Recent advances in heterogeneous catalysis of solar-driven carbon dioxide conversion.

Solar-driven carbon dioxide (CO2) conversion including photocatalytic (PC), photoelectrochemical (PEC), photovoltaic plus electrochemical (PV/EC) systems, offers a renewable and scalable way to produce fuels and high-value chemicals for environment and energy sustainability. This review summarizes the basic fundament and the recent advances in the field of solar-driven CO2 conversion. Expanding the visible-light absorption is an important strategy to improve solar energy conversion efficiency. The separation and migration of photogenerated charges carriers to surface sites and the surface catalytic processes also determine the photocatalytic performance. Surface engineering including co-catalyst loading, defect engineering, morphology control, surface modification, surface phase junction, and Z-scheme photocatalytic system construction, have become fundamental strategies to obtain high-efficiency photocatalysts. Similar to photocatalysis, these strategies have been applied to improve the conversion efficiency and Faradaic efficiency of typical PEC systems. In PV/EC systems, the electrode surface structure and morphology, electrolyte effects, and mass transport conditions affect the activity and selectivity of electrochemical CO2 reduction. Finally, the challenges and prospects are addressed for the development of solar-driven CO2 conversion system with high energy conversion efficiency, high product selectivity and stability.

Promoting jet fuel production by utilizing a Ru-doped Co-based catalyst of Ru-Co@C(Z-d)@Void@CeO2 in Fischer Tropsch synthesis.

In this study, the MOF-derived hollow void catalyst Co@C(Z-d)@Void@CeO2 is promoted using ruthenium (Ru) for application as an efficient catalyst for the Fischer Tropsch synthesis (FTS). The reducibility of Co active sites is significantly improved in the presence of the Ru nanoparticles (NPs), leading to a higher degree of reduction (DOR) and dispersion. Hence, the catalyst performance, i.e., CO conversion, was enhanced by 56% at 12 bar in comparison with the catalyst without Ru. Moreover, the Ru-doped catalyst promotes the jet fuel production yields more than the other FTS products. Remarkably, both the experimental results and the molecular dynamics (MD) simulation confirmed the desired effects, where the calculated Gibbs free energy (ΔG) of paraffinic hydrocarbon formation, particularly in the jet fuel range, was lower in the presence of Ru. The thermal stability of the Ru-doped catalyst was characterized by thermogravimetric analysis (TGA) and confirmed by a dramatic low-performance loss of 4.2% at 17.5 bar during TOS of 192 h.

A hollow void catalyst of Co@C(Z-d)@void@CeO2 for enhancing the performance and stability of the Fischer-Tropsch synthesis.

To enhance the catalyst performance of Fischer-Tropsch synthesis (FTS), removing the mass-transfer restriction in the catalysis synthesis is essential. Although the core-shell nanostructures can improve the activity and stability of the catalyst, they can restrict the reactants' diffusion towards the active sites and the transfer of the products from these sites in FTS. Creating an adequate porosity between the core and the outer shell of the catalyst structure can tackle this issue. In this work, the synthesized cobalt-based nano-catalyst is encapsulated with two shells and a middle porous shell. The first shell is a carbon shell at the core of the catalyst derived from ZIF-67, the second one is the outer shell of ceria, and the middle porous shell is formed by removing the sacrificial silica shell through the etching technique. The characterization and performance tests represent significant evidence of the etching treatment's impact on the FTS catalyst performance. Besides, molecular dynamics simulation is also utilized to clarify its effect. The FTS catalytic performance is enhanced more than 2 times with the etched catalyst versus the catalyst without it at 17.5 bar and a (H2/CO) ratio of 1.2. In addition, not only does the etched catalyst with high porosity play the role of a nanoreactor and intensify its catalytic performance, but it also has higher stability.

Durable Perovskite UV Sensor Based on Engineered Size-Tunable Polydimethylsiloxane Microparticles Using a Facile Capillary Microfluidic Device from a High-Viscosity Precursor.

In this work, size-tunable polydimethylsiloxane (PDMS) microparticles are fabricated from a high-viscosity oil phase using a facile coflowing capillary microfluidic device and optimized aqueous phase composition. The dispersity of the microparticle size is tuned by engineering of the viscosity of the continuous phase and flow rate ratio that leads us to achieve monodisperse microparticles. Regarding the high potential of the PDMS microparticles for optical applications, efficient environmentally durable perovskite-based UV sensors are fabricated employing the designed size-tunable microparticles. Surprisingly, the UV sensors comprising CH3NH3PbBr3 perovskite quantum dots as UV-sensitive nanocrystals embedded in transparent PDMS microparticles are water resistant because of the high hydrophobicity of PDMS. Remarkably, the UV sensors show a photoluminescence quantum yield as high as 75% that can be employed effortlessly as reusable leak detectors in different fluidic working systems.