INTERNATIONAL JOURNAL OF LATEST TECHNOLOGY IN ENGINEERING,  
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ISSN 2278-2540 | DOI: 10.51583/IJLTEMAS | Volume XIV, Issue XII, December 2025  
A Comprehensive Review of SnSexTe1-x Chalcogenide Thin Films for  
Next-Generation Photovoltaics  
Meena Gupta, Naresh Padha*, Zahoor Ahmed, Dimple Singh  
Jammu University, Jammu, Jammu and Kashmir, India  
Received: 09 December 2025; Accepted: 16 December 2025; Published: 27 December 2025  
ABSTRACT  
Global energy demand is projected to increase by nearly 1.5-fold by 2050, driven by fossil fuel depletion and  
the urgency of climate mitigation, thereby positioning thin-film photovoltaics as a critical component of  
sustainable energy transitions. This review traces the progression of solar-cell absorber materials-from  
crystalline silicon with efficiencies of ~27% and CdTe/CuInxGa1-xSe2 (CIGS) nanoparticle thin films with ~22%-  
toward earth-abundant chalcogenide ternaries such as SnSexTe1-x alloys. These materials exhibit tunable band  
gaps (0.9-1.5 eV), high absorption coefficients (>10⁵ cm⁻¹), and theoretical efficiencies approaching 36% in  
optimised heterostructures. However, experimental power conversion efficiencies remain limited to about 2.5%,  
primarily due to intrinsic defects, non-radiative recombination, and challenges in scalable fabrication. Drawing  
on 2024-2025 data from the Energy Institute and the International Renewable Energy Agency (IRENA), this  
analysis underscores the non-toxic and earth-abundant advantages of SnSexTe1-x, while contrasting them with  
the instability issues in perovskites and the phase complexity in kesterites. The review further highlights  
strategies such as bandgap engineering, atomic layer deposition (ALD)-based passivation, and multi-junction  
tandem architectures, along with scalable pulse laser deposition (PLD) routes, as promising approaches to  
achieving power conversion efficiencies exceeding 30%.  
Keywords: SnSexTe1-x thin films, chalcogenide photovoltaics, bandgap engineering, thin-film solar cells,  
renewable energy transition, defect passivation.  
INTRODUCTION  
The world energy requirements have evolved significantly over the past decade, reflecting changes in  
technology, population, and economic development. In the pre-industrial era, global energy demand was very  
low and was mainly met through available natural resources. The Industrial Revolution marked a significant  
shift, with coal emerging as the dominant energy source and driving rapid industrial and urban growth. After  
World War II, energy consumption rose sharply as oil became the primary fuel for industrialisation and modern  
lifestyles. The energy crises of the 1970s prompted diversification toward natural gas, nuclear power, and early  
renewable technologies. However, the global energy landscape has undergone a drastic transformation due to  
the depletion of fossil fuel reserves, rising greenhouse gas emissions, and climate change. The global population,  
which is growing at about 2% annually, continues to intensify demand for energy, economic development, and  
improved living standards, driving rising consumption. Industrialised nations, which comprise roughly 25% of  
the global population yet account for approximately 75% of global energy use, are driving this trend. World  
population is expected to double by the middle of the 21st century [1,2], and economic development will almost  
certainly continue to grow. Global demand for energy services is expected to increase by as much as an order of  
magnitude by 2050, while primary-energy demands are expected to increase by 1.5-3 times [2-4]. In the twenty-  
first century, rising demand from emerging economies and growing awareness of climate change accelerated the  
shift towards sustainable energy. The rapid expansion of renewable energy, the increasing electrification of  
transport and industry, the integration of digital technologies, and widespread commitments to carbon neutrality  
collectively indicate a global transition toward a cleaner, more efficient, and technologically advanced energy  
system. These challenges have shifted global focus toward sustainable, cleaner, and environmentally compatible  
energy sources. Renewable energy technologies-especially solar, wind, hydro, geothermal, biomass, and tidal-  
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are being adopted globally to ensure energy security, reduce emissions, and support economic development.  
Solar energy, in particular, is receiving unprecedented attention due to its abundance, scalability, and declining  
costs.  
METHODOLOGY  
This review paper was prepared through a systematic literature review across academic databases, including  
Web of Science, Scopus, Google Scholar, and ScienceDirect, focusing on publications from 2010 to 2025 on  
thin-film photovoltaics, with particular emphasis on chalcogenide semiconductors such as SnSe, SnTe, and  
SnSexTe1-x alloys [5]. Relevant studies were selected based on material properties (bandgap, absorption  
coefficient), device performance (PCE, stability), and synthesis techniques, yielding over 150 primary sources,  
which were categorised into silicon-based, CdTe/CIGS, perovskites, kesterites, and emerging IV-VI compounds.  
Data extraction involved compiling quantitative metrics-such as efficiency records, toxicity profiles, elemental  
abundance, and theoretical vs. experimental PCE gaps-into comparative tables and figures, including  
chronological flowcharts of material evolution. At the same time, qualitative analysis synthesised challenges,  
such as secondary phase formation, and proposed scalability solutions via bandgap engineering and interface  
passivation. Synthesis of findings employed a comparative framework to evaluate absorber materials against  
key performance indicators (e.g., absorption coefficient ~10⁵ cm⁻¹, bandgap 0.9-1.5 eV), integrating recent 2024-  
2025 reports from IRENA and the Statistical Review of World Energy to contextualise global renewable trends.  
Gaps in the current literature, such as the disparity between SnSe's theoretical efficiency (36.45%) and  
experimental values (~2.5%), were identified by cross-referencing simulation studies with empirical data,  
informing future directions such as multi-junction heterostructures and non-toxic deposition methods (e.g.,  
thermal evaporation, sputtering).  
Global energy 2024  
The Statistical Review of World Energy 2025 provides a comprehensive assessment of global energy supply,  
demand, and emissions for 2024, as shown in Fig. 1, revealing an energy system undergoing a rapid yet uneven  
transition. Global total energy demand grew by 2% in 2024, reaching 592 EJ (Exa joules, 1 EJ = 1018 joules),  
with non-OECD (Organisation for Economic Co-operation and Development) countries accounting for 63% of  
total supply and driving global consumption growth. Fossil fuels continued to underpin the energy landscape,  
accounting for 87% of global energy demand, while renewables expanded at a significantly faster pace than  
conventional fuels. Electricity demand grew 4%, outpacing total energy demand growth and signalling ongoing  
global electrification. Asia Pacific remained the central driver of energy trends, contributing 47% of global  
demand and 68% of global annual demand growth. Renewable energy continued to show the strongest  
momentum, with wind and solar growing by 16% and accounting for 53% of the global increase in electricity  
generation. China led global renewable expansion, accounting for 57% of global renewable additions and nearly  
60% of renewable power supply growth. Over the past decade, renewable energy has grown at four to five times  
the rate of total energy demand. Since 2010, renewables and nuclear energy have collectively helped avoid 1,371  
EJ of fossil fuel use. significantly improving global energy efficiency. Despite this, carbon emissions reached a  
record 40.8 GtCO₂e, up 1% from 2023 [6]. China and India were responsible for 62% of the global increase in  
emissions, while Europe and the US recorded modest declines. Fossil fuel combustion remained the dominant  
source of emissions, accounting for 87% of total energy-related greenhouse gas emissions. The report highlights  
that global emissions have grown by 2.3% annually since COVID-19, underscoring the difficulty of decoupling  
energy demand growth from emissions. Oil remained the most significant single energy source, meeting 34% of  
global demand. Global oil demand grew 0.7%, surpassing 101 Mbb l/d for the first time. OECD oil consumption  
plateaued, while non-OECD demand increased by 1%. The United States emerged as the world’s largest oil  
producer, accounting for 20% of global output, roughly equal to the combined output of SaudiArabia and Russia.  
Oil prices declined by 3%, though they remained significantly above pre-COVID levels. Natural gas production  
grew to 4,124 bcm, while global demand rose 2.5% after falling the previous year. The US, Russia, Iran, and  
China accounted for 53% of total production. Asia Pacific recorded the strongest regional growth in gas demand,  
while African gas demand declined slightly. Gas remained crucial to the global energy mix, meeting 29% of  
fossil fuel consumption and 25% of total energy demand. Coal demand reached a historic high of 165 EJ, with  
Asia Pacific accounting for 83% of global consumption and producing the largest regional surplus. China alone  
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accounted for 67% of global coal consumption. Despite record renewable investment, coal remained central to  
electricity generation in China (58% of output) and India (~75%). In contrast, Europe’s coal consumption fell  
7%, dropping below nuclear energy’s contribution for the first time. In the electricity sector, global generation  
grew 2.6% annually over the past decade. In 2024, renewables (including hydro) supplied 32% of electricity,  
while wind and solar contributed 15%, a fourfold increase over ten years. Installed solar capacity rose to 1,865  
GW, four times the rate of wind additions, with China accounting for 47% of global wind and solar capacity.  
Grid-scale battery storage saw remarkable growth, doubling to 126 GW, again led by China, which accounted  
for 60% of global installed capacity [7]. Investment in renewables is increasingly associated with energy security,  
reducing reliance on imported fuels. China avoided 87 EJ of imports over five years due to renewable expansion,  
while Europe and the US avoided 63 EJ and 34 EJ, respectively. However, countries heavily reliant on imports-  
such as Japan and South Korea-realised limited avoided fuel imports, highlighting missed opportunities in  
renewable deployment. Overall, the 2025 Review concludes that although renewables are accelerating and  
electrification is expanding rapidly, these advances are not yet sufficient to offset growing global energy demand  
and continued reliance on fossil fuels. The world remains in a phase of “energy addition” rather than substitution,  
leading to a disorderly, uneven transition toward a low-carbon future.  
Fig. 1: Global energy consumption [5]  
Accelerating clean energy transitions  
The "Climate Action Support 2025" report by IRENA outlines urgent global efforts to address climate change  
by accelerating the adoption of renewable energy and improving energy efficiency. Key points include: The  
world is experiencing record-high greenhouse gas levels and a warming trend, with 2024 the warmest year on  
record, necessitating urgent climate action to keep warming below 1.5°C. Renewable power capacity grew by  
582 GW in 2024, primarily driven by solar PV and wind, with Asia leading growth (especially China). Global  
renewable power reached 4,443 GW by the end of 2024, but a more rapid scale-up is required to meet the COP28  
UAE Consensus target of tripling capacity by 2030. Energy transition investment surpassed $2 trillion in 2024  
but remains well below the $5.6 trillion annually needed through 2030 to stay on a net-zero emissions path by  
2050. Technological advances have dramatically lowered costs, making most renewables more competitive than  
fossil fuels. Battery energy storage systems and digitalisation are essential technology enablers for grid flexibility  
and higher renewable integration.  
The report highlights the importance of Nationally Determined Contributions (NDCs) under the Paris Agreement  
[8]. As of late 2025, 104 countries had submitted updated NDCs 3.0 with more ambitious renewable energy and  
energy efficiency targets, aligned with the UAE Consensus. These NDCs outline sectoral commitments,  
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including renewable energy expansion, electric vehicles, clean cooking, and a phase-out of fossil fuels.  
Challenges include mobilising finance, addressing regulatory frameworks, and building capacity. IRENA  
actively supports countries worldwide (102 countries engaged) with technical assistance on NDC development,  
renewable resource assessment, policy, finance, energy transition technologies, and capacity building. Regional  
overviews show varying but progressive renewable energy additions and energy efficiency improvements, with  
Africa focusing on expanding access and resource assessment, Asia Pacific on scaling deployment, and Europe  
and Latin America setting ambitious climate targets and policy measures. The report also addresses the critical  
roles of climate finance, carbon markets, and international co-operation in bridging investment gaps and  
facilitating technology deployment, emphasising that clean energy transitions will bring socioeconomic and  
environmental co-benefits globally. Ecological and health concerns have driven a global shift toward renewable  
energy, offering cleaner, more sustainable alternatives. Renewable sources like solar, wind, and hydropower  
produce little to no pollution or greenhouse gases, mitigate climate change, and have rapidly declining costs,  
making them increasingly competitive. The shift to renewables also promotes energy security by diversifying  
supply and reducing dependence on finite resources. Though renewable energy also faces challenges such as  
intermittency and infrastructure needs, it is critical for achieving sustainable development and a low-carbon  
future, offering a necessary transition away from the disadvantages of conventional fuels, from extraction to  
global environmental impact and ultimately to sustainable alternatives.  
Renewable energy sources derive from natural processes that continuously replenish themselves, offering  
sustainable alternatives to finite fossil fuels. Primary renewable sources include solar, wind, hydropower,  
biomass, and geothermal energy, each harnessing natural phenomena to produce electricity, heat, or fuel with far  
lower environmental impacts. Solar energy is captured via photovoltaic cells or concentrated solar power  
systems, providing a vast, widely accessible resource. Wind energy utilises the kinetic energy of moving air to  
generate power, often in land-based and offshore installations. Hydropower exploits the energy from flowing or  
falling water, historically the largest source of renewable electricity worldwide. Biomass energy derives from  
organic materials such as plant residues and waste, which can be converted into heat, electricity, or biofuels.  
Geothermal energy taps into the Earth's internal heat for power generation and direct use applications.  
Collectively, these renewables help reduce greenhouse gas emissions, enhance energy security, and provide  
cleaner energy options, which are essential for mitigating climate change and achieving sustainable development  
goals. Solar energy is the radiant light and heat from the Sun, harnessed as one of the most abundant and versatile  
renewable resources, capable of meeting global energy needs many times over with minimal environmental  
impact. The IRENARenewable Capacity Statistics 2025 report highlights record growth and ongoing challenges  
in the worldwide energy transition. In 2024, renewable energy capacity increased by a historic 585 GW, as shown  
in Fig.2, expanding global renewable power stock by 15.1%. Renewables accounted for 92.5% of all new power  
additions, predominantly driven by solar (452 GW) and wind (113 GW) energy. Despite this progress, major  
disparities remain, with China, the United States, and the European Union responsible for 83.6% of new capacity,  
while Africa and other regions lag. By the end of 2024, renewables accounted for 46.2% of total installed power  
capacity globally, rapidly approaching fossil fuels, which stood at 47.3%. Yet, the current growth trajectory  
remains insufficient to meet the COP28 goal of tripling renewable capacity to over 11 TW by 2030. To achieve  
this, annual additions must exceed 1,120 GW, requiring an accelerated growth rate of 16.6% per year, above the  
15.1% recorded in 2024. Solar and wind dominate expansion, accounting for 97.5% of renewable capacity  
growth, reflecting their cost-effectiveness and scalability. Other renewables, such as hydropower, bioenergy, and  
geothermal, grew modestly but remain quantitatively less significant. The report underscores the urgency for  
faster deployment globally, addressing financing and technology access disparities to ensure a just and inclusive  
transition [8].  
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Fig. 2: Renewable power capacity growth [8]  
Solar energy harvesting  
Its limitless supply and global accessibility set solar energy apart. The Earth receives approximately 173,000  
TW of solar energy continuously-thousands of times higher than present global energy requirements. Efficient  
capture, conversion, and storage of this energy are essential for achieving long-term sustainability. The Sun emits  
electromagnetic radiation across the UV, visible, and IR spectra via nuclear fusion, providing an inexhaustible  
source of clean power [9]. Only about 51% of solar radiation reaches Earth's surface, creating both a technical  
challenge and a design opportunity for efficient solar energy conversion systems.  
Global mission of solar energy  
The global mission of solar energy programs, as depicted in Fig.3, seeks to harness the Sun's inexhaustible  
energy to realise a sustainable, clean, and secure energy future, confronting pressing challenges such as climate  
change, energy insecurity, and environmental degradation while advancing green economic growth and universal  
energy access. Central to this vision is the promotion of clean, renewable power generation to curtail greenhouse  
gas emissions and mitigate global warming, alongside reducing fossil fuel dependence to enhance energy  
security, particularly in developing nations abundant in solar resources yet constrained by infrastructure deficits.  
These initiatives prioritise equitable energy access for underserved populations, spur technological innovation  
in photovoltaics, energy storage, and smart grids, and catalyse international collaboration to fortify the renewable  
ecosystem, ultimately fostering green employment and alignment with Sustainable Development Goals (SDGs)  
for an environmentally responsible, economically viable, and socially inclusive global energy transformation  
[9,10].  
Fig. 3: Global mission of solar energy  
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Solar energy harvesting  
The Sun, a massive sphere of hot plasma at the heart of our solar system, emits energy in the form of photons  
that make up the solar spectrum. If even a fraction of the Sun’s immense energy could be efficiently harnessed,  
it would be sufficient to meet all global electricity demands. The Sun’s composition primarily includes about  
75% hydrogen and 25% helium, structured into four key layers: the core, photosphere, chromosphere, and  
corona, as depicted in Fig. 4. Solar energy is generated in the Sun’s core through nuclear fusion, where hydrogen  
nuclei fuse to form helium, releasing tremendous heat and light energy. This fusion occurs at extremely high  
temperatures reaching approximately 15 million degrees Celsius in the core, while the Sun’s surface temperature  
is about 5,505 °C (5,778 K) [11]. The dominant fusion pathway is the proton-proton (PP) chain reaction, which  
converts hydrogen into helium and emits vast amounts of energy as electromagnetic radiation. Energy produced  
in the core travels outward through the radiation and convection zones to the photosphere, from which it radiates  
into space. Additionally, the Sun employs the carbon-nitrogen-oxygen (CNO) cycle, which uses these elements  
as catalysts to facilitate hydrogen-to-helium fusion. The Sun fuses around 620 million metric tonnes of hydrogen  
every second, powering the constant flow of radiant energy.  
Fig. 4: Structure of the Sun, Nuclear Fusion Process, Solar Spectrum, and Solar Energy Flow to Earth  
Upon reaching Earth, solar energy appears as electromagnetic waves encompassing a broad spectrum of  
wavelengths. This solar spectrum varies with atmospheric conditions and altitude, and is often classified by air  
mass (AM) units. Outside Earth’s atmosphere (AM0), the solar constant-total solar irradiance-is about 1353  
W/m². At the Earth’s surface, this value decreases to around 1000 W/m² under AM1 conditions and further to  
about 832 W/m² under AM1.5 due to atmospheric absorption and scattering [12]. The solar spectrum is divided  
into three primary regions: ultraviolet (UV, <0.38 µm), visible light (0.38–0.78 µm), and infrared (IR, >0.78  
µm). The UV region contributes approximately 2% of the total energy, the visible region accounts for about  
47%, and the IR region delivers the largest share at 51% of the solar energy reaching Earth. Fig. 5 (a-b) illustrates  
these spectral components, highlighting the colour band visible to the human eye. Of the total solar radiation  
incident on Earth, about 51% passes through and reaches the surface, while the atmosphere reflects roughly 35%  
back into space and absorbs the remaining 14%.  
Earth continuously receives an average of about 173,000 terawatts (TW) of solar energy, which exceeds global  
energy consumption by thousands of times. This vast, renewable energy source, derived directly from the Sun's  
fusion process, is the most plentiful and sustainable resource for powering human civilisation.  
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Fig. 5: (a) The spectrum of solar radiation, (b) spectral distribution of solar energy and atmospheric effects  
Photovoltaic effect and solar cells  
Photovoltaic (PV) solar cells convert incident photons into electrical energy via semiconductor materials,  
typically structured as p-n junctions [13,14]. The operation hinges on bandgap properties and carrier-separation  
mechanisms, which are influenced by material composition, crystal structure, and thin-film architecture.  
Photovoltaic principle  
The photovoltaic effect is the process by which solar cells convert sunlight directly into electricity. When  
sunlight, composed of photons, strikes a semiconductor solar cell (usually silicon), the photons' energy is  
absorbed, exciting electrons and freeing them from their atomic bonds. This generates electron-hole pairs [15].  
The solar cell has a p-n junction formed by p-type and n-type semiconductor layers as shown in Fig. 6, which  
creates an internal electric field. This electric field drives the separated electrons towards the n-type layer and  
holes towards the p-type layer, thus preventing recombination and enabling charge separation. The free electrons  
are then collected by metal contacts on the solar cell surface, generating an electric current that can flow through  
an external circuit to power electrical devices. This flow of electrons constitutes usable electrical energy [15,16].  
Fig. 6: Principle of photovoltaic effect  
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Semiconductors in photovoltaics  
There is a rising demand for renewable energy as fossil fuel assets and other resources are insufficient to meet  
the world's increasing energy requirements. Developing renewable and sustainable energy sources and devices  
has been essential to meet global energy demands [17]. Photovoltaic electricity is considered one of the most  
promising solutions for sustainable energy needs. Extensive research has been dedicated to the development of  
thin-film photovoltaics, which not only lowers the production costs of solar cells but also supports green energy  
initiatives worldwide. In recent years, significant progress has been achieved in this field [18-20]. Power  
generation from photovoltaic (PV) solar cells has gained attention due to rapid technological advances and the  
development of alternative materials [21].  
Initially, the Silicon industry dominated 80% of the solar market, with crystalline silicon solar cells reaching a  
record efficiency of 25%. However, silicon-based solar cells utilise an absorber layer thickness of 100 μm.  
Furthermore, the requirement for producing single-crystal absorber substrates significantly increased  
manufacturing costs [22]. On the contrary, thin-film solar cell (TFSC) technology relies on direct-bandgap  
absorber materials such as cadmium telluride (CdTe) and copper indium gallium diselenide (CIGS). Due to these  
materials' high absorption coefficient (~10⁵ cm⁻¹), a thicker absorber layer is not required, enabling reliable  
performance with thin films of 1-2 μm that absorb nearly all incident solar radiation [6]. CdTe has reached a  
maximum power conversion efficiency (PCE) of 22.1%, while CIGS has 22.6% [23]. However, CdTe contains  
the toxic element Cadmium (Cd) and the rare-earth element Telluride (Te), and CIGS contains the expensive  
elements Indium (In) and Gallium (Ga); further, Selenium (Se) is toxic [24,25]. Further, researchers around the  
globe are exploring earth-abundant, cheap, and non-toxic materials-based solar cells. Perovskite thin films have  
recently garnered significant attention for their potential in next-generation solar cells, surpassing their Silicon  
counterparts due to their promising advantages, including high efficiency, lower costs, flexibility, and tunable  
optoelectronic properties [26,27]. However, perovskite-based solar cells face stability and toxicity challenges,  
limiting their commercial viability. Kesterite materials, Copper zinc tin Sulphide (CZTS), are also a part of the  
present initiative [25,28]. The parameters of some key absorber layers used for the fabrication of photovoltaic  
cells are presented in Table 1 [29].  
Table 1: Key parameters of single-junction terrestrial cell measured under the global AM1.5 spectrum (1000  
W/m2 ) at 25C (IEC 60904-3: 2008 or ASTM G-173-03 global) [29]  
Classification  
Efficiency  
25.0 ± 0.5  
23.6 ± 0.4  
20.3 ± 0.4  
22.4 ± 0.3  
11.4 ± 0.3  
12.1 ± 0.3  
26.1 ± 0.5  
19.2 ± 0.3  
13.0 ± 0.4  
Area  
Voc (V)  
0.706  
0.767  
0.683  
0.900  
0.746  
0.538  
1.201  
0.914  
1.040  
Jsc (mA/cm2)  
42.7  
FF (%)  
82.8  
80.5  
75.1  
79.3  
69.9  
63.6  
84.6  
79.0  
80.4  
Si (crystalline)  
4.00 (da)  
0.899 (da)  
526.7 (ap)  
0.450 (da)  
0.204 (da)  
1.066 (da)  
0.051 (da)  
0.033 (da)  
0.116 (da)  
CIGS (thin-film)  
CIGSSe (sub module)  
CdTe (thin-film)  
CZTS (thin-film)  
CZTSSe (cell)  
38.30m  
39.55  
31.4  
21.79  
35.29k  
25.73  
Perovskite (thin-film)  
Organic (thin-film)  
Dye sensitised  
26.61  
15.55  
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ap (aperture)  
da (designated illuminated area)  
However, the probability of the formation of secondary phases in the (CZTS) is high due to the involvement of  
more elements (Cu, Zn, Sn and S). The pure CZTS phase has a narrow region in the phase diagram, but  
controlling its composition is challenging [25]. Thus, the research efforts have been focused on identifying  
alternative materials to address these challenges. Efforts are on to explore alternative materials that are less toxic  
and more cost-effective. Some binary IV-VI compounds are attracting more attention in the pursuit of new  
semiconductor thin-film materials for solar energy [30-33]. Among these, Tin chalcogenides, especially SnSe  
and SnTe, have emerged as promising candidates. In addition to their desirable physical properties, the  
abundance, low toxicity, and low environmental impact of the constituent elements are additional advantages  
for large-scale application [34-38]. The SnSexTe1-x (0 ≤ x ≤ 1) semiconductor alloy-based thin films show  
variation in their energy bandgap (Eg) due to changes in composition and thus absorb different regions of the  
E.M. spectrum [39]. The element Sn, which has been replaced with Cd in research on IV-VI semiconductor  
compounds to create ecologically friendly absorber layers for photovoltaic devices [33]. Due to its high  
absorption coefficient (105 cm-1 at the visible region) and forbidden gap energy in the range of 0.9-1.5 eV, SnSe,  
a p-type semiconductor material, has been studied as an additional alternative absorber layer for the  
heterojunction solar cells in addition to the alternative material SnTe [39]. The highest theoretical simulation-  
based efficiency reported to date for the SnSe solar cell is about 36.45% for the n-CdS/p-SnSe/p+/CuInSe2/p++-  
WSe2 heterostructure device—modelling and efficiency enhancement of SnSe thin-film solar cell with a thin  
CIS layer. At the same time, its experimental efficiency is only 2.5%, providing ample scope for further research  
on thin-film solar cells. SnSexTe1-x has shown improvements in high photosensitivity, crystalline structure, and  
strength [40]. With a direct bandgap of roughly 1.24 eV and a high absorption coefficient (~10⁴ cm⁻¹), tin  
selenide (SnSe) has been used successfully as an absorber layer in solar cell topologies [41]. By altering the  
tellurium (Te) and selenium (Se) composition, the alloy equivalent SnTexSe1-x (0 ≤ x ≤ 1) exhibits a variable  
bandgap, enabling it to absorb light across the entire electromagnetic spectrum [42]. SnTexSe1-x thin films have  
demonstrated potential for thermoelectric devices that convert waste heat into energy, as well as for solar  
applications. Zinc Telluride (ZnTe) is a chalcogenide material belonging to AII-BVI semiconductors. It exhibits  
a direct bandgap of 2.26 eV, an absorption coefficient of ~105 cm-1, and an electron affinity of ~ 3.53 eV [43-  
47]. It is a promising material due to its potential applications in various electronic devices, including light-  
emitting diodes, solar cells, photosensors, photodetectors, thin-film transistors, and laser diodes [48]. The  
chronology of the different materials for photovoltaic applications is shown in Fig. 7.  
Fig. 7: Evolution of photovoltaic absorber materials: Chronological timeline  
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In addition to the above text, the historical improvement in photovoltaic technologies is commonly summarised  
using the National Renewable Energy Laboratory’s chart (Fig. 8), which compiles record conversion efficiencies  
reported by leading laboratories across all prominent solar-cell families. This dataset shows that multi-junction  
devices based on III–V compound semiconductors occupy the very top of the efficiency landscape, with recent  
concentrator cells from institutes such as Fraunhofer ISE approaching efficiencies near one-half under high  
illumination, but at the expense of complex epitaxial growth, sophisticated device designs and correspondingly  
high costs that confine them mainly to space and concentrator applications. In contrast, crystalline silicon  
technologies, which dominate commercial deployment because of mature manufacturing and material  
abundance, have progressed steadily from early values around 10% in the 1970s to nearly 27–28% in today’s  
champion cells, thus operating close to the Shockley-Queisser limit for a single-junction Si device. Thin-film  
technologies such as CdTe and CIGS occupy an intermediate position, combining lower material use and  
potentially cheaper module fabrication with record efficiencies in the low-to-mid-20% range. Over roughly the  
past decade, the NREL chart also documents the rapid ascent of perovskite and perovskite/silicon tandem cells,  
with perovskite single-junction records moving from a few percent to above 25% and monolithic tandems  
recently surpassing 33%, clearly indicating that tandem and multi-junction concepts based on perovskites and  
silicon are emerging as leading candidates for next-generation high-efficiency photovoltaic technologies.  
Fig.8: Efficiencies of various photovoltaic cells documented by the National Renewable Energy Laboratory  
(NREL), USA.  
Challenges  
Chalcogenide semiconductors, particularly SnSexTe1-x ternary alloys, exhibit promising optoelectronic  
properties for thin-film photovoltaic applications, yet several persistent challenges impede their transition from  
laboratory prototypes to commercial viability. A primary limitation lies in the short carrier lifetimes, primarily  
due to high recombination rates induced by intrinsic defects, such as vacancies and anti-site disorders, prevalent  
in these multi-component systems. These defects elevate non-radiative recombination centres, significantly  
reducing the open-circuit voltage (Voc) and fill factor (FF) in fabricated devices, with experimental efficiencies  
stagnating around 2.5% compared to theoretical maxima exceeding 36% in simulated heterostructures.  
Concurrently, elevated defect densities—often exceeding 1016 cm-3-arise from challenges in achieving  
stoichiometric control during deposition processes such as thermal evaporation or sputtering, exacerbating band  
tailing and energy broadening, and thereby degrading absorption efficiency across the visible spectrum. Scalable  
synthesis represents another formidable barrier, as current laboratory-scale techniques, including molecular  
beam epitaxy (MBE) and chemical bath deposition, struggle to achieve uniformity over large areas (>100 cm²)  
required for industrial roll-to-roll processing. Interface passivation at critical junctions, such as SnSexTe1-x /CdS  
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or SnSexTe1-x /back contact interfaces, remains suboptimal, leading to Fermi-level pinning and increased series  
resistance that curtail short-circuit current density (Jsc). Moreover, environmental stability under accelerated  
conditions reveals rapid degradation due to oxidation of Sn and Se/Te chalcogens, resulting in phase segregation  
and up to 50% efficiency loss within 1000 hours, underscoring the need for robust encapsulation strategies.  
Future scope  
To overcome these hurdles, future investigations must prioritise bandgap engineering through precise  
compositional tuning of the Se:Te ratio, enabling tunable absorption from 0.9-1.5 eV to optimise lattice matching  
in tandem architectures with wide-bandgap perovskites or a-Si. Integration into multi-junction devices holds  
transformative potential, where SnSexTe1-x could serve as a mid-bandgap absorber (Eg ≈1.2 eV) in triple-junction  
configurations, potentially surpassing 30% efficiency via current matching and spectral splitting, as validated by  
recent SCAPS-1D simulations incorporating thin CIS interlayers. Advancements in interface engineering,  
including atomic layer deposition (ALD) of Al2O3 or ZnO passivation layers, are imperative to suppress surface  
recombination velocities below 103 cm/s and enhance hole selectivity at the rear contact. Scalable synthesis  
optimisation-via high-throughput methods such as close-space sublimation (CSS) or pulsed laser deposition  
(PLD)-should target defect densities <1015 cm-de 3 and film thicknesses of 1-2 μm with >95% uniformity,  
facilitating the development of pilot-scale modules. Long-term stability enhancements through alloying with  
earth-abundant dopants (e.g., Na, Cu) and hybrid encapsulation with graphene barriers will be crucial, alongside  
comprehensive techno-economic analyses to benchmark against CdTe/CIGS benchmarks under IEC 61646  
standards. These concerted efforts, informed by ongoing global research, position SnSexTe1-x as a frontrunner in  
sustainable, non-toxic thin-film photovoltaics.  
CONCLUSIONS  
Chalcogenide semiconductors, exemplified by SnSexTe1-x ternary thin films, have emerged as a compelling class  
of earth-abundant, non-toxic absorber materials poised to address the limitations of conventional thin-film  
photovoltaics, such as CdTe and CIGS, which face toxicity and scarcity concerns. Their tunable bandgap, high  
absorption coefficient, and p-type conductivity enable efficient photon harvesting across the solar spectrum, with  
theoretical efficiencies approaching 36% in advanced heterostructures, far surpassing current experimental  
benchmarks of ~2.5%. This review has elucidated the evolution of photovoltaic absorber materials, from silicon  
dominance to thin-film innovations, underscoring SnSexTe1-x's potential in fostering sustainable energy solutions  
amid escalating global demands projected to rise 1.5-fold by 2050. Despite these advantages, persistent  
challenges-including short carrier lifetimes, high defect densities, scalability constraints, suboptimal interface  
passivation, and environmental instability-must be systematically resolved to unlock commercial viability.  
Future research trajectories emphasise bandgap engineering via Se:Te compositional gradients, integration into  
multi-junction tandems with perovskites, atomic layer deposition for interface optimisation, and scalable  
techniques such as close-space sublimation for large-area deposition with defect densities below 1015 cm-3.  
Concurrently, alloying strategies and graphene-based encapsulation promise enhanced stability under IEC 61646  
protocols, bridging the gap to efficiencies competitive with established technologies. In summary, SnSexTe1-x  
chalcogenides represent a paradigm shift toward eco-friendly, cost-effective photovoltaics, aligning with global  
sustainability goals and the COP28 target to triple renewable capacity by 2030. Sustained interdisciplinary efforts  
in materials synthesis, device architecture, and techno-economic modelling will propel these materials from  
niche research to widespread deployment, significantly advancing the transition to a low-carbon energy future.  
ACKNOWLEDGMENTS  
The authors are grateful to the Department of Science & Technology, the Government of India, for funding the  
X-ray diffractometer under the PURSE & FIST programs. We are also thankful to the Ministry of Education,  
Government of India, for RUSA 2.0 grants, University of Jammu for the research grant.  
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