Sangam: A Confluence of Knowledge Streams

Integrating Diverse Materials for Carbon Perovskite Solar Cells: Examining the Performance and Stability

Show simple item record

dc.contributor Sundaram, Senthilarasu
dc.contributor Mallick, Tapas Kumar
dc.contributor Tahir, Asif
dc.creator Bhandari, S
dc.date 2022-06-15T08:43:10Z
dc.date 2022-06-13
dc.date 2022-06-14T14:20:17Z
dc.date 2022-06-15T08:43:10Z
dc.date.accessioned 2023-02-23T12:14:26Z
dc.date.available 2023-02-23T12:14:26Z
dc.identifier ORCID: 0000-0002-3347-9682 (Bhandari, Shubhranshu)
dc.identifier ScopusID: 57210261568 (Bhandari, Shubhranshu)
dc.identifier http://hdl.handle.net/10871/129949
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/258535
dc.description The emergence of perovskite solar cells (PSCs) in a "catfish effect" of other conventional photovoltaic technologies with the massive growth of power conversion efficiency (PCE) with a simple manufacturing process has given a new direction to the entire solar energy field. Usually, PSC components such as electron transport material (ETM), perovskite sensitizer, hole transport material (HTM), and electrode materials need to be appropriately aligned according to the electron transfer and recombination process in order to achieve the best out of the device. Despite the enormous amount of research, the stability, reactivity, and cost issues of noble metal (Au, Ag) electrode-based traditional PSC devices are becoming obstacles to marketization. Due to the low fabrication cost and enhanced ambient stability, carbon counter electrode-based PSC (CPSC) evolved as a suitable alternative in such scenarios. These CPSCs are still in a stage of development where different fabrication engineering, designs and materials are being investigated to attain a comparable state with the standard commercialized photovoltaics. To date, hardly any report is available on ambient CPSC with PCE over 15% and stability of ~1000h without encapsulation, which opens up the window for more research. The fundamental objective of this thesis work was to develop high-performance ambient CPSC with PCE > 15% under 1SUN AM 1.5 illumination, maintaining the stability of ~1000h. This was achieved using alternative ETM and HTM with strategic incorporation instead of traditional ones. Noticeably, the temperature is a crucial parameter to attain and, at the same time, retain the aimed PV performance and stability. Therefore, a physico-thermal investigation was performed to understand the effect of temperature on the fabricated CPSC devices. The understanding further helped to examine the possible futuristic application of CPSC as the semi-transparent device for energy savings build environment. To achieve the goals of this thesis, the 1st step involved finding out suitable combination of HTM and carbon counter electrodes highlighted in chapter 3. For the first time, the fully printable mesoporous CPSCs are demonstrated with concentration-dependent WO3 (5, 7.5, and 10% by volume) nanoparticles incorporated in carbon electrodes fabricated under ambient conditions. The highest PCE ~10.5% was obtained with the 7.5% WO3/carbon device; however, the 10% WO3/carbon device exhibited better ambient stability of ~600h. Besides, graphene/ poly(3,4-ethylene dioxythiophene) polystyrene sulfonate (PEDOT: PSS) was introduced as an alternative HTM with novel light soaking and surface wettability strategies, and an enhanced PV performance with PCE >11% was achieved. In search of an alternative HTM/carbon combination with more superior performance, a novel and cost-effective synthesis process of graphitic CNP as a suitable counter electrode and its combination with NiO was visualized. The stability test of the high-temperature counter electrode strategy of CNP/NiO showed ~1000 h air stability with negligible efficiency loss having a maximum PCE of 13.2%, whereas the low-temperature strategy of CNP/NiO devices showed 14.2% PCE with ~650 h air stability. Thus CNP/NiO combination achieved performance very close to the aims of this thesis, which was enhanced to the required performance by introducing alternative ETM for the devices. Chapter 4 describes the strategic incorporation of morphology modulated BaSnO3 (BSO) and brookite TiO2 (BTO) nanostructures in place of conventional anatase TiO2 as ETM to successfully achieve PCE >13.5% and >15%, respectively, with stability >1000 h. The enhanced electron transport and reduced charge recombination by rod-based nanostructures of BSO and BTO displayed the best performance for the types to date in CPSC. Along with performance improvement, the understanding of CPSC’s temperature behaviour was considered in this thesis to understand the real-world feasibility of CPSC for the first time. The temperature coefficients (TC) of photovoltaic parameters for MAPbI3-based devices are demonstrated in chapter 5 with a detailed physico-chemical understanding. Besides CH3NH3PbI3, other perovskites such as CH3NH3PbI3-xClx and Cs0.05(FA0.83MA0.17)0.95Pb(I0.83Br0.17)3 were applied as an alternative sensitizer for the CPSCs and studied their temperature coefficients across a wide range of real-world temperatures to obtain behavioural differences between the halide perovskites. Finally, the suitability of semi-transparent CPSC for fenestration integration was evaluated for the first time via fabrication engineering and thickness control with the highest reported average visible transmittance/PCE combination to date, as discussed in chapter 6. Finally, in this thesis work, CPSC devices are explored, which highlights fascinating ambient fabrication processes and significant device performance with new series of HTMs, ETMs and designs for futuristic applications.
dc.publisher University of Exeter
dc.publisher Renewable Energy
dc.rights http://www.rioxx.net/licenses/all-rights-reserved
dc.title Integrating Diverse Materials for Carbon Perovskite Solar Cells: Examining the Performance and Stability
dc.type Thesis or dissertation
dc.type PhD in Renewable Energy
dc.type Doctoral
dc.type Doctoral Thesis


Files in this item

Files Size Format View
BhandariS.pdf 19.26Mb application/pdf View/Open

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse