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Featured researches published by Shenqiang Ren.


Nano Letters | 2011

Inorganic–Organic Hybrid Solar Cell: Bridging Quantum Dots to Conjugated Polymer Nanowires

Shenqiang Ren; Liang-Yi Chang; Sung-Keun Lim; Jing Zhao; Matthew W. Smith; Ni Zhao; Vladimir Bulovic; Moungi G. Bawendi; Silvija Gradečak

Quantum dots show great promise for fabrication of hybrid bulk heterojunction solar cells with enhanced power conversion efficiency, yet controlling the morphology and interface structure on the nanometer length scale is challenging. Here, we demonstrate quantum dot-based hybrid solar cells with improved electronic interaction between donor and acceptor components, resulting in significant improvement in short-circuit current and open-circuit voltage. CdS quantum dots were bound onto crystalline P3HT nanowires through solvent-assisted grafting and ligand exchange, leading to controlled organic-inorganic phase separation and an improved maximum power conversion efficiency of 4.1% under AM 1.5 solar illumination. Our approach can be applied to a wide range of quantum dots and polymer hybrids and is compatible with solution processing, thereby offering a general scheme for improving the efficiency of nanocrystal hybrid solar cells.


Nano Letters | 2011

Toward Efficient Carbon Nanotube/P3HT Solar Cells: Active Layer Morphology, Electrical, and Optical Properties

Shenqiang Ren; Marco Bernardi; Richard R. Lunt; Vladimir Bulovic; Jeffrey C. Grossman; Silvija Gradečak

We demonstrate single-walled carbon nanotube (SWCNT)/P3HT polymer bulk heterojunction solar cells with an AM1.5 efficiency of 0.72%, significantly higher than previously reported (0.05%). A key step in achieving high efficiency is the utilization of semiconducting SWCNTs coated with an ordered P3HT layer to enhance the charge separation and transport in the device active layer. Electrical characteristics of devices with SWCNT concentrations up to 40 wt % were measured and are shown to be strongly dependent on the SWCNT loading. A maximum open circuit voltage was measured for SWCNT concentration of 3 wt % with a value of 1.04 V, higher than expected based on the interface band alignment. Modeling of the open-circuit voltage suggests that despite the large carrier mobility in SWCNTs device power conversion efficiency is governed by carrier recombination. Optical characterization shows that only SWCNT with diameter of 1.3-1.4 nm can contribute to the photocurrent with internal quantum efficiency up to 26%. Our results advance the fundamental understanding and improve the design of efficient polymer/SWCNTs solar cells.


ACS Nano | 2012

Nanocarbon-Based Photovoltaics

Marco Bernardi; Jessica Lohrman; Priyank V. Kumar; Alec Kirkeminde; Nicola Ferralis; Jeffrey C. Grossman; Shenqiang Ren

Carbon materials are excellent candidates for photovoltaic solar cells: they are Earth-abundant, possess high optical absorption, and maintain superior thermal and photostability. Here we report on solar cells with active layers made solely of carbon nanomaterials that present the same advantages of conjugated polymer-based solar cells, namely, solution processable, potentially flexible, and chemically tunable, but with increased photostability and the possibility to revert photodegradation. The device active layer composition is optimized using ab initio density functional theory calculations to predict type-II band alignment and Schottky barrier formation. The best device fabricated is composed of PC(70)BM fullerene, semiconducting single-walled carbon nanotubes, and reduced graphene oxide. This active-layer composition achieves a power conversion efficiency of 1.3%-a record for solar cells based on carbon as the active material-and we calculate efficiency limits of up to 13% for the devices fabricated in this work, comparable to those predicted for polymer solar cells employing PCBM as the acceptor. There is great promise for improving carbon-based solar cells considering the novelty of this type of device, the high photostability, and the availability of a large number of carbon materials with yet untapped potential for photovoltaics. Our results indicate a new strategy for efficient carbon-based, solution-processable, thin film, photostable solar cells.


Nano Letters | 2011

Heterojunction Photovoltaics Using GaAs Nanowires and Conjugated Polymers

Shenqiang Ren; Ni Zhao; Samuel Crawford; Michael J. Tambe; Vladimir Bulovic; Silvija Gradečak

We demonstrate an organic/inorganic solar cell architecture based on a blend of poly(3-hexylthiophene) (P3HT) and narrow bandgap GaAs nanowires. The measured increase of device photocurrent with increased nanowire loading is correlated with structural ordering within the active layer that enhances charge transport. Coating the GaAs nanowires with TiO(x) shells passivates nanowire surface states and further improves the photovoltaic performance. We find that the P3HT/nanowire cells yield power conversion efficiencies of 2.36% under white LED illumination for devices containing 50 wt % of TiO(x)-coated GaAs nanowires. Our results constitute important progress for the use of nanowires in large area solution processed hybrid photovoltaic cells and provide insight into the role of structural ordering in the device performance.


Nano Letters | 2014

Polychiral semiconducting carbon nanotube-fullerene solar cells

Maogang Gong; Tejas A. Shastry; Yu Xie; Marco Bernardi; Daniel Jasion; Kyle A. Luck; Tobin J. Marks; Jeffrey C. Grossman; Shenqiang Ren; Mark C. Hersam

Single-walled carbon nanotubes (SWCNTs) have highly desirable attributes for solution-processable thin-film photovoltaics (TFPVs), such as broadband absorption, high carrier mobility, and environmental stability. However, previous TFPVs incorporating photoactive SWCNTs have utilized architectures that have limited current, voltage, and ultimately power conversion efficiency (PCE). Here, we report a solar cell geometry that maximizes photocurrent using polychiral SWCNTs while retaining high photovoltage, leading to record-high efficiency SWCNT-fullerene solar cells with average NREL certified and champion PCEs of 2.5% and 3.1%, respectively. Moreover, these cells show significant absorption in the near-infrared portion of the solar spectrum that is currently inaccessible by many leading TFPV technologies.


ACS Applied Materials & Interfaces | 2012

Synthesis and optoelectronic properties of two-dimensional FeS2 nanoplates.

Alec Kirkeminde; Brian A. Ruzicka; Rui Wang; Sarah Puna; Hui Zhao; Shenqiang Ren

There is a growing interest in the earth abundant and nontoxic iron disulfide (FeS(2)) photovoltaic materials. Here, we report the synthesis of FeS(2) nanoplates with different spectral features which we have associated with thicknesses and crystallization. The structure and crystalline order of ultrathin FeS(2) nanoplates have a strong influence on the carrier lifetime, electronic and optical properties. We demonstrate that two-dimensional FeS(2) nanoplates show great promise for fabrication of hybrid bulk heterojunction solar cells. This opens up a host of applications of these materials as inexpensive solar cells and photocatalysts.


Advanced Materials | 2013

Broad‐Spectral‐Response Nanocarbon Bulk‐Heterojunction Excitonic Photodetectors

Yu Xie; Maogang Gong; Tejas A. Shastry; Jessica Lohrman; Mark C. Hersam; Shenqiang Ren

High-performance broad-spectrum nanocarbon bulk-heterojunction photovoltaic photodetectors are reported. These reported photodetectors consist of a semiconducting single-walled carbon nanotube (s-SWCNT) and a PC71 BM blended active layer. Magnetic-field effects and the chirality of the s-SWCNTs play an important role in controlling the photoresponse time and photocurrent improvement.


ACS Nano | 2013

Lattice-matched bimetallic CuPd-graphene nanocatalysts for facile conversion of biomass-derived polyols to chemicals.

Xin Jin; Lianna Dang; Jessica Lohrman; Bala Subramaniam; Shenqiang Ren; Raghunath V. Chaudhari

A bimetallic nanocatalyst with unique surface configuration displays extraordinary performance for converting biomass-derived polyols to chemicals, with potentially much broader applications in the design of novel catalysts for several reactions of industrial relevance. The synthesis of nanostructured metal catalysts containing a large population of active surface facets is critical to achieve high activity and selectivity in catalytic reactions. Here, we describe a new strategy for synthesizing copper-based nanocatalysts on reduced graphene oxide support in which the catalytically active {111} facet is achieved as the dominant surface by lattice-match engineering. This method yields highly active Cu-graphene catalysts (turnover frequency = 33-114 mol/g atom Cu/h) for converting biopolyols (glycerol, xylitol, and sorbitol) to value-added chemicals, such as lactic acid and other useful co-products consisting of diols and linear alcohols. Palladium incorporation in the Cu-graphene system in trace amounts results in a tandem synergistic system in which the hydrogen generated in situ from polyols is used for sequential hydrogenolysis of the feedstock itself. Furthermore, the Pd addition remarkably enhances the overall stability of the nanocatalysts. The insights gained from this synthetic methodology open new vistas for exploiting graphene-based supports to develop novel and improved metal-based catalysts for a variety of heterogeneous catalytic reactions.


Scientific Reports | 2013

Symmetry-Defying Iron Pyrite (FeS2) Nanocrystals through Oriented Attachment

Maogang Gong; Alec Kirkeminde; Shenqiang Ren

Iron pyrite (fools gold, FeS2) is a promising earth abundant and environmentally benign semiconductor material that shows promise as a strong and broad absorber for photovoltaics and high energy density cathode material for batteries. However, controlling FeS2 nanocrystal formation (composition, size, shape, stoichiometry, etc.) and defect mitigation still remains a challenge. These problems represent significant limitations in the ability to control electrical, optical and electrochemical properties to exploit pyrites full potential for sustainable energy applications. Here, we report a symmetry-defying oriented attachment FeS2 nanocrystal growth by examining the nanostructure evolution and recrystallization to uncover how the shape, size and defects of FeS2 nanocrystals changes during growth. It is demonstrated that a well-controlled reaction temperature and annealing time results in polycrystal-to-monocrystal formation and defect annihilation, which correlates with the performance of photoresponse devices. This knowledge opens up a new tactic to address pyrites known defect problems.


Nano Letters | 2012

Extraordinary photocurrent harvesting at type-II heterojunction interfaces: toward high detectivity carbon nanotube infrared detectors.

Rongtao Lu; Caleb Christianson; Alec Kirkeminde; Shenqiang Ren; Judy Z. Wu

Despite the potentials and the efforts put in the development of uncooled carbon nanotube infrared detectors during the past two decades, their figure-of-merit detectivity remains orders of magnitude lower than that of conventional semiconductor counterparts due to the lack of efficient exciton dissociation schemes. In this paper, we report an extraordinary photocurrent harvesting configuration at a semiconducting single-walled carbon nanotube (s-SWCNT)/polymer type-II heterojunction interface, which provides highly efficient exciton dissociation through the intrinsic energy offset by designing the s-SWCNT/polymer interface band alignment. This results in significantly enhanced near-infrared detectivity of 2.3 × 10(8) cm·Hz(1/2)/W, comparable to that of the many conventional uncooled infrared detectors. With further optimization, the s-SWCNT/polymer nanohybrid uncooled infrared detectors could be highly competitive for practical applications.

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Guoliang Yuan

Nanjing University of Science and Technology

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Jeffrey C. Grossman

Massachusetts Institute of Technology

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