All-inorganic halide perovskite solar cells (PerSCs) have achieved rapid development in recent years. However, limited by narrow absorption bands, the power conversion efficiency (PCE) of all-inorganic halide PerSCs lag behind the organic–inorganic hybrid ones. In this contribution, to expand their absorption spectra and enhance the PCE, tandem solar cells (TSCs) with inorganic perovskite and organic conjugated molecules are constructed, utilizing CsPbI2Br as an ultraviolet–visible light absorber and a PTB7-Th:IEICO-4F bulk-heterojunction (BHJ) active layer as a near-infrared light absorber. To physically and electronically connect the front and rear subcells, P3HT/MoO3/Ag/PFN-Br is introduced as an interconnecting junction. Finally, the TSCs exhibit a remarkably higher PCE of 17.24% compared to that of the single junction PerSCs (12.09%) and organic solar cells (OSCs) (10.89%). These results indicate that the combination of all-inorganic perovskite and a low bandgap organic active layer for TSCs is a feasible approach to realize broad spectra utilization and efficiency enhancement.

All-inorganic perovskite (CsPbX 3 , X = Br or I) solar cells demonstrate superior stability, while the power conversion efficiency (PCE) lags behind the organic−inorganic hybrid counterparts mainly due to the limitation of narrow absorption bands. To broaden their absorption spectrum and improve their PCE, all-inorganic perovskite/organic integrated solar cells utilizing CsPbI 2 Br as an ultraviolet−visible light absorber and PBDTTT-E-T:IEICO as a near-infrared light absorber are demonstrated in this work. The integrated solar cells exhibit a broadened photoresponse to over 900 nm, attributed to the integration of PBDTTT-E-T:IEICO. The additional absorption enhances the short-circuit current density from 14.78 to 15.98 mA/cm 2 , resulting in greatly improved PCE of 14.03% for integrated solar cells, much higher than that of the control perovskite solar cells (12.53%) and organic solar cells (7.51%). An in-depth understanding of the charge-transfer dynamic process in the CsPbI 2 Br/PBDTTT-E-T:IEICO film is comprehensively analyzed by photoinduced transient absorption spectroscopy. Furthermore, the air stability and thermal stability of the integrated solar cells are greatly enhanced. For unencapsulated integrated solar cells, the PCE still preserves 95% of its initial value after aging for 300 h in an ambient environment and retains about 90% of its original value even after aging at 85 °C for 180 h in nitrogen.

The emerging perovskite materials present great opportunities for cost‐saving and efficient photovoltaic devices. However, perovskite solar cells (PSCs) suffer from the limitation of short optical absorption edge, resulting in most of the near‐infrared (NIR) light being wasted. Recently, strategies toward broadening the NIR spectra response and further improve the power conversion efficiency of PSCs have attracted extensive attention. In this review, the unique features of perovskite materials are first introduced; subsequently, the current developments of organic–inorganic hybrid PSCs and all‐inorganic PSCs are highlighted. Then, a detailed summary of the strategies toward enhancing the NIR light harvesting of PSCs, namely, perovskite/Si and perovskite/Cu(In1–x, Gax)Se2 tandem solar cells (TSCs) and the integrated perovskite/organic solar cells (IPOSCs), is presented. After an in‐depth understanding of the working mechanism of TSCs and IPOSCs, a comprehensive overview about their recent developments, key detrimental factors restricting their further performance enhancement, and feasible countermeasures to conquer these scientific and technological problems are given. In the end, the perspectives on the related materials and devices are addressed.