Su Liu

Graphene has been predicted to play a role in post-silicon electronics due to the extraordinary carrier mobility. Chemical vapor deposition of graphene on transition metals has been considered as a major step towards commercial realization of graphene. However, fabrication based on transition metals involves an inevitable transfer step which can be as complicated as the deposition of graphene itself. By ambient-pressure chemical vapor deposition, we demonstrate large-scale and uniform depositon of high-quality graphene directly on a Ge substrate which is wafer scale and has been considered to replace conventional Si for the next generation of high-performance metal-oxide-semiconductor field-effect transistors (MOSFETs). The immiscible Ge-C system under equilibrium conditions dictates graphene depositon on Ge via a self-limiting and surface-mediated process rather than a precipitation process as observed from other metals with high carbon solubility. Our technique is compatible with modern microelectronics technology thus allowing integration with high-volume production of complementary metal-oxide-semiconductors (CMOS).

Salinity gradient power (SGP) has been identified as a promising renewable energy source. Reverse electrodialysis (RED) and pressure retarded osmosis (PRO) are two membrane-based technologies for SGP harvesting. Developing nanopores and nanofluidic membranes with excellent water and/or ion transport properties for applications in those two membrane-based technologies is considered viable for improving power generation performance. Despite recent efforts to advance power generation by designing a variety of nanopores and nanofluidic membranes to enhance power density, the valid pathways toward large-scale power generation remain uncertain. In this review, we introduce the features of ion and water transport in nanofluidics that are potentially beneficial to power generation. Subsequently, we survey previous efforts on nanofluidic membrane synthesis to obtain high power density. We also discuss how the various membrane properties influence the power density in RED and PRO before moving on to other important aspects of the technologies, i.e., system energy efficiency and membrane fouling. We analyze the importance of system energy efficiency and illustrate how the delicately designed nanofluidic membranes can potentially enhance energy efficiency. Previous studies are reviewed on fabricating antifouling and antimicrobial membrane for power generation, and opportunities are presented that can lead to the design of nanofluidic membranes with superior antifouling properties using various materials. Finally, future research directions are presented on advancing membrane performance and scaling-up the system. We conclude this review by emphasizing the fact that SGP has the potential to become an important renewable energy source and that high-performance nanofluidic membranes can transform SGP harvesting from conceptual to large-scale applications.

Abstract Direct synthesis of light olefins from syngas (STO) using a bifunctional catalyst composed of oxide and zeolite has attracted extensive attention in both academia and industry. It is highly desirable to develop robust catalysts that could enhance the CO conversion while simultaneously maintain high selectivity to C2-C4 olefins. Herein, we report a bifunctional catalyst consisting of ZnCr binary oxide (ZnCrO x ) and low-Si AlPO-18 zeolite, showing both satisfying selectivity to C2-C4 olefins of 45.0% (86.7%, CO 2 free) and high olefin/paraffin ratio of 29.9 at the CO conversion of 25.2% under mild reaction conditions (4.0 MPa, 390 °C). By optimizing the reaction conditions, the CO conversion could be markedly increased to 49.3% with a slight drop in selectivity. CD 3 CN/CO-FTIR characterizations and theoretical calculations demonstrate that low-Si AlPO-18 zeolite has lower acid strength, and is therefore less reactive toward the hydride transfer in the STO reaction, leading to a higher olefin/paraffin ratio.

Abstract The direct synthesis of light olefins from syngas over a bifunctional catalyst containing an oxide and zeolite has been proven to be a promising strategy. Nevertheless, an unclear reaction network hinders any further enhancement in catalytic performance, such as increasing the conversion of CO. We herein report a novel bifunctional catalyst composed of a InZr binary oxide and SAPO‐34 zeolite displaying superior CO conversion (27.7 %) with selectivity to light olefins (73.6 %) at 400 °C, 2.0 MPa. We demonstrate that the Zr‐doped body‐centered cubic In 2 O 3 phase, exhibiting higher stability than pure In 2 O 3 under a reducing atmosphere, is the active oxide component for the initial activation of CO. A complete reaction network is proposed by DFT calculations and model reactions, revealing that CO activation over Zr‐In 2 O 3 follows a quasi‐CO 2 hydrogenation pathway and methanol is the key intermediate to be transformed into light olefins in zeolites. Moreover, inhibiting excessive hydrogenation is an effective strategy to achieve higher performance.