A mechanistic study of the dopant-induced breakdown in halide perovskites using solid state energy storage devices. Issue 10 (13th September 2022)

• Record Type: Journal Article
• Authors: Mathieson, Angus G. M.; Dose, Wesley M.; Steinrück, Hans-Georg; Takacs, Christopher J.; Feldmann, Sascha; Pandya, Raj; Merryweather, Alice J.; Mackanic, David; Rao, Akshay; Deschler, Felix; De Volder, Michael
• Is Part Of: Energy & environmental science. Volume 15:Issue 10(2022)
• Page Start: 4323
• Page End: 4337
• Publication Date: 2022-09-13
• Subjects: Energy conversion -- Periodicals; Fuel switching -- Periodicals; Environmental sciences -- Periodicals; Environmental chemistry -- Periodicals; 333.79
• DOI: 10.1039/d2ee01754g
• Languages: English
• ISSNs: 1754-5692

Abstract

Abstract : Elucidating and quantifying the effects of doping on halide perovskites using lithium ion batteries. Abstract : Doping halide perovskites (HPs) with extrinsic species, such as alkali metal ions, plays a critical, albeit often elusive role in optimising optoelectronic devices. Here, we use solid state lithium ion battery inspired devices with a polyethylene oxide-based polymer electrolyte to dope HPs controllably with lithium ions. We perform a suite of operando material analysis techniques while dynamically varying Li doping concentrations. We determine and quantify three doping regimes; a safe regime, with doping concentrations of <10 20 cm −3 (2% Li : Pb mol%) in which the HP may be modified without detrimental effect to its structure; a minor decomposition regime, in which the HP is partially transformed but remains the dominant species; and a major decomposition regime in which the perovskite is superseded by new phases. We provide a mechanistic description of the processes mediating between each stage and find evidence for metallic Pb (0), LiBr and LiPbBr2 as final decomposition products. Combining results from synchrotron X-ray diffraction measurements with in situ photoluminescence and optical reflection microscopy studies, we distinguish the influences of free charge carriers and intercalated lithium independently. We find that the charge density is equally as important as the geometric considerations of the dopant species and thereby provide a quantitative framework upon which the future design of doped-perovskite energy devices should be based.