Two-Dimensional Amorphous SnOx from Liquid Metal: Mass Production, Phase Transfer, and Electrocatalytic CO2 Reduction toward Formic Acid.

Liquid metal forms a thin layer of oxide skin via exposure to oxygen and this layer could be exfoliated by mechanical delamination or gas-injection/solvent-dispersion. Although the room-temperature fabrication of two-dimensional (2D) oxide through gas-injection and water-dispersion has been successfully demonstrated, a synthetic protocol in nonaqueous solvent at elevated temperature still remains as a challenge. Herein we report the mass-production of amorphous 2D SnOx nanoflakes with Bi decoration from liquid Sn-Bi alloy and selected nonaqueous solvents. The functional groups of the solvents play a key role in determining the final morphology of the product and the hydroxyl-rich solvents exhibit the best control toward 2D SnOx. The different solvent-oxide interaction that facilitates this phase-transfer process is further discussed on the basis of DFT calculation. Finally, the as-obtained 2D SnOx is evaluated in electrocatalytic CO2 reduction with high faradaic efficiency (>90%) of formic acid and stable performance over 10 h.

PdO/SnO2 heterostructure for low-temperature detection of CO with fast response and recovery.

In this paper, we developed a simple two-step route to prepare a PdO/SnO2 heterostructure with the diameter of the SnO2 and PdO nanoparticles at about 15 nm and 3 nm, respectively. In the evaluation temperature window between 80 °C and 340 °C, PdO/SnO2 shows the best response to 100 ppm of CO at 100 °C with fast response time (14 s) and recovery time (8 s). Furthermore, the PdO/SnO2 nanoparticles exhibit a low detection limit and good selectivity to CO against interfering gases as well as rarely-seen low-temperature stability and reversibility. Such enhanced gas sensing performance could be attributed to both the ultrafine structure of PdO and the synergy between PdO and SnO2. The results clearly indicate the application of PdO/SnO2 as a pratical low-temperature sensing material for CO.

Ultrafine nanoparticles of W-doped SnO2 for durable H2S sensors with fast response and recovery.

Ultrafine nanoparticles of W-doped SnO2 with an average diameter of 6 nm were fabricated via a facile hydrothermal method. The material shows a reduced particle size and enhanced response to H2S gas as compared to the pristine SnO2 nanoparticles. The detection limit can be down to 100 ppb while the response time and recovery time of the 5%-doped one are reduced to 17 s and 7 s respectively. In addition, the material shows impressive long-term stability of the response through 40 cycles of injection with 10 ppm H2S, which is attractive for designing a durable hydrogen sulfide sensor. The doping of W results in the reduction of size and modification of the electronic band structure of SnO2, which reduces the response time and recovery time and further improves the sensing durability of the materials.