Alloy tetrahexahedral Pd–Pt nanocrystals (THH Pd–Pt NCs) mainly enclosed by {10 3 0} high-index facets were prepared by electrochemistry. The as-prepared THH Pd–Pt NCs exhibit a catalytic activity that is at least three times higher than the tetrahexahedral Pd catalysts, and six times higher than commercial Pd black catalysts for the electrooxidation of formic acid. The significant enhancement in catalytic activity has been attributed to the synergy effect of high-index facets and electronic structure of the alloy.

A facile, economical, and one-step hydrothermal method was used to prepare highly luminescent nitrogen-doped carbon quantum dots (N-CQDs) with chitosan as both carbon and nitrogen sources. The as-prepared N-CQDs have an average size of 2 nm and exhibit excitation wavelength-dependent fluorescence with a maximum excitation and emission at 330 and 410 nm, respectively. Furthermore, due to the effective quenching effect of Fe³⁺ ions, the prepared N-CQDs can be used as a fluorescent sensor for Fe³⁺ ion-sensitive detection with a detection limit of 0.15 μM. The selectivity experiments revealed that the fluorescent sensor is specific to Fe³⁺ even with interference by high concentrations of other metal ions. Most importantly, the N-CQD-based Fe³⁺ ion sensor can be successfully applied to the determination of Fe³⁺ in real water samples. With excellent sensitivity and selectivity, such stable and cheap carbon materials are potentially suitable for the monitoring of Fe³⁺ in environmental application.

Water-soluble and reductive carbon quantum dots (CQDs) were fabricated by the hydrothermal carbonization of chitosan. Acting as a reducing agent and stabilizer, the as-prepared CQDs were further used to synthesize gold nanoparticles (AuNPs). This synthetic process was carried out in aqueous solution, which was absolutely “green”. Furthermore, the CQDs/AuNPs composite was used to detect iodine ions by the colorimetric method. A color change from pink to colorless was observed with the constant addition of I⁻ ions, accompanied by a decrease in the absorbance of the CQDs/AuNPs composite. According to the absorbance change, a favorable linear relationship was obtained between ΔA and I⁻ concentration in the range of 20–140 μM and 140–400 μM. The detection limit of iodide ions, depending on the 3δ/slope, was estimated to be 2.3 μM, indicating high sensitivity to the determination of iodide. More importantly, it also showed good selectivity toward I⁻ over other anion ions, and was used for the analysis of salt samples. Moreover, TEM results indicated that I⁻ ions induced the aggregation of CQDs/AuNPs, resulting in changes in color and absorbance.

Selenium (Se) is an essential trace element in most organisms but has to be carefully handled since there is a thin line between beneficial and toxic concentrations. Many bacteria have the ability to reduce selenite (Se(IV)) and (or) selenate (Se(VI)) to red elemental selenium that is less toxic. A strictly aerobic bacterium, Comamonas testosteroni S44, previously isolated from metal(loid)-contaminated soil in southern China, reduced Se(IV) to red selenium nanoparticles (SeNPs) with sizes ranging from 100 to 200 nm. Both energy dispersive X-ray Spectroscopy (EDX or EDS) and EDS Elemental Mapping showed no element Se and SeNPs were produced inside cells whereas Se(IV) was reduced to red-colored selenium in the cytoplasmic fraction in presence of NADPH. Tungstate inhibited Se(VI) but not Se(IV) reduction, indicating the Se(IV)-reducing determinant does not contain molybdenum as co-factor. Strain S44 was resistant to multiple heavy and transition metal(loid)s such as Se(IV), As(III), Cu(II), and Cd(II) with minimal inhibitory concentrations (MIC) of 100 mM, 20 mM, 4 mM, and 0.5 mM, respectively. Disruption of iscR encoding a transcriptional regulator negatively impacted cellular growth and subsequent resistance to multiple heavy metal(loid)s. C. testosteroni S44 could be very useful for bioremediation in heavy metal(loid) polluted soils due to the ability to both reduce toxic Se(VI) and Se(IV) to non-toxic Se (0) under aerobic conditions and to tolerate multiple heavy and transition metals. IscR appears to be an activator to regulate genes involved in resistance to heavy or transition metal(loid)s but not for genes responsible for Se(IV) reduction.

Bimetallic nanocrystals bound by high-index facets are promising catalysts, as they have both electronic effects from alloying and surface structure effects from high-index facets. Herein, we mainly focused on electrochemical preparation of two new Pt–Rh nanocrystals with high-index facets: {830}-bound tetrahexahedron and {311}-bound trapezohedron, and their excellent electrocatalytic properties for ethanol oxidation, especially the ability to break C–C bonds. Combining previous results about surface-modified tetrahexahedral Pt nanocrystals, we discuss the correlation of alloy and surface effects of the bimetallic system.