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可可西里

木虫之王 (文学泰斗)

甾体者说

是我自己找到的

在他们学校的主页上

这个应该算什么呢?
求助文献下载后,及时评分和EPI。
11楼2006-09-23 14:19:21
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zbzhaono1

木虫 (正式写手)

0.5

若能将此文献给大家共享一下那就太理想了,谢谢!
12楼2006-09-27 14:09:27
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mvpworm

木虫 (著名写手)

1

辛苦
13楼2006-09-27 16:28:32
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涛声依旧771224

金虫 (正式写手)

0.25

(377) Z.Lei, G. Ma, M. Liu, W. You, H. Yan, G. Wu, T. Takata, M. Hara, K. Domen, C. Li,
“Sulfur-substituted and zinc-doped In(OH)3: A new class of catalyst for photocatalytic H2 production from water under visible light illumination"
J. Catal., 2006, 237, 322-329.
日本的?搞清楚再说!!!
14楼2006-09-27 19:03:28
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可可西里

木虫之王 (文学泰斗)

甾体者说

引用回帖:
Originally posted by 涛声依旧771224 at 2006-9-27 07:03 PM:
(377) Z.Lei, G. Ma, M. Liu, W. You, H. Yan, G. Wu, T. Takata, M. Hara, K. Domen, C. Li,
“Sulfur-substituted and zinc-doped In(OH)3: A new class of catalyst for photocatalytic H2 production from w ...

是你做的吧

呵呵

确实有日本人Domen啊

呵呵

都是互相挂名字

呵呵

虽然大化所很牛

但是李灿也是一直和Domen合作的吧

呵呵

里边应该也有Domen的建议吧
求助文献下载后,及时评分和EPI。
15楼2006-09-27 22:30:04
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limeng

铜虫 (初入文坛)

八错!
请问怎样复合氧化铝和二氧化硅来制备以氧化铝为主体的复合载体?谢谢
16楼2006-11-25 14:15:13
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limeng

铜虫 (初入文坛)

请教制备复合载体方面的问题

请问有没有制备以氧化铝为主体的复合载体(氧化铝-二氧化硅)
17楼2006-11-25 14:17:10
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bss

铁虫 (初入文坛)

日本人做这方面的确有一手,
我做固体碱催化剂方面的,日本人的研究深度和分析方法要超过我们好多年!
其实关键就是人家有钱,有设备,有样就分析,自然就有得写了
兄弟们,要努力哦
18楼2006-11-25 16:58:30
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lizijing9527

日本人就是强!
19楼2006-11-25 17:36:22
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starfry

木虫 (小有名气)

楼主辛苦了,很值得参考的资料。我找了06年的摘要,这是给endnote的,存成档案可直接import。
--------------------------------------------------------------------------------------------------------------------

FN ISI Export Format
VR 1.0
PT J
AU Maeda, K
   Teramura, K
   Saito, N
   Inoue, Y
   Domen, K
AF Maeda, Kazuhiko
   Teramura, Kentaro
   Saito, Nobuo
   Inoue, Yasunobu
   Domen, Kazunari
TI Improvement of photocatalytic activity of (Ga1-xZnx)(N1-xOx) solid
   solution for overall water splitting by co-loading Cr and another
   transition metal
SO JOURNAL OF CATALYSIS
AB Modification with a two-component cocatalyst consisting of Cr and
   another transition metal was examined in an attempt to improve the
   photocatalytic activity of (Ga1-xZnx)(N1-xOx) for overall water
   splitting. The activity of (Ga1-xZnx)(N1-xOx) modified with various
   transition metals is enhanced by co-loading of Cr, although
   modification with Cr alone is not effective for promoting activity in
   this reaction. The activity of the co-loaded catalyst is found to be
   strongly dependent on the amount of loaded Cr, which in turn varies
   according to the paired transition metal. The improvement in activity
   is attributed to the formation of suitable reaction sites by intimate
   interaction between Cr and the paired metal component. (c) 2006
   Elsevier Inc. All rights reserved.
PD OCT 25
PY 2006
VL 243
IS 2
BP 303
EP 308
UT ISI:000241591900009
ER

PT J
AU Saito, N
   Arai, N
   Nishiyama, H
   Domen, K
   Inoue, Y
AF Saito, Nobuo
   Arai, Naoki
   Nishiyama, Hiroshi
   Domen, Kazunari
   Inoue, Yasunobu
TI Photocatalytic overall water splitting on ruthenium oxide-loaded P-type
   gallium nitride
SO ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY
PD MAR 26
PY 2006
VL 231
UT ISI:000238125908027
ER

PT J
AU Arai, N
   Saito, N
   Nishiyama, H
   Inoue, Y
   Domen, K
   Sato, K
AF Arai, Naoki
   Saito, Nobuo
   Nishiyama, Hiroshi
   Inoue, Yasunobu
   Domen, Kazunari
   Sato, Kazunori
TI Overall water splitting by RuO2-dispersed divalent-ion-doped GaN
   photocatalysts with d(10) electronic configuration
SO CHEMISTRY LETTERS
AB Divalent-metal-ion (Zn2+ or Mg2+)-doped GaN with d(10) electronic
   configuration was found to make a high and stable photocatalyst for
   overall water splitting when combined with RuO2 as a promoter, whereas
   neither undoped nor tetravalent-metal-ion (Si4+ or Ge4+)-doped GaN
   showed photocatalytic activity upon loading of RUO2. The present work
   clearly demonstrated the marked effects of dopants on photocatalytic
   performance of the metal nitride GaN for water splitting.
PD JUL 5
PY 2006
VL 35
IS 7
BP 796
EP 797
UT ISI:000240439900051
ER

PT J
AU Lee, YG
   Watanabe, T
   Takata, T
   Hara, M
   Yoshimura, M
   Domen, K
AF Lee, Yungi
   Watanabe, Tomoaki
   Takata, Tsuyoshi
   Hara, Michikazu
   Yoshimura, Masahiro
   Domen, Kazunari
TI Effect of high-pressure ammonia treatment on the activity of Ge3N4
   photocatalyst for overall water splitting
SO JOURNAL OF PHYSICAL CHEMISTRY B
AB The photocatalytic activity of beta-Ge3N4 powder for overall water
   splitting is successfully enhanced by ammonia treatment at 823 K for
   5-24 h at ammonia pressures of 20 MPa or greater. The surface and bulk
   nitrogen content in the treated samples varies according to the
   treatment temperature and treatment time, related to the stability of
   beta-Ge3N4 powder under pressurized ammonia. The change in nitrogen
   content resulted in a change in the photocatalytic activity for overall
   water splitting. A beta-Ge3N4 powder treated at 823 K for 5 h under
   ammonia at 20 MPa exhibited a photocatalytic activity 4 times higher
   than that of the as-synthesized powder, attributable to a decrease in
   the density of anion defects in the bulk and surface.
PD SEP 7
PY 2006
VL 110
IS 35
BP 17563
EP 17569
UT ISI:000240158600040
ER

PT J
AU Liu, MY
   You, WS
   Lei, ZB
   Takata, T
   Domen, K
   Li, C
AF Liu Meiying
   You Wansheng
   Lei Zhibin
   Takata, Tuyoshi
   Domen, Kazunari
   Li Can
TI Photocatalytic water splitting to hydrogen over a visible light-driven
   LaTaON2 catalyst
SO CHINESE JOURNAL OF CATALYSIS
AB LaTaON2 with a perovskite structure has been successfully prepared by a
   high-temperature ammonolysis technique using NH2Cl as the mineralizer.
   The optical absorption edge of LaTaON2 is significantly red-shifted
   compared to that of LaTaO4. Under visible light irradiation, LaTaON2
   with Pt or Ru as a co-catalyst shows high activity for reduction of
   water to H-2 in the presence of ethanol as a sacrificial electron
   reagent. A remarkable improvement in production efficiency was observed
   when both Pt and Ru are present.
PD JUL
PY 2006
VL 27
IS 7
BP 556
EP 558
UT ISI:000239715600006
ER

PT J
AU Maeda, K
   Teramura, K
   Lu, DL
   Takata, T
   Saito, N
   Inoue, Y
   Domen, K
AF Maeda, Kazuhiko
   Teramura, Kentaro
   Lu, Daling
   Takata, Tsuyoshi
   Saito, Nobuo
   Inoue, Yasunobu
   Domen, Kazunari
TI Characterization of Rh-Cr mixed-oxide nanoparticles dispersed on
   (Ga1-xZnx)(N1-xOx) as a cocatalyst for visible-light-driven overall
   water splitting
SO JOURNAL OF PHYSICAL CHEMISTRY B
AB The structure of Rh-Cr mixed-oxide (Rh2-yCryO3) nanoparticles dispersed
   on (Ga1-xZnx)(N1-xOx) is characterized by electron microscopy and X-ray
   spectroscopy. The Rh2-yCryO3 nanoparticle is an efficient cocatalyst
   for photocatalytic overall water splitting on the (Ga1-xZnx)(N1-xOx)
   solid solution and is loaded onto the catalyst by impregnation from an
   aqueous solution containing Na(3)RhCl(6)(.)2H(2)O and
   Cr(NO3)(3)(.)9H(2)O followed by calcination in air. Impregnation of the
   (Ga1-xZnx)(N1-xOx) with 1 wt % Rh and 1.5 wt % Cr followed by
   calcination at 623 K for 1 h provides the highest photocatalytic
   activity. Structural analyses reveal that the activity of this
   photocatalyst is strongly dependent on the generation of trivalent
   Rh-Cr mixed-oxide nanoparticles with optimal composition and
   distribution.
PD JUL 20
PY 2006
VL 110
IS 28
BP 13753
EP 13758
UT ISI:000239001700013
ER

PT J
AU Maeda, K
   Teramura, K
   Masuda, H
   Takata, T
   Saito, N
   Inoue, Y
   Domen, K
TI Efficient overall water splitting under visible-light irradiation on
   (Ga1-xZnx)( N1-xOx) dispersed with Rh-Cr mixed-oxide nanoparticles:
   Effect of reaction conditions on photocatalytic activity
SO JOURNAL OF PHYSICAL CHEMISTRY B
AB The photocatalytic activity of (Ga1- xZnx)(N1-xOx) loaded with Rh-Cr
   mixed-oxide (Rh(2-y)CryO(3)) nanoparticles for overall water splitting
   under visible-light irradiation (lambda > 400 nm) is investigated with
   respect to reaction pH and gas pressure. The photocatalytic performance
   of the catalyst is found to be strongly dependent on the pH of the
   reactant solution but largely independent of gas pressure. The present
   photocatalyst exhibits stable and high photocatalytic activity in an
   aqueous solution of pH 4.5 for 72 h. The photocatalytic performance is
   much lower at pH 3.0 and pH 6.2, attributable to corrosion of the
   cocatalyst and hydrolysis of the catalyst. The dispersion of Rh2-yCryO3
   as a cocatalyst on the (Ga1-xZnx)(N1-xOx) surface promotes hydrogen
   evolution, which is considered to be the rate-determining step for
   overall water splitting on this catalyst.
PD JUL 6
PY 2006
VL 110
IS 26
BP 13107
EP 13112
UT ISI:000238645700045
ER

PT J
AU Lee, Y
   Nukumizu, K
   Watanabe, T
   Takata, T
   Hara, M
   Yoshimura, M
   Domen, K
TI Effect of 10 MPa ammonia treatment on the activity of visible light
   responsive Ta3N5 photocatalyst
SO CHEMISTRY LETTERS
AB The photocatalytic activity of tantalum nitride (Ta3N5) for H-2
   evolution under visible-light irradiation (lambda > 420nm) is improved
   fivefold by 10 MPa ammonia treatment at 823 K. The rate of H-2
   evolution of the treated samples is highly related to the treatment
   time and treatment temperature.
PD APR 5
PY 2006
VL 35
IS 4
BP 352
EP 353
UT ISI:000237721500004
ER

PT J
AU Bao, NZ
   Shen, LM
   Takata, T
   Lu, DL
   Domen, K
TI Highly ordered Pt-loaded CdS nanowire arrays for photocatalytic
   hydrogen production under visible light
SO CHEMISTRY LETTERS
AB Highly ordered crystalline Pt-loaded US nanowire arrays were prepared
   using a hard template of mesoporous silica and show good photocatalytic
   activity for hydrogen production under visible-light irradiation.
PD MAR 5
PY 2006
VL 35
IS 3
BP 318
EP 319
UT ISI:000237207000037
ER

PT J
AU Yashima, M
   Maeda, K
   Teramura, K
   Takata, T
   Domen, K
TI Crystal structure analysis of (Ga0.93Zn0.07)(N0.9O0.10) oxynitride
   photocatalyst
SO MATERIALS TRANSACTIONS
AB Gallium zinc oxynitride (Ga0.937Zn0.07)(N0.90O0.10) is a new type of
   photocatalyst that is capable of overall water splitting under visible
   light. The crystal structure of the (Ga0.93Zn0.07)(N0.90O0.10) was
   refined by Rietveld analyses of neutron powder diffraction data. The
   (Ga0.93Zn0.07)(N0.90O0.10) was confirmed to have a wurtzite-type
   Structure (space group: P6(3)mc). The present work demonstrates that
   oxygen substitutes for nitrogen in the crystal structure, and may be
   responsible for the desirable optical properties of
   (Ga0.93Zn0.07)(N0.90O0.10) as a photocatalyst for visible light-driven
   overall water splitting. The neutron scattering amplitude distribution
   through the maximum-entropy method (MEM) and MEM-based pattern fitting
   revealed that the crystal structure of the (Ga0.93Zn0.07)(N0.90O0.10)
   is free of interstitial sites and large disorder.
PD FEB
PY 2006
VL 47
IS 2
BP 295
EP 297
UT ISI:000236784700014
ER

PT J
AU Maeda, K
   Teramura, K
   Lu, DL
   Takata, T
   Saito, N
   Inoue, Y
   Domen, K
TI Photocatalyst releasing hydrogen from water - Enhancing catalytic
   performance holds promise for hydrogen production by water splitting in
   sunlight.
SO NATURE
PD MAR 16
PY 2006
VL 440
IS 7082
BP 295
EP 295
UT ISI:000235997600041
ER

PT J
AU Teramura, K
   Maeda, K
   Saito, T
   Takata, T
   Saito, N
   Inoue, Y
   Domen, K
TI Characterization of ruthenium oxide nanocluster as a cocatalyst with
   (Gal(1-x)Zn(x))(N1-xOx) for photocatalytic overall water splitting (vol
   109, pg 21915, 2005)
SO JOURNAL OF PHYSICAL CHEMISTRY B
PD MAR 9
PY 2006
VL 110
IS 9
BP 4500
EP 4501
UT ISI:000235944500095
ER

PT J
AU Lei, ZB
   Ma, GJ
   Liu, MY
   You, WS
   Yan, HJ
   Wu, GP
   Takata, T
   Hara, M
   Domen, K
   Li, C
TI Sulfur-substituted and zinc-doped In(OH)(3): A new class of catalyst
   for photocatalytic H-2 production from water under visible light
   illumination
SO JOURNAL OF CATALYSIS
AB Sulfur-substituted In(OH)(3) [hereafter denoted as In(OH)(y)S-z] and
   Zn-doped In(OH)(y)S-z [hereafter denoted as In(OH)(y)S-z:Zn] are
   synthesized in an aqueous Solution of ethylenediamine via the
   hydrothermal method. The photoactivities of these catalysts for H,)
   production are investigated in the presence of Na2S and Na2SO3
   sacrificial reagent under visible light illumination (lambda > 420 nm).
   The absorption edge of In(OH)(y)S-z shifted monotonically from 240 nm
   for In(OH)(3) to 570 nm for In(OH)(y)S-z when the atomic ratio of S/In
   in the synthesis solution is increased from 0 to 2.0. But the
   absorption edge of In(OH)(y)S-z:Zn shifted from 570 to 470 nm as the
   atomic ratio of Zn/In in the synthesis solution was increased from 0 to
   1.0. The catalyst In(OH)(y)S-z is active for H-2 production, with an
   average rate of H-2 of 0.9-1.8 mu mol/h, under visible light
   illumination. The The rate of H-2 production is 35.8 and 67 mu mol/h on
   2wt% Pt-loaded In(OH)(y)S-z:Zn photoactivity of In(OH)(y)S-z is
   enhanced by doping with Zn2+ catalyst when X = 0.2 and 0.5,
   respectively, corresponding to a quantum efficiency of 0.32 and 0.59%
   at 420 +/- 10 nm, respectively. (c) 2005 Elsevier Inc. All rights
   reserved.
PD JAN 25
PY 2006
VL 237
IS 2
BP 322
EP 329
UT ISI:000235330600012
ER

PT S
AU Nakajima, K
   Lu, D
   Hara, M
   Domen, K
   Kondo, JN
TI Synthesis and application of thermally stable mesoporous Ta2O5
   photocatalyst for overall water decomposition
SO MOLECULAR SIEVES: FROM BASIC RESEARCH TO INDUSTRIAL APPLICATIONS, PTS A
   AND B
SE STUDIES IN SURFACE SCIENCE AND CATALYSIS
AB Thermally stable mesoporous Ta2O5 is prepared by a sol-gel technique
   using a neutral block copolymer P123 as a template. N-2 adsorption
   analysis reveals that this material has a BFT surface area of 145
   m(2.)g(-1), mesopore diameter of 3.5 nm, and mesopore Volume or 0.20
   mL(.)g(-1) The wall thickness of rnesoporous Ta2O5 is estimated to be
   ca. 3.5 mm based oil the repeat distance in the X-ray diffraction
   Pattern and the pore diameter. The formation of thicker walls results
   in higher thermal stability than tantalum oxides prepared by a
   ligand-assisted templating method. The NiO-Ioaded mesoporous Ta2O5
   photocatalyst exhibits high photocatalytic activity for the
   decomposition of water under ultraviolet (UV) light, comparable to that
   of crystallized nonporous Ta2O5 particles. The influence of wall
   thickness oil the activity or some mesoporous Ta2O5 photocatalysts is
   discussed.
PY 2005
VL 158
PN Part A-B
BP 1477
EP 1484
UT ISI:000234827501066
20楼2006-11-27 13:41:48
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