Thermosensitive microgels consisting of a solid core of polystyrene and a shell of cross-linked poly(N-isopropylacrylamide) (PNIPA) were synthesized as nano-reactors, in which Ag–Pd bimetallic nanoparticles were prepared through simultaneous in situ reduction reaction. The spatial distribution of metallic nanoparticles in the microgels was analyzed by small angle X-ray scattering (SAXS) and the results indicated that metal nanoparticles were mainly located in the inner layer of microgels. The catalytic activity of Ag–Pd bimetallic nanoparticles was investigated using the reduction of p-nitrophenol to p-aminophenol by NaBH₄ as model reaction. The data demonstrated that Ag–Pd bimetallic nanoparticles showed enhanced catalytic activity compared to each monometallic nanoparticle alone and their catalytic activity was controllable by temperature due to the volume transition of PNIPA microgels.

Highly efficient energy-saving windows with high solar modulation properties (ΔT_sol) are the everlasting pursuit of research for industrial applications in the smart window field. Hybridization is an effective means of improving both ΔT_sol and luminous transmittance (T_lum). In this paper, hybrid thermochromic films were synthesized using tungsten-doped VO₂ nanoparticles (NPs) and starch derivatives. Thermoresponsive 2-hydroxy-3-butoxypropyl starch (HBPS) was prepared with a low critical solution temperature (LCST) varying from 32 to 21 °C by the substitution of reactive groups. The hybrid film was obtained by dispersing W-doped VO₂ NPs in HBPS hydrogels, which exhibiting remarkable solar modulation property (ΔT_sol = 34.3%) with a high average luminous transmittance (T_{lum, average} = 53.9%).

Heavy metal detection has become very important for the protection of water resource. In this work, a novel controllable probe is presented for the sensitive detection of Pb²⁺ in aqueous solutions. The probe was synthesized via the immobilization of surface functionalized carbon dots (named as CAEA-Hs) into the shell of the spherical polyelectrolyte brushes (SPB). The fluorescence of CAEA-H was firstly “turned off” via electrostatic interaction induced quenching. Based on the aggregation induced emission enhancement (AIEE), the fluorescence of the immobilized CAEA-H could be specifically turned on via the aggregation of the SPB particles. This fluorescence “turn on” sensor could selectively detect Pb²⁺ among five different metal ions with a relatively wide detecting range (0–1.67 mM) and good linear relationship (R² = 0.9958). Moreover, the aggregating behavior and nano-structure of CAEA-H loaded SPB have been systematically analyzed via small angle X-ray scattering, turbidity titration, and Zeta-potential measurement. Based on a series of control experiments, we finally gain an insight into the sensing mechanism of this novel sensing probe. This contributed a proof of concept demonstration that sensitive and selective chemical detection can be achieved via a C-dot/SPB synergistic platform.