Bhaskar Akkisetty, Deepa Melepurath, Rao Tata Narasinga
Department of Materials Science and Metallurgical Engineering, Indian Institute of Technology Hyderabad, Ordnance Factory Estate, Yeddumailram, 502205, Andhra Pradesh, India.
Nanoscale. 2014 Sep 21;6(18):10762-71. doi: 10.1039/c4nr02505a. Epub 2014 Aug 7.
Tin oxide hollow spheres (SnO₂ HS) with high structural integrity were synthesized by using a one pot hydrothermal approach with organic moieties as structure controlling agents. By adjusting the proportion of acetylacetone (AcAc) in the precursor formulation, SnO₂ HS of 200 and 350 nm dimensions, with a uniform shell thickness of about 50 nm, were prepared. Using the optimized solution composition with a Sn precursor, heating duration dependent structural evolution of SnO₂ was performed at a fixed temperature of 160 °C, which revealed a transition from solid spheres (1 h) to aggregated spheres (4 h) to porous spheres (10 h) to optimized HS (13 h) and finally to broken enlarged HS (24 h). A heating temperature dependent study carried out with a constant heating span of 13 h showed a metamorphosis from spheres with solid cores (140 °C) to ones with hollow cores (160 °C), culminating with fragmented HS, expanded in dimensions (180 °C). A growth mechanism was proposed for the optimized SnO₂ HS (2.5 or 5.0 mL of AcAc, 160 °C, 13 h) and the performance of these HS as anodes for Li ions batteries was evaluated by electrochemical studies. The 200 nm SnO₂ HS demonstrated an initial lithium storage capacity of 1055 mA h g(-1) at a current density of 100 mA g(-1), and they retained a capacity of 540 mA h g(-1) after 50 charge-discharge cycles. The SnO₂ HS also showed excellent rate capability as the electrode exhibited a capacity of 422 mA h g(-1) even at a high current density of 2000 mA g(-1). The notable capacity of SnO₂ HS is a manifestation of the mono-disperse quality of the SnO₂ HS coupled with the high number of electrochemically addressable sites, afforded by the large surface area of the HS and the striking cyclability is also attributed to the unique structure of HS, which is resistant to degradation upon repeated ion insertion/extraction. The SnO₂ HS were also found to be luminescent, thus indicating their usefulness for not only energy storage but also for energy harvesting applications.
采用一锅水热法,以有机部分作为结构控制剂,合成了具有高结构完整性的氧化锡空心球(SnO₂ HS)。通过调整前驱体配方中乙酰丙酮(AcAc)的比例,制备了尺寸为200和350 nm、壳层厚度均匀约为50 nm的SnO₂ HS。使用含锡前驱体的优化溶液组成,在160 °C的固定温度下进行了加热时间依赖性的SnO₂结构演变研究,结果表明其从实心球(1小时)转变为聚集球(4小时),再到多孔球(10小时),然后到优化的空心球(13小时),最后到破碎扩大的空心球(24小时)。在恒定加热时间为13小时的情况下进行的加热温度依赖性研究表明,其从具有实心核的球(140 °C)转变为具有空心核的球(160 °C),最终以尺寸扩大的破碎空心球(180 °C)告终。针对优化的SnO₂ HS(2.5或5.0 mL的AcAc,160 °C,13小时)提出了生长机制,并通过电化学研究评估了这些空心球作为锂离子电池阳极的性能。200 nm的SnO₂ HS在100 mA g(-1)的电流密度下表现出1055 mA h g(-1)的初始锂存储容量,在50次充放电循环后仍保持540 mA h g(-1)的容量。SnO₂ HS还表现出优异的倍率性能,因为即使在2000 mA g(-1)的高电流密度下,该电极仍表现出422 mA h g(-1)的容量。SnO₂ HS的显著容量体现了其单分散质量以及由空心球大表面积提供的大量可电化学寻址位点,而出色的循环稳定性也归因于空心球的独特结构,该结构在反复的离子插入/脱出过程中抗降解。还发现SnO₂ HS具有发光性,因此表明它们不仅对能量存储有用,而且对能量收集应用也有用。