The ongoing research activities in the field of lignocellulosic biomass for production of value-added chemicals and polymers that can be utilized to replace petroleum-based materials are reviewed.
King Abdullah University of Science and Technology
ORCID: 0000-0003-0787-7991Publishes on Perovskite Materials and Applications, Conducting polymers and applications, Organic Electronics and Photovoltaics. 75 papers and 9.3k citations.
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The ongoing research activities in the field of lignocellulosic biomass for production of value-added chemicals and polymers that can be utilized to replace petroleum-based materials are reviewed.
Stacking solar cells with decreasing band gaps to form tandems presents the possibility of overcoming the single-junction Shockley-Queisser limit in photovoltaics. The rapid development of solution-processed perovskites has brought perovskite single-junction efficiencies >20%. However, this process has yet to enable monolithic integration with industry-relevant textured crystalline silicon solar cells. We report tandems that combine solution-processed micrometer-thick perovskite top cells with fully textured silicon heterojunction bottom cells. To overcome the charge-collection challenges in micrometer-thick perovskites, we enhanced threefold the depletion width at the bases of silicon pyramids. Moreover, by anchoring a self-limiting passivant (1-butanethiol) on the perovskite surfaces, we enhanced the diffusion length and further suppressed phase segregation. These combined enhancements enabled an independently certified power conversion efficiency of 25.7% for perovskite-silicon tandem solar cells. These devices exhibited negligible performance loss after a 400-hour thermal stability test at 85°C and also after 400 hours under maximum power point tracking at 40°C.
We report on bulk-heterojunction (BHJ) organic photovoltaics (OPVs) based on the self-assembled monolayer (SAM) 2PACz as a hole-selective interlayer functionalized directly onto the indium tin oxide (ITO) anode. The 2PACz is found to change the work function of ITO while simultaneously affecting the morphology of the BHJ deposited atop. Cells with PM6:N3 BHJ and ITO-2PACz anode exhibit a power conversion efficiency (PCE) of 16.6%, which is greater than that measured for bare ITO (6.45%) and ITO/PEDOT:PSS (15.94%) based devices. The enhanced performance is attributed to lower contact-resistance, reduced bimolecular recombination losses, and improved charge transport within the BHJ. Importantly, the ITO-2PACz-based OPVs show dramatically improved operational stability when compared with PEDOT:PSS-based cells. When the ITO-2PACz anode is combined with the ternary PM6:BTP-eC9:PC71BM BHJ, the resulting cells exhibit a maximum PCE of 18.03%, highlighting the potential of engineered SAMs for use in hole-selective contacts in high-performance OPVs.