期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 608, 期 -, 页码 40-47出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.09.117
关键词
Power conversion efficiency; CsPbIBr2; Carbon electrode; All-inorganic perovskite solar cell; N-doping
The addition of an appropriate amount of Cd2+ into the CsPbIBr2 precursor solution can improve the film quality, enhance the efficiency of CsPbIBr2 PSCs, reduce trap density, suppress carrier recombination, exhibit n-type doping, and optimize energy level alignment, leading to higher PCE and improved stability.
High efficiency and stability have long been the key issues faced by perovskite solar cells (PSCs). It is found that the CsPbIBr2 all-inorganic perovskite has a suitable band gap and satisfactory stability, so it has attracted much attention. However, the many defects in the CsPbIBr2 film are one of the main prob-lems hindering the improvement of power conversion efficiency (PCE) of the CsPbIBr2 PSCs. The substi-tution of trace impurities is undoubtedly a simple, cost-effective and efficient strategy. In this work, an appropriate amount of Cd2+ (1.0% mol of Pb2+) is added into the CsPbIBr2 precursor solution to fabricate high quality CsPbIBr2 film with improved crystallinity, reduced trap density, suppressed photo-generated carrier recombination, displayed n-type doping and optimized energy level alignment. The corresponding carbon-based all-inorganic Cd2+-doped CsPbIBr2 PSCs achieve a maximum PCE of 10.63% with a high open circuit voltage (V-OC) of 1.324 V, which are much higher than those of the control one with a PCE of 8.48% and an V-OC of 1.235 V. The unencapsulated device can still retain more than 92% of the initial PCE when stored at ambient atmosphere (25 degrees C, relative humidity about 30%) for 40 days. (C) 2021 Elsevier Inc. All rights reserved.
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