TY - JOUR
T1 - Low-loss contacts on textured substrates for inverted perovskite solar cells
AU - Park, So Min
AU - Wei, Mingyang
AU - Lempesis, Nikolaos
AU - Yu, Wenjin
AU - Hossain, Tareq
AU - Agosta, Lorenzo
AU - Carnevali, Virginia
AU - Atapattu, Harindi R.
AU - Serles, Peter
AU - Eickemeyer, Felix T.
AU - Shin, Heejong
AU - Vafaie, Maral
AU - Choi, Deokjae
AU - Darabi, Kasra
AU - Jung, Eui Dae
AU - Yang, Yi
AU - Kim, Da Bin
AU - Zakeeruddin, Shaik M.
AU - Chen, Bin
AU - Amassian, Aram
AU - Filleter, Tobin
AU - Kanatzidis, Mercouri G.
AU - Graham, Kenneth R.
AU - Xiao, Lixin
AU - Rothlisberger, Ursula
AU - Grätzel, Michael
AU - Sargent, Edward H.
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2023/12/14
Y1 - 2023/12/14
N2 - Inverted perovskite solar cells (PSCs) promise enhanced operating stability compared to their normal-structure counterparts1–3. To improve efficiency further, it is crucial to combine effective light management with low interfacial losses4,5. Here we develop a conformal self-assembled monolayer (SAM) as the hole-selective contact on light-managing textured substrates. Molecular dynamics simulations indicate that cluster formation during phosphonic acid adsorption leads to incomplete SAM coverage. We devise a co-adsorbent strategy that disassembles high-order clusters, thus homogenizing the distribution of phosphonic acid molecules, and thereby minimizing interfacial recombination and improving electronic structures. We report a laboratory-measured power conversion efficiency (PCE) of 25.3% and a certified quasi-steady-state PCE of 24.8% for inverted PSCs, with a photocurrent approaching 95% of the Shockley–Queisser maximum. An encapsulated device having a PCE of 24.6% at room temperature retains 95% of its peak performance when stressed at 65 °C and 50% relative humidity following more than 1,000 h of maximum power point tracking under 1 sun illumination. This represents one of the most stable PSCs subjected to accelerated ageing: achieved with a PCE surpassing 24%. The engineering of phosphonic acid adsorption on textured substrates offers a promising avenue for efficient and stable PSCs. It is also anticipated to benefit other optoelectronic devices that require light management.
AB - Inverted perovskite solar cells (PSCs) promise enhanced operating stability compared to their normal-structure counterparts1–3. To improve efficiency further, it is crucial to combine effective light management with low interfacial losses4,5. Here we develop a conformal self-assembled monolayer (SAM) as the hole-selective contact on light-managing textured substrates. Molecular dynamics simulations indicate that cluster formation during phosphonic acid adsorption leads to incomplete SAM coverage. We devise a co-adsorbent strategy that disassembles high-order clusters, thus homogenizing the distribution of phosphonic acid molecules, and thereby minimizing interfacial recombination and improving electronic structures. We report a laboratory-measured power conversion efficiency (PCE) of 25.3% and a certified quasi-steady-state PCE of 24.8% for inverted PSCs, with a photocurrent approaching 95% of the Shockley–Queisser maximum. An encapsulated device having a PCE of 24.6% at room temperature retains 95% of its peak performance when stressed at 65 °C and 50% relative humidity following more than 1,000 h of maximum power point tracking under 1 sun illumination. This represents one of the most stable PSCs subjected to accelerated ageing: achieved with a PCE surpassing 24%. The engineering of phosphonic acid adsorption on textured substrates offers a promising avenue for efficient and stable PSCs. It is also anticipated to benefit other optoelectronic devices that require light management.
UR - http://www.scopus.com/inward/record.url?scp=85177679159&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85177679159&partnerID=8YFLogxK
U2 - 10.1038/s41586-023-06745-7
DO - 10.1038/s41586-023-06745-7
M3 - Article
C2 - 37871614
AN - SCOPUS:85177679159
SN - 0028-0836
VL - 624
SP - 289
EP - 294
JO - Nature
JF - Nature
IS - 7991
ER -