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An extremely simple sonication method is reported to hydroxylate a hematite surface without affecting its bulk properties. The surface hydroxyl groups serve as a hole collection layer that mediates the transfer of photoinduced holes, resulting in a considerably enhanced photocurrent. [ABSTRACT FROM AUTHOR]

A Cu-doped CeO2 solid solution was constructed by co-precipitation and additional acid treatment to investigate the behavior of doped copper under thermal treatment. Acid treatment was used to intentionally remove the surface Cu species. Surface properties and fundamental characteristics of the catalysts were characterized by several techniques, as well as the CO oxidation performance. The results reveal that doped Cu ions could gradually migrate from the matrix to the catalyst surface during calcination. The degree of migration was mostly dependent on the calcination temperature, and also the concentration gradient of Cu between the surface and matrix. Catalytic testing in CO oxidation showed that the migration induced a distinct promotional effect on the activities of catalysts, supposedly closely related to the increased surface active Cu species and improved redox properties generated by the Cu migration. The present study offers renewed understanding of the dynamic behavior of ceria-based solid solution catalysts. [ABSTRACT FROM AUTHOR]

Two different precursors, manganese nitrate (MN) and manganese acetate (MA), were employed to prepare two series of catalysts, i.e., xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2, by a co-impregnation method. The catalysts were characterized by XRD, LRS, CO-TPR, XPS and EPR spectroscopy. The results suggest that: (1) both xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2 catalysts exhibit much higher catalytic activities than an unmodified Cu/TiO2 catalyst in the NO + CO reaction. Furthermore, the activities of catalysts modified with the same amount of manganese are closely dependent on manganese precursors. (2) The enhancement of activities for Mn-modified catalysts should be attributed to the formation of the surface synergetic oxygen vacancy (SSOV) Cu+–□–Mny+ in the reaction process. Moreover, since the formation of the SSOV (Cu+–□–Mn3+) in the xCuyMn(N)/TiO2 catalyst is easier than that (Cu+–□–Mn2+) in the xCuyMn(A)/TiO2 catalyst, the activity of the xCuyMn(N)/TiO2 catalyst is higher than that of the xCuyMn(A)/TiO2 catalyst. This conclusion is well supported by the XPS and EPR results. [ABSTRACT FROM AUTHOR]

FeMnTiOx mixed oxide is prepared by the CTAB-assisted co-precipitation method, and the transformation of anatase into rutile is inhibited by CTAB to some extent. The catalyst obtained in the present work shows nearly 100% NO conversion at 100–350 °C, more than 80% N2 selectivity at 75–200 °C, and excellent H2O durability for the selective catalytic reduction of NO by NH3 with a space velocity of 30 000 mL g−1 h−1. [ABSTRACT FROM AUTHOR]

An in situ technique is employed to tailor the valence states of copper in CuOδ/γ-Al2O3 catalysts with the purpose of inducing superior catalytic performance for simultaneous elimination of NO and CO. The catalyst with zero-valent copper exhibits excellent catalytic performance, which is comparable with the conventional supported noble-metal catalysts. [ABSTRACT FROM AUTHOR]

Chromium oxide nano-particles with an average diameter of 3 nm covered by amorphous carbon (CrO x /C) were successfully synthesized. The synthesized CrO x /C materials were used for the selective catalytic reduction of NO x by NH 3 (NH 3 -SCR), which shows superb NH 3 -SCR activity and in particular, satisfactory regeneration ability in the presence of SO 2 compared with Mn-based catalysts. The as-prepared catalysts were characterized by XRD, HRTEM, Raman, FTIR, BET, TPD, TPR, XPS and in situ FTIR techniques. The results indicated presence of certain amounts of unstable lattice oxygen exposed on the surface of CrO x nano-particles with an average size of 3 nm in the CrO x /C samples, which led to NO being conveniently oxidized to NO 2 . The formed NO 2 participated in NH 3 -SCR activity, reacting with catalysts via a "fast NH 3 -SCR" pathway, which enhanced th NH 3 -SCR performance of the CrO x /C catalysts. Furthermore, the stable lattice of the CrO x species made the catalyst immune to the sulfation process, which was inferred to be the cause of its superior regeneration ability in the presence of SO 2 . This study provides a simple way to synthesize stable CrO x nano-particles with active oxygen, and sheds light on designing NH 3 -SCR catalysts with highly efficient low temperature activity, SO 2 tolerance, and regeneration ability., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

A Cu-doped CeO 2 solid solution was constructed by co-precipitation and additional acid treatment to investigate the behavior of doped copper under thermal treatment. Acid treatment was used to intentionally remove the surface Cu species. Surface properties and fundamental characteristics of the catalysts were characterized by several techniques, as well as the CO oxidation performance. The results reveal that doped Cu ions could gradually migrate from the matrix to the catalyst surface during calcination. The degree of migration was mostly dependent on the calcination temperature, and also the concentration gradient of Cu between the surface and matrix. Catalytic testing in CO oxidation showed that the migration induced a distinct promotional effect on the activities of catalysts, supposedly closely related to the increased surface active Cu species and improved redox properties generated by the Cu migration. The present study offers renewed understanding of the dynamic behavior of ceria-based solid solution catalysts.

Two different precursors, manganese nitrate (MN) and manganese acetate (MA), were employed to prepare two series of catalysts, i.e., xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2, by a co-impregnation method. The catalysts were characterized by XRD, LRS, CO-TPR, XPS and EPR spectroscopy. The results suggest that: (1) both xCuyMn(N)/TiO2 and xCuyMn(A)/TiO2 catalysts exhibit much higher catalytic activities than an unmodified Cu/TiO2 catalyst in the NO + CO reaction. Furthermore, the activities of catalysts modified with the same amount of manganese are closely dependent on manganese precursors. (2) The enhancement of activities for Mn-modified catalysts should be attributed to the formation of the surface synergetic oxygen vacancy (SSOV) Cu(+)-□-Mn(y+) in the reaction process. Moreover, since the formation of the SSOV (Cu(+)-□-Mn(3+)) in the xCuyMn(N)/TiO2 catalyst is easier than that (Cu(+)-□-Mn(2+)) in the xCuyMn(A)/TiO2 catalyst, the activity of the xCuyMn(N)/TiO2 catalyst is higher than that of the xCuyMn(A)/TiO2 catalyst. This conclusion is well supported by the XPS and EPR results.

FeMnTiOx mixed oxide is prepared by the CTAB-assisted co-precipitation method, and the transformation of anatase into rutile is inhibited by CTAB to some extent. The catalyst obtained in the present work shows nearly 100% NO conversion at 100-350 °C, more than 80% N2 selectivity at 75-200 °C, and excellent H2O durability for the selective catalytic reduction of NO by NH3 with a space velocity of 30,000 mL g(-1) h(-1).

An in situ technique is employed to tailor the valence states of copper in CuOδ/γ-Al2O3 catalysts with the purpose of inducing superior catalytic performance for simultaneous elimination of NO and CO. The catalyst with zero-valent copper exhibits excellent catalytic performance, which is comparable with the conventional supported noble-metal catalysts.