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Different Morphologies of SnS2 Supported on 2D g-C3N4 for Excellent and Stable Visible Light Photocatalytic Hydrogen Generation
ACS Sustainable Chemistry & Engineering ( IF 7.1 ) Pub Date : 2018-02-13 00:00:00 , DOI: 10.1021/acssuschemeng.7b04792 Liquan Jing , Yuanguo Xu , Zhigang Chen , Minqiang He , Meng Xie , Jie Liu , Hui Xu , Shuquan Huang , Huaming Li
ACS Sustainable Chemistry & Engineering ( IF 7.1 ) Pub Date : 2018-02-13 00:00:00 , DOI: 10.1021/acssuschemeng.7b04792 Liquan Jing , Yuanguo Xu , Zhigang Chen , Minqiang He , Meng Xie , Jie Liu , Hui Xu , Shuquan Huang , Huaming Li
Highly efficient different morphologies of SnS2 (nanoparticles, nanosheets, and 3D flower-like)/g-C3N4 composites were, respectively, prepared via an elementary hydrothermal method that was integrated with the calcination means. The XRD results showed that the relative intensities of several diffraction peaks, especially (001), (100), (101), and (102), indicated that the as-prepared samples (SnS2 nanoparticle, SnS2 nanosheet, and 3D flower-like SnS2) should be dominated by different specific preferred growth of facets. In comparison with SnS2 and pure g-C3N4, the SnS2/g-C3N4 composites exhibited much higher H2 development performance under visible light irradiation in the presence of Na2SO3 and Na2S as the sacrificial agent. The SnS2 nanoparticles/g-C3N4 composites exhibit the highest visible-light-driven H2-generation rate of 6305.18 μmol h–1 g–1 without any noble metal as cocatalyst, which is approximately 16.98 times higher than that of SnS2 nanoparticles. In all, the SnS2 nanoparticles (SnS2 nanoparticle/g-C3N4 composite) dominated by (001) and (100) preferred growth of facets exhibit significant photocatalytic activity resulting from their suitable band edges to realize the photocatalytic redox reaction. The analysis of photocurrent response, linear sweep voltammograms, and photoluminescence demonstrated that the low recombination rate and the efficacious charge transfer of photogenerated carriers could be assigned to the interactive impact of g-C3N4 and SnS2.
中文翻译:
二维gC 3 N 4上负载的SnS 2的不同形态,可产生稳定且稳定的可见光光催化氢
通过与煅烧装置集成的基本水热法分别制备了SnS 2(纳米颗粒,纳米片和3D花状)/ gC 3 N 4复合材料的高效不同形貌。XRD结果表明,几个衍射峰的相对强度,特别是(001),(100),(101)和(102),表明所制备的样品(SnS 2纳米颗粒,SnS 2纳米片和3D花类SnS 2)应以不同的特定小平面优先增长为主。与SnS 2和纯gC 3 N 4相比,SnS 2 / gC在作为牺牲剂的Na 2 SO 3和Na 2 S的存在下,在可见光照射下,3 N 4复合材料表现出更高的H 2显影性能。SnS 2纳米颗粒/ gC 3 N 4复合材料在没有任何贵金属作为助催化剂的情况下,可见光驱动的H 2生成速率最高,为6305.18μmolh –1 g –1,约为SnS 2的16.98倍纳米粒子。总之,SnS 2纳米颗粒(SnS 2纳米颗粒/ gC 3以(001)和(100)为主的N 4复合物)的优选小面生长由于其合适的能带边缘实现光催化氧化还原反应而表现出显着的光催化活性。对光电流响应,线性扫描伏安图和光致发光的分析表明,低重组率和光生载流子的有效电荷转移可以归因于gC 3 N 4和SnS 2的相互作用。
更新日期:2018-02-13
中文翻译:
二维gC 3 N 4上负载的SnS 2的不同形态,可产生稳定且稳定的可见光光催化氢
通过与煅烧装置集成的基本水热法分别制备了SnS 2(纳米颗粒,纳米片和3D花状)/ gC 3 N 4复合材料的高效不同形貌。XRD结果表明,几个衍射峰的相对强度,特别是(001),(100),(101)和(102),表明所制备的样品(SnS 2纳米颗粒,SnS 2纳米片和3D花类SnS 2)应以不同的特定小平面优先增长为主。与SnS 2和纯gC 3 N 4相比,SnS 2 / gC在作为牺牲剂的Na 2 SO 3和Na 2 S的存在下,在可见光照射下,3 N 4复合材料表现出更高的H 2显影性能。SnS 2纳米颗粒/ gC 3 N 4复合材料在没有任何贵金属作为助催化剂的情况下,可见光驱动的H 2生成速率最高,为6305.18μmolh –1 g –1,约为SnS 2的16.98倍纳米粒子。总之,SnS 2纳米颗粒(SnS 2纳米颗粒/ gC 3以(001)和(100)为主的N 4复合物)的优选小面生长由于其合适的能带边缘实现光催化氧化还原反应而表现出显着的光催化活性。对光电流响应,线性扫描伏安图和光致发光的分析表明,低重组率和光生载流子的有效电荷转移可以归因于gC 3 N 4和SnS 2的相互作用。