Nan Wang

Bio: Nan Wang is an academic researcher from Tianjin University. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 2, co-authored 3 publications receiving 55 citations. Previous affiliations of Nan Wang include Chinese Academy of Sciences.

Recent Advances in Covalent Organic Frameworks for Catalysis

Abstract: Covalent organic frameworks (COFs) as an emerging type of crystalline porous materials, have obtained considerable attention recently. They have exhibited diverse structure and attractive performance in various catalytic reactions. It is highly expected to have a systematic and comprehensive review summing up COFs-derived catalysts in homogeneous and heterogeneous catalysis, which is favorable to the judicious design of an efficient catalyst for targeted reaction. Herein, we focus on summarizing recent and significant developments in COFs materials, with an emphasis on both the synthetic strategies and targeted functionalization, and categorize it in accordance with the different types of catalytic reactions. Their potential catalysis applications are reviewed thoroughly. Moreover, a personal view about the future development of COFs catalysts with respect to the large-scale production is also discussed.

A review on biomass-derived levulinic acid for application in drug synthesis

Abstract: Levulinic acid (LEV) has been identified as a key building block chemical produced entirely from biomass. Its derivatives can be used to synthesize a variety of value-added chemicals, such as 2-but...

The international energy agency

Abstract: This chapter surveys the role of the IEA as a key component of the international energy security system. First, it gives an overview of the nature of the energy security challenges and the key governance regimes that have been set up historically to manage these challenges, including the IEA. Then, it elaborates on the specific roles taken up by the IEA in global energy governance, particularly in light of the dramatic changes that characterize the global energy security system. Finally, it gives a comparative overview of the three oil market interventions that the IEA has so far coordinated, before presenting the conclusions.

Recent Progress in Metal‐Free Covalent Organic Frameworks as Heterogeneous Catalysts

Abstract: Covalent organic frameworks (COFs), connecting different organic units into one system through covalent bonds, are crystalline organic porous materials with 2D or 3D networks. Compared with conventional porous materials such as inorganic zeolite, active carbon, and metal-organic frameworks, COFs are a new type of porous materials with well-designed pore structure, high surface area, outstanding stability, and easy functionalization at the molecular level, which have attracted extensive attention in various fields, such as energy storage, gas separation, sensing, photoluminescence, proton conduction, magnetic properties, drug delivery, and heterogeneous catalysis. Herein, the recent advances in metal-free COFs as a versatile platform for heterogeneous catalysis in a wide range of chemical reactions are presented and the synthetic strategy and promising catalytic applications of COF-based catalysts (including photocatalysis) are summarized. According to the types of catalytic reactions, this review is divided into the following five parts for discussion: achiral organic catalysis, chiral organic conversion, photocatalytic organic reactions, photocatalytic energy conversion (including water splitting and the reduction of carbon dioxide), and photocatalytic pollutant degradation. Furthermore, the remaining challenges and prospects of COFs as heterogeneous catalysts are also presented.

Covalent organic frameworks with high quantum efficiency in sacrificial photocatalytic hydrogen evolution

Abstract: Organic semiconductors offer a tunable platform for photocatalysis, yet the more difficult exciton dissociation, compared to that in inorganic semiconductors, lowers their photocatalytic activities. In this work, we report that the charge carrier lifetime is dramatically prolonged by incorporating a suitable donor-acceptor (β-ketene-cyano) pair into a covalent organic framework nanosheet. These nanosheets show an apparent quantum efficiency up to 82.6% at 450 nm using platinum as co-catalyst for photocatalytic H2 evolution. Charge carrier kinetic analysis and femtosecond transient absorption spectroscopy characterizations verify that these modified covalent organic framework nanosheets have intrinsically lower exciton binding energies and longer-lived charge carriers than the corresponding nanosheets without the donor-acceptor unit. This work provides a model for gaining insight into the nature of short-lived active species in polymeric organic photocatalysts.