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Small · 2023 · IF 13.3

n-Si/SiOx/CoOx-Mo Photoanode for Efficient Photoelectrochemical Water Oxidation

Shuyang Peng,Di Liu,Keyu An,Zhiqin Ying,Mingpeng Chen,Jinxian Feng,Kin Ho Lo,Hui Pan

Green hydrogen is considered to be the key for solving the emerging energy and environmental issues. The photoelectrochemical (PEC) process for the production of green hydrogen has been widely investigated because solar power is clean and renewable. However, mass production in this way is still far away from reality. Here, a Si photoanode is reported with CoO x as co-catalyst for efficient water oxidation. It is found that a high photovoltage of 350 mV can be achieved in 1.0 m K 3 BO 3 . Importantly, the photovoltage can be further increased to 650 mV and the fill factor of 0.62 is obtained in 1.0 m K 3 BO 3 by incorporating Mo into CoO x . The Mo-incorporated photoanode is also highly stable. It is shown that the incorporation of Mo can reduce the particle size of co-catalyst on the Si surface, improve the particle-distribution uniformity, and increase the density of particles, which can effectively enhance the light absorption and the electrochemical active surface area. Importantly, the Mo-incorporation results in high energy barrier in the heterojunction. All of these factors are attributed to improved the PEC performance. These findings may provide new strategies to maximize the solar-to-fuel efficiency by tuning the co-catalysts on the Si surface.

研究领域: 材料科学 · 能源化学
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Journal of Energy Chemistry · 2025 · IF 14.9

Self-crosslinking strategy enabling high-performance inverted inorganic perovskite solar cells with fill factor exceeding 85%

Zhongyu Liu,Xiu Huang,Yuchen Zhao,Jianwei Wang,Jiaying Liu,Chenyu Zhou,Hongwei Wang,Tian Cui,Xiaohui Liu

Inorganic CsPbI 3 perovskite with superior thermal stability and photoelectric properties has developed into a promising candidate for photovoltaic applications. Nevertheless, the power conversion efficiency (PCE) of CsPbI 3 perovskite solar cells (PSCs) still lags far behind that of both organic-inorganic hybrid counterparts and the theoretical PCE limit, primarily restricted by severe fill factor (FF) and open-circuit voltage ( V OC ) deficits. Herein, an in-situ self-crosslinking strategy is proposed to construct high-performance inverted inorganic PSCs by incorporating acrylate monomers as additives into CsPbI 3 perovskite precursors. During the thermal annealing process of perovskite films, acrylate monomers can form network structures by breaking the C=C groups through an in-situ polymerization reaction, mainly anchored at the grain boundaries (GBs) and on the surfaces of perovskite. Meanwhile, the C=O groups of acrylate polymers can favorably coordinate with uncoordinated Pb 2+ , thereby decreasing defect density and stabilizing the perovskite phase. Particularly, with multiple crosslinking and passivation sites, the incorporation of dipentaerythritol pentaacrylate (DPHA) can effectively improve the perovskite film quality, suppress nonradiative recombination, and block moisture erosion. Consequently, the DPHA-based PSC achieves a champion PCE of 20.05% with a record-high FF of 85.05%, both of which rank among the top in the performance of inverted CsPbI 3 PSCs. Moreover, the unencapsulated DPHA-based device exhibits negligible hysteresis, remarkably improved long-term storage, and operational stability. This work offers a facile and useful strategy to simultaneously promote the efficiency and device stability of inverted inorganic PSCs.

研究领域: 材料科学 · 光伏技术
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SOLAR ENERGY MATERIALS AND SOLAR CELLS · 2024 · IF 6.3

Interfacial engineering with a ferrocene derivative for air-stable inverted perovskite solar cells with high fill factor of 83.57 %

Kexin Hu,Jin Peng,Qi Wang,Lu Deng,Chen Deng,Maoxia Xu,Zetan Zhang,Haorong Ren,Chengbin Yang,Jingyu Chen,Hua Yu

Perovskite solar cells have demonstrated exceptional photovoltaic performance , but stability remains a challenge due to insufficient interfaces. In this work, a UV-resistance ferrocene derivative, 1,1′-bis (diphenylphosphine) ferrocene (DPPF), is introduced between the electron transport layer and the perovskite, reducing defect density by interaction with undercoordinated Pb 2+ , suppressing non-radiative recombination of charge carriers, and enhancing electron extraction. Desirable interfacial properties and homogeneous perovskite grains are formed, resulting in a champion power conversion efficiency (PCE) of 20.82 % and a significantly improved fill factor of 83.57 %. Moreover, DPPF can optimize the interfaces, provide a brand-new morphology with exceptional air durability, cover the active layer to restrain water and oxygen intrusion, and suppress metal electrode corrosion. Resultant devices without encapsulation have remained above 80 % of their initial PCE for 1400 h under 25 °C air and 50–60 % relative humidity conditions.

CAS / MDL: 12150-46-8 141-43-5
研究领域: 材料科学 · 能源技术
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ADVANCED FUNCTIONAL MATERIALS · 2024 · IF 18.5

Li, Ag Co-Doping Enables Efficient Kesterite Solar Cell with a High Fill Factor of 74.30%

Xinyi Zhong,Jinlin Wang,Litao Han,JinJin Chi,Tong Liu,Dongxing Kou,Wenhui Zhou,Zhengji Zhou,Shengjie Yuan,Yuena Meng,Yafang Qi,Qingbo Meng,Sixin Wu

In addition to open-circuit voltage (V OC ) loss, fill factor (FF) loss is considered another major factor restricting the further optimization of Cu 2 ZnSn(S,Se) 4 (CZTSSe) device efficiency. In this work, a comprehensive investigation into the loss mechanisms of FF has been conducted, and implemented a Li&Ag co-doping approach to enhance FF. The results indicate that the FF loss caused by insufficient carrier extraction is higher than that caused by non-radiative recombination. The carrier extraction capability is significantly influenced by the band alignment of the CdS/CZTSSe interface and has little relationship with the carrier concentration of the absorber. Therefore, although Ag doping reduces the hole concentration and conductivity, it reduces the FF loss caused by carrier extraction due to the improvement of band alignment. Ag doping is also superior to Li in passivating harmful defects, which helps reduce FF losses caused by non-radiative recombination. Correspondingly, Li performs better than Ag in increasing the hole carrier concentration and optimizing band alignment, greatly reducing FF losses caused by insufficient carrier transport. Finally, the Li and Ag co-doping strategy enables a 14.91% efficient kesterite solar cell with the highest reported FF to date of 74.30% through collaborative optimization of carrier extraction and suppression of non-radiative recombination.

研究领域: 材料科学 · 光伏技术
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