The relationship between positive workplace gossip and job satisfaction: The mediating role of job insecurity and organizational identity.

From the perspective of social information processing theory and social identity theory, 1,267 employees were selected as the subjects, and the data were statistically analyzed by using Mplus8.0 and SPSS25.0 to explore the relationship between positive workplace gossip and job satisfaction and the role of job insecurity and organizational identity in this relationship. The results showed that there was a significant positive correlation between positive workplace gossip and job satisfaction. Furthermore, job insecurity and organizational identity independently mediated the relationship between positive workplace gossip and employee job satisfaction. In addition, job insecurity and organizational identity played a serial mediating role in the relationship between positive workplace gossip and job satisfaction. The results of the study shed light on how job insecurity and organizational identity were associated with the process of the positive workplace gossip-job satisfaction relationship. Based on the findings, implications and avenues for future research were discussed.

Preparation of LDO@TiO2 core-shell nanosheets for enhanced photocatalytic degradation of organic pollution.

TiO2-based nanosheet materials with a core-shell structure are expected to be one of the promising photocatalysts for the degradation of organic pollution. It is a challenge to synthesize TiO2 by the desired nucleation and growth process, so most reported TiO2 core-shell photocatalysts are prepared using TiO2 as a core material. Layered double hydroxides (LDHs) are considered ideal platforms to grow TiO2in situ and further serve as additional components to improve the separation of photogenerated charge carriers. In this work, we report the design and fabrication of anatase TiO2-coated ZnAl-layered double oxide (LDO@TiO2) nanosheets, which involve the in situ growth of TiO2 on ZnAl-LDH followed by subsequent calcination treatment. The resulting LDO@TiO2 photocatalyst yields typical core-shell nanosheet morphology with a mesoporous structure, exhibiting excellent photodegradation and mineralization efficiency for organic pollution.

The effect of the photochemical environment on photoanodes for photoelectrochemical water splitting.

Besides photoelectrode materials, realizing the synergy of the photochemical environment and photoelectrodes for high charge carrier utilization is crucial for enhancing the performance of photoelectrochemical (PEC) water splitting systems. However, few researchers have focused on this important aspect. Herein, the effect of the photochemical environment on photoanodes in PEC water splitting, including the redox potential of electrolytes and light direction, is rationally discussed. A combined study of the potential distribution and electrochemical impedance spectroscopy reveals that the low redox potential of electrolytes facilitates the interior charge transfer and surface charge utilization by enlarging the depletion layer. In addition, it is found that the optimum thickness of semiconductors in photoelectrodes is the length of the depletion layer plus diffusion layer.

A Bicadmium-Substituted Polyoxometalate Network Based on a Vanadosilicate Cluster for the Selective Oxidation of Styrene to Benzaldehyde.

A new bicadmium-substituted vanadosilicate, [Cd(en)2]2[(en)2Cd2Si8V12O40(OH)8(H2O)0.5]·5H2O (1; en = ethylenediamine), had been hydrothermally synthesized and characterized. Structural analysis revealed that the kind of new [(en)2Cd2Si8V12O40(OH)8(H2O)0.5]4- polyoxoanionic cluster was derived from the classical {V18O42} cluster by replacing six {VO5} square pyramids with four {Si2O7} and two [Cd(en)]2+ groups. Notably, such mixed substitution of both main-group and transition metals in polyoxovanadates is much less developed. Furthermore, compound 1 displays efficient catalytic activity toward the selective oxidation of styrene to benzaldehyde with a conversion of 97% and a selectivity of 87% in 8 h.

Impact of oxygen vacancies on TiO2 charge carrier transfer for photoelectrochemical water splitting.

Oxygen vacancies are recognized as the most prevalent defects in oxide materials. The effect of oxygen vacancies on the physicochemical properties of metal oxide semiconductors has attracted considerable attention in the photocatalysis field. But so far, the impact of oxygen vacancies on charge carrier transfer for photoelectrochemical water splitting has been unclear. In this work, TiO2 photoanodes with various oxygen vacancy concentrations were studied as metal oxide models to clarify the impact of oxygen vacancies on charge carrier transfer behaviors. The potential distribution and electrochemical impedance spectroscopy results indicate that the oxygen vacancies facilitate charge carrier diffusion in TiO2, but are disadvantageous for the charge carrier drift in the TiO2/electrolyte interface. The TiO2-400 photoanode with intermediate oxygen vacancy concentration exhibits the highest photocurrent density. It is expected that this work will provide reference to design and fabricate oxide semiconductors as photoanodes for higher charge carrier utilization in the field of solar-to-chemical energy conversion.