Interfacial charge collection efficiency has demonstrated significant effects on the power conversion efficiency (PCE) of perovskite solar cells (PSCs). Herein, crystalline phase‐dependent charge ...collection is investigated by using rutile and anatase TiO2 electron transport layer (ETL) to fabricate PSCs. The results show that rutile TiO2 ETL enhances the extraction and transportation of electrons to FTO and reduces the recombination, thanks to its better conductivity and improved interface with the CH3NH3PbI3 (MAPbI3) layer. Moreover, this may be also attributed to the fact that rutile TiO2 has better match with perovskite grains, and less trap density. As a result, comparing with anatase TiO2 ETL, MAPbI3 PSCs with rutile TiO2 ETL delivers significantly enhanced performance with a champion PCE of 20.9 % and a large open circuit voltage (VOC) of 1.17 V.
A rutile TiO2 electron transport layer (ETL) was prepared. The thickness and crystallinity can be controlled by deposition time and sintering temperature. Rutile TiO2 has higher conductivity than anatase for faster electron transfer, better interface contact with the perovskite layer, and a lower trap density. These facilitate the charge extraction and collection and reducing carrier recombination.
Listening to the Brain With Photoacoustics Hu, Song
IEEE journal of selected topics in quantum electronics,
2016-May-June, 2016-5-00, Letnik:
22, Številka:
3
Journal Article
Recenzirano
Photoacoustic imaging (PAI), providing the unique contrast of optical absorption and the superb scalability of spatial resolution and penetration, has emerged as an enabling technique in both basic ...and translational brain research. In this paper, first, mechanisms behind neuro-PAI of endogenous absorber-encoded functional information (e.g., the concentration of hemoglobin, the oxygen saturation of hemoglobin, blood flow, oxygen metabolism, and water accumulation) and exogenous probe-labeled molecular targets (e.g., neural activity, glucose uptake, aberrant protein aggregation, and malignancy) are introduced. Then, two technical innovations-functional connectivity photoacoustic tomography and high-speed functional photoacoustic microscopy-for spatio-temporal interrogation of the brain at resting and activated states are highlighted, and two application niches in vascular cognitive impairment and brain cancer are discussed. Finally, the prospect of neuro-PAI is envisioned.
ConspectusHydrogen is an ideal energy carrier and plays a critical role in the future energy transition. Distinct from steam reforming, electrochemical water splitting, especially powered by ...renewables, has been considered as a promising technique for scalable production of high-purity hydrogen with no carbon emission. Its commercialization relies on the reduction of electricity consumption and thus hydrogen cost, calling for highly efficient and cost-effective electrocatalysts with the capability of steadily working at high hydrogen output. This requires the electrocatalysts to feature (1) highly active intrinsic sites, (2) abundant accessible active sites, (3) effective electron and mass transfer, (4) high chemical and structural durability, and (5) low-cost and scalable synthesis. It should be noted that all these requirements should be fulfilled together for a practicable electrocatalyst. Much effort has been devoted to addressing one or a few aspects, especially improving the electrocatalytic activity by electronic modulation of active sites, while few reviews have focused on the synergistic modulation of these aspects together although it is essential for advanced electrochemical water splitting.In this Account, we will present recent innovative strategies with an emphasis on our solutions for synergistically modulating intrinsic active sites, electron transportation, mass transfer, and gas evolution, as well as mechanical and chemical durability, of non-precious-metal electrocatalysts, aiming for cost-effective and highly efficient water splitting. The following approaches for coupling these aspects are summarized for both cathodic hydrogen evolution reaction (HER) and anodic oxygen evolution reaction (OER). (1)
. The electronic structure of a catalytic site determines the adsorption/desorption of reactive intermediates and thus intrinsic activity. It can be tuned by heterogeneous doping, strain effect, spin polarization, etc. Coupling these effects to optimize the reaction pathways or target simultaneously the activity and stability would advance electrocatalytic performance. (2)
. The crystallinity, crystalline phase, crystalline facets, crystalline defects, etc. affect both activity and stability. Coupling these effects with electronic modulation would enhance the activity together with stability. (3)
. It will focus on concurrently modulating electronic structure for improving the intrinsic activity and morphology for increasing accessible active sites, especially through single action or processing. The mass transfer and gas evolution properties can also be enhanced by morphological modulation to enable water splitting at large output. (4)
. Electrocatalytic reaction generally consists of a couple of elementary reactions. Each one may need a specific active site. Designing and combining various components targeting every elementary step on a space-limited catalyst surface will balance the intermediates and these steps for accelerating the overall reaction. (5)
Taking all these strategies together into account is necessary to integrate all above essential features into one electrocatalyst for enabling high-output water electrolysis. Beyond the progress made to date, the remaining challenges and opportunities is also discussed. With these insights, hopefully, this Account will shed light on the rational design of practical water-splitting electrocatalysts for the cost-effective and scalable production of hydrogen.
Electroless deposition via a spontaneous redox reaction between the metal precursor and support is believed to be a promising approach for the syntheses of supported metal nanoparticles (SMNPs). ...However, its widespread applications are significantly prohibited by the low reductivity and high cost of support. To overcome these shortcomings, a porous carbon (PC) is herein developed as a promising matrix for the electroless deposition of metal NPs. Benefiting from abundant oxygen‐based surface functional groups, the PC shows stronger reducibility (low redox potential) than conventional carbon substrate such as carbon nanotubes or graphene oxide, enabling a facile electroless deposition of Ir, Rh, and Ru NPs on its surface. These SMNPs exhibit an impressive electrocatalytic activity for the hydrogen evolution reaction (HER) or hydrogen oxidation reaction (HOR). For example, the Rh NP/PC can deliver an HER current density of 10 mA cm−2 with a small overpotential of 21 mV in 0.5 m H2SO4, while the Ru NP/PC exhibits excellent HOR activity in 0.1 m KOH in terms of high mass and surface specific exchange current density of 263 A g−1Ru and 0.227 mA cm−2Ru. The present strategy may open up opportunities for mass production of efficient supported NPs for diverse applications.
Ultrafine well‐dispersed Ir, Rh, and Ru nanoparticles (NPs) are synthesized by cost‐effective room‐temperature electroless deposition using the support itself as the reducing agent. Rh NP/PC (porous carbon) shows superior hydrogen evolution reaction activity with a small overpotential (21 mV) at 10 mA cm−2 whereas Ru NP/PC exhibits excellent hydrogen oxidation reaction activity in terms of high exchange current density.
Although single-atomically dispersed metal-N
on carbon support (M-NC) has great potential in heterogeneous catalysis, the scalable synthesis of such single-atom catalysts (SACs) with high-loading ...metal-N
is greatly challenging since the loading and single-atomic dispersion have to be balanced at high temperature for forming metal-N
. Herein, we develop a general cascade anchoring strategy for the mass production of a series of M-NC SACs with a metal loading up to 12.1 wt%. Systematic investigation reveals that the chelation of metal ions, physical isolation of chelate complex upon high loading, and the binding with N-species at elevated temperature are essential to achieving high-loading M-NC SACs. As a demonstration, high-loading Fe-NC SAC shows superior electrocatalytic performance for O
reduction and Ni-NC SAC exhibits high electrocatalytic activity for CO
reduction. The strategy paves a universal way to produce stable M-NC SAC with high-density metal-N
sites for diverse high-performance applications.
Thermally-induced tensile strain that remains in perovskite films following annealing results in increased ion migration and is a known factor in the instability of these materials. ...Previously-reported strain regulation methods for perovskite solar cells (PSCs) have utilized substrates with high thermal expansion coefficients that limits the processing temperature of perovskites and compromises power conversion efficiency. Here we compensate residual tensile strain by introducing an external compressive strain from the hole-transport layer. By using a hole-transport layer with high thermal expansion coefficient, we compensate the tensile strain in PSCs by elevating the processing temperature of hole-transport layer. We find that compressive strain increases the activation energy for ion migration, improving the stability of perovskite films. We achieve an efficiency of 16.4% for compressively-strained PSCs; and these retain 96% of their initial efficiencies after heating at 85 °C for 1000 hours-the most stable wide-bandgap perovskites (above 1.75 eV) reported so far.
Photoacoustic tomography (PAT) can create multiscale multicontrast images of living biological structures ranging from organelles to organs. This emerging technology overcomes the high degree of ...scattering of optical photons in biological tissue by making use of the photoacoustic effect. Light absorption by molecules creates a thermally induced pressure jump that launches ultrasonic waves, which are received by acoustic detectors to form images. Different implementations of PAT allow the spatial resolution to be scaled with the desired imaging depth in tissue while a high depth-to-resolution ratio is maintained. As a rule of thumb, the achievable spatial resolution is on the order of 1/200 of the desired imaging depth, which can reach up to 7 centimeters. PAT provides anatomical, functional, metabolic, molecular, and genetic contrasts of vasculature, hemodynamics, oxygen metabolism, biomarkers, and gene expression. We review the state of the art of PAT for both biological and clinical studies and discuss future prospects.
Practical electrochemical water splitting requires cost‐effective electrodes capable of steadily working at high output, leading to the challenges for efficient and stable electrodes for the oxygen ...evolution reaction (OER). Herein, by simply using conductive FeS microsheet arrays vertically pre‐grown on iron foam (FeS/IF) as both substrate and source to in situ form vertically aligned NiFe(OH)x nanosheets arrays, a hierarchical electrode with a nano/micro sheet‐on‐sheet structure (NiFe(OH)x/FeS/IF) can be readily achieved to meet the requirements. Such hierarchical electrode architecture with a superhydrophilic surface also allows for prompt gas release even at high output. As a result, NiFe(OH)x/FeS/IF exhibits superior OER activity with an overpotential of 245 mV at 50 mA cm−2 and can steadily output 1000 mA cm−2 at a low overpotential of 332 mV. The water‐alkali electrolyzer using NiFe(OH)x/FeS/IF as the anode can deliver 10 mA cm−2 at 1.50 V and steadily operate at 300 mA cm−2 with a small cell voltage for 70 h. Furthermore, a solar‐driven electrolyzer using the developed electrode demonstrates an exceptionally high solar‐to‐hydrogen efficiency of 18.6%. Such performance together with low‐cost Fe‐based materials and facile mass production suggest the present strategy may open up opportunities for rationally designing hierarchical electrocatalysts for practical water splitting or diverse applications.
A 3D hierarchical NiFe(OH)x/FeS/IF electrode with a nano/micro sheet‐on‐sheet structure exhibits superior oxygen evolution reaction activity and durability with a low overpotential of 261 mV at 100 mA cm−2 and 332 mV at 1000 mA cm−2. The water‐alkali electrolyzer, using it as an anode, achieves stable overall water splitting at 300 mA cm−2 with a small cell voltage.
Low‐threshold two‐photon‐pumped (TPP) perovskite microcavity lasers are achieved in crystal perovskite 1D or 2D microstructures fabricated through a liquid‐phase self‐assembly method assisted by two ...distinct surfactant soft templates. The lasing actions from the perovskite materials exhibit a shape‐dependent microcavity effect, which is subsequently utilized for the modulation of the lasing modes and for the achievement of two‐photon‐pumped single‐mode perovskite microlasers.
Tin halide perovskites are rising as promising materials for lead‐free perovskite solar cells (PSCs). However, the crystallization rate of tin halide perovskites is much faster than the lead‐based ...analogs, leading to more rampant trap states and lower efficiency. Here, we disclose a key finding to modulate the crystallization kinetics of FASnI3 through a non‐classical nucleation mechanism based on pre‐nucleation clusters (PNCs). By introducing piperazine dihydriodide to tune the colloidal chemistry of the FASnI3 perovskite precursor solution, stable clusters could be readily formed in the solution before nucleation. These pre‐nucleation clusters act as intermediate phase and thus can reduce the energy barrier for the perovskite nucleation, resulting in a high‐quality perovskite film with lower defect density. This PNCs‐based method has led to a conspicuous photovoltaic performance improvement for FASnI3‐based PSCs, delivering an impressive efficiency of 11.39 % plus improved stability.
We disclosed a key finding to modulate the crystallization kinetics of FASnI3 through a non‐classical nucleation mechanism based on pre‐nucleation clusters. A direct link between the colloids in the perovskite precursor solution and final optoelectronic quality of the perovskite films was established. Finally, power conversion efficiency of 11.39 % was obtained for FASnI3‐based perovskite solar cells.
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