Enhanced Coloration for Hybrid Niobium-Based Electrochromic Devices

被引:36
|
作者
Mjejri, Issam
Grocassan, Romain
Rougier, Aline [1 ]
机构
[1] CNRS, UMR 5026, ICMCB, 87 Ave Dr Albert Schweitzer, F-33600 Pessac, France
来源
ACS APPLIED ENERGY MATERIALS | 2018年 / 1卷 / 08期
关键词
polyol synthesis; nanoparticles; niobium oxide; dip coating; electrochromic performances; hybrid device; NB2O5; THIN-FILMS; OXIDE; V2O5; GROWTH; METAL;
D O I
10.1021/acsaem.8b00967
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Niobium pentoxide, Nb2O5, exists in many polymorphs with diverse properties and morphologies that are dependent on the synthesis route. In this work, we design a new approach to fabricate and stabilize the metastable polymorph hexagonal nano-niobium pentoxide using soft chemistry and in particular the polyol synthesis. The electrochromic properties of homogeneous niobium pentoxide thin films deposited by dip coating, from as-synthesized hexagonal powder, are studied in lithium trifluoromethanesulfonimide (LiTFSI) in 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMITFSI) ionic liquid electrolyte versus Pt as counter electrode. The structure and morphology of the Nb2O5 thin films before and after cycling are characterized by ex-situ XRD and SEM while their optical and electrochemical properties are investigated by in-situ transmittance and cyclic voltammetry (CV), respectively. Thin films made from hexagonal Nb2O5 with a sphere architecture exhibit good cycling stability, high transmittance modulations (Delta T approximate to 33% at 550 nm), fast switching speeds (2-3 s for coloration and bleaching at 550 nm), and high coloration efficiency (CE approximate to 26 cm(2) C-1) with a good quality factor G((lambda)) = 10.4 cm(2) C-1 s(-1). Finally, novel electrochromic devices based on hybrid thin films combining poly(ethylene-3,4-dioxythiophene):poly(styrenesulfonicacid) (PEDOT:PSS) and oxides are assembled showing enhanced coloration and simultaneous color change due to their double-sided configuration.
引用
收藏
页码:4359 / 4366
页数:15
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