超高感度CCD摄像传感器的特性分析

介绍了超高感度 CCD(EXview HAD CCD)摄像传感器的概念、结构特点和性能特征。比较了常规的基底为 Nsub、Psub的 CCD传感器和超高动态 CCD传感器各自的灵敏度、饱和信号和暗电流 ,给出了量子转化效率与光波长的关系曲线。结果表明 :超高感度 CCD摄像传感器在减小拖影方面具有突出的优点。

碘激光的H2振动受激拉曼阈值研究

首次实现了脉冲光解碘激光作为基频光的氢气振动受激拉曼变频,对碘激光的波长转换有着重要意义。在碘激光单脉冲能量100~130mJ(脉宽100ns)的条件下,采用双次聚焦技术降低了高压氢气的振动受激拉曼变频的阈值,获得了波长为2900nm中红外激光,光子转化效率最高达到8.7%。实验发现当拉曼介质氢气气压大于1 MPa后,一级斯托克斯光的拉曼转化效率不再随气压变化,并对这一现象进行了理论分析和归属。

秀优杂交稻与富士光光谱特性的比较研究

本文研究了秀优杂交稻和富士光两个水稻品种的光谱特性。实验结果表明,这两个不同产量水平的水稻品种,其光谱特性具有明显差别。在含等量叶绿素的情况下,高产的秀优杂交稻比低产的富士光对光的吸收能力更大,前者的叶片具有更高的潜在光合作用量子转化效率;叶绿体的PSⅡ潜在活性和PSⅡ原初光能转化效率也高。与富士光相比,Mg^(2+)不仅能较大幅度地提高秀优杂交稻叶绿体上述两个光合作用参数,而且对它两个光系统之间的激发能分配也有较大的调节能力。

Synergistic high efficiency and low energy loss of all-small-molecule organic solar cells based on benzotriazole-basedπ-bridge unit

Reducing energy loss(V_(loss))is one of the most crucial challenges in organic photovoltaic cells.The V_(loss),determined by the differences between the optical band gap(E_(g))of the active layer material and the open-circuit voltage(V_(oc))of the device,is generally alleviated by lowering the energy difference between the lowest unoccupied molecular orbital(LUMO)and highest occupied molecular orbital(HOMO)level of the donor(D)and acceptor(A).In this work,we synthesized two A-π-D-π-A-type small-molecule donors(SMDs)SM-benzotriazole(BTz)-1 and SM-BTz-2 by introducing a BTzπ-bridge unit and terminal regulation.The BTzπ-bridge unit significantly lowers the HOMO energy level of SMDs,resulting in high V_(oc)and high mobility,achieving a balance of low energy loss(<0.5 eV)and high efficiency.Ultimately,the organic solar cells based on SM-BTz-2 as the donor and Y6 as the acceptor obtain a high V_(oc)of 0.91 V,J_(sc) of 22.8 mA cm^(−2),fill factor of 68%,and power conversion efficiency(PCE)of 14.12%,which is one of the highest efficiencies based on the SMDs with triazoleπ-bridges to date.What’s more,the BTzπ-bridge unit is a potential unit that can improve mobility and reduce energy loss.

Enhanced performance of CdS/CdSe quantum dotsensitized solar cells by long-persistence phosphors structural layer

Light absorption plays an important role in improving the power conversion efficiency(PCE)of quantum dot-sensitized solar cells(QDSSCs).In this study,a multifunctional long-persistence phosphor(LPP)layer was introduced into the CdS/CdSe QDSSCs via a simple doctor blade method.The LPP layer can simultaneously improve the light harvesting and photo charge transfer in CdS/CdSe QDSSCs.As a result,their short-circuit current and corresponding PCE are effectively enhanced.The PCE can reach up to 5.07%,which is about 24%larger than that of the conventional CdS/CdSe QDSSCs without LPP layer.The solar cells can work in dark for a while due to the long-lasting fluorescence of the LPP layer.This research provides an effective way to improve the PCE of QDSSCs,and finds the possibility for all-weather QDSSCs.

Optimizing the component ratio of PEDOT:PSS by water rinse for high efficiency organic solar cells over 16.7%

For the state-of-the-art organic solar cells(OSCs),PEDOT:PSS is the most popularly used hole transport material for the conventional structure.However,it still suffers from several disadvantages,such as low conductivity and harm to ITO due to the acidic PSS.Herein,a simple method is introduced to enhance the conductivity and remove the additional PSS by water rinsing the PEDOT:PSS films.The photovoltaic devices based on the water rinsed PEDOT:PSS present a dramatic improvement in efficiency from 15.98%to 16.75%in comparison to that of the untreated counterparts.Systematic characterization and analysis reveal that although part of the PEDOT:PSS is washed away,it still leaves a smoother film and the ratio of PEDOT to PSS is higher than before in the remaining films.It can greatly improve the conductivity and reduce the damage to substrates.This study demonstrates that finely modifying the charge transport materials to improve conductivity and reduce defeats has great potential for boosting the efficiency of OSCs.

15.3% efficiency all-small-molecule organic solar cells enabled by symmetric phenyl substitution

Synergistic optimization of donor-acceptor blend morphologyis a hurdle in the path of realizing efficient non-fullerene small-molecule organic solar cells(NFSMOSCs)due to the anisotropic conjugated backbones of both donor and acceptor.Therefore,developing a facile molecular design strategy to effectively regulate the crystalline properties of photoactive materials,and thus,enable the optimization of blend morphology is of vital importance.In this study,a new donor molecule B1,comprising phenyl-substituted benzodithiophene(BDT)central unit,exhibits strong interaction with the non-fullerene acceptor BO-4 Cl in comparison with its corresponding thiophene-substituted BDT-based material,BTR.As a result,the B1 is affected and induced from an edgeon to a face-on orientation by the acceptor,while the BTR and the acceptor behave individually for the similar molecular orientation in pristine and blend films according to grazing incidence wide angle X-ray scattering results.It means the donor-acceptor blend morphology is synergistically optimized in the B1 system,and the B1:BO-4 Cl-based devices achieve an outstanding power conversion efficiency(PCE)of 15.3%,further certified to be 15.1%by the National Institute of Metrology,China.Our results demonstrate a simple and effective strategy to improve the crystalline properties of the donor molecule as well as synergistically optimize the morphology of the all-small-molecule system,leading to the high-performance NFSM-OSCs.

Quantum dot-sensitized solar cells employing Pt/C_(60) counter electrode provide an efficiency exceeding 2%

A microporous platinum/fullerenes (Pt/C 60) counter electrode was prepared by using a facile rapid thermal decomposition method,and the quantum-dot sensitized solar cell (QDSSC) of Pt/C 60-TiO 2-CdS-ZnS and Pt/C 60-TiO 2-CdTe-ZnS was fabrication.The technique forms a good contact between QDs and TiO 2 films.The photovoltaic performances of the as-prepared cells were investigated.The QDSSCs with Pt/C 60 counter electrode show high power conversion efficiency of 1.90% and 2.06%,respectively (under irradiation of a simulated solar light with an intensity of 100 mW cm 2),which is comparable to the one fabricated using conventional Pt electrode.