Colloidal zinc oxide-copper(I) oxide nanocatalysts for selective aqueous photocatalytic carbon dioxide conversion into methane

被引:130
作者
Bae, Kyung-Lyul [1 ,2 ]
Kim, Jinmo [1 ,2 ]
Lim, Chan Kyu [1 ,2 ]
Nam, Ki Min [3 ]
Song, Hyunjoon [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Inst for Basic Sci Korea, Ctr Nanomat & Chem React, Daejeon 34141, South Korea
[3] Mokpo Natl Univ, Dept Chem, Jeonnam 58554, South Korea
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
新加坡国家研究基金会;
关键词
FIELD-EMISSION; CO2; PHOTOREDUCTION; TIO2; ADSORPTION; REDUCTION; SURFACE; ENERGY; NANOSTRUCTURES; NANOPARTICLES;
D O I
10.1038/s41467-017-01165-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Developing catalytic systems with high efficiency and selectivity is a fundamental issue for photochemical carbon dioxide conversion. In particular, rigorous control of the structure and morphology of photocatalysts is decisive for catalytic performance. Here, we report the synthesis of zinc oxide-copper(I) oxide hybrid nanoparticles as colloidal forms bearing copper (I) oxide nanocubes bound to zinc oxide spherical cores. The zinc oxide-copper(I) oxide nanoparticles behave as photocatalysts for the direct conversion of carbon dioxide to methane in an aqueous medium, under ambient pressure and temperature. The catalysts produce methane with an activity of 1080 mu mol g(cat)(-1) h(-1), a quantum yield of 1.5% and a selectivity for methane of >99%. The catalytic ability of the zinc oxide-copper(I) oxide hybrid catalyst is attributed to excellent band alignment of the zinc-oxide and copper(I) oxide domains, few surface defects which reduce defect-induced charge recombination and enhance electron transfer to the reagents, and a high-surface area colloidal morphology.
引用
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页数:8
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共 48 条
  • [1] [Anonymous], 2012, ANGEW CHEM-GER EDIT
  • [2] Opportunities and prospects in the chemical recycling of carbon dioxide to fuels
    Centi, Gabriele
    Perathoner, Siglinda
    [J]. CATALYSIS TODAY, 2009, 148 (3-4) : 191 - 205
  • [3] CO2 photo-reduction: insights into CO2 activation and reaction on surfaces of photocatalysts
    Chang, Xiaoxia
    Wang, Tuo
    Gong, Jinlong
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2016, 9 (07) : 2177 - 2196
  • [4] INTERACTION OF CO WITH CU+ CATIONS - CO ADSORPTION ON CU2O(100)
    COX, DF
    SCHULZ, KH
    [J]. SURFACE SCIENCE, 1991, 249 (1-3) : 138 - 148
  • [5] Cu2O/ZnO hetero-nanobrush: hierarchical assembly, field emission and photocatalytic properties
    Deo, Meenal
    Shinde, Deodatta
    Yengantiwar, Ashish
    Jog, Jyoti
    Hannoyer, Beatrice
    Sauvage, Xavier
    More, Mahendra
    Ogale, Satishchandra
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (33) : 17055 - 17062
  • [6] FORMATION OF 2-CARBON ACIDS FROM CARBON-DIOXIDE BY PHOTOREDUCTION ON CADMIUM-SULFIDE
    EGGINS, BR
    IRVINE, JTS
    MURPHY, EP
    GRIMSHAW, J
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (16) : 1123 - 1124
  • [7] Concurrent synthetic control of dopant (nitrogen) and defect complexes to realize broadband (UV-650 nm) absorption in ZnO nanorods for superior photo-electrochemical performance
    Game, Onkar
    Singh, Upendra
    Gupta, Anubha A.
    Suryawanshi, Anil
    Banpurkar, Arun
    Ogale, Satishchandra
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (33) : 17302 - 17310
  • [8] A review of the aqueous electrochemical reduction of CO2 to hydrocarbons at copper
    Gattrell, M.
    Gupta, N.
    Co, A.
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2006, 594 (01) : 1 - 19
  • [9] A review of one-dimensional TiO2 nanostructured materials for environmental and energy applications
    Ge, Mingzheng
    Cao, Chunyan
    Huang, Jianying
    Li, Shuhui
    Chen, Zhong
    Zhang, Ke-Qin
    Al-Deyab, S. S.
    Lai, Yuekun
    [J]. JOURNAL OF MATERIALS CHEMISTRY A, 2016, 4 (18) : 6772 - 6801
  • [10] Photocatalytic Reduction of CO2 on TiO2 and Other Semiconductors
    Habisreutinger, Severin N.
    Schmidt-Mende, Lukas
    Stolarczyk, Jacek K.
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (29) : 7372 - 7408