Vanadium nitride decorated carbon cloth anode promotes aniline degradation and electricity generation of MFCs by efficiently enriching electroactive bacteria and promoting extracellular electron transfer.

To increase the colonization of electroactive bacteria and accelerate the rate of extracellular electron transfer, a simple coated anode of microbial fuel cell was designed. Here, we took advantage of vanadium nitride (VN) particles to modify the carbon cloth (VN@CC). Compared with bare carbon cloth, the designed VN@CC bioanodes exhibited a larger electrochemically active area, better biocompatibility, and smaller charge transfer impedance. The MFC with VN@CC bioanodes achieved the maximum power density of 3.89 W m-2 and chemical oxygen demand removal rate of 84% when 1000 mg L-1 aniline was degraded, which were about 1.88 and 2.8 times that of CC. The morphology of biofilm and 16s rRNA gene sequence analysis proved that the VN@CC bioanodes facilitated the enrichment of electroactive bacteria (99.02%) and increased the ratio of fast electron transfer in the extracellular electron transfer, thus enhancing the MFC performance of aniline degradation and power output. This work disclosed that it was feasible to increase the overall performance of MFC by enhancing the EET efficiency and presented valuable insights for future work.

Active Sites Intercalated Ultrathin Carbon Sheath on Nanowire Arrays as Integrated Core-Shell Architecture: Highly Efficient and Durable Electrocatalysts for Overall Water Splitting.

The development of active bifunctional electrocatalysts with low cost and earth-abundance toward oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) remains a great challenge for overall water splitting. Herein, metallic Ni4 Mo nanoalloys are firstly implanted on the surface of NiMoOx nanowires array (NiMo/NiMoOx ) as metal/metal oxides hybrid. Inspired by the superiority of carbon conductivity, an ultrathin nitrogen-doped carbon sheath intercalated NiMo/NiMoOx (NC/NiMo/NiMoOx ) nanowires as integrated core-shell architecture are constructed. The integrated NC/NiMo/NiMoOx array exhibits an overpotential of 29 mV at 10 mA cm-2 and a low Tafel slope of 46 mV dec-1 for HER due to the abundant active sites, fast electron transport, low charge-transfer resistance, unique architectural structure and synergistic effect of carbon sheath, nanoalloys, and oxides. Moreover, as OER catalysts, the NC/NiMo/NiMoOx hybrids require an overpotential of 284 mV at 10 mA cm-2 . More importantly, the NC/NiMo/NiMoOx array as a highly active and stable electrocatalyst approaches ≈10 mA cm-2 at a voltage of 1.57 V, opening an avenue to the rational design and fabrication of the promising electrode materials with architecture structures toward the electrochemical energy storage and conversion.

Hydrophobic and Hydrophilic Conjugated Polymer Dots as Binary Photocatalysts for Enhanced Visible-Light-Driven Hydrogen Evolution through Förster Resonance Energy Transfer.

Organic semiconducting polymers exhibited promising photocatalytic behavior for hydrogen (H2) evolution, especially when prepared in the form of polymer dots (Pdots). However, the Pdot structures were formed using common nonconjugated amphiphilic polymers, which have a negative effect on charge transfer between photocatalysts and reactants and are unable to participate in the photocatalytic reaction. This study presents a new strategy for constructing binary Pdot photocatalysts by replacing the nonconjugated amphiphilic polymer typically employed in the preparation of polymer nanoparticles (Pdots) with a low-molecular-weight conjugated polyelectrolyte. The as-prepared polyelectrolyte/hydrophobic polymer-based binary Pdots truly enhance the electron transfer between the Pt cocatalyst and the polymer photocatalyst with good water dispersibility. Moreover, unlike the nonconjugated amphiphilic polymer, the photophysics and mechanism of this photocatalytic system through time-correlated single-photon counting (TCSPC) and transient absorption (TA) measurements confirmed the Förster resonance energy transfer (FRET) between the polyelectrolyte as a donor and the hydrophobic polymer as an acceptor. As a result, the designated binary Pdot photocatalysts significantly enhanced the hydrogen evolution rate (HER) of 43 900 µmol g-1 h-1 (63.5 µmol h-1, at 420 nm) for PTTPA/PFTBTA Pdots under visible-light irradiation.

Ultrasensitive Gas Sensors Based on Vertical Graphene Nanowalls/SiC/Si Heterostructure.

Gas sensors, which play an important role in the safety of human life, cover a wide range of applications including intelligent systems and detection of harmful and toxic gases. It is known that graphene is an ideal and attractive candidate for gas sensing due to its high surface area and excellent mechanical, electrical, optical, and thermal properties. However, in order to fully realize its potential as a commercial gas sensor, demand for a graphene-based device of low-limit detection, high sensitivity, and fast response time needs to be met. Here, we demonstrate a metal/insulator/semiconductor (MIS) based gas sensor consisting of as-grown epitaxial graphene nanowalls (EGNWs)/silicon carbide (SiC)/silicon (Si) structure. The unique edge dominant three-dimensional (3D) EGNWs based MIS device achieved an extraordinarily low limit of detection (0.5 ppm) and unprecedented sensitivity (82 µA/ppm/cm2 for H2) with a fast response of shorter than 500 ms. These unique properties of our MIS device are attributed to the abundance of vertically oriented nanographitic edges and structural defects that act as extra-favorable adsorption sites and exhibit fast electron-transfer kinetics through the edges. Our experimental findings can pave the way for the realization of high-performance 3D graphene-based gas sensor devices.