Peimei Da

Bio: Peimei Da is an academic researcher from Fudan University. The author has contributed to research in topics: Perovskite (structure) & Nanowire. The author has an hindex of 20, co-authored 22 publications receiving 3011 citations. Previous affiliations of Peimei Da include University of Oxford.

Planar perovskite solar cells with long-term stability using ionic liquid additives

Abstract: Solar cells based on metal halide perovskites are one of the most promising photovoltaic technologies(1-4). Over the past few years, the long-term operational stability of such devices has been gre ...

Reduced Mesoporous Co3O4 Nanowires as Efficient Water Oxidation Electrocatalysts and Supercapacitor Electrodes

Abstract: While electrochemical water splitting is one of the most promising methods to store light/electrical energy in chemical bonds, a key challenge remains in the realization of an efficient oxygen evolution reaction catalyst with large surface area, good electrical conductivity, high catalytic properties, and low fabrication cost. Here, a facile solution reduction method is demonstrated for mesoporous Co3O4 nanowires treated with NaBH4. The high-surface-area mesopore feature leads to efficient surface reduction in solution at room temperature, which allows for retention of the nanowire morphology and 1D charge transport behavior, while at the same time substantially increasing the oxygen vacancies on the nanowire surface. Compared to pristine Co3O4 nanowires, the reduced Co3O4 nanowires exhibit a much larger current of 13.1 mA cm-2 at 1.65 V vs reversible hydrogen electrode (RHE) and a much lower onset potential of 1.52 V vs RHE. Electrochemical supercapacitors based on the reduced Co3O4 nanowires also show a much improved capacitance of 978 F g-1 and reduced charge transfer resistance. Density-functional theory calculations reveal that the existence of oxygen vacancies leads to the formation of new gap states in which the electrons previously associated with the Co-O bonds tend to be delocalized, resulting in the much higher electrical conductivity and electrocatalytic activity.

A piperidinium salt stabilizes efficient metal-halide perovskite solar cells.

Abstract: Longevity has been a long-standing concern for hybrid perovskite photovoltaics. We demonstrate high-resilience positive-intrinsic-negative perovskite solar cells by incorporating a piperidinium-based ionic compound into the formamidinium-cesium lead-trihalide perovskite absorber. With the bandgap tuned to be well suited for perovskite-on-silicon tandem cells, this piperidinium additive enhances the open-circuit voltage and cell efficiency. This additive also retards compositional segregation into impurity phases and pinhole formation in the perovskite absorber layer during aggressive aging. Under full-spectrum simulated sunlight in ambient atmosphere, our unencapsulated and encapsulated cells retain 80 and 95% of their peak and post-burn-in efficiencies for 1010 and 1200 hours at 60° and 85°C, respectively. Our analysis reveals detailed degradation routes that contribute to the failure of aged cells.

Controlled Sn-Doping in TiO2 Nanowire Photoanodes with Enhanced Photoelectrochemical Conversion

Abstract: We demonstrate for the first time the controlled Sn-doping in TiO2 nanowire (NW) arrays for photoelectrochemical (PEC) water splitting. Because of the low lattice mismatch between SnO2 and TiO2, Sn dopants are incorporated into TiO2 NWs by a one-pot hydrothermal synthesis with different ratios of SnCl4 and tetrabutyl titanate, and a high acidity of the reactant solution is critical to control the SnCl4 hydrolysis rate. The obtained Sn-doped TiO2 (Sn/TiO2) NWs are single crystalline with a rutile structure, and the incorporation of Sn in TiO2 NWs is well controlled at a low level, that is, 1–2% of Sn/Ti ratio, to avoid phase separation or interface scattering. PEC measurement on Sn/TiO2 NW photoanodes with different Sn doping ratios shows that the photocurrent increases first with increased Sn doping level to >2.0 mA/cm2 at 0 V vs Ag/AgCl under 100 mW/cm2 simulated sunlight illumination up to ∼100% enhancement compared to our best pristine TiO2 NW photoanodes and then decreases at higher Sn doping levels. ...

WO3 Nanoflakes for Enhanced Photoelectrochemical Conversion

Abstract: We developed a postgrowth modification method of two-dimensional WO3 nanoflakes by a simultaneous solution etching and reducing process in a weakly acidic condition. The obtained dual etched and reduced WO3 nanoflakes have a much rougher surface, in which oxygen vacancies are created during the simultaneous etching/reducing process for optimized photoelectrochemical performance. The obtained photoanodes show an enhanced photocurrent density of ∼1.10 mA/cm2 at 1.0 V vs Ag/AgCl (∼1.23 V vs reversible hydrogen electrode), compared to 0.62 mA/cm2 of pristine WO3 nanoflakes. The electrochemical impedance spectroscopy measurement and the density functional theory calculation demonstrate that this improved performance of dual etched and reduced WO3 nanoflakes is attributed to the increase of charge carrier density as a result of the synergetic effect of etching and reducing.

Plasma-Engraved Co3 O4 Nanosheets with Oxygen Vacancies and High Surface Area for the Oxygen Evolution Reaction.

Abstract: Co3O4, which is of mixed valences Co2+ and Co3+, has been extensively investigated as an efficient electrocatalyst for the oxygen evolution reaction (OER). The proper control of Co2+/Co3+ ratio in Co3O4 could lead to modifications on its electronic and thus catalytic properties. Herein, we designed an efficient Co3O4-based OER electrocatalyst by a plasma-engraving strategy, which not only produced higher surface area, but also generated oxygen vacancies on Co3O4 surface with more Co2+ formed. The increased surface area ensures the Co3O4 has more sites for OER, and generated oxygen vacancies on Co3O4 surface improve the electronic conductivity and create more active defects for OER. Compared to pristine Co3O4, the engraved Co3O4 exhibits a much higher current density and a lower onset potential. The specific activity of the plasma-engraved Co3O4 nanosheets (0.055 mA cm−2BET at 1.6 V) is 10 times higher than that of pristine Co3O4, which is contributed by the surface oxygen vacancies.

Transition-Metal (Co, Ni, and Fe)-Based Electrocatalysts for the Water Oxidation Reaction

Abstract: Increasing energy demands and environment awareness have promoted extensive research on the development of alternative energy conversion and storage technologies with high efficiency and environmental friendliness. Among them, water splitting is very appealing, and is receiving more and more attention. The critical challenge of this renewable-energy technology is to expedite the oxygen evolution reaction (OER) because of its slow kinetics and large overpotential. Therefore, developing efficient electrocatalysts with high catalytic activities is of great importance for high-performance water splitting. In the past few years, much effort has been devoted to the development of alternative OER electrocatalysts based on transition-metal elements that are low-cost, highly efficient, and have excellent stability. Here, recent progress on the design, synthesis, and application of OER electrocatalysts based on transition-metal elements, including Co, Ni, and Fe, is summarized, and some invigorating perspectives on the future developments are provided.

Defect Chemistry of Nonprecious-Metal Electrocatalysts for Oxygen Reactions

Abstract: Oxygen electrocatalysis, including the oxygen-reduction reaction (ORR) and oxygen-evolution reaction (OER), is a critical process for metal-air batteries Therefore, the development of electrocatalysts for the OER and the ORR is of essential importance Indeed, various advanced electrocatalysts have been designed for the ORR or the OER; however, the origin of the advanced activity of oxygen electrocatalysts is still somewhat controversial The enhanced activity is usually attributed to the high surface areas, the unique facet structures, the enhanced conductivities, or even to unclear synergistic effects, but the importance of the defects, especially the intrinsic defects, is often neglected More recently, the important role of defects in oxygen electrocatalysis has been demonstrated by several groups To make the defect effect clearer, the recent development of this concept is reviewed here and a novel principle for the design of oxygen electrocatalysts is proposed An overview of the defects in carbon-based, metal-free electrocatalysts for ORR and various defects in metal oxides/selenides for OER is also provided The types of defects and controllable strategies to generate defects in electrocatalysts are presented, along with techniques to identify the defects The defect-activity relationship is also explored by theoretical methods

High-Efficiency Perovskite Solar Cells.

Abstract: With rapid progress in a power conversion efficiency (PCE) to reach 25%, metal halide perovskite-based solar cells became a game-changer in a photovoltaic performance race. Triggered by the development of the solid-state perovskite solar cell in 2012, intense follow-up research works on structure design, materials chemistry, process engineering, and device physics have contributed to the revolutionary evolution of the solid-state perovskite solar cell to be a strong candidate for a next-generation solar energy harvester. The high efficiency in combination with the low cost of materials and processes are the selling points of this cell over commercial silicon or other organic and inorganic solar cells. The characteristic features of perovskite materials may enable further advancement of the PCE beyond those afforded by the silicon solar cells, toward the Shockley-Queisser limit. This review summarizes the fundamentals behind the optoelectronic properties of perovskite materials, as well as the important approaches to fabricating high-efficiency perovskite solar cells. Furthermore, possible next-generation strategies for enhancing the PCE over the Shockley-Queisser limit are discussed.