Facile Phase-Selectable Chemical Synthesis of Tin Selenide Nanosheets toward Nanostructured Materials for Energy-Related Applications

油胺 成核 硒化物 三辛基氧化膦 材料科学 相(物质) 带隙 化学工程 硫系化合物 金属 纳米技术 分析化学(期刊) 化学 纳米晶 光电子学 有机化学 萃取(化学) 冶金 工程类
作者
Simon Moore,Keiji Kobayashi,Mari Takahashi,Koichi Higashimine,Shinya Maenosono
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:127 (25): 12394-12403 被引量:1
标识
DOI:10.1021/acs.jpcc.3c03026
摘要

Here, we present a facile, phase-selectable, size-controllable chemical method for the synthesis of Sn-Se nanosheets (NSs). The resultant NSs were characterized using XRD, SEM, TEM, STEM, and EDS. Phase control was achieved by changing the input molar ratio of Sn:Se. At ratios of 1:1 and 1:2, pure-phase, rectangular SnSe NSs; at ratios of 1:6 and 1:10, pure-phase, hexagonal SnSe2 NSs; and at a ratio of 1:4, a mix of the two NSs were produced. The produced NSs were large (a few hundred nm in diameter) and thin (10–20 nm), although there was no significant increase in the optical band gap calculated from UV–vis–NIR spectroscopy, indicating an absence of quantum confinement effects. Size control of both phases was achieved by changing the amount of the ligand, trioctylphosphine oxide (TOPO). Increasing the amount of TOPO decreased the size of the SnSe NSs and increased the size of the SnSe2 NSs. Finally, the formation mechanism was investigated and it was found that the formation of metal-ion complexes, namely, Sn-TOPO and Se-oleylamine, played an important role in the phase selectivity and size distribution of the NSs by changing the effective ratio of Sn:Se and slowing the nucleation of the NSs.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
xjcy应助橙子采纳,获得10
1秒前
老睿智发布了新的文献求助10
1秒前
啊啊啊应助风清扬采纳,获得10
1秒前
2秒前
wwwteng呀完成签到,获得积分10
2秒前
Sunny完成签到,获得积分10
3秒前
慕青应助lzy采纳,获得10
3秒前
ndrise发布了新的文献求助10
4秒前
4秒前
4秒前
Mdead完成签到,获得积分10
5秒前
5秒前
脑洞疼应助落寞丹烟采纳,获得10
5秒前
5秒前
星辰大海应助无糖可乐采纳,获得10
6秒前
Baneyhua发布了新的文献求助10
6秒前
于呆呆完成签到,获得积分10
8秒前
土豆兵应助研友_RLN4OZ采纳,获得10
8秒前
8秒前
乐乐应助醉熏的烤鸡采纳,获得10
9秒前
刻苦书白发布了新的文献求助10
9秒前
DengLipan应助懵懂的柚子采纳,获得10
9秒前
许xxxx完成签到 ,获得积分10
9秒前
9秒前
9秒前
背后三问完成签到,获得积分10
10秒前
风清扬发布了新的文献求助10
11秒前
江仁媛完成签到,获得积分20
11秒前
11秒前
12秒前
12秒前
汉堡包应助棣月永远采纳,获得10
13秒前
老睿智完成签到,获得积分10
15秒前
Orange应助Baneyhua采纳,获得10
16秒前
海贼王的男人完成签到 ,获得积分10
16秒前
fabian完成签到,获得积分10
16秒前
Jasper应助吉吉国王的跟班采纳,获得10
17秒前
17秒前
雷霆万钧发布了新的文献求助20
17秒前
光年完成签到,获得积分10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Governing Growth: Us Industrial Policy from Hamilton to Trump 500
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7624654
求助须知:如何正确求助?哪些是违规求助? 9199729
关于积分的说明 19723509
捐赠科研通 7195622
什么是DOI,文献DOI怎么找? 3273562
关于科研通互助平台的介绍 2435731
邀请新用户注册赠送积分活动 2269409