Enzymatic and Bioinspired Systems for Hydrogen Production.

The extraordinary potential of hydrogen as a clean and sustainable fuel has sparked the interest of the scientific community to find environmentally friendly methods for its production. Biological catalysts are the most attractive solution, as they usually operate under mild conditions and do not produce carbon-containing byproducts. Hydrogenases promote reversible proton reduction to hydrogen in a variety of anoxic bacteria and algae, displaying unparallel catalytic performances. Attempts to use these sophisticated enzymes in scalable hydrogen production have been hampered by limitations associated with their production and stability. Inspired by nature, significant efforts have been made in the development of artificial systems able to promote the hydrogen evolution reaction, via either electrochemical or light-driven catalysis. Starting from small-molecule coordination compounds, peptide- and protein-based architectures have been constructed around the catalytic center with the aim of reproducing hydrogenase function into robust, efficient, and cost-effective catalysts. In this review, we first provide an overview of the structural and functional properties of hydrogenases, along with their integration in devices for hydrogen and energy production. Then, we describe the most recent advances in the development of homogeneous hydrogen evolution catalysts envisioned to mimic hydrogenases.

Significantly Enhanced Thermoelectric Properties of Copper Phthalocyanine/Single-Walled Carbon Nanotube Hybrids by Iodine Doping.

The copper phthalocyanine/single-walled carbon nanotube (CuPcI/SWCNT) hybrids were fabricated through doping the CuPc/SWCNT mixture using iodine vapor. It was found that both CuPc and SWCNTs were oxidized by iodine vapor resulting in great increase in carrier concentration. Moreover, the strong π-π conjugation interactions between CuPcI- and I-doped SWCNTs make the CuPcI molecules to assemble on the surface of SWCNTs in an ordered face-on packing, which benefits decreasing the carrier transport barrier across the CuPcI/SWCNT interfaces. The combination of iodine bidoping and the ordered face-on packing of CuPcI on the SWCNT surface realizes the synergetic enhancement of carrier concentration and carrier mobility and therefore the great improvement of electrical conductivity. The maximum electrical conductivity (6281 S cm-1) and thermoelectric power factor (∼304 µW m-1 K-2) at room temperature were obtained at a composition of 60 wt % SWCNTs. The power factor value is 3 orders of magnitude higher than the pure CuPcI and 1 order of magnitude higher than SWCNTs. Consequently, the highest ZT value of CuPc/SWCNT hybrids is up to 0.03, which is among the highest value of organic small-molecule complexes.