles (NPs) are deposited on PDA surfaces via in situ reduction by mussel-inspired PDA layers. High catalytic activity and fast adsorption of a model dye methylene blue (MB) at different pH values are achieved mainly due to the presence of monodisperse Ag NPs and electrostatic interactions between PDA and MB. The as-prepared Fe3O4@PDA-Ag microspheres also show high cyclic stability (>27 cycles), good acid stability, and fast regeneration ability, which can be achieved efficiently within several minutes by using NaBH4 as the desorption agent, showing great potentials in a wide range of applications.

Poly­(vinylidene fluoride) (PVDF)-based piezoelectric materials are promising candidates for sensors, transducers, and actuators, due to several distinctive characteristics such as good flexibility, easy processability, and high mechanical resistance. In the present work, PVDF-based nanocomposites loaded with BaTiO3 nanoparticles (NPs) of various weight fractions were prepared by the electrospinning technique and used for the fabrication of a flexible piezoelectric pressure tactile sensor (PPTS). The addition (5, 10, and 20 wt %) of piezoelectric BaTiO3 NPs improves the piezoelectric performance, especially the β phase crystals of PVDF/BaTiO3 (10 wt %) nanocomposites that can reach 91.0%. In addition, the mechanical strength of PVDF/BaTiO3 nanocomposites is up to 26.7 MPa, which is an increase of 66% compared to neat PVDF. It should be emphasized that the elongation at break continuously increases from 71% to 153% with increasing BaTiO3 NPs. More importantly, the PPTS (piezoelectric pressure tactile sensor) with the combination of electrospun PVDF/BaTiO3 nanocomposite membranes and polydimethylsiloxane (PDMS) displays excellent flexibility and linear response to external mechanical force. The flexible PPTS devices capable of detecting different music sounds have potential uses in wide fields, such as voice recognition, speech therapy, and ultrasound imaging.