Edge interface microenvironment regulation of CoOOH/commercial activated carbon nano-hybrids enabling PMS activation for degrading ciprofloxacin.

Peroxymonosulfate (PMS) is widely employed to generate oxygen-containing reactive species for ciprofloxacin (CIP) degradation. Herein, cobalt oxyhydroxide @activated carbon (CoOOH@AC) was synthesized via a wet chemical sedimentation method to activate PMS for degradation of CIP. The result suggested AC can support the vertical growth of CoOOH nanosheets to expose high-activity Co-contained edges, possessing efficient PMS activation and degradation activity and catalytic stability. In the presence of 3.0 mg of optimal CoOOH@AC and 2 mM PMS, 96.8 % of CIP was degraded within 10 min, approximately 11.6 and 9.97 times greater than those of CoOOH/PMS and AC/PMS systems. Notably, it was disclosed that the optimal CoOOH@AC/PMS system still exhibited efficient catalytic performance in a wide pH range, different organics and common co-existing ions. Quenching experiments and electron paramagnetic resonance indicated that both radical and non-radical processes contributed to the degradation of CIP, with 1O2 and direct electron transfer accounting for the non-radical pathway and SO4•- and •OH serving as the main radical active species. Finally, possible CIP degradation pathways were proposed based on high-performance liquid chromatography-mass spectrometry. This study provided an alternate method for wastewater treatment based on PMS catalyzed by cobalt-based hydroxide.

Constructing Cu-CuO heterostructured skin on Cu cubes to promote electrocatalytic ammonia production from nitrate wastewater.

Electroreducting nitrate (NO3-) into ammonia (NH3), i.e. NO3-RA, can not only relieve NO3- pollution but also produce high value-added NH3. Cu-based species have been taken as a promising catalyst for NO3-RA because of their relatively high Faradaic efficiency (FE), benefiting from the weak side hydrogen evolution reaction (HER). However, their NH3 yield rates are still unsatisfactory due to the multiple electron paths of NO3-RA. Herein, we report a Cu cube with Cu-CuO heterostructured skin, prepared by electrochemically induced reconstruction from a Cu2O cube. This novel Cu-based catalyst presents a mol-level NH3 yield rate of 3.17 mol h-1 g-1 ranking at the top level among non-noble metal catalysts and an ultrahigh FE of 98.7 %. These excellent performances attribute to the Cu-CuO heterostructured skin of Cu cubes, which has favorable energy for the hydrogenation of *NO to *NOH during the NO3-RA process and an unfavorable one for HER. For the NO3- removal of real river water, this novel Cu-based catalyst presents a high NO3- removal rate of 95.5 % after the NO3-RA test for 12 h, resulting in a lower NO3- concentration than the maximum residual amount of NO3- in drinking water limited by WHO and China. This study provides a feasible strategy by the electrochemical reconstruction method to prepare superior Cu-based electrocatalysts with mol-level NO3-RA performances for the purification of nitrate wastewater.

A bamboo-inspired hierarchical nanoarchitecture of Ag/CuO/TiO(2) nanotube array for highly photocatalytic degradation of 2,4-dinitrophenol.

The optimized geometrical configuration of muitiple active materials into hierarchical nanoarchitecture is essential for the creation of photocatalytic degradation system that can mimic natural photosynthesis. A bamboo-like architecture, CuO nanosheets and Ag nanoparticles co-decorated TiO2 nanotube arrays (Ag/CuO/TiO2), was fabricated by using simple solution-immersion and electrodeposition process. Under simulated solar light irradiation, the 2,4-dinitrophenol (2,4-DNP) photocatalytic degradation rate over Ag/CuO/TiO2 was about 2.0, 1.5 and 1.2 times that over TiO2 nanotubes, CuO/TiO2 and Ag/TiO2, respectively. The enhanced photocatalytic activity of ternary Ag/CuO/TiO2 photocatalyst was ascribed to improved light absorption, reduced carrier recombination and more exposed active sites. Moreover, the excellent stability and reliability of the Ag/CuO/TiO2 photocatalyst demonstrated a promising application for organic pollutant removal from water.

Cellulose Tailored Anatase TiO2 Nanospindles in Three-Dimensional Graphene Composites for High-Performance Supercapacitors.

The morphologies of transition metal oxides have decisive impact on the performance of their applications. Here, we report a new and facile strategy for in situ preparation of anatase TiO2 nanospindles in three-dimensional reduced graphene oxide (RGO) structure (3D TiO2@RGO) using cellulose as both an intermediate agent eliminating the negative effect of graphene oxide (GO) on the growth of TiO2 crystals and as a structure-directing agent for the shape-controlled synthesis of TiO2 crystals. High-resolution transmission electron microscopy and X-ray diffractometer analysis indicated that the spindle shape of TiO2 crystals was formed through the restriction of the growth of high energy {010} facets due to preferential adsorption of cellulose on these facets. Because of the 3D structure of the composite, the large aspect ratio of the TiO2 nanospindles, and the exposed high-energy {010} facets of the TiO2 crystals, the 3D TiO2@RGO(Ce 1.7) exhibited excellent capacitive performance as an electrode material for supercapacitors, with a high specific capacitance (ca. 397 F g(-1)), a high energy density (55.7 Wh kg(-1)), and a high power density (1327 W kg(-1)) on the basis of the masses of RGO and TiO2. These levels of capacitive performance far exceed those of previously reported TiO2-based composites.